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Dear Norman,
Since this syndrome (The excruciating pain) was described in 1906, so many treatemt either fully or partially failed to controlControl Control rx it , and the main reason was not the pain itself but also because the thalamus is a compacted area with different functions ..so if a small infarction happen would not only affect one area e.g sensory but also may affect the mood, behaviour, or tolerability as well..so your tolerance threshold would be much lower compared to other people with central neurogenic pain..which lead to call several trials in thalamic pain as a failure or poorly benifecial...One of the last thing used was DBS a deep brain stimulation which helped other type of neurogenic pain , but with some negative remarks in cases like yours....try first to disscuss with your pain management specialist about the meds you used in the past and see if any of them could have been given more time to work better, then ask him about DBS.
I had a thalamic stroke 4 years ago and shortly after developed thalamic pain syndrome.
Sx I have are constant pins and needles on my left side, deep burning pain and tighting of my muscles.
To get relief from the deep buring pain I take 900 mg of gabapentin four tmes a day and lomotrigine 100 mg three times a day. These are anti-culvasants drugs.
When my wife had a stroke that hit her thalmus we found narcotics to be somewhat helpful & lyrica (gabapentin) was better. For better or worse marijuana worked infinitely better than anything. Fortunately, where we live one can get a prescription & marijuana is legal for medical uses.
I had hypothalamic lacunar stroke on 01/09/09 with subsequent thalamic pain syndrome on my right side arm/hand & leg/foot/toes. Constant tingling/burning/tightness/numbness & cold my entire right side of body. After stroke, my doctor immediately put me on 75 mg Plavix same day. After putting up with syndrome for 4 weeks, I went to my neurologist Thursday, 02/05/09 & told him the pain was really getting to me. He prescribed Lyrica 75 mg twice a day. He told me it would relive the tingling/burning, but not the tightness/numbness. He was right on! I've been on it for 3 days now and the tingling/burning sensations are just about unnoticeable now.
Hope this helps someone.
Since this syndrome (The excruciating pain) was described in 1906, so many treatemt either fully or partially failed to control it , and the main reason was not the pain itself but also because the thalamus is a compacted area with different functions ..so if a small infarction happen would not only affect one area e.g sensory but also may affect the mood, behaviour, or tolerability as well..so your tolerance threshold would be much lower compared to other people with central neurogenic pain..which lead to call several trials in thalamic pain as a failure or poorly benifecial...One of the last thing used was DBS a deep brain stimulation which helped other type of neurogenic pain , but with some negative remarks in cases like yours....try first to disscuss with your pain management specialist about the meds you used in the past and see if any of them could have been given more time to work better, then ask him about DBS.
Bob Hilton
Sx I have are constant pins and needles on my left side, deep burning pain and tighting of my muscles.
To get relief from the deep buring pain I take 900 mg of gabapentin four tmes a day and lomotrigine 100 mg three times a day. These are anti-culvasants drugs.
I would suggest seeing a good neurologist.
Pat Morlock
Good luck,
trustedfriend
Hope this helps someone.