Home Forums General Discussion Rash is starting to improve!!!

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  • #304587
    BJK7493@aol.com
    Participant

    Well the rash is starting to fade alittle but they bumped my steroids up to 65mg daily! I'm jumping out of my skin and already have the lovely moon face. We are still awaiting to see if we can get approval for for the IVIG.  Interestingly, my Rheumi agreed that mino helped my joints but said it did nothing for my dermatomyositis skin problems. He wasn't angry and even said he would refill the mino but could not give me the IV doxy.

    Hope everyone is having a great weekend.

    Julie

    #350501
    sjess
    Participant

    Hey Julie,

    That's great news the rash is clearing up a bit. I hope it continues. I can relate to how you feel taking that prednisone :shock:!  Hang in there.

    Hugs,

    Sharon

    #350502
    BJK7493@aol.com
    Participant

    Thanks! I don't know how long I can stand this high dose! He did give me some ATivan to calm me down which seems to help with the shakiness. How are you feeling? Can you tell any difference since the treatment?

     

    Julie

    #350503
    sjess
    Participant

    Hey Julie,

    I hope you are doing better on the prednisone. I know I always responded well to it though it was hard for me to sleep on it. Glad they have given you some stuff to counter the effects.

    I'm doing okay. Nothing big to report. I had several good half-days and then some not so good days. Today was pretty good. My hip/back is doing better so I am thankful for that. I hope that is due to the IV. The PT gals said that that was due to arthritis, so that would definitely be a good sign that the IVs are working.

    I'm just trying to be patient. 😕

    Take care of yourself!!!!!!! Please keep us posted on how you are doing.

    Sharon

    Oh, have you posted the pic yet?

    #350504
    BJK7493@aol.com
    Participant

    I'm glad you are doing good! My daughter downloaded the pictures but now I have to figure out how to get them to the Roadback website.  I will let you know as soon as I get them posted!

     

    Julie

    #350505
    lynnie_sydney
    Participant

    Julie – Tom (tbird) posted a 'how to post a picture' thread a while back. Here's the link: http://www.rbfbb.org/view_topic.php?id=2791&forum_id=1&highlight=post+your+picture Lynnie

     

    Be well! Lynnie

    Palindromic RA 30 yrs (Chronic Lyme?)
    Mino 2003-2008 100mg MWF - can no longer tolerate any tetracyclines
    rotating abx protocol now. From Sep 2018 MWF - a.m. Augmentin Duo 440mg + 150mg Biaxsig (roxithromycin). p.m. Cefaclor (375mg) + Klacid 125mg + LDN 3mg + Annual Clindy IV's
    Diet: no gluten, dairy, sulphites, low salicylates
    Supps: 600mg N-AC BID, 1000mg Vit C, P5P 40mg, zinc picolinate 60mg, Lithium orotate 20mg, Magnesium Oil, Bio-identical hormones (DHEA + Prog + Estrog)

    #350506
    BJK7493@aol.com
    Participant

    Thanks, I will have my daughter try putting them on tonight

Viewing 7 posts - 1 through 7 (of 7 total)

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