Nicely done. I don't have EDS, and can't even begin to imagine how debilitating it is, but I have been in severe chronic pain since 21. Were you able to get SSDI and health insurance? Hope you're doing well.
Well said only people with EDS can understand people with EDS, and even then there are varying degrees of EDS with people affected far less than others. I have many dislocations per day, migraines that feel like my head is going to explode like a bomb, neurological pain and many more. I feel what you're saying and mean it. Thank you for the video.
As we all know there are many extremes of Eds, with many so affected that its not possible to function efficiently, no matter how hard they try. Lovely video which sums up chronic pain most elequently :)
i have eds:) and i dont take pain pills, and im a gymnast...i just pretend to be normal and do what i love!!! a lot of people are diagnosed with eds when they just have a little hyper extending joint...but i got it full blown!!! migrains and dislocations!!! it seems like this doesnt exist outside of my family...but yeah:)
I am a fellow EDSer in chronic pain and it affects every aspect of my life. Your video said it beautifully!
OzarksUSA 1 year ago
Nicely done. I don't have EDS, and can't even begin to imagine how debilitating it is, but I have been in severe chronic pain since 21. Were you able to get SSDI and health insurance? Hope you're doing well.
longlakeshore 2 years ago
Well said only people with EDS can understand people with EDS, and even then there are varying degrees of EDS with people affected far less than others. I have many dislocations per day, migraines that feel like my head is going to explode like a bomb, neurological pain and many more. I feel what you're saying and mean it. Thank you for the video.
Shandy1bob2 2 years ago
As we all know there are many extremes of Eds, with many so affected that its not possible to function efficiently, no matter how hard they try. Lovely video which sums up chronic pain most elequently :)
Elfins 2 years ago
i have eds:) and i dont take pain pills, and im a gymnast...i just pretend to be normal and do what i love!!! a lot of people are diagnosed with eds when they just have a little hyper extending joint...but i got it full blown!!! migrains and dislocations!!! it seems like this doesnt exist outside of my family...but yeah:)
amgymonkey 2 years ago
Said beautifully!
shellybeep 3 years ago 2
thank you i worked very hard on it
EDSGIRL021 3 years ago