i was told i have a pinched nerve in my neck
Goodness this is going on for some time now, unless u had a break in there?
What has ur Dr said in regards to this symptom?
I have not had the "dead" feeling, but the weakness to lift something like a teacup, I have and it is not fun...plus it hurts....and u feel so helpless...
Have u been dx'd with Ehlers-danlos?I know I asked this b4, but wondered if u have been to the dr since?
"selma"
oh dear, my arm has now had the 'dead arm' feeling for the past 3 days, my wrist is painfull and even lifting a cup is putting strain on it. feel like one giant bruise.... ;-(
Ah cause i also have hypermobility [ mild ] along with skin elasticity or sumin like that, the reumo diagnosed that last year. i'll have a look at the link now thanks Selma xx
I am sure what u r experiencing could be either of the 2 or something we haven't considered.....
EDS is first dx'd with a neuro exam, then confirmed getting a skin biopsy...A NL does the initial exam, sends u to a rheumatoid Dr who in turn sends u to a geneticist....
There r many types of EDS and like chiari no one will have all the listed symptoms.
Here is a link where they added criteria for hypermobility to the EDS testing.....-http://www.reumatologia-dr-bravo.cl/para%20medicos/crit%20y%20diag/DIAGCRITJHS.htm
"selma"
Hey Selma, erm i it's like my muscles are burning but then the sharp pain is in my knees/ankles/wrists ..... but the comes and goes intermitdley if that makes sense.
How do docs test for EDS and is that something that is connected with chiari, im more leaning towards the nerve and spinal cord impingment i have, im womdering could this be now compressing causing this pain?
Hi....is this more in ur muscles or joints?
If it is ur joints, I would say have ur Drs look into EDS- Ehlers-Danlos Syndrome....it is a connective tissue disorder that can abruptly flare up....
I have noticed the sharp pains in my ankle as I sit...and it hurts quite a bit....I also have TC, so I am not sure if mine is brought on by the TC or EDS but if it is my joints, I feel it is the EDS.