I have no dexterity. Can't type or hold glasses. Can't walk. My wife feeds me. Dresses me. Pretty much everythings me. Life is hard at times for MSers. Perspective and humor are keys. Fight on! And smile. #MS #MultipleSclerosis. #LifewithMS #ChronicIllness #MSwarrior #MSawareness

Shout out to PourBros for hosting, what seemed like, an awesome event! #MultipleSclerosis #MSawareness #PPMS yahoo.com/news/jeeping-m…

Fully-accessible resort, first of its kind, opens in Ely, Minnesota! #AmericansWithDisabilitiesAct #ADA mprnews.org/episode/2024/0…

I just registered for the upcoming #MSActivist Webinar: "Voting Without Barriers!" I hope you'll join me for the virtual event! Register today at: p2a.co/la0IHFZ

Patient liability, treatment adherence, and treatment persistence associated with state bans of copay accumulator adjustment programs | Journal of Managed Care & Specialty Pharmacy jmcp.org/doi/10.18553/j…

This study found that in states making #AllCopaysCount, patients paid 41%-63% less for their medicine. They were also more likely to keep taking their medicine correctly and less likely to stop taking it. #WILEG #MNLEG jmcp.org/doi/10.18553/j…

WOW --> "Copay accumulators were initially focused in specific specialty therapeutic areas, such as autoimmune diseases or #multiplesclerosis; however, use has expanded to other diseases as well". Isn't that discrimination & denial of care?jmcp.org/doi/10.18553/j…

ABC News should not influence your vote. Taylor Swift should not influence your vote. Your vote… is YOURS.

Update: CVS Caremark is now charging $7,636 for a $17 multiple sclerosis drug. CVS Health why are you marking up this MS drug by a record 47,000%? #PharmacistsFightBack

Hey Jaime Imitola MD., FAAN FANA do you know about this? Is there anything we can do to stop this?

Literally just testified about this yesterday for the Illinois House Committee on Healthcare Availability & Accessibility. Something has to be done. These back room deals that PBMs are directly impacting the wallets of patients. It’s time for #PBMReform! #MSActivist

Diagnosed with MS in November 2012 at 30 years old. One and only treatment so far is still Gilenya. You?

Thank you Rep. Jake Auchincloss 🟧 for continuing to highlight the issues of access & affordability of MS meds. The availability of generic disease-modifying meds should mean greater affordability for those with MS. 🚨The time for #PBMReform is now!🚨 #MSActivist

Good question - I introduced the bipartisan Pharmacists Fight Back Act to block PBM price-gouging abuses that raise premiums & co-pays and bankrupt community pharmacies. How you can help: call your Member of Congress & encourage them to co-sponsor the #PharmacistsFightBack Act.

nationalmssociety.org/news-and-magaz…

I’m up against the lobby for PBMs. I need 25 Ds & 25 Rs signed on by Thanksgiving — call your Member of Congress & ask them to sponsor the Pharmacists Fight Back Act, HR 9096. Use the hashtag #PharmacistsFightBack with the most appalling Rx drug markup you’ve seen. Keep the

The FDA, the US Food & Drug Administration, has approved the use of Ocrevus as a 2x/year '10 minute injection' vs an hours-long infusion. Ocrevus treats relapsing & primary progressive MS. This week a woman in Wales was the 1st in UK to get the injection. bbc.com/news/articles/…

We are celebrating with other #MSwarriors and supporters at US Bank Stadium in #Minneapolis after two glorious days of #biking . Thanks to the ⁦National MS Society⁩ for making the 2024 Tour of Champions a great success! #multiplesclerosis #IRideWithMS

The FDA approved Ocrevus Zunovo, a subcutaneous formulation of Ocrevus, for adults with relapsing forms of MS and PPMS bit.ly/3XkuP5e #news