MSU group member shares their testimony

This group of wonderful people took me in when was lost and alone and unsure of where to turn with Myositis. They educated me, cared for me and my family. They inspired and supported me and gave me a place to turn in the dark days. They gave me a place to vent when I was down on myself and depressed. They gave me a place to come when I needed to share my accomplishments and cheered me on. There is no way I could repay them for all they have done to give me the spirit to go on. As far as I’m concerned they’re as much of my family as my wife and children. God Bless them all.

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

© Myositis Support and Understanding Association, Inc. 2010-2018. All Rights Reserved. MSU is a patient-centered 501(c)(3) nonprofit organization.

You agree to our Terms,Privacy Policy, and Cookie Policy by using and viewing our site.

Log in with your credentials

or    

Forgot your details?

Create Membership

Join our email updates and newsletter

Subscribe to our general myositis-related email updates. If you are a member of MSU, you will automatically recieve these updates and there is no need to subscribe here. To register for your free MSU membership and access to The Myositis Community Network, visit UnderstandingMyositis.org/register

You have been subscribed successfully!

Please look at your entries. There was an error.

Send this to a friend