Virtual Group Meetings Via Video Conferencing programs Like Zoom, Web-ex, and Skype will keep the sharing of information and support from group meetings. I have worked with several groups facilitating these meetings. Contact Mike Delp for help with setting up these conference calls.
In person meetings have started back up (Slowly)
South County (Affton), West County Welcomers, (Chesterfield), Casual Cup (Ballwin), Metro East (Swansea)
the remaing groups are still meeting virtually
Welcome to the St. Louis Area MS Community website. After being diagnosed a few years ago, and keeping quiet to what has been going on with my life, I posted an article on the Multiple Sclerosis .Net site about my journey with this disease, and showed social media the results. The responses have been awesome, and it made me want to push further to make it easier for others affected by this disease to have a source of information, and a place to speak out on blogs to let the world know what it is like to live with a serious illness, and share the obstacles that we face.
Editors NOTE November 1, 2020 the Celebrities with MS page has been updated with embedded links to your tube videos. Please check it out and let me know of other celebrities I can add to this resource.
I can be reached at mikedelp@gmail.com or admin@stlmsgroups.com
By phone 636-748-7345 Calls that from unknown numbers might go to voicemail, but i will check the Voice Mail and call back quickly. You can also check out the Contact Us link to get more information.
Everything is centered on the menu. Find it, and you can see links to the groups, or start with events to see what is happening in in chronological order (by date) sorry for the big words. Feel free to leave a comment on any of the pages or posts and i will follow up on it. The posts are my blog entries about my journey, or group functions or information relative to the MS community.
My husband have MS and ulcerative colitis
Debbie, Thank you for reaching out. Do you guys attend any of the Local STL meetings? The men with MS are definitely the minority. Stay cool this summer. Mike
I looked into this. How long do you need to take this set of herbs? Is it life long? He told me the cost and wanted to know how long I needed to do this.
Is this something you take the rest of your life or….?
Monica, I do not have any personal information on this. I don’t have Sully’s email to ask him.
good job mikey. makes me wonder if there are sites like this for my malady.