“I don’t expect to see a cure in my lifetime… but I will never give up hope.” Some conversations feel bigger than the milestone they represent. As we reach Episode 100 of the A Couple Takes on MS Podcast, we…
In this episode of A Couple Takes on MS, we’re honored to welcome Sarah Locke, founder of Locke’s Promise, a New Hampshire–based nonprofit born from her own lived experience with Multiple Sclerosis. Sarah shares how Locke’s Promise came to life,…
When Allié McGuire was 41 years old and learned the reason behind years of unexplained symptoms was Multiple Sclerosis, that moment didn’t silence her. It sparked a mission. Today, Allié uses storytelling to elevate voices and causes that often go…
You say flare. I say exacerbation. Or is it relapse? Whatever you call it, MS is progressing. All it took was the recent Healthline article Is an MS Flare-Up the Same as a Relapse? to make us remember that…
Always believe in the power of your voice and your story to influence change. Whether it’s at the local, state or national level, your experiences are valuable in making things better for you and many others dealing with the same…
We’ve never met Sarah Kirwan and Carl Deriso as a married couple, let alone had a shared conversation with the two of them. But less than two minutes into our chat with the Arizona couple, it was like we were…
This episode released on Valentine’s Day so of course it embraces a theme related to maintaining loving relationships when you or your significant other are living with Multiple Sclerosis. Just think about it: all committed relationships present their share of…
We all know Multiple Sclerosis is a relentless, unpredictable, frustrating disease. It can make living with it seem impossible, but we can regain some control in how we manage our MS. Shortly after she was diagnosed more than 26 years…
When people ask who in the MS community inspires us, Jenn Powell is always among the top names on our list. For real. Seriously. Jenn is for real. She is living with Secondary Progressive MS and truly speaks our language:…
It’s one thing to not be included in social activities, but the perceived intention shifts for people who are living with visible or invisible disabilities. Questions like, “How much did my disability play into me being excluded?” or “Do my…