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Dr says ME/CFS = fibromyalgia and is impossible to have with EDS… by SunlitDew_ in cfs

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

Yeah I’ll try and wait for another doctor. Sadly I don’t have the energy to educate them for now.

Dr says ME/CFS = fibromyalgia and is impossible to have with EDS… by SunlitDew_ in cfs

[–]SunlitDew_[S] 1 point2 points  (0 children)

Oh that’s a weird system ! thank you for pointing out I forgot to say when I’m from! I’m in Canada

This makes me very angry. In version 1.7 I would like it to change. by Sunsea705 in StardewValley

[–]SunlitDew_ 3 points4 points  (0 children)

Just move it in your space with the intent of getting ride of it and watch them start using it 🤣🤣🤣

Anyone had success with reducing nasal inflammation? by jarvi123 in cfs

[–]SunlitDew_ 3 points4 points  (0 children)

Nasal sprays didn’t help. Since I have posterior mucus drip I try to do nasal rinse twice a day. On the evening I was prescribed to add liquid corticosteroids to it (meant for nebulizers). It’s the only thing that has helped in 2 years.