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I tried to post this reply to a comment to my MS story, but it was rejected several times. Can you tell me why? I would also like to know how some people use their full names an post their stories with pictures.
Thank you.
I tried to post this reply to a comment to my MS story, but it was rejected several times. Can you tell me why? I would also like to know how some people use their full names an post their stories with pictures.
Thank you.
This is the reply I tried to post:
Thank you for sharing that. I don't know that I've "met" anyone who's had MS longer then me, so I'm impressed, if I can say that! Is this pain from MS or something else... Am I just clumsy or is it the MS... etc, etc. It keeps me guessing. I don't bother with doctors too much because of my feeling of what's the point, there is nothing that can "be done" anyway, and I do fine most of the time, so there's really nothing TO be done, but EAT YOUR VEGGIES! Keep smiling!
I've had PPMS for almost 21 years 10 of those years I was misdiagnosed with rheumatoid arthritis. But I agree with you - why bother going to the doctors. It takes me longer to get out of my bed than it does actually being in front of my doctor trying to squeeze in as many questions or issues that I'm having before they say okay well next patient. I am the people that can just keep smiling ☹️. I'm in pain 24 hours a day and when you're hurting it's hard to smile, it's hard to get out of bed. Well enough of boohoo me. I would just like to wish Joy, Smiles, and Love to everyone who suffers from this to debilitating disease ✌️🌻
