Information on Cavernous Hemangioma
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Mycoplasma in synovium / cartilage/ Myelium sheath have compound excreations which can be tagged electronically for 3D modeling population densities at - and migrating between - affected sites IE spine / Knee etc. Especially in cases of traumatic paralisis where CNS regrowth is inhibited.
Mycoplasma are undetectable via standard lab procedures as they die so quickly. Mapping routes and high densities for intervention in real time may save mobility for many patients.
There are some connections to HPV / adapose / connective tissues and bacterial migrations /spread, MRI traces of combined elements or overlapping separate models have promise of high diagnostic accuracy /for treatment protocols.
Are there any research projects of mapping Human bacteria with MRI currently under study?
Thank You for your time and response
Will
Approximately 3 years ago I suffered a stroke which involved a hemorrhage in the brain. After many visits to the hospital and numerous MRI's, the problem eventually was diagnosed by a neurologist as a cavernous malformation. (Initially the bleeding was suspected to have been caused by a tumor in the brain.)
Within a month or so of my original stroke, I began to experience seizures...and tegretol was prescribed as my anti-seizure medicine. The first seizures involved a temporary numbnous in one of the arms, a drooping lip, a drooping eyelid, and a temporary loss of speech. My dosage of tegretol was increased from 1 pill a day, to 2 pills a day, and finally to 3 pills a day. 3 tegretols a day seemed to prevent any further seizures until December 10 of last year.
On December 10, 1999, I passed out in a restaurant. I was unconscious for 5 minutes or so. Paramedics were called and they revived me with oxygen. Because of my stroke history, they insisted on taking me to the emergency clinic. Neither the paramedics nor the doctor in the emergency clinic could find any apparent cause of the passing out. Nor could my regular doctor the next day. In each case, all my vital signs were normal. My regular doctor suspected, however, that the passing out was another form of seizure, different than any previous manifestations of a seizure.
Last week, I took another MRI as part of my annual medical checkup. The neurologist told me that he could see signs of a new bleed in December. Moreover, he suggested to me that the time for a surgical removal of the cavernous malformation had come. But, the final decision should be made by me because I am 74 years old this year. If I do not have the cavernous malformation removed, I am likely to have more frequent and more serious seizures. On the other hand, he cannot tell how many years of a quality life I will have even if the cavernous malformation is removed. (Except for the cavernous malformation problem, I am in excellent health and physical condition.)
The cavernous malformation is in the left temporal area. I would guess that it is located about inch or so below the skullbone.
What would you recommend that I do about surgery vs. just letting the malformation remain in place and hoping that the tetretol will prevent a seizure so bad that it will not result in either death or a major paralysis? I am looking for another neurologist's insight.
Bert