We can’t say enough about Tyler Campbell and the impact he is having on us and members of the Multiple Sclerosis community. You need to hear him for yourself. We are so honored to share with you in this podcast…
These three thoughts keep going through Jennifer’s mind after ever since Dan turned 50 in September: “Here we go again.” “If it is worth doing, it is worth doing again.” “Nothing worth having is easy to get.” Seeing Dan hitting…
We celebrated with the Multiple Sclerosis community as TG Therapeutics announced in the final days of 2022 that the FDA approved Briumvi (ublituximab-xiiy), putting the number of available MS disease-modifying therapies to more than 25. Hooray, right? Of course! But…
We’re going beyond New Year’s resolutions in 2023. Who’s with us? OK, so what we’re talking about technically isn’t a resolution. It really is more of a commitment to hold ourselves accountable to our personal challenges to improve ourselves in…
It’s hard to conceptualize, but Multiple Sclerosis doesn’t hold the market on our health concerns. In fact, we see other health care providers a lot more often than we connect with our neurologist. For real. On the surface, these scheduled…
New segment – MS in Their Voices – launches A new segment for our podcast is MS in Their Voices. This segment features the writing of MS authors who will read to you the powerful words of their personal essays,…
In this episode, we pull in our friend Louie Preciado to share his perspectives as a person recently diagnosed with Multiple Sclerosis. He was formally diagnosed December 1, 2021. This diagnosis didn’t stop him from achieving his goal to ride…
This one is another Ketchup Episode where Dan, Jennifer, and Ryan just chit-chat. This talk starts with the Digmann’s discussing their diagnosis of Covid. That leads into Ryan sharing news about his Grandma, it’s sad, so be warned. They do…
It’s one thing to connect with a mental health provider when you’re living with a chronic medical condition, but it’s even better when you find one who truly understands the realities you’re facing. Dr. Meghan Beier gets it, and the…
More than 22 years have passed since the first time we each heard the life-altering phrase, “You have Multiple Sclerosis.” That’s more than two decades, so conversations about being newly diagnosed with MS really have nothing to do with either…