#Medcan - #Vera - #MultipleSklerose & #EhlersDanlos #Cannabis #Freude #Leben #Medzin #Gesundheit
@karl-theodor.mastodon.social.ap.brid.gy
@karl-theodor.mastodon.social.ap.brid.gy
@ellkjell.eurosky.socialKanke vente til mandagens uambisiøse lyspunkt: legen var enig i at nok er nok så nå skal jeg få ha sekstimersdager i lang tid fremover 🥳 Og time til røntgen av en hel masse ledd. Og artrodese i foten over nyttår. Og skifte hofta om en god stund. Og fått meg fysiotimer. Bring it. #EhlersDanlos
@sammillinson.bsky.socialWhen the tremor in your leg makes you think that your phones going off but the phones actually in your hand...
@fernaenova.bsky.socialFound the big one with the screenshots and such
tagging again sorry #EDS #hEDS #ehlersdanlos #hypermobileEDS I'm posting this because I feel like the owner of this sub is not a safe person, and these subs often have people posting personal details or images.
@footdocdana.bsky.socialWhich one was your favorite? 🤔 #amazing #extraordinary #quirky #believeitornot #abilities #ehlersdanlos #hyperflexible #doctor #doctors #reaction #react
@halcionandon.bsky.socialI’d really like a chance at life.
I need a stable, safe environment. Without it, I will continue to decline & die.
#MutualAid #ChronicIllness #MyalgicEncephalomyelitis #MECFS #MCAS #POTS #EhlersDanlos #LongCovid #Endometriosis #ChronicPain #Dysautonomia
@richardmonvoisin.bsky.social#Kiné #santé #Ehlersdanlos #suisse
@ldruart.bsky.social @lvercueil.bsky.social
@richardmonvoisin.mastodon.social.ap.brid.gyqui pratique vers Vevey. Bonne écoute
https://www.ligues-rhumatisme.ch/news/syndrome-dehlers-danlos-quand-lhypermobilite-devient-une-maladie-invisible.html
@magicalunicorns.bsky.socialSo my kiddo was diagnosed with Vascular Ehlers Danlos and i have Hypermobile type. I feel for him and kids like him there needs more awareness so im posting awareness vids to platforms in hopes to help
youtube.com/shorts/izIHc... #ehlersdanlos #veds #heds #vascularehlersdanlos #awarenessmatters
@achronicvoice.com"“A bad #pain day is asking my husband to please not touch me, not even put a blanket on it. My #skin hurts so bad I can’t even take the weight.” – Gail W.": buff.ly/cSH28Q4
via @TheMightySite.bsky.social
#ChronicPain #EhlersDanlos #ChronicIllness #EDS #touch #InvisibleIllness