Thanks so much for taking the time to send a message – sorry to hear that you have this stupid disease as well – it really can be truly annoying at times! I don’t know if you were aware, but I just wrote a book – it’s about my first years of having this disease. It can be found on Amazon: Segway Into My New Life: A Story of Diagnosis Perhaps there are some stories in there that you might relate to as well.

I hope you stick around! And keep going to the gym and moving. It is when I STOPPED moving (because i had to go back to work full time and being a singe mom, there wasn’t time for gym workouts and swims and that is when my pain started to creep in. It is for sure why it got so bad for a few years, but i’m thankfully now back out walking 3+ miles a day and along with cannabis, cbd, and diet it’s made a huge difference!!

Hey Bruce!
Can completely empathize about humidity. Having grown up on the East coast (and now visiting my folks back there every summer) I know it all too well. Although I must confess that when we do go now, I pretty much live at the beach and in the water to battle getting over heated. And to think that I used to head out almost daily for 6+ mile runs while there. Can NOT even imagine that at this point.

I know that for others it is the COLD weather that causes issues. I have to say that even with the vision tanking and other symptoms cranking up, I would take feeling hot over being cold any day of the week. But that is more because I have NEVER liked feeling cold irrelevant of the MS shit:)

Thanks for taking the time to read and share!

Cheers,
Meg (aka BBH)

Thanks for sharing Lisa!

Cheers!
Meg (aka BBH)

Cheers!
Meg (aka BBH)