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Old 07-03-2012, 11:08 PM #1
xliquidx22 xliquidx22 is offline
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Originally Posted by ginnie View Post
Welcome to Neuro Talk. I am so sorry that you are experiencing all those symptoms at such a young age. In general county hospitals are not the source for diagosing neruological problems. I don't know if you can, but I would seek a teaching institute, and or Mayo Clinic. Your PCP could refer you to that facility. I went to Mayo myself, and did get a dianosis, and really good care. It would be worth the trip to any good location, to find out what is wrong with you. The not knowing is terrible. I can't believe they made you wait for 7 months. You can get into Mayo quicker than that. Have you had a lumbar puncture? What others tests have they given you besides the MRI? I hope you can find some resolution with your symptoms. Neruo talk will stick by you no matter what as you go through all this. I found this site two years ago and never left. It has been a souce of compassion and understanding. Glad you found us. ginnie

Thanks for the response ginnie whats a mayo clinic and where are they located? im broke so if its anything that requires money i wont be bale to do it , havent had a lumbar puncture they said its not needed since my MRI came back normal , ya the worst part of this all is not knowing what you have and just going crazy , the only real diagnosis i have is b12 deficiency at 242 but ive been taking b12 shots and lozenges for a month now with very little improvement also i wouldent imagine how symptoms like facial numbness,heat sensitivity,sensitivity to sound ,vision problems, fast heartbeats,feeling like passing out when walking can be related to something simple like a vitamin b12 deficiency , if was it indeed b12 wouldent a month be enough time to see improvement in all those? so confusing....
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Old 07-05-2012, 10:39 PM #2
xliquidx22 xliquidx22 is offline
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xliquidx22 xliquidx22 is offline
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mrsD is there anyway of getting a personal email address of a memeber here who doesnt post anymore? theres one member here with the name of nerveendings he posted a thread about b12 deficiency causing sensitivity to loud noises and light besides all my other symptoms hes probly the other only person ive came across who has sensitivity to sound and has b12 deficiency would love to talk to that guy and see how hes progress is going he would probly also offer valuable advice any way to get in contact with him?
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Old 07-06-2012, 12:28 AM #3
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Originally Posted by xliquidx22 View Post
mrsD is there anyway of getting a personal email address of a memeber here who doesnt post anymore? theres one member here with the name of nerveendings he posted a thread about b12 deficiency causing sensitivity to loud noises and light besides all my other symptoms hes probly the other only person ive came across who has sensitivity to sound and has b12 deficiency would love to talk to that guy and see how hes progress is going he would probly also offer valuable advice any way to get in contact with him?

Sorry we don't give out personal information.
You can PM (private message ) that member, here's the profile page link - http://neurotalk.psychcentral.com/member.php?u=38460
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