This question is mainly for fun... what is one small task that you've done recently that felt great?
cleaned part of top of stove
Just curious as to what my fibro friends do for fun. Im single, and between the pain, and anxiety levels I have im having a tough time. I read, and do cross words. I can't stand on my legs for a long time without being in pain.
I recently discovered adult coloring books and I'm really enjoying them , helps relieve my stress and take my mind off the pain , I love watching the pages come to life , it makes me feel like I… read more
I can't drive at nighttime as I struggle to see the roads and my balance is rubbish with the sun and the nighttime.
Yes I have it too.
I am so grateful for this site. Just wondered when Myfibroteam began?
@A MyFibroTeam Member
We are still buddies! Enjoyed the fun chatting too. Go Dawgs! Love and hugs! ☺🌹💤💤💕
I have had less flare ups over the past couple years. Odd because I'm now 43 and I've dealt with this since I started my period. The worst part of the flares were my skin feeling like I was rolling in small shards of glass. To be touched or shower or loose clothing were hell! To this day without a flare for months I will still fret a shower!! Once in there I'm ok but getting there is a struggle!! Also I met someone and being touched or just held feels so foreign and although it doesn't hurt I… read more
Yes, I have experienced it. It is hard to get over it. Talk with your new friend. Teach him how you like it. Have fun. Gentle hugs.
I am 18 yrs old and all of a sudden I’ve been sweating in my sleep? Like every single time I go to sleep does anyone else have this problem?
My doctor suggested Evening Primrose. It has helped a lot.
I just go with the flow,if I can't remember it right then I will keep thinking till I remember😊 it,I just tell people I am having a fibro.fog day...
I've had 8 chest infections & 2 kidney infections in 12 months!
No. I haven't been sick in years, even through COVID. I do wash my hands and mask when around sick people or just a lot of people.
I can never tell if my aches and pains are from the scleroderma or fibro.
Thanks and have a great day.
El
Oh no, I just meant scleroderma is an autoimmune disease and fibromyalgia isn’t. That would make me wonder what other autoimmune diseases they might have overlooked. Like your arthritis, is it… read more
Fybromyalgia, chronic widespread pain syndrome, arthritis, gyeany problems,4 sleep disorders, agitated depression,wonky liver , 1 foot long umbilical hernia 😟,PTSD,Costochondritis, spinal headaches
Tests are oh so fun, right? Lol
Sorry you had to to go thru that.
Most tests don't show much often. Fibromyalgia is more an illness that's a "catch-all" to say we tested you for everything and you… read more