Author:

Jerry Williams, the Founder and President of MSU, was diagnosed with Polymyositis in 2003 at the age of 27. Since his diagnosis, Jerry has made it his mission to help others living with the rare disease, Myositis. To this effort, Jerry is involved in many different aspects such as education, writing, helping support and answer questions from patients and caregivers, social networking and website development, and much more. (NOTE: Some things are posted under Jerry Williams but he is not the true author. This is because he manages the website.)

View more information: Jerry Williams

5 Comments
  1. Renee Williams 2 years ago

    I was diagnosed with Dermatomyositis. I tried doing a full time sedentary job and went into a set back the first week. I had to leave the job. At this time, I did not understand why I could not handle the job. Now, thanks to you and other sources, I comprehend that stress played a major role. Thank you for sharing this information on stress and its effects on autoimmune. As for my coping skills, I turn to my faith. God gives me peace as I take one day at time along with acceptance of this disease (something that was difficult for me at the beginning). I look forward to reading more of the MSU site.

  2. James Hegarty 2 years ago

    Has anyone used Wellbutrin to manage the associated depression that can accompany the ups and downs of Dermatomyositis?

  3. Thelma Farfan 5 years ago

    I was recently diagnosed with polymyositis and im learning to cope with it althought at times it is very hard. Im on prednisone 60 mg. I find it hard to get around without the use of a walker, I am always scared of falling which I have several times and causes me to lose my confidence.

  4. Jerry Williams 13 years ago

    HI Karen and thank you for joining us! So sorry you have to go through all of this mess.
    I know, once I got down to 20 mg, my doctor started first by decreasing by 5mg’s until I got down to 10 and then did 1mg at a time to prevent any adrenal issues or cushings.

    Be sure to check out our Facebook Support Group: Polymyowhat: Understanding Myositis. It is a great group of over 120 people just like us!

  5. Karen Brown 13 years ago

    Thank you for being out there. I was diagnosed in June, 2013 with Polymyositis. Although I never had the biopsy that the doctor ordered. I did not need to have any other expensive test to give me a diagnosis, I had every symptom. The treatment would be identical whether or not I had the biopsy, so I have not done it. I wanted to treat the disease with diet. The rhuemotlogist told me that would not work. You fill me with hope! I am doing the Paleo diet, and am on 50 mg of Predsisone daily. I plan on tapering off slowly. Do you know of a safe taper schedule below 20 mg?

    Thanks for sharing your story, so others do not feel so alone.

    Karen Brown

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