Has anyone started a forum for Chemo in Dec 2008?
Comments
-
Firni - love your description of springtime in the Rockies! I used to live in Monument (north of Colo Spgs) and March and April were the snowiest months..... kept those snow shovels handy!!
I am now 2 months post chemo (3 weeks radiation) and virtually all SEs are gone. (Just in time for the Femara SEs to kick in). Though my skin is still drier and still a touch of tingling in a little toe. Fatigue is gone; so I need to get out and exercise to lose that chemo weight. I think my hair (including new hair for the thin eyebrows and eyelashes) is going to be slow in coming back in; and I've read where some women lose hair with Femara...... ARGHHH
You ladies that are having fatigue/ foot/ nail/ additional surgery issues - I admire your strength. How incredibly difficult to plan and do normal daily activities. YOU ARE TOTALLY AWESOME for sharing here and encouraging others!!!! Thank you.
Mary L
-
Since my plastic surgeon told me I had to wait 6 months post-radiation for reconstruction, I'm getting my port removed by my breast surgeon. He's doing it under local anesthetic a couple weeks after my last treatment.
Firni, my oncologist never mentioned the dark nail polish. I considered using a dark color throughout treatment and hindsight, it might have worked because my toenails got a little sore but they don't show near the damage. Might have something to do with wearing closed-toed shoes and them rarely being exposed to light?
Tricia, I hear you on the weakness. I have always been BIG into exercise and healthy diet. Now I can barely move and since nothing tastes good, I don't care what I eat. All that will change in a few weeks. I can't wait to reclaim my life!
-
That's right Firni, I guess I am still having chemo brain (or old age setting in). I knew you were finished. I guess I read something that made me think you had one more. (I would not wish that on anyone!
I am 7 weeks out from my last treatment and I can happily say I have no SE's (other than the hair issue). At times I still feel like I don't have the energy I used to but I think I just need to get my hiney to exercise.
All of you ladies still going through treatment are incredible. I pray for you each night that you will have the strength to finish. Please know that I am here cheering you on! You can finish!
I hope everyone has a great weekend and has very little side effects!
-
Mary, Monument usually gets the worst of the storms. North Metro where I am doesn't seem to get as much. Altho, IN is no walk in the park either for winter and spring.
I don't know if it's the light or chemicals in the polish. I'm using Hard as Nails now and there has been no progression in my nail beds except for the pain. I tried just clear polish and that did not help. I don't know if Hard as Nails can be clear and block the light. I hate to put something dark on my finger nails coz they're cut so far back and stubby now. As long as it's status quo I'm good.
-
I've been using Hard as Nails since starting the Taxotere. That hasn't stopped the damage but I wanted to monitor what was happening -- which I couldn't with the darker polish. (Plus, I'm a klutz anyway at putting on polish. Combine that with sore nails and numb fingertips, and whoa what a mess!)
Ironically, I am impressed with the nice quality of my nails since using Hard as Nails. Except for what's happening on the nail beds, they've never been in such great shape. I'll continue to use it long after this problem is resolved.
-
Hi ladies,
This is just a quick note to let you know that I had my exchange and port removal yesterday and feel almost normal today. I took half a Vicodin before leaving the hospital and no pain meds since. Surgery always aggravates my asthma, so that's my biggest issue today. The plastic surgeon had planned to do a lift on my right side too, but decided once he got me on the operating table that I wouldn't be happy with the results. Since there was no signed consent form for an implant, he left that side alone. I guess we can decide later whether to do the implant, probably after radiation when I know if there is damage to my new implant on the left. At this point I'm wrapped up and won't know how things look for a few days. Take care and enjoy the weekend.
~Bonnie
-
Has anyone heard from Elaine? I wonder how her RADs are going? Thinking about ya!
-
I saw the PS yesterday. Everything he said is healing well. He also told me that the cyst he removed was just that a cyst. I was pretty sure that was all it was, but you know how we let our minds wonder. He also said that if I was going to have the nipple done he would not do anything until after the summer. He said my body has been through so much, now it is time just to heal. H e said to think about it and that there is 3 different ways he can do it. Has anyone had this done yet? or are going to?
My mom had her scans and things are looking ok right now. The cancer has not spread and the fluid in her lung has decreased a little bit. He said she can go for 1 more tx (which will make 6) and that would be all. I just hope that this makes her comfortable. But she also asked when she can return to Florida. I really do not think she can live on her own anymore, but it may take her trying to do it for herself. Well we will see. She is totally amazing though, she has a very strong will.
Well I hope everyone is enjoying your weekend. The weather in NY feels like a fall day not spring, it is very windy and chilly. I am hoping tomorrow will be warmer. Bring on SPRING!!!!
Love to all,
Colleen
-
Colleen, glad your mom is doing better. I asked my PS about how she did nipples but didn't get a straight answer. Around here, they spoon feed you the 'next' information and stall about everything else. It's frustrating.
My last infusion is Tuesday morning. I am SO not looking forward to another couple of weeks of side effects. But at least it will be over and I can focus on getting my stamina back.
-
Colleen, if your mom insists on going home, see if she'll allow home health to come in a couple times a week to check on her. That will set your mind at ease and help her out as well. I will eventually have nipples done. I know my PS does a graft for the nipple and for the areola. Beyond that, I don't know. He really hasn't said any more. He likes to address what's going on now and not even bring up anything else.
Texas, I know waiting for that final tx is ridiculous. You're so mentally ready to be done and knowing that those SEs are going to hit all over again, it's hard to want to have that last Tx. I do have to say that I'm feeling better faster after the final Tx. I know it's mental. Coz the SEs that I do have are huge and they are going to run their full course of at least 3 weeks. Knowing it's the last time tho seems to make a difference for me. Only a couple days now till you are done too.
Bonnie, did your PS tell you before the surgery that he might not do the lift? It's a little unsettling to think that he's making decisions about your body without you. I hope you're happy with the results tho when you get unwrapped. It probably is smart to wait until after rads and make whatever adjustments are needed to both sides at the same time.
-
Elaine is on the April rads board. She's doing good.
-
Thanks Caroline for the update on Elaine. I'm glad she's doing good.
Texas - You're finally there! Only 1 more! We're all standing proud behind you!
Colleen - I am so happy to hear your mother is doing better.
Happy Monday!
-
Hey Divas. Thanks for asking about me. I feel a bit guilty because I have been all-consumed with rads these days. Last week I started and it was a little stressful but I think I'll handle it ok. I still have some side effects from the Taxol. Hopefully those will be gone soon.
I am catching up on some posts. I'm glad surgeries are going well.
*Hugs*
Elaine
-
Colleen - I had my nipples done 2+ weeks ago and today had the stitches removed and the ok to do whatever I want exercise wise. They look awesome but the PS said they eventually will flatten out - who cares!! I scheduled my tattoo sessions and start those in 3 weeks for 3-4 sessions. When I look in the mirror it just looks so much better than just those scars across my chest. Just my personal preference as I know lots of us choose not to reconstruct at all. My SO has been so patient and supportive and he likes the new girls so I feel I am doing something for him also. I do have some tips for anyone who has nipple recon in their future so post on here when you are ready to undergo that last step. I read everyday but have not been posting much as work is crazy and by nightime(like now) I'm just wiped out. Luck and love to all the December survivors - I couldn't have done this without all your support, suggestions and love.
Bobbi
-
Bobbi...just sent you a PM on the nips!
Well, it's been exactly two months since my last TX and my nails are feeling like they are going to fall off! I had this sensation a few weeks ago, but now they look like there are air bubbles under the nails and if I catch them on something, they feel like they are coming off! So I'm really trying to baby them. Typing is fun! NOT LOL
Guess time will tell!!!!!!!!!!
Hope everyone is doing well!
-
Bobbi, I'll be interested in all of your tips. My reconstruction is not until the end of the year, so if it's okay I'll PM you too so I don't forget.
Lisa, I hear you on the nails. Several of mine are black, and the rest are white beneath the nail which tells me they are no longer resting on the nail bed. I'm also babying them like crazy, but after all we've been through, I've come to peace with losing them if I must. Like my hair, they'll grow back.
-
I'm with you Texas...I know they will grow back...but they look so good now with polish! LOL Some of mine had black stripes through them, but up until last week they were fine...then the white spots showed up!
Just another bump in the journey!
-
Lisa, What a drag about your nails. I would have thought at this point you would be done with the surprises. Here I am not quite 3 weeks from my last Tx and wondering why I still feel like crap. I guess I'd better relax a little. I cut my nails REAL short so they can't catch on anything. I never had short nails before. I'm still getting used to the look. How is your hair doing at two months out?
-
Firni - encouragement here: At two months out the nails seem to be more brittle, but look normal and are holding on just fine. My hair is growing, I don't need a magnifying glass to see it anymore! It is about an 1/8 of an inch long. My eyebrows/eyelashes are still losing hair, but not gone. Even though I am on Femara I am beginning to feel normal.
Got big fluffy snowflakes here today.
Mary L
-
Firni my hair is growing in...I just stopped shaving it about 5 weeks ago! LOL It is probably close to a 1/4 of an inch. I updated my photo...but it is hard to tell!
Mary my eyelashes and eyebrows are starting to come back in! yeah!
Oh and snow...I'm so sick of it!!!! We got a couple inches over night and are due for about 6 more!
-
Day 2 of LAST CHEMO!!!! YAY!!! of course, I know there's SE's still to come, and going into the unknown of Femara after my next appointment with the onco in 3 weeks, so am back into the jitters about what that will bring, but trying to concentrate on celebrating the end of this phase
I have an awesome support group of family and friends but still don't think I could have gotten through this and stayed at least somewhat sane without all of you divas - as so many have said better than I can, there's just no one who can help as much as someone who's going through the same things, plus reading of how so many of you are contending with so much more than I have had to has really been inspiring - THANK YOU ALL!
Elaine - hope the rads go well, and the Taxol SE's go away soon
Texas - thinking of you today and your LAST TX! hope all goes well
Lisa - looked up Zumba in my area and gonna try it either this week or next - they charge $10 per session around here if you're not a member of their club, and the cost of membership is way out of my means! have to drive about 25 miles to get to it, so will probably only go once a week, figure anything is better than nothing, and will also try to get back to walking
blessings and thanks again to all...
-
Hi everyone,
Just wanted to say that I'm thinking of all of you and wishing you a good week with as little discomfort as possible.
I'm about 6 weeks out from last Tx and have about a quarter inch of hair that is still filling in. My nails are brittle and soft, but otherwise intact. Exchange surgery was last Friday and I'm a little disappointed that the lift was not done because my chest is still uneven. PS wants to do a small implant on the right side in a couple of weeks, but I have decided to wait until after radiation, which should start in 2-3 weeks. It is possible that the new foob will drop enough to even things out or that there will be damage from rads that will require surgery anyway. Anyway, I'm happy to have the implant -- it's nice and soft and looks great and also thrilled to have the chemo port gone, but still a little bummed that things didn't go quite as expected. Take care.
~Bonnie
-
Thinking about you TEXAS! Let's yell LAST ONE!!!!!!!
Congratulations Grancy11! I know what you mean. I certainly could not have made it without all of the ladies here! You all have kept me strong! Thank you all!!!
Sonia
-
Checking in ladies: the last treatment almost didn't happen! My white blood count was pretty low. I had to promise to add a 3rd Neulasta shot to my schedule this week then the infusion began. I had quite the parade of people leading to the front desk for me to ring the bell. Then there were lots of hugs and words of encouragement. I love the nurses at my oncologist's office.
My hair's about 1/2 inch. I can still see plenty of bald. Can't wait for the return of eyelashes!!!!!
WOOOO HOOOOOO! Congratulations Grancy! Simvog, your day is coming SOON
-
Grancy11 CONGRATS on your last chemo
For me, it was the easiest one as far as SEs goes so wishing you the same. -
Grancy11 - Congratulation on finishing chemo!
Texas357: thank you! I am counting the days.
Lisasayers: I am more terrified for loosing my nails than my hair! I hope yours come back soon and no pain!
I am day 4 after TX4 and I am tired and have bone pain, but I can manage without pills. I also had some tingling in my left hand and foot but not for long and only on the 3rd day. My last dose was cut to 60 mg since the one before was 100 mg and it was supposed to be only 80 mg. Unfortunately my blood is not good. I am borderline anemic but the white count is high to 6.8. I just hope I can manage without blood transfusion.
I saw my surgeon yesterday, I schedule my port removal for June 12, and we discussed about right mastectomy for September. Both my onc and surgeon gave me the ok to go on vacation in July (Anguilla), I am so happy! I hope my nails are not falling off since July is only 2 months away from my last tx May 29. If you are interested, I found on Victoria Secrets Bandeau top with removable padding that actually have pockets and they look great. I do snorkel a lot and for that, I will not need extras since I wear a west. I am not staying in the sun, but I love the water.
Wish everybody no SEs and speedy recovery.
-
Hey Ladies...I have a question for all of you. I'm a bit worried about my sister and confused as to how things were done with her surgery, but maybe things are different than what I had.
My sister was diagnosed two weeks before me. She has ILC, 7 cm tumor and they did neoadjuvant chemo (6 AC followed by 12 weekly taxol). Before surgery they knew the tumor had shrunk. Last week she had her bilateral mastectomy...no expanders as they knew she would be getting 6 weeks of radiation. When she got out of surgery I asked her about her lymph nodes...she didn't have any information
Now when I had surgery they did a quick frozen dissection of the nodes to make sure they were clear...so my surgeon only removed two. My sister said they didn't do that.
Today she met with her doctor for the first time since she had surgery...to find out that they want her to go back and have more surgery, as her nodes were positive. Is this typcial to go and remove more instead of just proceeding with rads?
Any insight would be helpful...as she is scared!
Thanks!
Lisa
-
Lisa,
I thought it was common to check lymph nodes when you have surgery. Looks like extra money for the hospital and the doctors since they didn't do it the first time.
Question for all? I started Femara on 4/2. Anyone else? Those that have been on it was awhile, SEs??????????????
Linda
-
Lisa - Wow! That's not how mine went. They did SNB while I was out for the Mx. Where does she live?
Wishing your sister a speedy recovery!
-
Thanks! That is what I thought! My sister lives in Michigan and she is going to Karmanos Cancer Institute, which has a great reputation. I'm really confused!!!!!!!!!!!! And angry!!!!!!!!!
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team