View Full Version : Help Prevent Breast Cancer
IronCaballo4
04-08-05, 11:04 PM
I lost a friend yesterday to Breast Cancer, she was only 42. I ask of you all to click on this link:
http://www.thebreastcancersite.com/cgi-bin/WebObjects/CTDSites
Then click on the button that says "Fund Free Mammograms".
It's absolutely free, and if you click once a day, it'll help pay for free mammograms for women who cannot afford them. So bookmark this site, send it to your friends, and with something as simple as the click of a mouse, we can all make a difference.
Thanks,
Chris
Archer1979
04-08-05, 11:07 PM
I lost a friend yesterday to Breast Cancer, she was only 42. I ask of you all to click on this link:
http://www.thebreastcancersite.com/cgi-bin/WebObjects/CTDSites
Then click on the button that says "Fund Free Mammograms".
It's absolutely free, and if you click once a day, it'll help pay for free mammograms for women who cannot afford them. So bookmark this site, send it to your friends, and with something as simple as the click of a mouse, we can all make a difference.
Thanks,
Chris
Done. And I'm sorry for your loss.
Cancer is such an insidious disease, I hope we can find a cure for it, and soon.
Again, my condolences.
WashingtonYankee
04-09-05, 02:35 AM
Chris- I am really sorry. I know what it's like to have someone who has/had breast cancer. My aunt is going through it. If you ever need to talk to anyone, I'm always here.
And my thoughts are with you and your family.
This would be a good thread to "sticky."
Breast cancer has touched most of our lives. I lost my Mom to it 12 years ago, and a friend (45 years old) in November. She left two young children.
I'm sorry for the loss of your friend.
I'm truly sorry about the loss of your friend.
Coincidentally, I received an e-mail from a friend today that will also help with funding for breast cancer research. I wasn't aware of these until I got the e-mail.
Breast Cancer research needs all the support it can get...
Please keep this going for a good cause!
New M&M colors
Pass this on to all of your friends. There are many women out there who have breast cancer. Let's do all we can to support this cause.
New Pink & White M&M's
The maker of M&M candies has teamed up with the Susan G. Komen Breast Cancer Foundation to raise funds through the sale of their new "pink & white" M&M candies.
For each 8-ounce bag of the special candies sold, the makers of M&M (Masterfoods) will donate 50 cents to the foundation. The next time you want a treat, please pick up a bag (now sold in stores nationwide) - you will be donating to a great cause and satisfying your sweet tooth.
Please pass on to all your family and friends. -- Thank you.
Anything that can be done to help funding is a big plus.
Sorry to hear about your friend. Its a horrible disease.
IronCaballo4
04-09-05, 10:45 PM
This would be a good thread to "sticky."
How do I do this?
And thanks a lot for your help and your kind words everyone, it means a lot, y'all are the best
Dooley Womack
04-10-05, 12:06 AM
Sorry for your loss. I clicked.
FreeYayo
04-10-05, 02:39 AM
Chalk up another click
Sorry about your loss
Dave Visbeck
04-10-05, 06:14 AM
I lost a friend yesterday to Breast Cancer, she was only 42. I ask of you all to click on this link:
http://www.thebreastcancersite.com/cgi-bin/WebObjects/CTDSites
Then click on the button that says "Fund Free Mammograms".
It's absolutely free, and if you click once a day, it'll help pay for free mammograms for women who cannot afford them. So bookmark this site, send it to your friends, and with something as simple as the click of a mouse, we can all make a difference.
Thanks,
Chris
Sorry for the loss of your friend. I clicked.
How do I do this?
And thanks a lot for your help and your kind words everyone, it means a lot, y'all are the best
I don't think us mere mortals can sticky a thread. It has to be done by a moderator or the administrator of the site, and I'm not sure what type of thread qualifies. I don't see why this one wouldn't though, since there's an ALS thread "stickied." You could email Jim and see if he'd allow it.
yankees27
04-10-05, 10:45 AM
Very sorry for your loss. I clicked last night and this morning.
IronCaballo4
04-11-05, 03:50 PM
Thanks for your help so far everyone...I hope you all remember to click on the site everyday, it only takes a few seconds and it's free...so help some people out, and send this site to your friends too
jlw1980
04-11-05, 04:00 PM
So sorry to hear about your friend. :(
I used to click on this site every day, and haven't for some time. There's a lot of causes you can help at that site just by clicking once each day. :NY:
IronCaballo4
04-12-05, 10:36 PM
Please don't let this thread die, guys...keep on clicking...and share this site with everyone!
Please don't let this thread die, guys...keep on clicking...and share this site with everyone!
I added the site to my signature, so this way at least I'm sure that I'm clicking it every day.
Have you asked a moderator of this could be stickied?
YankeeClemens22
04-13-05, 07:49 AM
I've clicked every day this week so far. Regular bumping of the thread should keep it going.
Luvtino
04-13-05, 06:27 PM
I am so sorry about your friend. Very sad news. :(
I clicked yesterday and again today. I will do so every day from here on out. Anything I can do to help. Great idea sweetie. :)
I've only clicked twice so far but I'm really trying to make this part of my daily routine.
NYYRules#1
04-13-05, 06:59 PM
I just clicked too, second time today.
Luvtino
04-13-05, 07:15 PM
I added the site to my signature, so this way at least I'm sure that I'm clicking it every day.
Have you asked a moderator of this could be stickied?
Your sig actually helped remind me sweetie. :)
IronCaballo4
04-13-05, 10:07 PM
Thanks for all the help everyone, keep clicking and a BIG thanks to whoever stickied this thread for me!
Luvtino
04-17-05, 10:21 PM
I have been vg about clicking. It is nice to see the numbers rise each and every day. :)
ladyleo
04-17-05, 10:33 PM
I'm sorry to hear of your loss.
As a breast cancer survivor, I go to this site a lot. They even send me frequent reminders (although I can't remember now how I got on their mailining list).
IronCaballo4
04-17-05, 10:49 PM
I have been vg about clicking. It is nice to see the numbers rise each and every day. :)
Yeah, the numbers have been shooting up...thanks for clicking everyone!
YankeeGalSC
04-19-05, 10:05 AM
I clicked.
I have heard of so many women losing their lives to breast cancer but don't know anyone personally who has been affected.
Also, there is supposed to be a postage stamp that is coming out. It will cost .40 vice the normal .37. The extra 3 cents goes to fund breast cancer research. I don't know if the stamp is out yet.
I clicked again but I am not ordering those pink shorts though .
I had a little umm, interruption in my routine but I'm back on track with clickey-click. :)
I'm sorry it took me so long to see this. I am clicking...
Luvtino
04-23-05, 08:56 PM
When I started clicking it was at 57 and we have now gotten it up to 124. That is awesome!! :cheer:
I clicked.
I have heard of so many women losing their lives to breast cancer but don't know anyone personally who has been affected.
Also, there is supposed to be a postage stamp that is coming out. It will cost .40 vice the normal .37. The extra 3 cents goes to fund breast cancer research. I don't know if the stamp is out yet.
That stamp is out and available at the post office.
That stamp is out and available at the post office.
That's all well and fine, but I think you should order those pink shorts. Think of it as supporting the cause ;) :D
That stamp is out and available at the post office.
That stamp has generated 10.4 million dollars to breast cancer research as of December 2004. It's the highest volume stamp sale ever......followed by the tribute to the fallen heros of 9/11.
Luvtino
04-26-05, 10:30 PM
Thanks for the info on the stamps everyone. I am going to go and pick some up this weekend. :)
Luvtino
05-18-05, 07:27 PM
Let's try and break 100 this month!! :)
I hope everyone is continuing to click.
I can tell you firsthand that breast cancer can happen to anyone. My wife had her first mammogram in March which detected a "cluster" which led to a biopsy that proved to be cancerous. Fortunately it was detected at stage zero and will not be terminal. She did have to have a mastectomy and will be going through reconstructive surgery for the next 8 months or so. Small price to pay to get cancer out of our life. Had she waited another year to get a mammogram it would've been a completely different story. Early detection is the key to survival.
EVERY woman should have access to a mammogram. Lets all get behind this great cause.:)
I hope everyone is continuing to click.
I can tell you firsthand that breast cancer can happen to anyone. My wife had her first mammogram in March which detected a "cluster" which led to a biopsy that proved to be cancerous. Fortunately it was detected at stage zero and will not be terminal. She did have to have a mastectomy and will be going through reconstructive surgery for the next 8 months or so. Small price to pay to get cancer out of our life. Had she waited another year to get a mammogram it would've been a completely different story. Early detection is the key to survival.
EVERY woman should have access to a mammogram. Lets all get behind this great cause.:)
Thank God she's going to be ok! :)
I'll keep clicking, and I can't forget to call the doc to get my mammo prescription. I keep forgetting :o
Link is clicked.
My friend lost his mom in his senior year of HS.
My friend Alicia just got diagnosed. She's in her early 40's. It really sucks
in MO I trust 42
07-20-05, 04:21 PM
consider it clicked.
CTSoxFan
07-22-05, 06:02 PM
Clickety-click-click-click.
I made the site my homepage. Will think of you every time I click it. Godspeed.
yankeesfaninaz
07-23-05, 08:15 PM
I clicked. Im so sorry for your loss. I know what it is like to see someone go through cancer. My mom is a leukemia survivor.
Boricua21
08-03-05, 12:50 PM
Done as well. My condolences. I will make sure I try to click everyday and will try to tell others.
My friend Alicia just got diagnosed. She's in her early 40's. It really sucks
Quoting myself, I ran into Alicia, she's doing well, they caught in early and she's nearly done with radiation treatment and was lucky not to have to go through chemo.
She's a nurse and got a job working at the hospital where she's being treated.
Yanks Lifer
11-22-05, 04:36 PM
I lost a friend yesterday to Breast Cancer, she was only 42. I ask of you all to click on this link:
http://www.thebreastcancersite.com/cgi-bin/WebObjects/CTDSites
Then click on the button that says "Fund Free Mammograms".
It's absolutely free, and if you click once a day, it'll help pay for free mammograms for women who cannot afford them. So bookmark this site, send it to your friends, and with something as simple as the click of a mouse, we can all make a difference.
Thanks,
Chris
Very sorry on the loss of your friend. Folks should also be familiar with the American Cancer Society (www.cancer.org). I've been a volunteer and board member of my local unit for nearly 15 years now and can tell you there is much more help, information and best of all support available than most people realize. PLEASE support any legitimate cancer fighting cause.
Gringaloca
11-23-05, 07:31 PM
I cannot stress enough how important mammograms and self examinations can be..
I was recently diagnosed with Stage II BC...underwent a 'partial' masectomy/lumpectomy on Nov 11th. I say 'partial' because the tumor was over 2 cm and the tissue surrounding had to be removed.
I also had 4 lymp nodes under my right arm removed...thankfully, they were all negative.
I felt a small lump about 10 months ago, but my alter ego, 'Cleopatra-the Queen of 'Denial' set in as there is no history in my family, and both my sister and Mom suffered from 'Fibrocystic tumors' in their breast.
But in the last 10 weeks is seemed to be getting larger, and when I finally made the appointment with my PP (primary physcian) it had grown to 2 cm., and I was feeling an occasional burning sensation in the area.
When I hear women say they don't have yearly mammograms because...'It hurts'...wah wah wah"...I want to slap them! :mad:
"Let me tell you about pain, Girlfriend"... ;) Thank God for Percocet & Darvocet.. :D
My prognosis is good...I will start radiation therapy the first week in Dec. Five days a week...for 6 - 8 weeks. No 'day at the beach' for sure, but I'm a 'tough ol' broad' and this WILL NOT GET THE BEST OF ME!!.. :)
Bottom line...If you have a Mother, Sister, Wife or Girlfriend over 40 years old...PLEASE!! PLEASE....tell them how important a yearly mammogram is, and God forbid...they feel a lump, no matter how small...GET IT CHECKED OUT!!!.
As my 'treatment' progresses, I'll post again.
Thanks for reading 'my' story...pass it on. ;)
I cannot stress enough how important mammograms and self examinations can be..
I was recently diagnosed with Stage II BC...underwent a 'partial' masectomy/lumpectomy on Nov 11th. I say 'partial' because the tumor was over 2 cm and the tissue surrounding had to be removed.
I also had 4 lymp nodes under my right arm removed...thankfully, they were all negative.
I felt a small lump about 10 months ago, but my alter ego, 'Cleopatra-the Queen of 'Denial' set in as there is no history in my family, and both my sister and Mom suffered from 'Fibrocystic tumors' in their breast.
But in the last 10 weeks is seemed to be getting larger, and when I finally made the appointment with my PP (primary physcian) it had grown to 2 cm., and I was feeling an occasional burning sensation in the area.
When I hear women say they don't have yearly mammograms because...'It hurts'...wah wah wah"...I want to slap them! :mad:
"Let me tell you about pain, Girlfriend"... ;) Thank God for Percocet & Darvocet.. :D
My prognosis is good...I will start radiation therapy the first week in Dec. Five days a week...for 6 - 8 weeks. No 'day at the beach' for sure, but I'm a 'tough ol' broad' and this WILL NOT GET THE BEST OF ME!!.. :)
Bottom line...If you have a Mother, Sister, Wife or Girlfriend over 40 years old...PLEASE!! PLEASE....tell them how important a yearly mammogram is, and God forbid...they feel a lump, no matter how small...GET IT CHECKED OUT!!!.
As my 'treatment' progresses, I'll post again.
Thanks for reading 'my' story...pass it on. ;)
Gring :( :(
I know you're a tough cookie, but I'm sorry that you have to deal with this. Damn....I just don't understand this disease...
I'll be keeping you in my thoughts.
twinks34
11-23-05, 08:29 PM
Two of my teachers are currently battling breast cancer. My neighbor had breast cancer.
Gringaloca, I'll keep you in my thoughts. :(
Women, please please please get your yearly mammograms and do self examinations.
CptCrunch
11-23-05, 10:02 PM
I cannot stress enough how important mammograms and self examinations can be..
I was recently diagnosed with Stage II BC...underwent a 'partial' masectomy/lumpectomy on Nov 11th. I say 'partial' because the tumor was over 2 cm and the tissue surrounding had to be removed.
I also had 4 lymp nodes under my right arm removed...thankfully, they were all negative.
I felt a small lump about 10 months ago, but my alter ego, 'Cleopatra-the Queen of 'Denial' set in as there is no history in my family, and both my sister and Mom suffered from 'Fibrocystic tumors' in their breast.
But in the last 10 weeks is seemed to be getting larger, and when I finally made the appointment with my PP (primary physcian) it had grown to 2 cm., and I was feeling an occasional burning sensation in the area.
When I hear women say they don't have yearly mammograms because...'It hurts'...wah wah wah"...I want to slap them! :mad:
"Let me tell you about pain, Girlfriend"... ;) Thank God for Percocet & Darvocet.. :D
My prognosis is good...I will start radiation therapy the first week in Dec. Five days a week...for 6 - 8 weeks. No 'day at the beach' for sure, but I'm a 'tough ol' broad' and this WILL NOT GET THE BEST OF ME!!.. :)
Bottom line...If you have a Mother, Sister, Wife or Girlfriend over 40 years old...PLEASE!! PLEASE....tell them how important a yearly mammogram is, and God forbid...they feel a lump, no matter how small...GET IT CHECKED OUT!!!.
As my 'treatment' progresses, I'll post again.
Thanks for reading 'my' story...pass it on. ;)
Wow, that's really scary. Best of luck to you, I'm sure you'll beat this horrible disease.
#1PaFan
11-25-05, 04:36 PM
Whoa! :( Damn, Gring, you're definitely in my thoughts and prayers.
Here's a nice article that USAToday wrote about Deanna Favre.
http://www.usatoday.com/sports/football/nfl/packers/2005-10-19-deanna-favre-cover_x.htm
Here's a link to Deanna's Hope Foundation:
http://www.favrefoundationgear.com/?gclid=CODT0KO7zYECFSYMGgodnzfu3w
Archer1979
11-25-05, 05:07 PM
I cannot stress enough how important mammograms and self examinations can be..
I was recently diagnosed with Stage II BC...underwent a 'partial' masectomy/lumpectomy on Nov 11th. I say 'partial' because the tumor was over 2 cm and the tissue surrounding had to be removed.
I also had 4 lymp nodes under my right arm removed...thankfully, they were all negative.
I felt a small lump about 10 months ago, but my alter ego, 'Cleopatra-the Queen of 'Denial' set in as there is no history in my family, and both my sister and Mom suffered from 'Fibrocystic tumors' in their breast.
But in the last 10 weeks is seemed to be getting larger, and when I finally made the appointment with my PP (primary physcian) it had grown to 2 cm., and I was feeling an occasional burning sensation in the area.
When I hear women say they don't have yearly mammograms because...'It hurts'...wah wah wah"...I want to slap them! :mad:
"Let me tell you about pain, Girlfriend"... ;) Thank God for Percocet & Darvocet.. :D
My prognosis is good...I will start radiation therapy the first week in Dec. Five days a week...for 6 - 8 weeks. No 'day at the beach' for sure, but I'm a 'tough ol' broad' and this WILL NOT GET THE BEST OF ME!!.. :)
Bottom line...If you have a Mother, Sister, Wife or Girlfriend over 40 years old...PLEASE!! PLEASE....tell them how important a yearly mammogram is, and God forbid...they feel a lump, no matter how small...GET IT CHECKED OUT!!!.
As my 'treatment' progresses, I'll post again.
Thanks for reading 'my' story...pass it on. ;)
Gringa,
You are in my thoughts and prayers. Beat this thing! Please.
Tim
Gringaloca
11-30-05, 08:38 PM
Whoa! :( Damn, Gring, you're definitely in my thoughts and prayers.
Here's a nice article that USAToday wrote about Deanna Favre.
http://www.usatoday.com/sports/football/nfl/packers/2005-10-19-deanna-favre-cover_x.htm
Here's a link to Deanna's Hope Foundation:
http://www.favrefoundationgear.com/?gclid=CODT0KO7zYECFSYMGgodnzfu3w
Thanks, 'Uncle' George for the 'sites'..and your and all my nyyfans friends support. :ga-ga:
I ordered three items to help Deanna's Foundation. The tshirt, jersey for me & the wool beanie cap for my niece who lives in Duluth,Mn. She's a half-hearted Vike's fan but I'm sure she won't have a problem wearing it in her 'Aunt Vickie's' honor.
Unfortunately...the prognosis is not as good/easy (if any radiation treatment can be considered 'easy' ) as my Surgeon had led me to believe.
After my appt with my Oncologist today, I've been told that 6 months of 'chemo' is recommended. One treatment (Taxol) every 3 weeks for a 12 week period...and then once weekly (Taxol & Herceptin)for another 12 weeks.
I will have a 'vascular access port' inserted in the chest area for 'easy administration of medication'..hope that thing picks up the YES channel.. ;)
When that 6 month treatment has completed, they'll start the radiation treatment. Following that, 5 years of 'hormonal therapy'...but from what I've read...the jury's still out on that.
Just reading about the side effects of Taxol & Herceptin...pretty hairy stuff, or should I say 'hairless'... :D :dunno: :lol: (As you can see, I haven't lost my sense of humor. Hopefully, it will help get me through this. :D
Again...I cannot stress enough how important 'breast cancer awareness', ie, mammograms, self-exams can be to you or your loved ones.
I am a true testament that it does not have to be prevalent in your family...it certainly was not in mine.
Ok..probably TMI...I'll post again in a few weeks/months.
Thanks, 'Uncle' George for the 'sites'..and your and all my nyyfans friends support. :ga-ga:
I ordered three items to help Deanna's Foundation. The tshirt, jersey for me & the wool beanie cap for my niece who lives in Duluth,Mn. She's a half-hearted Vike's fan but I'm sure she won't have a problem wearing it in her 'Aunt Vickie's' honor.
Unfortunately...the prognosis is not as good/easy (if any radiation treatment can be considered 'easy' ) as my Surgeon had led me to believe.
After my appt with my Oncologist today, I've been told that 6 months of 'chemo' is recommended. One treatment (Taxol) every 3 weeks for a 12 week period...and then once weekly (Taxol & Herceptin)for another 12 weeks.
I will have a 'vascular access port' inserted in the chest area for 'easy administration of medication'..hope that thing picks up the YES channel.. ;)
When that 6 month treatment has completed, they'll start the radiation treatment. Following that, 5 years of 'hormonal therapy'...but from what I've read...the jury's still out on that.
Just reading about the side effects of Taxol & Herceptin...pretty hairy stuff, or should I say 'hairless'... :D :dunno: :lol: (As you can see, I haven't lost my sense of humor. Hopefully, it will help get me through this. :D
Again...I cannot stress enough how important 'breast cancer awareness', ie, mammograms, self-exams can be to you or your loved ones.
I am a true testament that it does not have to be prevalent in your family...it certainly was not in mine.
Ok..probably TMI...I'll post again in a few weeks/months.
Ah dammit Gring...
It's not TMI, I thank you for sharing with us. I just wish I could blink my eyes and make it go away for you.
It sounds like you're going to have a bit of a tough road, but you sound so strong. I admire your bravery. I will be praying for you every day, and sending good vibes your way. Please keep us posted.
And hey, look at it this way...if you lose your hair, you can get a variety of wigs, and be a gorgeous redhead, blonde, brunette, whichever you feel like that day ;)
#1PaFan
12-01-05, 08:12 PM
Ah dammit Gring...
It's not TMI, I thank you for sharing with us. I just wish I could blink my eyes and make it go away for you.
It sounds like you're going to have a bit of a tough road, but you sound so strong. I admire your bravery. I will be praying for you every day, and sending good vibes your way. Please keep us posted.
And hey, look at it this way...if you lose your hair, you can get a variety of wigs, and be a gorgeous redhead, blonde, brunette, whichever you feel like that day ;)
Wigs? I always wanted to pork a BaldyBabe! The fact that it's Gring will make it just that much Sweeter! :D
Let me know when the hair's gone, Woman! :gulp: :gulp:
You have my prayers Gring. You will beat this.
#1PaFan
12-02-05, 10:15 PM
I LOVE my CyberNiece Gring! She's my Hero.
If you want to learn what Gring is gonna go thru, here's some links:
This is a link about Taxol (Paclitaxel)
http://www.cancerbacup.org.uk/Treatments/Chemotherapy/Individualdrugs/Paclitaxel
Here is a link about Herceptin.
http://www.cancer.gov/clinicaltrials/digestpage/herceptin
The side effects of these two powerful drugs can be excrutiating, man.
I have NO doubts about Gring. Hell, she's a diehard Lions Fan. She's been thru worse in her life just cheering for these guys!!! :lol: :D
This is terrible news Gring. You have a good outlook and sense of humor though and that will definitely help in your fight against this thing.
My prayers are with you!
texasyankee
12-03-05, 06:29 AM
My thoughts & prayers go out to you, Gringaloca. Though I dont know you, I recognize your name and I sense your mental strength and toughness. I am confident you can overcome this bad time. My sister-in-law successfully fought breast cancer just in the past couple of years and her diagnosis was similar to yours.
I notice you reside in Florida - I hope you are happy & satisfied with your doctors and the medical department there. We have a highly regarded cancer center at Houston - M D Anderson Cancer Hospital - that is second only to Sloan-Kettering in NY. Many people from around the nation visit just for the fact they are a research hospital with the latest available cancer treatment procedures & programs. I am really impressed with the staff there and the beautiful way patients & visitors are receieved.
Best of luck & may your Christmas be one of the best ever.
Gringaloca
12-14-05, 07:44 PM
Had the appointment with the Nurse Oncologist last Wednesday. It seems I was half-listening to Dr. Abel about the upcoming program and the drugs that would be used for Chemo.
Taxol & Herceptin are the 2nd half of the 6 month program..weekly dosages for a 12 week period
Prior to that I'll have a Adriamycin/Cytoxan 'cocktail' every 3 weeks...4 dosages..over a 12 week period.
Adriamycin has some serious side effects regarding the heart. Hence, I am scheduled for a MUGA scan tomorrow afternoon. Going to check out if the "ol' ticker" can handle it.
http://heartdisease.about.com/cs/otherriskfactors/l/blmuga.htm
If I pass the test...it's back to Dr Levine (surgeon) to have the 'Port' installed. Hopefully, we can get the treatment underway by mid January.
"Nurse Debbie" has told me that the effects of each treatment won't be a problem until 2/3 days after...so I'll be scheduling them for late Wednesday afternoons. At least that will give me the weekend to rest/recuperate.
Advantage: No housecleaning, laundry, or cooking meals on the weekends! :lol:
Disadvantage: I should be able to 'work' Mon-Fri.. :(
I've been doing a lot of research on the 'Net. Maybe too much... Just anxious to get it started & over with. I've been healthy all my life...this is all new & strange. I have to take it one 'dose' at a time, I guess.
Hopefully the side effects I keep reading about will be minimal for me..but I have to say it is very intimidating & scary from what I've already read & heard.
Anyway...that's the latest. I'll post with updates as they happen.
Thanks for all your support, prayers & good thoughts. I can't tell you how much it is appreciated. :ga-ga: I love you guys!.
V.
True Yankee-ette13
12-15-05, 07:35 PM
Aw, sweetheart. I decided to come into this thread because my mom's aunt had surgery today (had the cancer removed) and then I saw this news.
I wish you the best and please keep us updated. You'll be in my thoughts this holiday season. :)
Had the appointment with the Nurse Oncologist last Wednesday. It seems I was half-listening to Dr. Abel about the upcoming program and the drugs that would be used for Chemo.
Taxol & Herceptin are the 2nd half of the 6 month program..weekly dosages for a 12 week period
Prior to that I'll have a Adriamycin/Cytoxan 'cocktail' every 3 weeks...4 dosages..over a 12 week period.
Adriamycin has some serious side effects regarding the heart. Hence, I am scheduled for a MUGA scan tomorrow afternoon. Going to check out if the "ol' ticker" can handle it.
http://heartdisease.about.com/cs/otherriskfactors/l/blmuga.htm
If I pass the test...it's back to Dr Levine (surgeon) to have the 'Port' installed. Hopefully, we can get the treatment underway by mid January.
"Nurse Debbie" has told me that the effects of each treatment won't be a problem until 2/3 days after...so I'll be scheduling them for late Wednesday afternoons. At least that will give me the weekend to rest/recuperate.
Advantage: No housecleaning, laundry, or cooking meals on the weekends! :lol:
Disadvantage: I should be able to 'work' Mon-Fri.. :(
I've been doing a lot of research on the 'Net. Maybe too much... Just anxious to get it started & over with. I've been healthy all my life...this is all new & strange. I have to take it one 'dose' at a time, I guess.
Hopefully the side effects I keep reading about will be minimal for me..but I have to say it is very intimidating & scary from what I've already read & heard.
Anyway...that's the latest. I'll post with updates as they happen.
Thanks for all your support, prayers & good thoughts. I can't tell you how much it is appreciated. :ga-ga: I love you guys!.
V.
Crap. I never really checked out this thread before. :o
I will add you to my prayer list, mi amiga.
LilChief
01-08-06, 04:16 PM
Crap. I never really checked out this thread before. :o
I will add you to my prayer list, mi amiga.
I hadn't seen it either...I feel awful! I am so sorry Gringa, and please know that my thoughts and prayers are with you. Let me know if there is anything you need that I can help with, or pm me if you just feel like talking sometime...Big Hugs, hang in there sweetie!
Steph
Gringaloca
01-29-06, 10:42 PM
Ok..latest update:
I finally had the 'port' inserted this past Wednesday. Feels kinda weird..just under the skin below the left 'clavical'. Still a little sore, tender, bruised after 4 days...ouch. Not to mention the surgical tape they used to cover the incision.
When removed took off two layers of skin... :eek: Some Neosporin and covering it with gauze bandages..but while healing it itches like...... ;)
'Nurse Debbie' wanted them to start this Wednesday.. :eek:
'No way, Sista!...I have plans for SuperBowl Weekend/Sunday and they don't involve hanging around the porcelain palace talkin' to Ralph & Beulah!".. :lol:
So.....I've delayed the treatments until Wednesday, Feb 8th. From what I've been told..the 'effects' won't occur until 2/3 days later. Jeeezzz..I can hardly wait :P
Actually, it's all a 'crap shoot', as from what I have read/heard, everyone reacts differently to their 'treats'. Hopefully, I'll be one of the more fortunate ones that don't experience the nausea, vomiting, hair loss, aches/pains, diarrhea, constipation, ..etc, etc...did I mention 'hair loss'??... :eek:
Thankfully, one of my girlfriends had found some really nice NYY scarfs on E-Bay. 'Doo-Rag' city..here I come. :) And another one has hooked me up with a 'wig-hat' maker in Miami. Can't wait to go for my first 'fitting'. :D
Upside is, I'll save a ton of $$$ on haircuts/colorings & tips at the salon over the next 12 months, not to mention time saved w/eyebrow maintenance/mascara application/ armpit & leg shaving. :)
Gotta keep a sense of humor... :D
LilChief
01-30-06, 05:07 AM
Ok..latest update:
I finally had the 'port' inserted this past Wednesday. Feels kinda weird..just under the skin below the left 'clavical'. Still a little sore, tender, bruised after 4 days...ouch. Not to mention the surgical tape they used to cover the incision.
When removed took off two layers of skin... :eek: Some Neosporin and covering it with gauze bandages..but while healing it itches like...... ;)
'Nurse Debbie' wanted them to start this Wednesday.. :eek:
'No way, Sista!...I have plans for SuperBowl Weekend/Sunday and they don't involve hanging around the porcelain palace talkin' to Ralph & Beulah!".. :lol:
So.....I've delayed the treatments until Wednesday, Feb 8th. From what I've been told..the 'effects' won't occur until 2/3 days later. Jeeezzz..I can hardly wait :P
Actually, it's all a 'crap shoot', as from what I have read/heard, everyone reacts differently to their 'treats'. Hopefully, I'll be one of the more fortunate ones that don't experience the nausea, vomiting, hair loss, aches/pains, diarrhea, constipation, ..etc, etc...did I mention 'hair loss'??... :eek:
Thankfully, one of my girlfriends had found some really nice NYY scarfs on E-Bay. 'Doo-Rag' city..here I come. :) And another one has hooked me up with a 'wig-hat' maker in Miami. Can't wait to go for my first 'fitting'. :D
Upside is, I'll save a ton of $$$ on haircuts/colorings & tips at the salon over the next 12 months, not to mention time saved w/eyebrow maintenance/mascara application/ armpit & leg shaving. :)
Gotta keep a sense of humor... :D
Vickie, you are one amazingly strong woman! Thanks for the update, and please let me know if there's anything I can do, or PM me if you want to talk.
Big Hugs,
Steph
Ok..latest update:
I finally had the 'port' inserted this past Wednesday. Feels kinda weird..just under the skin below the left 'clavical'. Still a little sore, tender, bruised after 4 days...ouch. Not to mention the surgical tape they used to cover the incision.
When removed took off two layers of skin... :eek: Some Neosporin and covering it with gauze bandages..but while healing it itches like...... ;)
'Nurse Debbie' wanted them to start this Wednesday.. :eek:
'No way, Sista!...I have plans for SuperBowl Weekend/Sunday and they don't involve hanging around the porcelain palace talkin' to Ralph & Beulah!".. :lol:
So.....I've delayed the treatments until Wednesday, Feb 8th. From what I've been told..the 'effects' won't occur until 2/3 days later. Jeeezzz..I can hardly wait :P
Actually, it's all a 'crap shoot', as from what I have read/heard, everyone reacts differently to their 'treats'. Hopefully, I'll be one of the more fortunate ones that don't experience the nausea, vomiting, hair loss, aches/pains, diarrhea, constipation, ..etc, etc...did I mention 'hair loss'??... :eek:
Thankfully, one of my girlfriends had found some really nice NYY scarfs on E-Bay. 'Doo-Rag' city..here I come. :) And another one has hooked me up with a 'wig-hat' maker in Miami. Can't wait to go for my first 'fitting'. :D
Upside is, I'll save a ton of $$$ on haircuts/colorings & tips at the salon over the next 12 months, not to mention time saved w/eyebrow maintenance/mascara application/ armpit & leg shaving. :)
Gotta keep a sense of humor... :D
Vic, you are an inspiration, you really are.
I'm keeping my fingers crossed that you'll be spared the chats with Beulah and Ralph :roflmao: My mom didn't have that lovely side effect, so maybe you won't either. She did lose her hair though, but she did have a lovely array of turbans. If you go that route, you can quote Young Frankenstein:
"Dr. Friedrich von Frankenstein: Igor, would you give me a hand with the bags?
Igor: [doing a Groucho Marx] Certainly, you take the blonde and I'll take the one in the turban."
:D
Luvtino
02-04-06, 08:38 PM
I just sent you a PM sweetie. You are in my thoughts and prayers. Pls know we all have your back. :)
#1PaFan
02-04-06, 08:46 PM
You are in my thoughts and prayers. Pls know we all have your back. :)
Ditto. I loves my Sweet Gring. :gulp:
Luvtino
02-04-06, 11:20 PM
Ditto. I loves my Sweet Gring. :gulp:
How could ya not love her?! She rocks as do you!! :)
LilChief
02-07-06, 09:50 PM
Vickie, I just want you to know you are in my thoughts and prayers, and I'll be thinking of you tomorrow when you got for your first treatment. Hope it goes as smoothly as possible, and your side efffects are minimal. Let us know how you're doing sweetie.
Hugs,
Steph
Gringaloca
02-11-06, 12:43 AM
As scheduled I had my first Chemo Treatment on Wednesday. All in all, it went very smoothly, and so far no ...'expected/predicted' side effects. ie no naseau/vomiting/diahrrea/ etc. Plus I keep checking my hairbrush for 'fallout'.. :) So far....so good.
They started me off with a 25(?) ml bag of Decadron...and anti-nauseau 'cocktail drip' Followed with the Adriamycin (push) and completed with Cytoxan 'drip'. Total time there was about 4 hours...picked up two more anti-nausea prescriptions at CVS on the way home. More Decadron (steriod) & Compazine
Had a 'huge' dinner at Roadhouse Grill ...appetizers, primerib, salad & baked potato. I figured it might be my last decent meal for a while...might as well 'load up'& enjoy :)
Back to work on Thursday...left a little early as the 'meds' make me very drowsy/dizzy. Put in the same hours today..left early..falling asleep at my desk, very difficult concentrating on work at hand.
Came home & slept for about 7 hours...now I'm wide awake :eek: at 2 a.m....
If it doesn't get any worse than this, I'll be a very happy camper, but I'm not fooling myself...just enjoying the easy part while I can.
Thanks for all your prayers, thoughts & support... :ga-ga: You guys are really awesome. :)
So far so good. I'm keeping my fingers crossed that you breeze through this :)
Luvtino
02-13-06, 06:48 PM
I am glad that things got off to a "good" start. Good is a relative term of course when discussing breast cancer, hair loss and diarrhea. ;)
Hang in there sweetie. I am sooo proud of the courage and strength you have shown through all of this. Cheers to you!! :cheer: :gulp: Better make that ginger ale just in case. :o :D
Gringaloca
02-23-06, 07:35 PM
Time for a brief update?
Two weeks & 1 day since the first 'Treat'..it went smoothly for the first couple of days...then...YIKES!!
The Compazine helped with the nausea/vomiting...none to speak of. But that 'Decadron'..is somethin' else. woooo. Nervousness, shakes & jittery on Saturday brought on a little bit of an 'anxiety attack'...Thankfully, Saturdays dose was the last one.
By Sunday afternoon it seemed to have cleared my system & things settled down. No problem with my appetite...I'm eating like a horse...put on 5 lbs in two weeks. ;)
And as told to me...two weeks to the day, my hair started to fall out. And I mean FALL OUT!! :eek: By the handful and the brush-full...maybe it'll ease up in a day or so and I won't lose all of it..but I've already made plans to go 'wig shopping' on Saturday. :D I've already shopped some 'on-line' so I've already picked the style/color similar to mine own.
Didn't realize that 'human hair' runs $700+.. :eek: so, I'll definitely be goin' for that 'synthetic look', and mostly likely pick up two of the cheaper model. This is not a lifetime investment...just something to get me thru the next 12 months or so, until it grows back enough to go without a wig at all. In the meantime I have my Yankee scarf/doo-rags & a couple of NYY caps, too. Might even breakdown & buy a Lions & Pistons cap to round out the look... :D
Keep smiling, amica mia.
You will beat this thing. :)
Gringaloca
02-23-06, 08:25 PM
Keep smiling, amica mia.
You will beat this thing. :)
I have no doubt that I will beat this, Lou :) Thanks to the fantastic support group that I have...Family, Friends & Co-Workers have been nothing short of spectacular. Not forgetting to mention the wonderful people at the Michael & Diane Bienes Cancer Center associated with Holy Cross Hospital here in Fort Lauderdale. I consider myself very lucky to have them all.
A friend sent me this email today...and I want to remind everyone that 'Breast Cancer Awareness' should not be designated just to the month of October.
Please tell ten friends to tell ten today
The Breast Cancer site is having trouble getting enough people to click on their site daily to meet their quota of donating at least one free mammogram a day to an underprivileged woman. It takes less than a minute to go to their site and click on "donating a mammogram" for free (pink window in the middle).
This doesn't cost you a thing. Their corporate sponsors/advertisers use the number of daily visits to donate mammogram in exchange for advertising.
Here's the web site! Pass it along to people you know.
http://www.thebreastcancersite.com/
AGAIN , PLEASE TELL 10 FRIENDS TO TELL 10 TODAY
#1PaFan
02-23-06, 10:41 PM
Time for a brief update?
Two weeks & 1 day since the first 'Treat'..it went smoothly for the first couple of days...then...YIKES!!
The Compazine helped with the nausea/vomiting...none to speak of. But that 'Decadron'..is somethin' else. woooo. Nervousness, shakes & jittery on Saturday brought on a little bit of an 'anxiety attack'...Thankfully, Saturdays dose was the last one.
By Sunday afternoon it seemed to have cleared my system & things settled down. No problem with my appetite...I'm eating like a horse...put on 5 lbs in two weeks. ;)
And as told to me...two weeks to the day, my hair started to fall out. And I mean FALL OUT!! :eek: By the handful and the brush-full...maybe it'll ease up in a day or so and I won't lose all of it..but I've already made plans to go 'wig shopping' on Saturday. :D I've already shopped some 'on-line' so I've already picked the style/color similar to mine own.
Didn't realize that 'human hair' runs $700+.. :eek: so, I'll definitely be goin' for that 'synthetic look', and mostly likely pick up two of the cheaper model. This is not a lifetime investment...just something to get me thru the next 12 months or so, until it grows back enough to go without a wig at all. In the meantime I have my Yankee scarf/doo-rags & a couple of NYY caps, too. Might even breakdown & buy a Lions & Pistons cap to round out the look... :D
Gring Baby, you'd look AWESOME in a Packer doo-rag! Hey, you could go to a karoke bar and do some Sinead O'Connor. :D :gulp:
I LOVES my Gring!!! :gulp:
LilChief
02-24-06, 11:28 AM
Vicki!!!! Thanks for the update, I was thinking about you! I'm so sorry you are getting the side effects :( but I know you're stong and it will all be worth it when the treats do their job and you are back to 100%!
My husbands cousin was bald for her (2nd) wedding...she went with a fancy white turban to match her gown. My Mom went with a few wigs, but I'm not sure she was ever reaaallllyyy comfortable with them. My husband's boss's wife (got that?LOL) always has her baseball caps on...it's a cute look and seems to work for her.
I know you'll look great no matter what you decide to do! Just remember it's temporary!
Super huge hugs! ((((((((((((((((((((((((((((((((((((((Vicki))))))))))))))))))))))))))))))))))))))))
Please continue to keep us posted on your progress, and know you are in my thoughts and prayers every day!
Steph
I'm glad you're doing better, Vic.
My mom had a wig, but really didn't wear it much. She wore a turban thingy or a scarf until it started to grow back. Don't be surprised if it comes back different somehow...hers did.
Please keep us posted, and know that I think of you every day, and say a prayer.
Gringaloca
03-02-06, 05:46 PM
Ok..update time:
Had the 2nd 'Treat' yesterday...some complications in getting the needles inserted into the 'port'. Seems there was a blockage at the end of the shaft and couldn't get the blood to draw back..
Finally around 1 p.m. they were able to start the administration of the Decadron/Adriamycin & Cytoxan. Finally got out of there after 5 hours but home in time to catch the last half of Judge Judy.... :D
Yep.Those 'bleached/blondew/thetrailer parkroots' locks are G-O-N-E!!...just stubs of dark brown & gray now... :) I can see why more women go with the doo-rag /baseball cap/turban look. My wig itches like a b*tch...and feels like one gigantic RubberBand is wrapped around my head. I know I'll only be wearing it to work on the days I absolutely HAVE to go in..but tomorrow being Casual Day, wonder what they'd say when I show up with my NYY doo-rag & Visor... Hey what's the worst they can do...Send me home!!??...Please, do me a favor... :)
Manny has been nothing short of spectacular in his support & humor over this whole thing...he actually has new lil' pet names for me now...Uncle Fester, Q-Ball, Chrome-Dome & my favorite...La GringalocaCalba...(the bald crazy white girl).. :D :D He actually helped me shave my head and even let me use his razor with a brand new blade...whoa!! How's that for being supportive... ;)
If I get up the nerve I'll post a before/after picture...I look like a cross between Uncle Fester & Melissa Ethridge... :eek:
Anyway, just wanted to give you all and update and thank everyone for their PM's...well not so much anymore..But thanks to all for your constant support & good thoughts & prayers.
Love & Hugs,
V.
I am so happy that you are keeping up your humor, mi amiga. I will keep up the praying. :)
Luvtino
03-02-06, 10:07 PM
Your attitude and bravery never cease to amaze me sweetie. And give Manny a hug for me. I love men who are there for their blad crazy white girls. Take out the bald and I am one of them too. ;) :D
I thought Melissa Etheridge never looked more beautiful than the time she came out on stage completely bald at the Grammys. She was glowing and I couldn't but think of the joy all those who were battling cancer would feel when seeing her perform. She was stunning and I am sure you are as well. :)
I am so happy to read that everyone has been as supportive and kind to you as they should be. I have read that the more women's lives remain the same when being treated for breast cancer that they quicker they recover and return to work in circumstances where they have to stop for a bit. And you wear that NYY doo rag and wear it proudly to the office. Trust me...they aren't going to take on a bald crazy white girl on major drugs. :o :lol:
LilChief
03-02-06, 11:52 PM
Hey Vicki! Thanks for the update! It will be worth all the hassles in the end, and I know I'm only one of many who are so very proud of you and your strength! Keep up the good work, and please continue to keep us posted...
(I keep wanting to PM you and then I remember I can't...;) )
#1PaFan
03-03-06, 04:54 AM
Send me some pics, my sexy Kojakloca!
I'm going to drink some beers for you as soon as I get this workday behind me. :gulp: :gulp: :gulp:
#1PaFan
03-25-06, 09:34 AM
It's been a few weeks, honey. I hope my lovely Gring is doing well!
It's only 10:30AM, but I'm having a Brew for YOU right now, LionsFan! :gulp:
LilChief
03-25-06, 10:09 AM
Hope everything's ok Vicki!
PLease give us an update when you can...we are thinking of you!
Barb51850
03-25-06, 01:11 PM
Time for a brief update?
Two weeks & 1 day since the first 'Treat'..it went smoothly for the first couple of days...then...YIKES!!
The Compazine helped with the nausea/vomiting...none to speak of. But that 'Decadron'..is somethin' else. woooo. Nervousness, shakes & jittery on Saturday brought on a little bit of an 'anxiety attack'...Thankfully, Saturdays dose was the last one.
By Sunday afternoon it seemed to have cleared my system & things settled down. No problem with my appetite...I'm eating like a horse...put on 5 lbs in two weeks. ;)
And as told to me...two weeks to the day, my hair started to fall out. And I mean FALL OUT!! :eek: By the handful and the brush-full...maybe it'll ease up in a day or so and I won't lose all of it..but I've already made plans to go 'wig shopping' on Saturday. :D I've already shopped some 'on-line' so I've already picked the style/color similar to mine own.
Didn't realize that 'human hair' runs $700+.. :eek: so, I'll definitely be goin' for that 'synthetic look', and mostly likely pick up two of the cheaper model. This is not a lifetime investment...just something to get me thru the next 12 months or so, until it grows back enough to go without a wig at all. In the meantime I have my Yankee scarf/doo-rags & a couple of NYY caps, too. Might even breakdown & buy a Lions & Pistons cap to round out the look... :D
Sending love Vickie. I know all about the cost of those wigs. I've had to wear one since I was 12 (not due to chemo). I buy mine from Jacquelyn (www.jacquelynwigs.com). They have synthetic/human hair blends that are very pretty. We're all here for you. Keep up that beautiful spirit. You are an inspiration.
LilChief
03-27-06, 09:31 AM
OK, has anyone heard from Vicki??? I emailed her a few days ago, but haven't heard back. I'm getting worried, I hope she's doing ok. If anyone has been in touch with her, please post to let us know if she's ok...:(
Gringaloca
03-27-06, 06:07 PM
Wow!...Didn't realize I hadn't posted in such a long time...
I was out of town on my mini-ST trip March 14th - 18th. I started off in Kissimee on Tuesday/Wednesday, Thursday in Lakeland (Yankees vs Tigers) and spent Friday & Saturday at the Yankee games in Jupiter. (vs Cardinals on Friday & Marlins on Saturday)..3 ST games in 3 days....
Unfortunately....I had forgotten how delicate my skin would be to the sun..due to the Chemo drugs, and absolutely 'fried' myself on Thursday. Friday & Saturday wore a big straw hat to both games. I'm sure the folks sitting behind me appreciated that...;) Oh well...girl's gotta do what a girl's gotta do. Finally stopped 'peeling my ears & neck last Monday....Yikes:eek:
Had the 3rd 'treat' last Wednesday...didn't go too well. My 'port' had shifted a little. Instead of laying flat against the upper chest it had tilted to the left and took some moving around to put it back into position in order to get the 'I-V's" going properly. That was an experience to say the least. Dr. Able changed the anti-nauseau med's and I had an adverse reaction to them. Yikes....hopefully the next time it'll be easier going. This past Friday & Saturday were pretty rough, but I seem to be back to normal today.
My next treatment is April 12th and then after that the 'weeklies' start. 12 more of those....should have Chemo completed by mid/late July. At that time, my hair should begin to grow back. Can't to see what color/texture it will be. It's been so long since I've seen my 'natural color'....dark brown with red highlights if I remember. :D Of course, I expect there to be quite a bit a gray mixed in there as well.
Thanks for the concern, and the wonderful words of encouragement. I have to admit I'm a little more than anxious as it gets closer to the 'weeklies'....I've read/heard that can be the worst part of all. But I have such a strong support group with family, friends & you guys are behind me...so I know it's gonna be okay. And opening day just around the corner to keep my mind off my own problems....:D
And....Like I said...' A girl's gotta do........;)
LilChief
03-28-06, 10:45 PM
Thanks for the update Vicki! I was getting worried when we didn't hear from you. Glad to hear you are hanging in there...You're doing great! Keep us posted as best you can.
Hugs,
Steph
Luvtino
03-30-06, 09:42 PM
Sorry ya had some trouble with the port and a bad reaction to one of the meds sweetie. :(
Glad to see that you are still a trooper with one of the best attitudes I have ever seen. You are amazing!! :)
Just think...your chemo will be over right around the All-Star break. We all know how fast the season goes so I pray time flies for you as well. You will be sporting a very chic short do by the time we head to the World Series. ;) :D
#1PaFan
03-31-06, 09:04 PM
Trouble with the port, Gring? Who put it there, Joey Harrington? ;)
Which antiemetics are ya taking? Just remember, when you get a little nausous, try not to think about the Lions Front Office. Or Jerry Jones. Or Terrell Owens.
Think about me! I'm a soothing influence. :) :gulp:
Gringaloca
03-31-06, 09:25 PM
Trouble with the port, Gring? Who put it there, Joey Harrington? ;)
Which antiemetics are ya taking? Just remember, when you get a little nausous, try not to think about the Lions Front Office. Or Jerry Jones. Or Terrell Owens.
Think about me! I'm a soothing influence. :) :gulp:
Stop making jokes on my very serious thread.....:D :D O cant evne tyep I';mn laughing so hard riht now
Soothing influence, my WASPA...more like 'nails on a blackboard'..:D
LilChief
04-03-06, 07:13 AM
Hi Vicki, Just checking in on you to let you know I'm thinking about you!Keep up that beautiful smile!
LilChief
04-11-06, 06:36 AM
Just checking in to see how you're doing Vicki...please give us an update when you can! Hugs! ;)
Gringaloca
04-14-06, 05:38 PM
Just checking in to see how you're doing Vicki...please give us an update when you can! Hugs! ;)
Hi Steph...
Yep...I'm back with the latest update.
Had the last treatment of the first cycle on Wednesday, April 12th. It went very smooth this time...no problems with the 'port' and I was outta there in under 3-1/2 hours this week.
Taking my Compazine every 6 hours faithfully to counteract the nausea...so far so good.
I have 3 weeks off, then start the 'weeklies'. At that point I'll be changing to different set of chemo drugs...Herceptin and Taxol..If the next 12 treats are as easy as the first ones...I'll breeze thru this and be finished just in time for my Birthday Weekend!!!...and I plan on celebrating, let me tell ya...:D :)
Thanks as usual for the thoughts & concern...I'm doing better than I ever expected...hairless or not.
( I am soooo over that part...it's actually pretty cool not having to worry about your hair..good days or bad ones...Us girls know what I;m talkin' 'bout, right?....;) Slap a scarf, doorag & baseball cap or visor & I'm out the door...
#1PaFan
04-14-06, 05:41 PM
I'm VERY happy to hear that you're doing well, SweetGring! :gulp: :gulp: :gulp:
LilChief
04-15-06, 08:19 AM
Thanks for the update Vickie! I'm so happy to hear things are going as well as they are! Keep up the great attitude and keep us posted when you can.
Maybe you can start your own line of Yankee related headwear!
Hugs! Steph
#1PaFan
04-15-06, 08:43 AM
I
( I am soooo over that part...it's actually pretty cool not having to worry about your hair..good days or bad ones...Us girls know what I;m talkin' 'bout, right?....;) Slap a scarf, doorag & baseball cap or visor & I'm out the door...
I wanna see some Bald Gringa pics, man! Please don't trash the pics with any Detroit Lions sh!t, either! I prefer my Gring hairless and lionless! :gulp:
Gringaloca
05-19-06, 05:54 PM
Time for an update:
Started the 'weeklies' on May 2nd. Every Wednesday for 12 weeks straight..I hope. I want this over with asap....:D
New chemo drugs..Taxol & Herceptin. Along with Tagamet/Benadryl & Kytril& Decadron....Decadron,Tagamet & Kytril for the nausea..Not sure what the Benadryl is for but twenty minutes after it hits the IV...I'm off to lala land..snzzzzzz....:snooze:
Still with the bald/chrome dome..and now the eyebrows & eyelashes are going as well. Oh well...still have my sense of humor..have to..'cuz I'm pretty scary lookin' without them..:D Thank God for eyebrow pencils/eyeliners.
"3 down & 9 more to go". If it goes this smoothly, I'll be done with this series on Wednesday, July 19th. At that point, the 'port' is removed and my hair will start growing back. Looking forward to nice salt&pepper spikey 'do.
Another 48 weeks of Herceptin...and 'maybe' radiation to follow. Jury's still out on that one.
More in a few weeks...time to watch the Yankees beat up on the Mets...:P
jlw1980
05-19-06, 09:43 PM
Hey! Benadryl's an OTC cold medicine that is often used for sleep. It's always nice to have something that zonks you out when you need it! :D
I'm late to say this, but I'm glad to hear that you're hanging in there. You are one brave lady, and an inspiration!
I wish you all the best in your fight; I can tell you're going to beat this thing!! :cheer:
LilChief
05-20-06, 08:33 AM
Great to hear from you Vicki!
Thanks for the update, I've been thinking about you often, just haven't been home or online much lately, what with the new job and all the running with the kids etc.
Keep on hanging tough my friend! You're doing GREAT! :D
Hugs!
Steph
#1PaFan
07-22-06, 11:18 AM
Update?:)
I echo Trishie's request.
Training Camps open within the next two weeks.
I want some Gring Updates!!! :gulp:
Gringaloca
07-28-06, 11:17 AM
Time for another 'update'...
Finally finished Round #2...the 12 weekly 'treats'. The first 6/7 weeks went fairly smooth...little or no side effects from the multiple anti-nausea drugs, the two Chemo drugs (Taxol & Herceptin). The second 1/2 was a little dicey...more intense muscle/joint pain, very tired/fatigued on Saturdays...so much so that I rarely got out of my p.j.'s all day.:o Worst part was the extreme diarrhea every weekend..sorry probably TMI,,,but you asked!..:D Dr. Able finally gave me a prescription for that...and it worked beautifully. I was at least able to leave the house on Sundays to go grocery shopping..
So....that Session is over. I started Round #3...the 48 weeks of just Herceptin this past Wednesday, and I can already feel the difference.
I've been able to sleep at night and have alot more energy during the day. My hair is already starting to grow back and will continue more rapidly now that the Taxol is out of my system.
The downside of Round #3...the 'port' stays in for another 48 weeks. I guess it's easier to use than having to set an IV each week, but it feels strange having that thing in my body..
Anywhooo...that's it for now.Things are progressing nicely...only 47 more weeks to go!..;)
LilChief
07-28-06, 03:25 PM
Wooohooo!!!! Great to hear from you Vicki!!! :D
Glad things are going relatively well under the circumstances. You keep hanging tough like you have been, and keep us posted when you can.
Keep up the great work!:clapping: :cheer: :clap: :clapping: :cheer: :clap:
Here's to you girl! :gulp: :gulp: :gulp:
Love & Hugs!
Steph
Hey Vicki! Glad to see an update from you. Hope you were able to enjoy "our" day last weekend. Hang in there! :)
#1PaFan
07-28-06, 06:31 PM
That is FANTASTIC news, Sweet Gring! :gulp:
I'm going to drink several in your Honor this weekend! :D
I'm very happy for you, Honey!
Yay for no more Taxol!!
You're really some chick, you know that?:)
Good to hear things are looking up for you. I know it's a long road, but you are a tough cookie and you'll make it through. :)
My continued good wishes are being sent your way!
Keep going strong, we're all with you.
Archer1979
07-29-06, 06:59 PM
Kick it's ass, Gringa!
We're all pulling for you!
Luvtino
07-29-06, 10:19 PM
I am glad things are looking a little brighter sweetie. I am so happy for you and so proud of you. You are a total trooper. :cheer:
Yeah to hair growth!! Boo to the port and the runs!! ;)
If you want the port out as it bothers you ask them to give you an IV instead as needed. I know people who have done this and were much more comfortable and much happier when this change was made. Hugs!! :)
fredgmuggs
07-30-06, 06:50 PM
Great news!
When so much in life is uncertain, this much I am certain about..... and that is how much I admire you and how hard I'm pulling for you. Be well....
Toaderly
09-19-06, 06:11 AM
Hi Gringa,
I just happened upon this thread and I do hope you will begin to update it again. Your courage, strength, and sense of humor in the face of such a terrible disease are all truly uplifting. My dad went through this battle (his was oral cancer) and fought it with the same character as you. He came out on top, as I am expecting you to do as well, and at 74 probably works harder everyday than I do.
My wife and I will be lifting you up daily in our prayers.
Toad
Gringaloca
10-04-06, 11:06 PM
Hey All!..Time for an update. :)
October begins and Breast Cancer Awareness Month is off to a great start. I'm sure you all have seen the commercials/news updates on what is going on in your community to sponsor or join the BC Awareness Walk this month. I will be 'walking' on Saturday, Oct 14th...Don't know if I'll finish, but I'll be there in all my "Pink".. I actually broke down and bought a 'pink' NY Yankee cap...and as it turns out...this is the perfect month to be wearing it..:D
One of the best Websites I've found is www.getbcfacts.com (http://www.getbcfacts.com). Please check it out...very informative, useful information. Not only for women, but everyone can learn something they did not know about this disease.
The numbers are absolutely staggering..200,00+ women will be diagnosed with BC this year.:eek: Of course, early detection is key to battling this dreadful disease. Whether it be monthly self-exams or the yearly mammogram.
And take it from me...family history is NOT always a factor. There is no history of BC in my family. On either side..hence my 'denial' when I first felt that small 'lump'.
My 'chemo treats' ended in mid/late July, so the worst is probably over as far as the side effects. I still receive the Herceptin infusion every week, and will until June 2007. MUGA scans every 3 months..had one today.:( They're a pain in the butt,,,but necessary as Herceptin 'side effect' is heart failure.
Funny story about the Herceptin tho'...I've been approached by Genentech (maker of Herceptin) to provide a 'testimonial' regarding my experience with treatment/dosage/side effects. They are offering me a trip to SanFrancisco in January..their 'annual stockholders meeting', I'm sure.:D Could possibly lead to tv commercials/print ads..per their Rep. "Okay..but only if I can wear this Pink NYY cap" How great will that be when the Yankees win the WS this year?;)
To make a long story short...I'm doing much better than I ever expected. My energy level is back..walking in the mornings while it's still somewhat 'cooler' here in So Fl...trying to lose the added pounds.
My hair is 'seriously' growing back...altho' alot more grey than I expected and 'curly'...but only on the left side of my head. What's that about?:P The top is soft & furry...like a lil' bunny rabbit..:D And I've got this weird Eddie Munster/Jay Leno dark 'widows peak' on my forehead...okay, probably TMI now.:lol:
But in closing...PLEASE..Ladies...make sure you do those monthly self-exams, and if you're old enough...SCHEDULE that Mammogram!
Guys...You can help the women in your lives, too. INSIST that they do the same.
Thanks again for all your prayers, support & good thoughts....:2thumbs:
I'm glad you're doing so well, Vick! You're my hero. Well, you and George:lol:
I had my yearly mammo on Tuesday. Of course, they had to take me in for a sono because they saw something. Now I have to worry until I see my gynecologist on Monday. The tech told me that it doesn't look worrisome though, that it looks like a cyst (she told me not to tell my doc that she told me so :lol: )
Nevertheless, I'll be worried until I know for sure.
Thanks for the update. I think of you all the time:)
LilChief
10-05-06, 07:01 AM
Thanks for the update Vickie! I haven't been around here much to post, but think of you daily! You are an amazing woman and an inspiration!
Keep up the good work, stay strong, and keep us posted! (Hopefully we'll get to see you on TV too!)
Off to drop my daughter off at school then to work...the Mommy-go-round begins!
Love ya!
Steph
Thanks for the update Vicki. Good to hear you are able to go out walking and your hair is growing back, although fuzzy and somewhat curly! :D
This reminds me I really need to schedule a mammo appt. I put it off way too long.
Luvtino
10-16-06, 05:39 PM
I am so glad that you doing well sweetie. I think and pray for you daily. Great news regarding your energy level being on the rise. I bet the walks feel really good. And your hair is growing back!! Yeah!! :)
Hope you get to go to SF. And wear that pink NY hat with pride. ;)
Luvtino
10-16-06, 05:40 PM
Trish,
You and your boobies ;) will be in my thoughts and prayers. I am sure you will be just fine. Hang in there. :)
46andygirl
10-29-06, 01:16 AM
Time for another 'update'...
Finally finished Round #2...the 12 weekly 'treats'. The first 6/7 weeks went fairly smooth...little or no side effects from the multiple anti-nausea drugs, the two Chemo drugs (Taxol & Herceptin). The second 1/2 was a little dicey...more intense muscle/joint pain, very tired/fatigued on Saturdays...so much so that I rarely got out of my p.j.'s all day.:o Worst part was the extreme diarrhea every weekend..sorry probably TMI,,,but you asked!..:D Dr. Able finally gave me a prescription for that...and it worked beautifully. I was at least able to leave the house on Sundays to go grocery shopping..
So....that Session is over. I started Round #3...the 48 weeks of just Herceptin this past Wednesday, and I can already feel the difference.
I've been able to sleep at night and have alot more energy during the day. My hair is already starting to grow back and will continue more rapidly now that the Taxol is out of my system.
The downside of Round #3...the 'port' stays in for another 48 weeks. I guess it's easier to use than having to set an IV each week, but it feels strange having that thing in my body..
Anywhooo...that's it for now.Things are progressing nicely...only 47 more weeks to go!..;)
Hi, Gringaloca. I just went onto this thread, and I am praying for you and wishing a fast and safe recovery.:cheer:
I lost my aunt to this horrible disease and all of the women in my family have breast issues. I hope you are doing okay and look forward to another update when you are feeling well.
If anyone here is interested on reading another couragous cancer story, go to www.tannerville.com (http://www.tannerville.com). This little one used to live near me and she has been fighting this for 3 years now. God bless everyone with this awful sickness.
Gringaloca
12-14-06, 09:34 PM
Time for an update?..
Still receiving the weekly Herceptin dosage thru the 'port' every Wednesday. Energy level is back & feelin' great! :)
My hair is coming in very nicely...although alot more grey than before. And CURLY!..:D As my friend, Jackie W says..."Girl, just put some 'product' in it. Lets get this salt n' peppa afro goin' on"...it really does look pretty sexy..with the gold hoop earrings & all.....watch out now!..:D
Going to SanFrancisco in mid January for the Genentech/Herceptin 'Patient Ambassador' training program. I've submitted all the 'patient/treatment documentation' and had a telephone interview with their marketing representatives...Snow & Associates.
Staying at the Ritz-Carlton. All expenses paid..airfare, ground trans, hotel & meals.
Even if I don't 'advance' to the 'spokesperson' level..And I honestly think that I will...because this is something that has not only affected me...but my family & friends for so many months, and I feel so strongly about BC awareness and the progress in treatments. If my story/experience helps just one other woman deal with this terrible disease..
It will still have been an great experience to meet other Breast Cancer patients/survivors. It's a 'win/win' if you ask me..:)
Only concern.... SanFrancisco weather in mid-January...? Isn't it cold/rainy?
Lou?...you would know.:D
CptCrunch
12-14-06, 09:59 PM
Glad to hear you're doing well. :)
I've said this before Gringy...you're my hero.
I'm so thrilled you're doing well. Not only just doing well, making something wonderful and positive come out of the experience. You make me smile, girl!:)
46andygirl
12-18-06, 04:33 PM
Time for an update?..
Still receiving the weekly Herceptin dosage thru the 'port' every Wednesday. Energy level is back & feelin' great! :)
My hair is coming in very nicely...although alot more grey than before. And CURLY!..:D As my friend, Jackie W says..."Girl, just put some 'product' in it. Lets get this salt n' peppa afro goin' on"...it really does look pretty sexy..with the gold hoop earrings & all.....watch out now!..:D
Going to SanFrancisco in mid January for the Genentech/Herceptin 'Patient Ambassador' training program. I've submitted all the 'patient/treatment documentation' and had a telephone interview with their marketing representatives...Snow & Associates.
Staying at the Ritz-Carlton. All expenses paid..airfare, ground trans, hotel & meals.
Even if I don't 'advance' to the 'spokesperson' level..And I honestly think that I will...because this is something that has not only affected me...but my family & friends for so many months, and I feel so strongly about BC awareness and the progress in treatments. If my story/experience helps just one other woman deal with this terrible disease..
It will still have been an great experience to meet other Breast Cancer patients/survivors. It's a 'win/win' if you ask me..:)
Only concern.... SanFrancisco weather in mid-January...? Isn't it cold/rainy?
Lou?...you would know.:D
Hello, thank you for the update. Glad to know you are doing well. Continue spreading the good news you are having, it educates people. I must do a monthly check and have since I was a teenager as it runs in my family. Keep your spirits up and know that you are a hero to many of us. :)
Yes SF weather is cold and rainy MOST of the year! Take a very warm jacket and a hat. Don't forget gloves and scarf. Since it is right on the water, the cold is extreme. Have a safe trip and a wonderful holiday
BTW, curly hair is great, it has personality.
yankeeschic12324
12-19-06, 03:43 PM
My best friend's mom is battling cancer right now so I am definately clicking this thing everyday. They caught it rather late(she was misdiagnosed twice) but shes doing better.
46andygirl
12-19-06, 05:50 PM
I hope she recovers and beats it. Long road, but hopefully she will get better news that it is fully gone.
Luvtino
12-25-06, 12:32 AM
Oh Gringa...your posts always make me smile. God bless you. May this year bring you only happiness, joy, and good health. You truly deserve it.
Any company would be lucky to have you represent them. I bet you will be lifting the spirits of many breast cancer survivors to come. May we all help to get the numbers down and ultimately wipe breast cancer off the map.
And as someone with wavy ringlets...welcome to my world. ;) Love ya!! :)
Gringaloca
01-13-07, 01:20 AM
Time for an update?..
Here I am in SanFancisco..freeezzzzin' my toes off~..:eek: This weekend has been the 'coldest' on record for over 15 years. woo hoo lucky me..
While it was sunny and 55 degrees all day..with the windchill factored in, it's about 28 degrees here tonight.
The first day of my training seminar was absolutely awesome. Can I say 'eye-opening' tooooo many times?
The numbers of BC patients per year is absolutely staggering. 300K plus..of which 41K die every year? The numbers are all relative..depending upon 'stage' 'mesastitis' 'lymphnodes affected',...etc
That in itself is just mind boggling, and the fact that there are definite progresses in the treatment..soooo many women are stilll suffering from this terrible disease.
My questions don't equate to 'treatment'..I've pretty much left that up to the 'experts'..whether it be AC/Cytoxan/Taxol/Herceptin, etc.. I'm willing to run the gamut of recommended treatments..no matter the 'side effects'.
The big question that I have is WHY?.when I have no BC history in my family? WHY? when I have no Cancer history in my family? WHY? when
Gringaloca
01-13-07, 01:32 AM
Time for an update?..
Here I am in SanFancisco..freeezzzzin' my toes off~..:eek: This weekend has been the 'coldest' on record for over 15 years. woo hoo lucky me..
While it was sunny and 55 degrees all day..with the windchill factored in, it's about 28 degrees here tonight.
The first day of my training seminar was absolutely awesome. Can I say 'eye-opening' tooooo many times?
The numbers of BC patients per year is absolutely staggering. 300K plus..of which 41K die every year? The numbers are all relative..depending upon 'stage' 'mesastitis' 'lymphnodes affected',...etc
That in itself is just mind boggling, and the fact that there are definite progresses in the treatment..soooo many women are stilll suffering from this terrible disease.
My questions don't equate to 'treatment'..I've pretty much left that up to the 'experts'..whether it be AC/Cytoxan/Taxol/Herceptin, etc.. I'm willing to run the gamut of recommended treatments..no matter the 'side effects'.
The big question that I have is WHY?.when I have no BC history in my family? WHY? when I have no Cancer history in my family? WHY? when I have always tried to try to 'eat right/excercise'..and limit the stress in my life.
WHY?...I've no answers and neither does anyone who researches this disease. Sure they have their 'benchmarks'..but we're all from such a diverse ethnicity/geographic/demographic background that they will never be able to tell me WHY?...do I have BC and not my older sister, Linda..came from the same 'parentals'..
Tomorrow is another day...I have to write 'My Story'...you can be sure I'll mention the NY Yankees in there somewhere
#1PaFan
01-13-07, 01:50 AM
Sweet Gring, you are ALWAYS in my thoughts & prayers, Woman!
I even mentioned you to St. Vincent Thomas Lombardi on my last pilgrimage! Unfortunately, I told him you were a Lions fan. He screamed at me, "What the Hell's going on down there???" ;)
YOU are Awesome, VB! Now, grab me a Beer, Wench! :gulp:
LilChief
01-13-07, 10:09 AM
Vicki darling, so wonderful to hear from you! You know you are my hero!
I thought about you even more than usual this week as I went for my 1st Mammogram...:eek: Not my favorite experience, but had to be done...;)
Please continue to keep us updated, I haven't been able to get online or to the forum much these past few months, but when I get your updates it always makes my day!
Always thinking of you my friend!
Hugs!
Steph
Everyone's pulling for you Gringa, Keep up the good fight.
jlw1980
01-13-07, 10:12 PM
You rock, Gring! :gulp:
Bernie51Williams
01-15-07, 12:01 AM
sorry bout your friend but I will be sure to click
BillBuckner
01-16-07, 04:12 PM
I'm sorry I didn't respond to this thread sooner. Just so you know I put the link at the top of my bookmark list and click it every morning after I wake up.
Gringaloca
01-19-07, 08:53 PM
Wow! I just read my post from SanFrancisco...can you tell I was more than a little
'emotional' when I typed it..:o
But seriously folks..What an eye opening and extremely emotional experience it was.
27 women chosen as "Patient Ambassadors" to speak on behalf of a fairly new BC drug called "Herceptin", discovered and produced/marketed by Genentech, a bio-oncology/medical firm located in South SanFrancisco.
27 women from all over the country..So Florida (me!) to Seattle...from Bridgeport, CT to SanDiego, CA. and various points in between. NYC, Memphis, Atlanta, Hilton Head, Cleveland, Minneapolis, HotSprings, Denver,Kansas City & SanAntonio, and many more I can't remember just now.
All ages..from 26 to 66. BC family history for some...none at all for others.
From those who were 'mis-diagnosed' (after countless visits to Primary/OB-GYN & Mammos) for two years...to 'Cleopatra's (Queen of Denial)..(me:o ) who convinced herself that 'lump' was nothing more than a fibroid tumor...I mean, afterall...My Mom & sister had them. 'That must be what it is....."...:eek:
The stories I heard were so inspiring...crying one minute and laughing the next.
Lori..who was mis-diagnosed for two years. By the time she had her 'double masectomy' at age 43..cancer had spread to her liver. After going thru a year of Chemo and radiation...she lost her only child, her son Colby, in a car accident.
Julie...who was 'cancer free' for 6 years only to be diagnosed AGAIN while 5 months pregnant with her second child. She had to make a choice...terminate the pregnancy..(Chemotherapy and pregnancy don't mix well:eek: ) or tuff it out and hope for the best.
Her daughter Alisa was born C-Section without complication...and while she was 'sportin' that bald/chrome-dome look'..the older daughter (13) applied temporary tattoos..."I'm to sexy for my..too sexy for my..." all over her body.
I cannot express how touched I am..how honored I feel to have met and shared with these brave and courageous women. I cannot express how fortunate I feel...to have NOT experienced some of their worst moments. My journey has been a 'day at the beach' compared to most. For that I am truly blessed and grateful.
If my 'Cleopatra Syndrome' Story (as I call it:)) ..my 'denial' at that first feeling of that lump..my 'denial' to take the time to get that Mammo..my 'denial' that it couldn't happen to me..
If my 'story' makes one women listen up and take notice and act...it's all I hope to achieve.
I apologize for rambling...but I am so excited about this opportunity that Genentech has given me. To tell 'HER Story'..and the benefits of Herceptin in the treatment of Breast Cancer.
Btw...attaching the Genentech website page regarding Herceptin.
http://www.gene.com/gene/products/information/oncology/herceptin/index.jsp
Thaaa Thaaa thaaa Thaaa's all folks...:D Stay tuned for further updates...
Thanks for the update and the touching stories. Glad you're doing well. :)
#1PaFan
01-20-07, 04:00 AM
I cannot express how touched I am..how honored I feel to have met and shared with these brave and courageous women. I cannot express how fortunate I feel...to have NOT experienced some of their worst moments. My journey has been a 'day at the beach' compared to most. For that I am truly blessed and grateful.
THAT was a Powerful Post, VB! :gulp:
I cannot express how touched and honored I am to know YOU, my Sweet, Lovely Gring!
God Bless YOU, Honey! :gulp: :gulp:
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