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Hi, just an introduction
Hi everyone! My name is Morgan and I'm new here. I joined to be able to talk to people with similar issues and get advice. Here is my story. I'm a school bus monitor and on 3/17 of this year I was attacked by a student. He beat my head off the inside window/wall of the bus and beat me in the head with his other hand. I don't remember most of it and the driver had to inform me of what exactly had happned. Initially it was diagnosed as just a neck sprain but as time went on it was diagnosed as a concussion but still ignored. When I went to the specialist he was very upset that it has been ignored for 2.5 weeks and said it was severe, and compounded by the fact I had a concussion 5 years prior. Fast forward to today, I've been diagnosed with PCS, and still have symptoms. Currently he's trying some prescriptions out, but I don't really know how well some of them are working. It's nice to meet you all, and I'll enjoy getting to know everyone. ^_^
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Hello Morgan,
Welcome to the NeuroTalk Support Groups. :Wave-Hello: I see you've found the TBI/PCS Forum and I'm sure you'll get lots of information and support from the members there. take care |
Welcome Akasya. :Wave-Hello:
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Nice to meet you!!
Morgan, :Wave-Hello: It is great to have you come and be with us. You will find a great number of dear friends to listen when you are in need of ears. Please let us know how we can help you out. You will find out we are supportive and relaxing place. Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
burning mouth syndrom
Good afternoon to all. I am a new member and very nervous because my mother language is french and I don't get to write english very often. Excuse my mistakes. I suffer of burning mouth syndrom since 5-6 years and I never had the chance to meet somebody that suffer the same sickness. I am medically treated at the Montreal General Hospital. I strongly beleive in support groups having myself with other patients created a support group in mental illness in my area.I have suffered before of a major severe depression for 13 years. Can somebody, with the help of God, get in touch with me if the suffer of that burning mouth syndrome because the doctors do not know wht else to suggest to me after trying all kinds of medication. I am waiting to see a specialist in ''medical cannabis'' to see if it could help me. The pain that I suffer of is rated 9-10 daily. PLEASE PLEASE SOMEONE HELP ME like the Beatles use to sing.:grouphug:
Robert (rocky) Brisebois |
Bonjour Robert, :Wave-Hello:
Welcome to the NeuroTalk Support Groups. You could try posting on the Peripheral Neuropathy Forum as there are posts there regarding Burning Mouth Syndrome. Another idea would be to do a forum search as there are posts by different members in different forums. http://neurotalk.psychcentral.com/search.php Just click on the links. If you need help navigating the forums, please just post again and someone will help you. p.s. As there are other medical illnesses where burning mouth syndrome may be a symptom, you could also look in that area. |
Welcome robert brisbois. :Wave-Hello:
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Nice to meet you!!
Robert, :Wave-Hello: It is great to have you come and be with us. You will find a great number of dear friends to listen when you are in need of ears. Please let us know how we can help you out. You will find out we are supportive and relaxing place. Please keep us up to date on your condition. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
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