User Tag List

Likes Likes:  0
Page 2 of 2 FirstFirst 12
Results 11 to 13 of 13

Thread: Feels like a set back...

  1. #11
    Join Date
    May 2011
    Posts
    266
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    ok but with the drugs, how am i to know when i'm getting better?
    Experience is the only way to survive. <3 Rini Orange

  2. #12
    Join Date
    Nov 2008
    Location
    Maryland, USA
    Posts
    10,836
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Rini, there are 3 types of indicators that our docs use to measure disease activity: 1) Signs and symptoms, 2) Lab tests (eg, inflammatory markers, creatinine, urine tests) and 3) Diagnostic tests (eg CT scans, x-rays)

    The ANCA is one lab test that is just not accurate for most people.

  3. #13
    Join Date
    Feb 2010
    Posts
    286
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Quote Originally Posted by oaktreehill View Post
    Went to see the Reaumy a week or so back.. Was complaining that I have been on Methotrexate for a year now and feel no better at all.. I was on a pred reduction plan by 1mg per month and was down to 8mg per day although starting to get side effects when I reuduced to 8mg. Nose starting to run again and getting so tired and lethargic...

    I know I shouldnt moan when I go see them as they took me off methotrexate and bumped up my pred to 10mg per day.. And I was doing so well on the reduction plan too.. Did a blood test and if all is well the plan is to start me on Imruan later on in July. Now I have a fear of the unknown again!! At least while I was on Mtx I knew what to expect and it was only a once a week thing.. Not so sure about this daily tablet business of imruan or aza-blahblah whatever its called. Would love to know when this thing will settle down so I can be "normal" again whatever that is.....
    Oak, I hear you, it is tedious. I had to increase the preds and now on 6 mgs daily. so will try and go slowly again as my goal is to get off the preds. I take cellcept and look forward to getting off it. last week had pain on inhalation and was like pleurisy, so thats when increased the preds to 10 and then to 6 until see how I do. argh do hate this but just can go as fast as body allows. do feel better now but hate that its due to increase in preds. its like an addiction.

Page 2 of 2 FirstFirst 12

Bookmarks

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts
  •