https://www.youtube.com/watch?v=AglexvIBq8U #scleroderma #raynauds
I'd like say this in advance, this goes beyond simple personal reasons that affect my life as a primary Raynaud's patient, it also affects my ability to work or even functions in conditions some feel would be normal but I find extreme.
I wish I could say I was made aware of the first video of this great and wonderful channel (and, no this is not a plug, I genuinely like TLDR News) covering this subject, but I wasn't.
If you decide to watch it and how you wish to act is entirely your decision. What I wanted to say is that everybody is lucky who never has to experience how your body feels your fingers and toes are invaders in need of being stopped. That's what greatly halted me last summer.
I mean, I know it's weird to pray for rain in a place where it rains a lot, but with that, you know what you get. I will try my best to be as thorough and fast with my work, yet I still have to count for such occasions.