My Personal Story of Disability With Narcolepsy and Multiple Sclerosis

Host Christina Brookman and Cohost Dr Nate Straus interview Eric Simpson about his personal story of disability with narcolepsy and multiple sclerosis. More information can be found on our website www.speakinginspoons.com

[@jobethdevore3913]

So many illnesses overlap too, it is hard for Dr s to discover these things .A Dr helped me find my immunodeficiency. There are Dr's out there, but because of legal and insurance companies saying where they can and cannot go and how much time to take a d just trying to full fill a percentage this happens.

[@jobethdevore3913]

I love your conversation, that is the best!! The way you guys are bouncing back and forth.

[@speakinginspoonsachronical216]

We have been having a lot of fun, been good friends for years so glad it shows!

[@jobethdevore3913]

I can't sleep much without a sleeping pill, but they say it's because of my TBI.

[@jobethdevore3913]

I was called a hypochondriac too. I hate going to the doctor so much.

[@speakinginspoonsachronical216]

its a shame so many people with chronic illness are called that when they are only looking for answers. hugs

[@jobethdevore3913]

I am borrowing that joke about the Corona beer and virus.

[@jobethdevore3913]

I like it, actually thought it was funny too.

[@jobethdevore3913]

I have taken the sleep test I snore, but I don't have to have a C-pap. My mother doesn't sweat much, and my grandmother did sweat either.

[@jobethdevore3913]

Like my mother, it's not fare but at least your not dead.sShe has had, so many car accidents.

[@jobethdevore3913]

We love board games too. If that applies.

[@jobethdevore3913]

He sounds like he is alot like me with his TOOLBOX. I do the same thing in way.

[@jobethdevore3913]

Do they know how MS starts in a person.

[@jobethdevore3913]

Please tell the DLCV if a place isn't accessible.

[@jobethdevore3913]

And polling places that you go to vote at.