I have a
trigeminalTrigeminal neuralgia neuralgiaCluster headaches
Neuralgia
Trigeminal neuralgia v1.v2 L. It came on stereotypically but with eye movement pain. At present I am only with the eye movement pain, using the eye for any amt of time causes severe pain for reading, looking from one person to another and so on or if something moves in front of it. Also have severe
photophobiaPhotophobia . It is at present sole reason I cannot work.
I have a
partialPartial (focal) seizure
Partial thromboplastin time (ptt)
Thyroid gland removal sturge weber and
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
First-progesterone vgs 200
First-progesterone vgs 25
First-progesterone vgs 400
First-progesterone vgs 50
First-testosterone
First-testosterone mc surgery of decompressing the vessels around the
nerveNerve biopsy
Nerve conduction velocity stopped all pain including eye.
(have had repeated decompressions,rhizolysis with injury 7 and 9, MVD with 100% facial paralysis, , trigeminal tractotomy, dorsal column stimulator-lost to infection, (which helped), narcotics, psychotrophics, anticonvulsants biofeedback hypnosis acupuncture. (currently on neurontin)
The vessels grew back after first op and the pain returned. (verified by return vascularized hamangioma v1 v2.) No surgery was successful after. I am currently with a R cortical sensory stimulator implant and have been told motor stimulation is not worth doing.
We have considered blinding and paralyzing the eye.
Do you have any suggestions?
Thank you.
All surgeries, etc have been done at Univ. centers. The sensory implant in fact was experimental.
My understanding is that, since I cannot have an MRI because of the implant, a gamma could not be done.
about numbness in the face.
I am not a dr. but shared with her my expereince....
I have been recommended to cut the Trigeminal... but I am really wanting to rule out other pathological causes first... it is not always just the nerve as in my case
ANNG
about numbness in the face.
I am not a dr. but shared with her my expereince....
I have been recommended to cut the Trigeminal... but I am really wanting to rule out other pathological causes first... it is not always just the nerve as in my case
ANNG
Thank you for your reply.
As someone with a 25 plus year experience with trigeminal neuralgia I can tell you that no surgeon with whom I have ever spoken would agree to cut the nerve. There are so many procedures out there that this is something that is rarely, if ever, done anymore. The attendant risks are too great.
That said I am not a medical person and you have to trust your own doctor.
You may be interested in my book, A Pained Life, a chronic pain journey, about my experience with TN. it is the first and only book written on the firsthand experience of living with and fighting against TN.
I do not know if you can post the addresses here but if you google the title you will come up with the book and can read the first chapter excerpted online.
Also Yahoo has a terrific online TN support group and you may find that of some help with your current situation.
Thanks again,
Thanks for your reply, Carol