Donna G. shares an open letter, Dear Dermatomyositis

Donna G. shares an open letter to Dermatomyositis for Myositis Awareness Month and MSU’s #MyositisLIFE project. 

In January 2015 I was diagnosed with Dermatomyositis at the age of 36. Of course I never heard of it. My initial reaction was mixed with confusion, sadness and anger. However the one thing I knew was I was not going to let the illness completely take away my quality of life. My family and friends were not going to allow it either. I decided to write a letter to Dermatomyositis:

Dear Dermatomyositis,

I am writing you because I found out in January 2015 you were the culprit behind my rash and muscle weakness. Apparently you will not be going anywhere anytime soon. So I think we need to set a few things straight. I was told there maybe days that I will battle getting out of bed. My regular daily battles usually include trying to get my 8 year old to do his homework, my teenage daughter with her busy schedule, and maybe my husband with paint colors. I like to keep it that way. I understand you are going to give me bad days, here’s the deal, I like to have the last word. I also have determined family and friends.

When you decide I am not making it up the stairs, my husband carries me up. My husband has been through deployments, he does not find you intimidating one bit. On the days you take a smile away from me, I have two amazing kids that replace it instantly. When you decide that you will not allow me to pick up the slack in the household, my mother moved in to help me. Did I mention she likes to drive? You are not keeping me in on the days I need to get somewhere and it is difficult for me to drive. There have been a few nights you wanted to keep me up but I did not get frustrated. My cousin works third shift, we text through it.

I have numerous friends and family that have adapted to the unpredicted schedule you have given me. What I am trying to say to you is you have a wall of people to get through to bring me down. Since they are not fond of you, my advice is to keep the flare-ups to a minimum. This flare that has been lasting a year is pushing it. Please do not get too comfortable, I have a life to enjoy with incredible people.



Author: Donna G.




Myositis Support and Understanding Association (MSU) is a 501(c)(3) nonprofit organization with a mission to improve the day-to-day lives of Myositis patients. MSU is a patient-centered organization, founded by Myositis patients, for Myositis patients, and believes education, support, advocacy, and assistance are key to helping patients and caregivers. As a nonprofit, we rely on donations for funding and volunteers to help manage our fast growing organization.

View more information: Myositis Support

1 Comment
  1. Jerry Williams 2 years ago

    I absolutely love this Open Letter! Great job Donna

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