Jarjar or others ? about scalp psorisis

Discussion in 'Fibromyalgia Main Forum' started by ckball, Jul 22, 2006.

  1. ckball

    ckball New Member

    Jarjar you replied to my foot problem and said it could be a co infection, that is possible, I see the Infectious Dr on MOn to get my results.

    In the last month I have developed several patch psorisis.
    It stated after I had a tick in my head. I have had several this year so I don't remember if it was that spot exactly.

    While checking for ticks in my head, I found this bump. I picked at it fearing it was a buried tick or one that I didn't get it all out.

    Now it has spread. When I went to the Infect Dr 2 weeks ago and she said it looked like cradle cap and didn't seem concerned.

    A freind has psorisis on her arms or legs sometimes. I did not know it was an autoimmune dd.

    Could this be part of a co-infection? Thanks Carla
  2. ckball

    ckball New Member

  3. ckball

    ckball New Member

    bump - can anyone help answer this
  4. jarjar

    jarjar New Member

    I'm sorry to hear about the psoriasis. Some in my family have to deal with it.

    Once again I mentioned how the MP helped my feet well if you visit the board you will see many others with psoriasis and lyme, FM, cfs or sarc. Has to do with the inflamational bacteria. You might want to spend some time studying the protocol and decide if you are up for it.

    Victoria is on the MP currently if you want to discuss it more with her.

    Its a big commitment with light avoidance etc.

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