Q2. Have you dealt with the trauma from diagnosis? What did this look like for you? Are you still dealing with it? #ChatMS

Q3. Have you ever shared your story with others? Was it therapeutic? What were the outcomes? #ChatMS

Q5. Who has been the most supportive/influential person in your life following diagnosis? How have they impacted your life? #ChatMS

Q6. Final #ChatMS question… What are your greatest sources of motivation? person-place-thing What keeps you thriving?

Thriving Over Surviving MS I love the mantra - Thriving over Surviving - I needed to see this, Thx!

A diagram explaining how the protein EBNA1 from Epstein–Barr virus (EBV) could contribute to MS by enhancing the proliferation and survival of autoreactive memory B cells. nature.com/articles/s4157…

#ChatMS A1 I use the wrong words a bunch. Occasionally slurred speech. Nothing too wild thank goodness. 🤞🏻🧡

A2 #ChatMS Comes and goes

Is a cure coming? ⁦Dr. Brandon Beaber⁩ #curems youtu.be/j5JIlA2r1x8

A2 No more contrast if I can help it! #ChatMS

A new study reveals that in MS, damage to the myelin sheath causes increased levels of VLCFAs, which are converted into an inflammation-driving molecule called S1P, presenting potential treatment options. buff.ly/3NsBLdb #multiplesclerosis #msnews #msawareness #msresearch

Just because you can’t see my scars doesn’t mean they aren’t there. Living with #MultipleSclerosis is a never ending battle. Please be patient with me. I’m going through a lot more than you can see.

For the first time in its history, MS therapies are now included on the World Health Organization’s Model Lists of Essential Medicines. buff.ly/3Kt7s3X #multiplesclerosis #msnews #msawareness #mscommunity

Be the magic 😁🧡

Data on Lemtrada after 13 years. mean EDSS only increased from 2.7 to 3.1 over 10 years, but people who got Rebif for 2 years and then Lemtrada had similar results

MRI day. To contrast or not to contrast. That is the question! #multiplesclerosis #ms #MRI

Findings: No significant relationship between gluten and dairy in multiple sclerosis progression or quality of life. Not sure how I feel about this. #MS