Nicole's Myositis Blog

Nicole Smith shares her Myositis blog for Myositis Awareness Month and MSU’s #MyositisLIFE project. 

Diagnosed with Dermatomyositis in 2012, I was looking for an easy (and interesting) way to share my story with friends, family and the world. So I attempted the whole blogging thing. Any way to get info out about Myositis is a good thing!

Check out Nicole’s blog here: https://nikilee766.wordpress.com/2012/05/


 

Tags:

Author:

Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization Empowering the Myositis Community. Founded by Myositis patients, for Myositis patients, MSU provides education, support, advocacy, access to research and clinical trial matching, and need-based financial assistance.

View more information: Myositis Support

0 Comments

Leave a reply

Your email address will not be published. Required fields are marked *

*

This site uses Akismet to reduce spam. Learn how your comment data is processed.

© 2024 Myositis Support and Understanding Association (MSU). All rights reserved. | View our Privacy Policy, Terms, and Non-Discrimination policy. MSU is a charitable organization with 501(c)(3) tax-exempt status. Federal ID #47-4570748.

View COVID-19 resources and updates, and stay tuned to your state, local, and federal health agencies, along with the CDC.

Log in with your credentials

or    

Forgot your details?

Register for Free Membership

Send this to a friend