But see that could all be EDS .....especially the fibro as I was misdx'd with it too....
Do u mean mitral valve prolapse...that is EDS too....same with the CFS...
I also torn the meniscus in my knee from a drop attack and had to have surgery, was told yrs prior I had tarsal tunnel,...I did not, it was the Chiari causing the issues....did they do a EMG study on u?
Always had slow healing ever since I can remember! I never gave it much thought before. A simple scratch always ended up a scar, bruises lasting forever ...the list goes on and on!! It's all starting to make sense now! Thanks for the answers. I've been diagnosed with Raynauds migraines osteoarthritis asthma fibromyalgia chronic fatigue mortal valve prolapse svt osteopenia carpal tunnel ...and more!! Had both my knees with ligaments torn, you name it I have it...
The easy bruising is an EDS symptom...so is the cold feelings...or known as Raynauds....so u could have EDS....
Are u slow to heal too...ur bruises last a long time b4 they go away?
Hopefully my NL will be up to date about everything when I see him Friday! My hands and feet are always freezing cold and numb. They even turn white like no blood flow! I've always bruised very easy. My doctors office always thought I was being abused by my husband!
U do not have to have all the flexability to have it as there r many types of EDS...so, u should have it ruled out....I said the same thing when I was first told about EDS, and then I was dx'd with it....so u never know.
I don't think I have that syndrome! I don't have all that flexibility. Thanks for the reply though.
Hi u had asked this on the other thread ...but so others reading this as well.....yes, as Mel has mentioned above...Chiari symptoms do cycle.....it can be based on ur stress levels or ur physical activities.....so it may be helpful to see what ur triggers may be...this will help u avoid some of the flares.
Testing for EDS is very important...as it can affect how u feel and heal should u have surgery....
Symptoms can come and go and are often are stronger based on the activities we do/or don't do. Have you been tested for Ehler Danlos Syndrome? You mentioned body aches which I have all the time from EDS.