loved the presentation.

I also am a member of PatientsLikeMe and it is a wonderful place because we all are sharing a disease and we help each other through the good time and not so good times, and we learn so much from one another, Presentation was "Awesome"......

I agree they cover so many diseases.

Hi Angela,



Good to see you my friend.....

I'm a member of PLM since 2007. At that time, we had 3000 members which has grown to over 14000! I find this site so beneficial in looking for the tools to cope with the disease. People post research and real-life patient experiences of current trials and treatments. Hope is a major focus of PLM and I encourage others to join. We are strong in numbers and we have a voice.
Great site.

Sean I am Charlene McNeil Pryor and I go by Pokie Too. I am in the Parkinson site with PLM. I too have been with PLM since 2007. It has been a God send to me and so many suffering....love pokie

I agree that patients like me is a great resource. There are so many symptoms listed. Only people who really have ms can understand the way it affects the body the mind, basically everything. When I do something stupid I can blame it on ms, or on being a senior moment.

PLM is a wonderful way to express what and how to live with this disease. It has changed my life for the better, have met wonderful individuals and we have shared, cried and grown by reaching out and expressing from our hearts, have made wonderful friends and have learned so much about the this "Silent Disease".
Have added Humor for we all need to laugh, it places a smile in our hearts.
I am one of those individuals that has a lot going on with this disease. Can't take any MS prescription drugs. I am very positive and driven and I will "Prevail" and I hold onto HOPE always.

PLM MS is a very special site and I am very glad to have found it. Although I am not on it as much as I would like to be, it always gives me wonderful insight whenever I need it.