"My name is Ayden Jude and I live with EDS, Ehlers Danlos Syndrome, a rare genetic condition that effects every part of my body, especially my collagen. I'm 29 years old and I was finally diagnosed at 27. I have many other chronic illnesses, but EDS covers a lot of them since it has so many co-morbidities. Everyday I deal with back And joint pain, muscle pain and spasms, joint instability, neck pain and instability, rolling and subluxing joints, heart rate spikes, blood pressure drops, dizziness, syncope, GI issues, mobility problems, and so much more. I get infusions through my central line to help manage some symptoms. I have multiple mobility aids to help with being independent and I have a task trained service dog named Lux Basil. Although EDS has completely changed my life, I'm learning my new limits and how to advocate for myself so much better than I used to. EDS isn't everything about me, but its definitely opened my eyes to a different part of life." @impossiblyspoonie
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#eds #pots #tbi #ptsd #adhd #pdd #autism #mooddisorderNOS #borderlinepersonalitydisorder #ocd #odd #psoriasis #muscularhypertension #posttraumaticheadaches #ticdisorder #torettes #ibs #GERD #delayedgastricemptying #restlesslegssyndrome #SCPE #osteoarthritis #tinnitus #chronicpain #port #salineinfusions #subclinicalhypothyroidism #nonbinary #wheelchairuser #servicedog
