ProDisc/synthes Problems

[Maria]

Was MS ruled out already by the Neuro? That would take a spinal tap I believe as part of the diagnosis ...

[Dlg2gldn]

I did have a Milogram after the surgery which came back good back in 2009 and think I'm on my way to another. They have never taken spinal fluid. When the Parkinson’s diagnosis was given all they did is a toxology on my urine.

[Maria]

A friend started to notice some weakness in his left hand when he played the guitar (dominant hand). He had a stiff neck upon waking at times and while didn't actually have pain felt that he had trouble positioning his neck for years while sleeping or to allow for a comfortable sleep position. He was diagnosed with cervical disc problems because he had disc changes on MRI. He was not recommended to have surgery as far as I know and he continued to have problems and progressive weakness. Finally he was advised to have surgery for his progressive weakness BUT he got a referral to a group at UCLA and someone decided to do a very full workup on him and including a spinal tap and lo and behold he actually had what was then called the "rare progressive form of MS".. (not called that now). This diagnosis came at least 3-4 years after initial disc related diagnosis (21 years ago).

I was just wondering with regard to your diagnosis. He had mostly weakness as his symptom and on one side of his body. Now it's well progressed into muscle wasting and he's in a motorized wheelchair most of the time.

It was thought that the MS might have actually stemmed from some orbital fracture he had in his face back when he was in his early 20's. You just never know what's going to happen in this life and why..

I know it's a bitter pill to swallow re what you're going thru.. I thought the same thing after my 2nd spine surgery failed and I was left with super horrific back pain and neuropathies that lasted nearly 17 years post 2nd surgery.

Again I do hope somehow things will get better for you and do keep plugging away the best able at having things checked out and "dealing with it" as best able too.

We do get some really crazy challenges thrown at us in this life though it's the only one we have so have to just keep "keeping on" and hoping a new day brings something better. That's what pretty much kept me going.

Again please keep us posted. I'm interested to read or hear about your endeavors and how things go.. good bad or indifferent. Wishing you all the best though!

Maria

[Dlg2gldn]

Maria,
This is all very interesting, l did specifically ask a movement disorder specialist at one time if this could be MS and was told no, but I've been misdiagnosed before.

More than anything I like to know if this thing in my neck is responsible for my pain, it sure seems like it! I'll keep you informed

[sahuaro]

I am very sorry to learn of your current problems post ADR.
And very concerned.
I had a Prestige-ST implanted at C5/C6 shortly before you had your surgery. I do not have the pain that you describe. But I have developed a tremor which waxes and wanes in intensity--it is worst when I am tired, dehydrated or very, very upset. At those times, I cannot write or lift a glass, etc. It is thus different from what you are describing, but it is a tremor. I did see a neurologist who sort of blew it off and just prescribed some sedative, which I haven't taken.

I wish Mark would weigh in as to whether he has heard of tremors developing post-ADR.

Please, please update.

[Maria]

Tremor Fact Sheet: National Institute of Neurological Disorders and Stroke (NINDS)

however if not please read.. it's good basic information

Barbara I'm wondering if the neurologist Mark knows in Germany ..Birnbaum??) might know more about anything like this since he might have been more informed with regard to the various cervical implants and possibilities... just a thought.

Hopefully Mark will see this thread.

[sahuaro]

Thanks so much for that link. I would guess that I was diagnosed with an essential tremor because he prescribed Propanolol.