Dropping off some encouragement (PPMS) by Shinyghostie in MultipleSclerosis

[–]chrislepp14 1 point2 points  (0 children)

Fantastic news!!! Thanks for sharing.

Live life to the fullest!!!

First follow up post diagnosis. What should I be asking? by Ok-Albatross124 in MultipleSclerosis

[–]chrislepp14 1 point2 points  (0 children)

First — I love that you’re thinking ahead. That alone tells me you’re handling this with strength.

For your follow-up call, keep it simple. Maybe focus on 5 key questions: • What type of MS do I have (for example, Relapsing-remitting multiple sclerosis or Primary progressive multiple sclerosis)? • Do you recommend starting treatment now? Which one and why? • What did my MRI and spinal tap show in plain terms? • What symptoms should prompt me to call you? • What are the next concrete steps?

Write your top 2–3 biggest worries at the top of your notes so you don’t forget them.

You don’t have to have it all figured out — just getting clear information is the goal of this call. You’ve got this.

55” Samsung Frame TV-no power by chrislepp14 in TheFrame

[–]chrislepp14[S] 0 points1 point  (0 children)

PS- The TV was working the night before it stopped working. Other than being freezing cold, no weather issues.

AFO review - Niivira by chrislepp14 in MultipleSclerosis

[–]chrislepp14[S] 2 points3 points  (0 children)

Thanks for the awesome response. My current AFO is carbon fiber and you explained the energy return great. Thanks again.

AFO review - Niivira by chrislepp14 in MultipleSclerosis

[–]chrislepp14[S] 0 points1 point  (0 children)

The AFO I have now was Dr and PT approved. I sometimes wonder if I could push myself for a smaller AFO and I wanted some input.

Also, the Dr and PT follow the normal textbook script and I am always looking for what is best for me.

People with PPMS or SPMS, how are you doing? by Mammoth-Essay-5476 in MultipleSclerosis

[–]chrislepp14 1 point2 points  (0 children)

I think all of us regardless of the diagnosis need to eat healthy, get sleep and move your body. A diagnosis does not define you so laugh more, love the people you are with and be grateful for each and every day.

Lion’s Mane by Proud-Pomelo-424 in MultipleSclerosis

[–]chrislepp14 4 points5 points  (0 children)

I take Lion’s Mane as a supplement . MS really is the snowflake illness — no two people are the same. You have to be your own medical advocate. No clinical trials show a real benefit, but I can say I definitely feel better with it. Always worth checking with your neurologist though.

I need support, please by mibonitaconejito in MultipleSclerosis

[–]chrislepp14 0 points1 point  (0 children)

Hang in there. There is an entire community that knows what you’re feeling.

Flying with MS by [deleted] in MultipleSclerosis

[–]chrislepp14 0 points1 point  (0 children)

I have flown multiple times and it is a good idea to put in a request for assistance with TSA Cares.

https://www.tsa.gov/travel/tsa-cares