@Jkoiou 

EditedLast reply

Jkoiou

Hello everyone

Hi MSers of the world. I just wanted to say hi, and that it is nice to know I am not alone in this silent, obscure, struggle... and neither are you. Personally, my RRMS plays a daily role in making me feel constant fatigue, random memory blips, and a lot of joint pains. But, I've learned that taking is slow, at your own pace, is ok. I was tested for 2 full years of MRIs and event told at one point I did not have MS, before a 3rd specialist said I had it, 100%. My question to you all is, how do you all deal with the daily ups and downs? Most days I am "ok", sometimes I feel the "tingles" all over my body, and 90% of the time my meds make me feel like I'm going through constant man-opause with heat flashes and lots of flushing (I'm taking Tecfidera). How I cope with it is "laziness", and having a fan literally on my face most of the day, even though I know exercise is the best medicine for us. My body gets tired very fast doing anything.
@DamianVaz

I've realized that I'm way more forgiving about myself taking it slow, or not having a productive day since my diagnost. It's ok to do things slow and on your time, that's how I deal with it.

1