When do start feeling better?
I'm almost to the end of my BC treatments. May 2nd will be, my last rad. Just wondering what will really be permanent side effects.. I'm on 11 of 25 rads
Tiredness is from rads. But sometime s my muscles burn and scream when walking up one flight of stairs. And sometimes my feet still fell tingly. I still dont like someone to touch my rt arm.
I'm not on tamoxifin yet.
I'm seeing a naturapath dr. next week. I feel better than I did before rads started
Looking back it feels like I've come so far..
Comments
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fredntan,
Congratulations on getting through treatment! It can be quite an ordeal. You HAVE come far.
I'm nearly four years out from diagnosis. What I can say, at this point, is that recovery time seems to vary greatly, and has a lot to do with your treatment and your reaction to the drugs you were given and the regimen your doctor prescribed. But good nutrition, regular exercise, and support from friends and family make a huge difference. Seeing a naturopathic dr. seems like a great idea.
At some point you'll realize that you're not thinking about your health or this frightening disease quite as often as you were. Keep focusing on regaining your good health. Sending best wishes for a smooth and speedy recovery!
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fred, the tired legs, for me, was a SE of the taxotere. According to my onc, it causes inflammation of the muscles. It went away fairly quickly, about 8 weeks or so. Just when I thought it would drive me around the bend, it eased up. It helps to keep moving, even if it is just a little every day. Also make sure to circle your shoulders, stretch your arms etc.
I am now 4 months past my last chemo, and 2 months past my rads and over all, I really feel pretty good. I have some slight, slight neuropathy in the tips of the fingers on my right hand, but not all the time. The nail on my right big toe still looks like hell, but is hanging on, hair is growing nicely, skin is fully recovered. I do still get sort of tired easily, and I can see from my latest blood work that my red and white blood cells are still pretty low. So hopefully I will feel less tired once I get those numbers up.
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You have come so far and congrats on that. I will be 2 yrs in July so maybe someone with more experience will chime in. I wish I could say that I feel awesome....the way I did before BC but I don't. I am on an AI and I know that has a lot to do with it but it does get better as the days go by. I still have some tingling in my fingertips and my ALND did a number on my arm...no LE yet but it does hurt. Rads left me with no energy but once I was done within a couple of weeks I started feeling better. Other than aches and pains ramdomly all over I have most of my energy back now and do everything I want to do. I do agree staying active helps but I think once you go through chemo it leaves lasting effects on us.
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Fredntan,
Septembersong said it very nicely. This is really the first time that I have seen others with a diagnoses that is close to mine.
I had mastectomy last April, chemo from May to Nov. then rads until mid January. Never broke down through any of it until about a month ago. On tamoxifin since the first of February. Coming here and hearing from others is the best thing I could have done. You can tell which forums to read on which days. If you are feeling down.....dont read the ones that will upset you. I was able to work through my 2 week funk that I was in from support of family and friends and this board.
Go to the American Cancer society webpage and sign up for "reach to recovery" they will match you with someone to talk to. Join any support groups that are in your area.............I have nothing due to the fact that I live in the sticks of Wisconsin and that is why I frequent the boards.
If you do not reguarly exercise........start now. My job is very active and we live on a dairy farm, so I thought that was enough. ITS NOT! Nothing better than a walk to clear your thoughts and stress. Wish someone would have told me that sooner and I could have avoided some of the tention.
Be sure to tell your onc of any medication that your primary doc puts you on. I was put on an antidepresant that would weaken the effect of the tamoxifin. Luckly I had only taken one.......Now Im on nothing except for an occational alprazolam for anxiety attacks.
Good luck to you.
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Your recovery really does depend on good nutrition, exercise and recognizing your limitations and not expecting too much too soon. I think I was pretty much back to regular life about 1 month after completing tx. The only ongoing issue I have is with my legs. Can't be sure if it was the chemo, Arimidex or just the natural effects of aging.
I definitely agree with Cindi. Walking is the best exercise for both the body and the brain. So keep moving!!
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I was wondering this as well. I will be finished with rads on the 23rd of April. Feeling great compared to chemo. But still finding it difficult keeping up with my 7 and4 year old. And since it is spring break from school I am really feeling it. Exhausted but really in a good way enjoying life a bit which a few months back I did not think would happen. But eagerly awaiting my energy to return fully.
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We're all so different! A/C wasn't that bad - lost hair, appetite and sense of taste and a little tired on day 3 & 4 but a nap took care of that. Surgery wasn't that bad either. # weeks after surgery started 12 weekly Taxol - all I could do for those 12 weeks was exist on the couch. A week after last Taxol I started feeling better. That was also the day I started rads and I kept felling better all the time. Also started Femara a week after starting rads. Felt better all the time til rads were over and I burned quite bad. But all that's done with now - next month will be 2 years since the deepest of the burns finally healed.
You might ask your Dr about adding a B Complex pill as it helps with energy. My Drs all said it was fine to take during TX but we are all different and our Drs are also. -
I take B complex. B6. Etc etc
I think I feelbetter tbis week compared to last . Had mylast big breakdown the weekofrads start.. Ready to start life again. 13 more rads to go. -
Pip,
Did you do any tamoxifin?
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