You’re in luck! I volunteer as a Disability advocate for EDS and Rising Voices of Narcolepsy.There’s a test for EDS called the Beighton Scale. If you have all 9, it’s a guarantee for the hypermobile type of it called hEDS. Even if you’ve got 5-6 on the scale, you probably have it. 9 is the worst, what I have. I’ve needed multiple surgeries and was designated as fully disabled by a judge in my early 20s.
Having answers brings peace of mind, but what’s even more important is that your treatments will change. People with Ehlers Danlos Syndrome ABSOLUTELY CANNOT use the antibiotics in the Cipro family. It causes vein collapse, circulatory system leakage, and aortic aneurysms. It can kill you. You also can’t do most stretches, so Yoga is a no go and physical therapy can only focus on strengthening your injured areas.
Here’s the test. Hope it helps!
https://www.ehlers-danlos.com/assessing-joint-hypermobility/
I’m immunocompromised and still mask indoors. I haven’t been sick at all since 2020 and it’s awesome! Between 40-60% of people have some form of permanent brain damage and 70-80% have long covid problems from Covid. The damage to the body compounds every time a person gest re-infected, so the numbers are terrifyingly high.
I have a postmortem science degree and it required 4 years of pre-med/pathology. With all that and what we know about the virus, I am honestly not sure I’ll stop wearing a mask indoors until we find a cure or better vaccine. I can’t stand that politicians are trying to ban masks, essentially sacrificing the elderly, disabled, and ill. A government making medical decisions, creating an environment where a person can’t mask up, regardless of if they have cancer and want to stay safe; or if they’re severely sick with something else but need to pick up medication at a pharmacy… it’s dark. It’s fucked up