Hypermobility Canada | Self Referrals Learn how to self-refer and see our Hypermobility team! Hypermobility Canada is a program designed to support individuals living with hypermobility disorders through personalized, whole-person care.

Hypermobility. Bookings can now be requested for a Core Assessment. Go to hypermobilitycanada.com/hypermobilit... Patients will get a written report to help them move into the next steps of care. #hypermobility #ehlerdanlossyndrome

Yeah it be like that sometimes.. #heds #sedh #ehlerdanlossyndrome #tattoolifestyle #tattooartist

Raising awareness one confused immune system at a time.
Join our support group 👉 www.facebook.com/share/g/1Abd...

#autoimmunedisease #chronicillnessawareness #immunesystem #rheumatoidarthritis #lupus #ehlerdanlossyndrome #sjogrenssyndrome #ulcerativecolitis

"It took 39 years for a doctor to actually listen; finally put my mental illness diagnosis to the side and focus on my physical health - or lack thereof. But, even after finally being diagnosed, finding EDS knowledgeable medical professionals was, and is, far from easy. Never mind figuring out how to pay for healthcare, especially since many of us are "unemployable," aka unemployed, and without insurance... And that is only going to get worse under the Trump administration and their funding cuts." - founder of The Zebra Alliance Community

Day 21 of #EDS & #HSD Awareness Month: Barriers to Care 👉 What challenges have you faced in getting diagnosed and the right treatment? People without EDS/HSD don't know, so we need to share our stories.
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Resources: @ehlersdanlos.bsky.social
#ehlerdanlossyndrome #hypermobilityspectrumdisorder

On parlera #EhlerDanlosSyndrome ce soir n’hésitez pas à passer !

Safe EDS Exercise Guide | Jeannie Di Bon Find out how to exercise well with EDS syndrome from movement specialist Jeannie Di Bon.

Low impact sports (such as pilates), tailored physical therapy, and sports like Tai Chi are perfect for many people with EDS. Ask your healthcare team/physical therapist about sports appropriate for you.

#EDS #ehlerdanlossyndrome #HSD #hypermobility #exercise #physicaltherapy

The rest of my life is suffering in pain because no one is willing to touch me and I have no money to pay someone to care #fuckthisshit #ehlerdanlossyndrome #mcas #itsactuallyworsethanyouthink #reasonsiwanttodie

Hello BlueSky,
We are The Zebra Alliance Community and we are excited to be here!
You can learn more about us here: linktr.ee/thezebraalli...
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#ehlerdanlossyndrome #raredisease #chronicillness #health

9 known and 1 unknown, so far!
Gotta keep the collection growing! 😂
#rarediseases #unknowndiseases #ehlerdanlossyndrome #Neuropathy #Raynaud's #medicalmystery #unicorn #zebra

Yep…

#fibromyalgia #ehlerdanlossyndrome #hypermobility #fatigue

Well I have a new pain from Ehlers Danlos Syndrome which is either Tietze Syndrome or Costochondritis which I have the Genes for both of because fuck this shit and my Great Grandparents were a bit inbred
#chronicillness #ehlerdanlossyndrome #disabled #fuckthisshit #costochondritis

I have applied to almost 20,000 jobs since July 2019.

Not a single job offer.

Have fun answering questions to INTERPOL.

#Discrimination

#EhlerDanlosSyndrome

#Nasdaq

#DowntownNYC