mcslo
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- New here and I don't know anything. I went through a chemotherapy treatment for hep c which kicked my butt. I can't seem to recover and no Drs seem to know what's wrong. I'm had to start 2 drugs for hypothyroid but still feel terrible and my body...
- I' m not on this side of DS much but I'm trying to learn more. What's the general consciences About Wilson's. I have read that most endo doctors don't believe it is real.I have been to 2 different endo drs and one says I'm hypo and one doesn't know...
- I just found out that karmah's son is in the hospital. She has been through so much with treatment and post treatment she needs all the prayers and good thoughts she can get
- Sometimes I feel like the left side of my head is going to explode. My body temperature runs 2 to 4 degrees below normal and Im always cold. I have body aches and pain and I have constant fatigue. My feet and legs swell at night and it is hard to...
- I was on 75 levothyroxine and 10 cytomel and switched endocrinologist. New doc took me off all meds and now I really feel like crap. I am suppose to wait until drugs leave system to take new labs. New doc can't see me for another month but I want...
- Do you think this applies to us Heppers ?http://www.theonion.com/video/aa-destroying-the-social-lives-of-thousands-of-onc,18349/
- I am now 8 months post treatment and no virus detected. If I knew then what I know now I WOULD NOT DO IT.I'm going to keep coming back to post here to warn people who are thinking about treatment. Read everything you can before making the commitment...
- I posted this about year ago but thought it was worth repostinghttp://www.elements4health.com/coffee-consumption-could-benefit-chronic-hepatitis-c-sufferers.html
- I don't want to take people away from this site (I don't know how I would of made it without all the support from here) but these are interesting post from another site.People need to consider all possibilities before treatment. I was one person who...
- http://articles.mercola.com/sites/articles/archive/2010/10/13/soy-controversy-and-health-effects.aspx
- I think I just joined this group both on ds and physically . I seem to have the symptoms. 6 months ago I completed a chemotherapy treatment for hep c. The DRs arent sure but my immune system seems to be attacking my thyroid.My liver dr, my GP doc...
- For the first six weeks or so after tx I felt better each week. Since then I've been going down hill. Now I have joint pain, muscle aches, fatigue and loss of any motivation.My muscles seem to tingle all the time and my feet seem to be swollen in...
- Im four months post treatment and still have many of the symptoms of treatment. I have joint pain, extreme fatigue, loss of motivation, brain fog and want to sleep more. It's hard to work and hard to do most of the stuff I use to do. I have been...
- I haven't been here much lately but I thought this is worth sharing with my hep friends:Imagine that you had won the following prize in a contest: Each morning your bank would deposit $86,400.00 in Your private account for your use. However, this...
- I was looking for that trial from Brisol Meyer Squibb that woman did for a week and was undetecable with no side effects. I didn't find it but these are sure looking promisinghttp://www.hcvadvocate.org/hepatitis/hepC/HCVDrugs.html