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 one of us, right?
Not so fast, we say.
Join us as we take a matter-of-fact honest look into the realities of living with an ever-changing unpredictable disease of the central nervous system. See why – with the experiences we’ve had – we conclude that no matter how long you have lived with MS, in many ways you forever can consider yourself newly diagnosed.
Here are the links to helpful MS resources we reference for you to follow up on:
• nmss.org – National Multiple Sclerosis Society
• msfocus.org – Multiple Sclerosis Foundation
• mymsaa.org – Multiple Sclerosis Association of America
• msviews.org – MS Views and News
• realtalkms.com – Real Talk MS podcast
• bezzyms.com – MS peer support community
• mymsteam.com – MS peer support community
• care.twill.health – MS health information