In nov 2001 i was attacked with a baseball bat leaving work that fractured the left side of my
skullCranial ct scan
Malignant otitis externa
Skull
Skull anatomy
Skull of a newborn
Skull of an adult
Skull x-ray. after that i've had short term
memoryMemory loss
Mental status tests loss, and was unable to speak correctly, knowin what i wanted to say, i was able to write it down,It took me a while to be able to speak correctly. in sept 2002 i started to have
partialPartial (focal) seizure
Partial thromboplastin time (ptt)
Thyroid gland removal complex seizures which seemed to happen every other month with my menstral cycle. the
partialPartial (focal) seizure
Partial thromboplastin time (ptt)
Thyroid gland removal complex siezures progressed to grand mal seizures in feb 2003 and since then i've had another grand mal in april 2003 which started out as a
partialPartial (focal) seizure
Partial thromboplastin time (ptt)
Thyroid gland removal complex, withthe
partialPartial (focal) seizure
Partial thromboplastin time (ptt)
Thyroid gland removal complex i am unable to speak correctly and my right side is numb. i've had several mri's and eegs, the mri has shown a 5mm sized fluid spot. my questions are, will the seizures go away or will i continue to have them the rest of my life? i am taking dilantin 500mg daily. Will the short term memory loss get better eventually? does the 5mm fluid spot need drained? does my menstral cycle screw with the medician makein me more siezure prone? and lastly does weather patterens high or low pressure cause my "dent" fracture to ache or is that coincident? thank you for time answering my questions hope i have given you enough information. i have been seeing a nurologist since the first seizure, just for get to ask these questions with i'm there, go figure. Thanks again
http://neuro-mancer.mgh.harvard.edu/cgi-bin/forumdisplay.cgi?action=topics&number=33&forum=Epilepsy&DaysPrune=1000&startpoint=0
chad
There is a very slow "classic chat" room provided by the mgh people at:
http://neuro-mancer.mgh.harvard.edu/brainchat/
It is slow in the method used, sorry don't know the tech jargon. It is so painfully slow that I only last a couple of minutes, but there are usually people there and they are often the people from the forum I mentioned in the above comment.
They, also, provide an "Advanced chat", which is much better, but I have never found anybody in the epilepsy room. However, I have found people with epilepsy in the "main lobby".
If you want live support you can check out your local hospitals or EFA, or ask your dr.
I hope that is of help to you.
Hugs
To the original "comment poster" I hope you are getting better and if you need to talk about these things please post follows ups and there are lots of us that will pray for you and try to help. 8-)
chad