She wanted to learn as much as she could about MS as she realized she didn’t know really anything about it. I was invited because I have MS and the podcast is called “Runners Without Limits” and this particular episode the host was covering her Dopey Challenge run at Disney and that she was running it with the MSAA to bring awareness around MS. Podcasts: Podcasts can be a great resource to learn from and a way to simply hear others’ stories about MS No one can explain themselves better than them so this is from their website: Mission Stadiums for Multiple Sclerosis (MS4MS) is a registered 501(c)(3) sports and entertainment-focused non-profit organization whose mission is to raise awareness of MS at all stadiums while raising funds directly for families with MS Warriors and for the advancement of research at the Johns Hopkins Project Restore MS Research Center in hopes of finding a cure. I discovered them on social and quickly began #SpreadingORANGE! It’s in my Amazon cart now!įundraising Organizations you can get involved with… She is another author as well that wrote MS Madness!, A ‘giggle more, cry less’ story of Multiple Sclerosis. I was recently told about her and quickly dove into her amazing website and blog filled with fun, light-hearted stories of life with MS. If you are looking to ‘find humor in a multiple sclerosis life’ look no further than Yvonne deSousa. writes about her MS, and others with MS, features books about MS and is an award winning author that tells her own story about MS.
So crazy you couldn’t make these symptoms up! Some are educational and I use them as guidance, other are humorous and keeps MS on the lighter side of things because if you think about it, it is a laughable disease. The best way I have found to stay tethered to this Earth and not lose myself in all the ‘what if's of having MS is by reading other MSer’s blogs.
There are great bloggers out there with MS! Truly a fantastic resource for anyone with MS (and their family members). They have podcasts, webinars, trainings, and guidance on what to expect when newly diagnosed. The Multiple Sclerosis Association of America is a great resource and they recently released an Ultimate MS Treatment Guide that allows you to compare drugs for disease-modified treatments. Looking for another great resource? The MSAA! The National MS Society is a fabulous place to turn to for information about Multiple Sclerosis! Where to start? The National MS Society that’s where In case you are - here are some links I find helpful along with some blogs and organizations I have run into that I have found pretty darn awesome to follow while having MS. You might just be here because you have MS and find my content of interest.
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