~Hypermobility EDS~For everyone with HEDS. Come here to talk about your daily lives, medications, doctor appointments etc. relating to this type of EDS.
Welcome To EDS-Kids
EDS Kids is a support group and community dedicated to helping children and young adult who suffer from chronic pain resulting from illnesses and genetic conditions like Ehlers Danlos Syndrome and Fibromyalgia. Ehlers-Danlos Syndrome (EDS for short) is a genetic connective tissue disorder which primarily causes chronic joint pain and joint dislocations. EDS Kids is a community dedicated to helping not only sufferers of EDS but their family and friends too.
I take
L-5-hydroxitriptofane
the name of the med itself is "Tript-OH" but i guess that changes from country to country.
that is quite mild, but they don't want me to take anything too strong...
Anyway it helps quite a lot.
__________________
Chiara, 18
EDS III type (or type I, they wonder about it)
Just Smile. ....and Always Stay Positive! Just think that life could be your worst enemy or your best love, it's up to you. And also the worst ailment could have its positive side.
I got diagnoised in June, so they haven't done anything for me.
A joint and muscles speclis diagnoised me, the doctors didn't know, which was really annoying.
I'm now trying ibeprofen (excuse my horrible spelling)
We have to wait and see if this works
Ouch. See Sophie, most of us are on high pain killers which can be VERY bad considering they are bad for you and they make us build a tolerance and soon we will have nothing to really work for us.
ANYWAYS- but as long as ibeprofen works for you...so be it!
Hope all goes well.
__________________ Brittany Lynn Stay Strong.
I am a site administrator and if you ever need anything please feel free to contact me.
"some of us are just trying to get through the day without falling apart."
A good friend is a connection to life - A tie to the past, a road to the future, the key to sanity in a totally insane world.
Its not working though :/
But mum is still making me keep on them. Pointless if you ask me.
I have tried a lot of stuff, but none of it seems to work :/
oh man. im on like 7 different kinds of meds, that i still dont know the names of by heart. i had oxycodone, i remember that one.
i used to take vicodin but it made me sick... it might have just been a wrong dosage?
i take tramadol after surgeries, and if my pain gets super bad one day.
i take 1200 mg of ibuprofen every day... as well as vitamin c. melatonin or something like that? and two migraine medicines b/c i get chronic migrains all the time from eds.
tramadol works wonders for me, but its not a good day to day medicine, it can make you kind of loopy sometimes =P
i was prescribed naprosyn 500 mg from my "family doctor" (i don't know whether this kind of doctor exists out of Italy)
(naprosyn = naproxene)
it is for rheumatic pain.
__________________
Chiara, 18
EDS III type (or type I, they wonder about it)
Just Smile. ....and Always Stay Positive! Just think that life could be your worst enemy or your best love, it's up to you. And also the worst ailment could have its positive side.
Dilaudid 4mg works for me as well as 7.5/700mg of Vicodin
__________________ Gwendolyn
*21 years old*
EDS (Hypermobility and Classical), POTS, NCS, CFS, IBS, GERD, Fibromyalgia, a sliding hiatal hernia, Depression, Gastroparisis
I am beginning to learn that it is the sweet, simple things of life which are the real ones after all.
~Laura Ingalls Wilder
The best and most beautiful things in the world cannot be seen or even touched. They must be felt within the heart.
~Helen Keller