Hello there community members!
It’s been awhile since my last post! For any of our new members, my name is Kaitlyn and I am the Public Relations & Marketing Coordinator at MSAA. It’s been so lovely to see this community grow and watch all of the wonderful support and friendships that have resulted over the past year!
As some of you may already know, MSAA is a member of the Spasticity Alliance, a group of patient advocacy organizations that have come together in support of those whose lives are affected by spasticity. If you would like to know more about the Alliance, feel free to visit their website at spasticityalliance.org.
The Alliance has asked us to share a story on their website from someone living with multiple sclerosis that regularly experiences spasticity as a symptom. You can see examples of the stories that the Spasticity Alliance has already featured on their website here: spasticityalliance.org/our-...
If anyone on this community feels comfortable using their name and sharing their story about their experiences with spasticity on the Spasticity Alliance website, please send me a direct message sometime this week. We can work together on writing a story so that anyone visiting the Alliance website with multiple sclerosis is able to see that they are not alone in their experiences with this symptom! If anyone has any questions, feel free to leave a comment below.
Thank you everyone!
-Kaitlyn, MSAA