Starting chemo January 2009?
Comments
-
Hello everyone. So many postings, such deep thoughts and I am forever grateful for this thread. JJS rock! Can you tell I am in my high school teacher mode? I have been planning a bike trip with about 12 of my students. I at first thought I could take them along a trail built along a river- I took my mountain bike along the trail and within about 10 minutes of a nicely groomed trail, I began a descent of about a 45 degree angle; I am thinking "okay, kids could have fun with this", until I hit the bottom and had to manueuver around an hairpin turn...so my thought, "Nah, this is probably too tough!"
Actually the trip turned out to be tough for me. I thought maybe the low wbc issue was starting to kick my in the butt again and I am a bit worried, because after that intermediate trail, I was quite bruised up. Never seemed to be so bruised before! I have done mountain biking before- all over the place- I've been in competitions before and never was I so bruised.,....and the fact that I wanted to stop. Halfway through the 15 mile trek I stopped. I swear I am going to go through that trail again. And I am not going to stop, dang nabit!
-
Jess, I think that sounds like a lot of great exercise. Yeah, maybe not what you would have done a couple of years ago, but, wow, sounds like a lot of good work to me
-
Had my check up today. The lab work was still cooking when I met with my Onc but absent anything on that he gave me a good bill of health and does not want to see me for 6 mths. I will get my, hopefully, last CAT scan then. He was not worried about my having had my period last month and not this month. He said break through bleeding not full menstrual periods is what they worry about and that in premenapausal woman they have actually not had any uterine issues and for now he still conciders me premenpausal since I must be making estrogen to have had a period last month. Of course I have been having hot flashes again since then, not bad but they had pretty much gone away.
At work we broke in new technology. We now have super duper conference phones so we can do remote digital recording of our hearings. Believe it or not we were using cassette tapes and recorders prior to today and will still have to for any hearings that were started that way and not completed.
DS had his second swim lesson today and was totally into it, unlike last week when he absoluted refused to do anything but sulk in the corner of the pool and mumble.
DH came home with a smart phone this evening. He lucked out and got one of the three new droid phones delivered to Cosco. The saleman said he had a list of 500 people wanting a call when they came in and would only sell it to my DH if he swore he would not return it.
So all in all it was a good day.
-
Renrel that sounds like a wonderful day. Congratulations
-
Renrel, yay for a clean bill of health! I have a follow-up next week. I am hoping he wants to run some tests. He usually does blood work, but it's been almost 2 years since diagnosis and I would like to be scheduled for a bone scan. I think I want one to put my mind at ease. Also, I have had a headache for over 3 weeks straight, every day, for most of the day. I even wake up with it and go to bed with it. I think it's iron deficiency anemia which I was dx's with 2 times before, so I started back on my iron, maybe my recent surgery put me into the anemia again, so I want the doc to run some tests on my iron to confirm. Please let it be anemia!! I have been drinking lots of water so I don't think that is the reason for the headaches. I take a mulitvitamin (and vit D and Vit C and iron pills) everyday but maybe it doesn't have enough iron to maintain my levels.
Anyway, have a great day ladies, better get back to work....
-
Just checking in to say hi to everyone. Its been a good week. The meds are helping with the neuropathy pain so I'm back plowing away at work. One of those weeks it was possible to almost forget you ever had cancer. Certainly a week when I could not let the worry get to me.
-
Two years ago today I was diagnosed. My emotions aren't as strong as last year. I still feel "why me?" alot, and feel very sad that I may be leaving life sooner than I'd planned. But I'm feeling OK, and today at our block party my neighbors all were saying I look better than before my surgery, which is weird because I sure have my aches and pains and exhaustion. Not sure what to think of that. I do remember how stressed I was after diagnosis, and all the waiting, and the worsening news with each test. I'm so grateful for a good year after all the treatment, took some fun trips, got back into work, really appreciating friends, family--and of course the JANUARY JEWELS!!
LadyJane--I'm having renewed insomnia too! I wonder why. I slept pretty well last year, and now with the start of the new school year I'm having those 4 am wake ups again. It's exhausting. Maybe as the school year goes on I'll get back into a better sleep routine . Hope you do too.
Renrel-I so relate to your post about eating well. I try, but as I was reading the posts I was eating a handful of choc. chips! Great news about the all clear.
Jilly-hopethe headaches go away. Does a painkiller like advil help?
kmmd-glad you had a good week! I hope we all have more of those as time goes by.
Jess--that bike ride sounds hard! I bruise easily too. My platelets are within range and so are my rbc, but my wbc dropped 2 points over the last 3 months.
Hugs!
-
Kim, it's hard to believe it's been 2 years! that made me tear up when you said you are sad that you may leave life sooner. You WILL survive this, and you WILL live to be a very old lady. 2 years is a huge milestone! Isn't the first 2 years the most important for grade 3 girls (me too!). Because it's faster growing and more aggressive (wait, I'm going somewhere positive with this....) we have recurrences earlier (hmmm, wait, that was supposed to be a GOOD thing). What I'm saying is once you reach 2 years your odds for a recurrence plummet! I wonder if I can find the stats on that. Anyway, I think 2 years is a huge thing and I am so happy for you!!!!!!!
Thoughts of "why me" are completely normal and I think we ALL have those days. I know I do.
This time of year is so mixed for all of us Jewels, but one thing we should feel is proud of ourselves. If you think back, all of us would have loved to fast forward 2 years and here we are, we've come out the other side, stronger, determined to survive, with a lot more friends than when we started this thing! I am so glad we all have each other and that we carried each other through the fires of hell. I sure know you have all carried me at some point, with your kind words and inspiring stories, and just the fact that you were "there" for me. Hugs to everyone,
Jill
-
Jilly--THANKS. I needed your positive words more than I realized yesterday. I agree that these milestones bring up lots of feelings, and I'm sure they'll get easier over time. I've been thinking about that grade 3 and the idea that if it was going to spread it would have shown up by now. I like that idea!! And you're so right about being carried through those fires on the back of the JJs.
Today my husband and a goodfriend and I went to do the bike part of the mini tri I'm going to attempt next weekend. It was 11 miles on flat road, and I did fine but my butt is sore. The lake looks clean enough, but there were lots of geese and cormorants and ducks. Ick. I get to start at 8 am with this group:"under 18, disabled, and over 50". OK.
Have a great week!
-
Oh--and I'm in the over 50 group!
-
Lol, Bk! You go, girl over 50! Yeah, I just finished the route I am taking the kids on...which has now grown to 20 of them. I decided to simplify the route and go around it twice if I have to. I went about 13 miles and my legs aches. Good news, though....no bruises!
My two year comes up next month. My mammo is two days before THE phone call. Yeah, I'll never forget for so many days, weeks and even months it seemed every test revealed more bad news.
My oncologist said the same thing about the first two years being the time when the risk for cancer returning is highest........I'll sigh a bit of relief after my mammo.
-
I just started listening to an audio production of LIttle Bee. The character Little Bee, a Nigerian Refugee, askes the reader to think of scars a beautiful because only survivors have them. You have to live to have scars, dead people don't form them. I thought it was a good sentiment to share.
-
I just started back to work today just pt it was all I could find but a start to reclaiming my life.
-
Mnmom- Hows work going? It great that you are able to take this step back into normacy.
-
Renel,
It is far from what 'normal' was for me before...but my former position is taken. I've had to start all over again. It is an awful job but I am making the best of it, got to do what you got to do. I had lost so much of myself during my 8yr marriage & since BC (chemo brain & physically)...that this is really important to my & my childrens survival. My thriving will take quite some time if ever
...but I am determined. I remind mmyself of all the lines I've told my children...... keep your chin up, do your best, believe in yourself, work for what you want, ...etc..... Surely if BC has only taken it's toll on me (be it big or little) no job is gonna take me down.
kmmd, glad you had a better week!
-
I am going for my routine follow-up with my surgeon tomorrow. He's a bc specialist and follows his patients for life, so I have been seeing him every 4 months since diagnosis.
My question for you ladies, is there any tests I should be asking for? I had a bone scan, and ultrasounds and x-rays, all that stuff when I was diagnosed. I haven't had any tests since, and I am wondering if there is any "2-year" tests anyone else is doing. I have had headaches for about a month but I'm convinced it's my iron levels, so I'll ask him to check that. Has anyone had a bone scan since diagnosis?
-
So glad there are those who are making a stab at claiming back life. That is good. For today, life is wonderful. Day to day is so entertaining. I car pool with a young woman who energizes me with laughter. I appreciate that. Hugs to the JJs. At this moment, I am alive and life is good.
-
mnmom--glad you found a job, and hope it's going well. And I know what you mean about reclaiming our lives!
Jilly-My old onc didn't do any follow ups. Only with symptoms, or if the blood work is abnormal. Forgot to ask my new one, but I think she's the same--just wants me to have a mammo in Dec and another MRI next June. She said that after that I might not need another MRI because the high risk period of 3 years would be over.
Jess-glad you're feeling good today!!! And that you have a happy carpool friend.
I reclaimed a bit of my old self (and maybe more since I've never done this!!) by FINISHING the mini tri--1/4 mile swim, 11 mile bike, and 3 mile run (more like a walk/jog for me).There were 1,000 women, and we raised over $10,000 for the Breast Cancer Fund. I finished in just under 2 hours, and know I could have been even faster but I stopped to shower off before biking (just a couple others did). It was really hot for the jog part, and that was hard for me. I'm not a runner any more, especially with the pain I've been having in my ankles--anyone else?? I think it must be from the Arimidex or the Boniva, but I'm gong to ask my onc at next visit.
I'm tired--but it's a good tired and so different from the tired during tx year.
-
Berkleykim - Way to Go Girl!!!!!!!!!! You Totally Rock!
-
Well ladies, I had my CT of the Brain this morning. I got it because I have had a non-stop headache for about a month so when I saw my surgeon the other day he ordered one. I got in within 24 hours of the requsition being faxed, so glad there wasn't a long wait for that. The tech said my doc should have the report by the end of the week. Cross your fingers for me!
I personally think my headaches are from iron deficiency anemia, which I've had in the past (twice). He ordered bloodwork as well and I did that on Friday. Between the CT and the bloodwork I hope I find the reason for the headaches. I started on my iron pills 3 weeks ago in case it's my anemia, but no improvement yet.
The contrast dye injection for the CT was yucky, got an instant metallic taste in the mouth.
Hope everyone is having a great day, I will post when I know more.....
-
Hi guys,
I hardly ever seem to get the time to check in nowadays with work being so busy but yesterday was my second anniversary of finding The Lump and it made me think of you all again. I can't begin to express how helpful this forum was when I was first diagnosed. I have wonderful friends and family but no-one can truly understand what it's like unless they are going through it too. Thanks so much to Lisa for kicking off the January Jewels.
It almost feels like an emotional rollercoaster to read your most recent posts. I can relate to so many of the things you are all writing. In some ways it's hard to believe two years have gone by. In other ways it seems like a lifetime ago.
Like Renrel I also got a clean bill of health at my latest check up - last week. It's amazing how nerve-wracking going to visit the specialist is and when I come out I can't stop smiling because - so far - it's always been good news.
I spoke to a woman the other day who is five years post breast cancer and she told me you do eventually put it to the back of your mind and forget about it. Just two years on that's hard to imagine but I guess I'm reminded of it every day when I take that Tamoxifen pill or when I have a hot flash!
Anyway, just wanted to touch base with you all - my thoughts are with you all.
K.
PS - Have been blogging for a while about my exercise comeback (the comeback isn't pretty but I'm getting there): http://aplodder.blogspot.com/ -
My leg has been threatening to cramp at night for months and I always managed to stretch it out before it siezed up on me. Last night it seized and OMG did it hurt. I think it was at least a full minute before we managed to get it to relax with DH pushing on my foot and my trying to will it to relax and rub it. Does anyone know if this is a tamoxaphin side effect? I have to say I a little scared to go to sleep tonight, though this seems like such a silly thing to freak about after dealing with masactomies and chemo, but it hurt more than I remember either of those hurting.
This weekend we are having a party to celebrate my IL's 60th wedding anniversary. It is a couple of months early but this will be more convenient for most guests than the following weekend is DS 7th b-day. We are doing it in the house for the first time and I am a bit scared. We invited 14 or so kids and I am hoping a good number of them will be out of town for the three day weekend.
-
Good luck this weekend Renrel. I think I've heard of the cramps being a tamox SE. I know what you mean because you just described me to a T. I've never had such a bad charlie horse in my life as the one a few months back. Hurt to walk on that leg for days after. Had another hit this week but not as bad. You're right most of the time I can catch it. They started for me with the taxotere and never really went away. I've tried magnesium supplements and potassium rich foods can't shake them.
KM47. Congrats on an anniversary passing. I'm getting better at keeping the memories at bay, so I'm hoping a few more years will help and I'll be just like the woman you met who is 5 years out
I had a first yesterday. Had my hair cut. I've been getting it trimmed and shaped up while growing it back out. Went in yesterday and said, its too long, give me a cut. That felt like such a blow for normal life.
-
Leg cramps are a SE of Tamoxifen for sure. It's pretty common. I have those as well, every few months I will go through bouts where I get a leg cramp every couple of nights and then it's gone again for another few months. One night it was so bad that the next day I was practically limping, it was so sore for a few days I had myself convinced I had a blood clot in the leg! I think I read something about leg cramps and potassium as well kmmd.
kmmd, less than 2 years ago we couldn't imagine saying our hair was "too long". That's a great feeling. I am still growing and haven't really got a real cut yet. I got it trimmed up in the back twice and that's it. It's curly and almost to my shoulders now.
My CT report should be back tomorrow or Monday, I hope I get the all clear sooner than later so I can stop worrying. I am SURE it's nothing but my iron deficiency anemia giving me trouble but I am getting nervous that he hasn't called me about my bloodwork yet, he would have gotten them back already. I was expecting a call saying 'yep, you're right, your low on iron'. I did the bloodwork on Friday and I know he would have gotten it that day or Monday. Cross your fingers for me!
Hugs Jewels,
Jill
-
I have had horrible times with leg cramps. It is a horrible feeling. I have found plenty of stretching throughout the day and lots of fluids seems to mitigate the pain.
BK!! You ROCK! Good for you. Photos????????????
Kmmd---I have kept my hair short, and it is nice to keep it how I want it. So much easier to keep going with short hair.
Jilly- I still struggle with wbc- flu cycling around school and with every ache and pain I think I am going to get sick.Good luck with results of the cat scan.
Hugs to you all
-
Yes, leg cramps....My foot has been cramping too even while driving (yikes) I got them when I was PG & the doc always said it was calcium deficiency does potassium work?
jillyG thinking of you ...hope your results come in Fri.
-
Hi Everyone: Kim - is sneaking up on two years since my diagnose also. (Nov. 17th) I am still confused as to how they calculate survival years. Is it from date of diagnose, surgery, or end of treatment? Well anyway two years ago in Nov, I got "the call". Does not seem possible.
Good news is I am feeling great and very excited about walking/running in the Susan G Komen race for the cure this weekend in Hunt Valley, Maryland. Any Jewels planning on being there? Myself, my husband, one of my sons, my two daughters and my grandbaby are all walking for the cause. It is gonna be a great experience I can already tell because just picking up packets today was great fun.
Say a little pray that all goes well.
Thanks.
Patti
p.s. we raised about $1,000.00 for the cause. Woo Hoo!
-
LadyJane - WooHOO on the $1000 bucks!!!!
Today is my 2 year anniversary of "The Call." Given that it is the first day of bc awarness month I doubt I will ever miss noticing the day. I was thinking about that day and realizing that all my strong memories of reaction had to do with other people. I was home because it was the second day of Rosh Hashona. It felt like a weekend since I was home, so the call suprised me. I remember telling my son he had to leave the room and let me talk which hurt is feelings because I am always a wet noodle about stuff like that. Feeling bad for my doctor who had to give me the news and who felt bad about doing it while my son was in the room. My husband breaking down and crying while doing the dishes as I told him. I felt so bad because I was so calm that I did not even think about how the new wouid effect him. At that moment he thought I was going to die. By evening he had changed his mind, decided I was going to l ive and that we just had a really really tough year to get through. I remember calling my parents and being so glad that I had told them that I was going for the tests so all I had to say was that the news was not good rather than put the news into words. I remember my father taking the call because my mom was out shopping. I usually go through her on big things like that.
Those are the memories that are imprinted in my brain from that day.
-
ladyjane, congrats on almost 2 yr & the walk
Renrel, congrats on 2 years.
-
My Mom crying when I told her the news still bothers me more than the memory of hearing it myself
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