i had a spinal fusion (t2-t12) in 1999, following that i...
Posted , 3 users are following.
i had a spinal fusion (t2-t12) in 1999, following that i was diagnosed with having M.E/C.F.S, i have had terrible neck pain since dec 07, with numbness in my hands & i get dizzy often too. i have panic attacks because of this & am currently having c.f.s. physio with acupuncture weekly for the pain. my g.p has referred me to a rheumatologist, i am waiting for an appointment.
i am 30 years old & my neck & shoulderblades are grinding & make crackling/popping noises. the pain is unbearable & i have to wear a neck collar when its at its worse. i currently take co-codamol & seractil (dexibruprofen)
[i:58f80b74d0]This message was automatically imported from the original Patient Experience[/i:58f80b74d0]
0 likes, 3 replies
Guest
Posted
Hi,
I found this site by just flicking around on the p.c.
I have scoliosis and in july 96 had a spinal fusion (between shoulder blades)...things were grand for a long time.
the past year or so,the pain in my neck has been unreal at times,not to mention the headache!!
ive had medication for it,pain killers,synflix and anti inflamitry tablets,not that they work.... this week i went to the hospital and on the note the doctor gave me it says principal diagnosis,,,cervical spondylosis and thoracic hermivertabra...so im going for mri and ct scans etc..reading the comments left on this site i now realsie the pain down my right upper arm (when in bed) is probably due to the above. I now have to hold my arm up when im in bed!!
Im so bloody angry,with my parents for not doing more about it when the scoliosis was first diagnosed in my early teens(im now 37),for the doctors who did the fusion in 96,that they did not put rods or pins in the curve just below my neck,to prevent further misery.
Im fed up of listening to myself complain and being restricted in what i can do...(as i learned the hard way,i cant go clearing up the garden or moving furniture or ill be almost bed ridden for a week or two)
im sick of the constant aches....
I came away from the hospital with tears in my eyes...
anyway who knows what the next step id..the doc says surgery is far too risky.
so just thought id let off a little steam here.
hope you dont mind,.
feel free to e.mail me,or anyone else that want to.
me e.mail is ****
take care[/b:ad5ff7b369]
(Sorry but Patient Admin have removed either a telephone number, an email address, and or web address, from this posting, as it is the policy of Patient UK not to publish these on this forum.
If you wish to communicate directly with people, you should register, for free, with the forum (click Register in the menu list below the green banner above). You and other registered members will then be able to communicate with each other via Private Messaging (PM) or e-mail.)
VANESSA_JANE
Posted
chris215a
Posted