Chemo May 2013
Comments
-
Kate it certainly does sound like you made the best decision in changing jobs. A huge Thanksgiving blessing.
Argynis it's wonderful that you are doing so well.
))
Pat February you are busy and I bet you will be busy in December too. I say January ought to be declared your month of rest.
A Blessed and joyful Thanksgiving to all.
Carla
-
Happy Thanksgiving to all of you wonderful ladies. Enjoy today - We have much to be thankful for!
Annie -
Hapoy Thanksgiving to all of you wonderful, amazing women!
I am sooooo thankful to have had you all be a part of my journey this year...
Laughter
Tears
Pain
Frustrations
Healing
And smiles
Thank you all!
Lorrie
-
I hope everyone is doing well.. been quiet fir a couple days..
-
I took a few days break and am catching up now. I hope everyone had a great Thanksgiving. I had a really nice one. I truly had lots to be thankful for this year. I did have to take my daughter to urgent care yesterday she has a sinus infection and bronchitis. She is feeling better today but Thanksgiving sucked for her.
Wow Lorrie I don't even know what to say. Prayers to you and her family. -
Enjoyed Thanksgiving with the family. Thankful we were all together. A few of us had physical or mental issues that could have prevented us to be together so that alone was a blessing.
Been in my own cocoon the last few days. Getting my head around the new therapy that will continue for 5 years. Anastrozole. The very possible side effects and what I can do to be proactive about them. Have started and hope to be diligent about exercise, excellent eating habits and taking care of myself. I'm in charge of me.
Peace and joy - Carla -
Hi Carla,
I've been on Anastrozole for 1 month now. No problems so far! I am a bit stiff and achey (old agebut I was that before my dx and it hasn't gotten worse on the AI. I've read that Claritin may help with any pain SE from anastrozole - much like it did with the neulestra (sp?) injection during chemo. Some people also take glucosomine for the same purpose. I haven't needed anything extra though. Hope it stays that way.
Annie -
Thanks Annie. Nice to hear. There's hope.
) Wouldn't that be wonderful if it stayed that way for you.
-
Hi everyone.
So I've been battling a cold all ThanksgivingMy body aches and my throat is REALLY sore again. I'm scared I might have that esophigial thrush...:( I'm tired of not feeling good - and I'm pretty sure everyone around me is tired of it too....
It was nice to have 4 days off though - I just wish I could've used the time more productively... -
Kate, do you have the prescription for thrush?
I purchased Manuka honey ....read about it on one of the boards here. It is from New Zealand, honey made from bees that use the Manuka trees. Supposedly it has "healing qualities". I used it in my tea when I had a cold coming on. 3x a day. My cold was gone within 2 days. (Results not typical? Lol). Here is a link to amazon http://www.amazon.com/s/ref=nb_sb_noss_1?url=search-alias%3Daps&field-keywords=Manuka+honey. Also I read if allergic to bees don't eat honey!
Zinc is also supposed to be good. The Zicam cold tablets work wonders.
As is typical, check with your doctor before medicating. Hope you feel better!
Carla, glad you had a good Thanksgiving. Good luck with your next step in this process.
Pat -
forgot to mention, I had read when buying the Manuka honey look for an "mgo" of 400 or greater.
Don't ask me what mgo means!
Pat -
Lorrie - so sorry. Will definitely keep your boss and his family in our prayers.
Anyone else on Herceptin feel having issues with numbness/tingling in hands/feet? Yes, I have had this with the taxol, but I thought it was getting better. Then, after my last Herceptin, I feel like it's getting worse. Just wondered...
Hope all had a good Thanksgiving!
-
MomofSam - I also still have some neuropathy...tingling and numbness in my fingertips and on one foot. I have not noticed any association with Herceptin though. My Doc told me that the Taxotere I took is famous for "latent" se's that show up or continue for months after the finish of chemo. He said it should resolve itself over time....just don't know how much time!
Annie -
Thanks Annie! Hopefully that's the same for me too -
Only thing I'm noticing on Tam is that when I take it on the am.... I have to eat a cracker or toast & I HATE eating in the morning... but my tummy feels yucky if I dont.
The other thing.. Chemo started me menopause.... but the hot flashes are more intense...now.... that's about all. Totally doable.... not sure if it's the brand of Tam.. but I'm good -
Did a good deed today... I try throughout the year, but I make it my mission during the holiday season to jump on every opportunity I can (if I can afford it.., haha)
A friend if my aunt on FB has rectal cancer... hes only 30, friend requested me when he saw my aunt and I talking on fb... he goes to the same chemo lounge & rads zapper that I did.... anyway he posted to his friends that he needed a ride to OHSU hospital in portland for an appointment.... an hour each way...no one responded so I private messaged him to offer to take time off work and drive him if he was comfortable with a stranger.... haha.... I took him today and he was so thankful... we had quite a while to talk & when I dropped him off back in salem, he thanked me again... I just saw a post on FB from him that said he was emotional tonight, not sad emotional, but grateful emotional that someone that didnt even kniw him would help him...... good deeds make me feel good! Its selfishly my christmas gifts to myself, because it makes me feel so giid
-
oh Lorrie, tears in my eyes! The gift of TIME is the best gift anyone can ever give. Add in a "therapy session" on that long drive and the guy had a double bonus gift. Keep up the good work. Thank you for inspiring!
Pat -
Lorrie and Pat-Inspiring is the perfect word for it. What you did affected him in so many good ways. Really touching and a motivator. Thank you Lorrie for doing and then sharing your story.
Carla -
Lorrie that is such a great story.
FYI Chemo has slammed me into menopause as well. The hot flashes on Tami have steadily gotten worse. My doc put me on a drug called Gabapentin for them. It is working well for me. -
Love those kind of good deeds...................so inspiring!! -
It has been so quiet in here lately - I guess that's a good thing - we are all busy living life...
I went for my infusion yesterday and it always makes me so reflective when I'm there. It's across the street from the hospital where I had my mastectomy. And I think about when Barry and I had Denny's across the street after meeting with the oncologist for the first time...or being wheeled downstairs to get into the car when I was discharged from the hospital, or the first seat I sat in at the clinic for my first chemo, talking to the pharmacist. It's incredible how quickly the time has gone by don't you think. This year is almost over...
My daughter turns 14 today - and I can't believe 14 years have gone by . I hope I get to see so many more of her birthdays....she is my oldest so I have been a mother for 14 years....
Okay - I told my boss at work about my cancer/wig etc so I am going wig free on Monday and I'll have to deal with all the shock/comments etc, but then I hope I can put my wigs away for good. I really want to ship them all off to someone that might need them but I feel like I should keep at least one...
Have a Dj gig tonight - a Holiday party...
Kate -
Hi All!! Right now I'm only on Herceptin every 3 weeks. I'll start Rads in Jan. I had my exchange on 10/30 and so far so good, I guess. I do experience stiffness in my legs after sleeping or sitting in one position for a time (where I didn't have this before diagnosis). Do any of you experience this? Does Herceptin cause achiness? Thanks!! -
Kate, great to here you will be wig free! I boxed up all my stuff to get rid of and then had a questionable scan...so I will hold onto the stuff for now. 14 years as a mom...I'm right there with you. My oldest will be 15 in May. My stepdaughter is 22 but her mother never let me take on a "motherly role" so I am more of an "adult figure" in her life, though could also be considered a mom as she only comes by if she wants something! Lol
Mcgis, glad things are moving along. I did not do herceptin so I can't speak to that. Did you mention this to your onc! Perhaps she has a vitamin recommendation to offer? Maybe search the boards and see if you can find someone else with similar experiences...I don't think the oncs know everything! Lol
Pat -
mcgis - I have the exact same issue with Hercepten so it must cause that -
patty - any updates on that scan? -
Kate, I posted a while back...did a scan early November and my oncologist referred me to a pulminologist.
The pulminologist said 1 of the lesions is looking like a ground glass nodule. So now I wait. I go back in early Febrary for another scan to see if anything changes. I am beside myself, life continues as normal for my hubby. I have finally gotten to the point that I will not think about it "all day". Did I mention the word cancer was never mentioned during this consult, or when I spoke to my oncologist? I googled ground glass nodule to see what that was all about.
I am trying to get "my life in order" which has always been a goal since I retired. Need to get my will updated (it is pre-kids!) and get my kids albums updated (last done when my daughter was 1, she is now 10 going on 11!).
Still have my next surgery stage for the DIEP scheduled for New Orleans and am going with friends. I have decided that regardless of the outcome of the next scan I will be going to New Orleans.
I've said it before and I will say it again. Cancer is a huge inconvenience! I'm a planner by nature and it sure sucks to plan with the "I don't know what is next".
Pat -
Sorry Patty - you did mention all of that. I swear, I had the sharpest memory before this year and now I have the hardest time remembering details...
I would be just like you too - to just "wait and see" is not a great place to be in....:(
I spend my downtime googling "reccurance rates" etc.
My husband and I don't have a will. We don't have anyone that would take the children incase of our dying together so we just decided to bury our heads in the sand and not think about it. Alicia is only 4 years away now from being able to take care of everyone so we just have to make it 4 more years (together)... -
Kate, I hear you! Memory? I'm lucky I remember my name sometimes! Stay off the recurrence rates and go enjoy what you can. It has taken me weeks to sleep through the night (well I still have the hot flash thing going on, but I'm not then dwelling on dying!). Save the worrying for when you really need it.
I know the importance of a will. Used to be that it would have been complicated with my stepdaughter in the picture as well...how to divide assets...who is determined to pre decease if both die first. What a PIA! I wanted the money (ha!) to go to the sucker (oops...important family member) that would take in my kids! 3 kids! Who needs that! No one has a house that can take on 3!
Anyhow, I better look into things, a trust, whatever. I am worth way more dead than alive...thanks to a good insurance policy...but I don't want the money wasted away by a spendthrift and the kids get nothing. Then again I don't need my kids turning 18 and getting a huge amount of money to spend on partying! Lol. I have read a book on ideas for trusts and it would appear there is no "easy answer" as the scenarios can vary so greatly...2 responsible kids wind up paying for 3rd who runs through his money etc. can lead to a lot of fights! Oh well, won't be MY problem?
Will also look at cemetery plots, why not, we all have to go sometime! One less thing for either of us to deal with when the time comes. I didn't like the funeral director when my dad died...I think they are up there with car salesmen...unscrupulous. (Hope I'm not offending anyone,though I did meet a GREAT car salesman once, I think he was burnt out, he practically paid me to take the brand new car off his lot! Lol) can you negotiate burial plots?
Christmas has really been disturbing to me this year, not just because of the cancer thing. I feel my kids have so much and I grew up poor (socks, underwear, ugly sweater and then one game to share under the tree). Their lists are waaaay out of any price range I would consider...these are things they need to work and save money and MAYBE I would match their savings or contribute a little toward the item). So do I NOT get them these things on their list and possibly give them their "worst Christmas ever" or do they get what they want and are then spoiled? I'm thinking if I make this their worst Christmas ever and then I die that is how they remember it.(me). But then I would love to leave a note for the next Christmas with instructions to get them whatever they want and a note to them to say "see, these are just things....we need to love the people in our lives while we can"....it's not about "stuff". Of course that would be really cruel. Sigh. I will keep begging them to revise their lists. So much easier to have the Christmas spirit when they were younger.
Tonight hubby and I are driving down to Queens to see the Boston Pops Symphony and a chorus for their Christmas production. Weather is supposed to be uncooperative, snow! Ugh! Will be packing the car with blankets in case we decide to pull off the road. You would think a suburb of NYC would take care of their highways, but they don't. Hate the white knuckle driving. And of course it's never me that's the a$$hole driver! Lol
Anyhow...discovered travelzoo.com for great discounts on tickets. Don't have to be a member either. Got my orchestra tickets for half price! Woo hoo! -
Have fun, Pat... & definately be careful! You didnt fight cancer to be a road statistic!
Yay Kate on ditching the wig..., my hair is only about 1/2-3/4", but I biught a bix of blonde dye.... still to chicken to go hatless outside the house, even tho everyone says I should. My excuse right now is our temps are in the teens - I need my hat!
Forcing myself to slow down this week.... since feeling better, ive been over doing it and I feel like im having a "chemo" week......
Hope everyone is feeling well!
Lorrie
-
Kate looking forward to hearing how your wig free day went at work. I'm guessing it went well. It has been nice not wearing my wig lately. Although I think I look better in my wig then I did before chemo or even now. My hair is about 1/4 to 1/2 in long and grey grey grey with a few sprinkles of dark brown. Thought I would dye it brown yesterday. It is now orange orange orange. Ha ha ha. Think I'll wear a hat out until I dye it again.
Pat my prayers for you to is to be in peace while waiting for your February scan. How did the Symphony go? It's great that you are getting a will and your cemetery plots taken care of. It is something I've wanted to do for a long time. But, alas, have failed to do so. We had a will from about 25 years ago. Before our 3rd daughter was even born. I mean,my hubby and I could die at the same time, then what? Last week we requested the paperwork to sign so that our 3rd daughter will be added to the beneficiary. Still need to redue the will etc. Takes money so who knows when it will happen It will feel good when it's taken care of. I too have one child that I am concerned how she would use the money. Possibly in an unhealthy way. Can hope for Devine intervention.
All of our chilren are out of the nest now. But I remember praying that both or at least one of us live until our youngest daughter was of age. And when she reached the age of 18 was thankful and then asked we live at least until she was on her own. She is on her own and now I am prayerful that I am still here for all our girls and grandchildren. I am grateful for all my days I'm given. But am sooo grateful that we made it until they all reached adulthood.
Made an appt with my onc on Thursday. My left (and remaining breast) nipple has been having burning sensations. Don't feel any lumps like I did in my right breast but thought I would check it out.
Looks like a beautiful day today. I'm going to take it on and enjoy.
Blessings to all.
Carla
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