Dalton, I just tried to mail an answer to a message and it was addressed to exactly the same people as you have mailed this message to, only mine came back as undeliverable. I used the same addresses as you have used. Is there anything you can do to help me? To answer your question, I thought the same thing. I mentioned electrical stimulation to my Dr. and she didn't seem too interested in it. I didn't think about the hyperbaric chamber. I was in one before, but don't remember what it was for. Maybe pressure sores that I got while in the nursing home recovering from surgery. I hope I never have to go back. Thank you for responding. I'm not used to being back here yet. Is there still good information coming through as far as changes or innovations regarding TM? It's good to hear from you. Judy in Michigan In a message dated 1/16/2013 12:53:54 P.M. Eastern Standard Time, [email protected] writes:
Judy; When at Texas A&M and dealing with migraines I would be put in a hyperbaric chamber where the pressure was set to two atmospheres in a pure oxygen state. And there beside me was this A&M football player with a broken leg. They used that device to greatly accelerate healing. While that may be unobtainable, small levels of electric current and/or magnets have been shown to work in boosting bone healing. Dg Dalton Garis Flushing, Queens New York, USA Mobile: 718-838-0437 From: <[email protected]_ (mailto:[email protected]) > Date: Wednesday, 16 January 2013 12:48 PM To: <[email protected]_ (mailto:[email protected]) >, Dalton Garis <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) >, <[email protected]_ (mailto:[email protected]) > Subject: Re: [TMIC] need for a neuroloist We are talking about the need for a neurologist. I just saw mine yesterday. For my pain he recommended a pain pump. I'm going to have a trial pump put in to see if it will work for me. If it does, they will implant a permanent one in my body, next to the spine with a catheter leading out to my abdomen where the pump can be refilled periodically. The medication last about six months before it must be refilled. I have so much pain because I have a broken leg that is not healing. It's been almost 1 & 1/2 years. The pain is intense on top of my TM pain. I'm taking strong medication to just get by. Guess I 'talked' your ears off. Will go for now. Judy in Michigan In a message dated 1/16/2013 8:16:47 A.M. Eastern Standard Time, [email protected]_ (mailto:[email protected]) writes: The description you gave sounds familiar. I didn't and could not have gone back to my banking job. My biggest anxiety in the early days of TM was my inability to think. It took four months before i could read And longer to comprehend. I got stuck or stumbled on words when trying to talk and literally sounded drunk. Had a hard time between left and right. Couldn't follow directions. Got lost in buildings, because I always turned the wrong way. Did things backwards. I had to have a note for everything. I worked hard to overcome those issues. I sat for hours reading tmic and the TM forum. Typed with two fingers to write my posts, tried for days to make a flow-chart, and even had a nine year old come after school two days a week to play kids games and build items with Legos. I felt like the steroids fried my brain. I'm much, much better and thank God everyday for the improvements. Patti V - Michigan Sent from my iPad On Jan 15, 2013, at 10:44 PM, Dalton Garis <[email protected]_ (mailto:[email protected]) > wrote: Cognitive problems, did you say??? Please elaborate. I was a high-flying associate professor economist in an engineering school when getting TM in 2010. Then I began to experience the unthinkable—literally. I could go into class and do the entire lecture from my head. But after TM I would get to a point in the delivery when it was time to pull out some element from my head and, it wouldn't be there! It had always been there, but now I couldn't recall it. It was shocking and humiliating to say the least. It finally did me in. Please tell me about these cognitive problems you mentioned. DG From: <[email protected]_ (mailto:[email protected]) > Date: Tuesday, 15 January 2013 9:53 PM To: tmic <[email protected]_ (mailto:[email protected]) > Subject: [TMIC] need for a neuroloist Resent-From: <[email protected]_ (mailto:[email protected]) > Resent-Date: Tue, 15 Jan 2013 18:53:27 -0800 I had the same neurologist for first five years of TM. I had several MRI's and he was satisfied that I didn't have MS (TM left me with cognitive problems). I had been on the same medications for two years, my primary said he would renew my rx when needed, and I didn't feel the need to contnue seeing my neuro (140 mile round trip). That worked for another two years until my primary moved and his replacement refused to write my rx for the Lyrica and Baclofen. She referred me to her neuro buddy, but I made an appointment with another neuro whom I had heard was "the best" from one of his MS patients. The new Neuro agreed with my med regime, agreed that there was no need for MRI's, and agreed that I didn't need to see him oftener than annually unless I had neurological changes. The new neuro also understood my frustraton with a primary who would not renew my Lyrica and Baclofen rx. I never went back to that primary and have since seen a Physicians Assistant for my regular illnesses. I didn't think I needed a neurologist. However, I realize that as long as I need Baclofen and Lyrica and it is wise to have one available. Patti V. - Michigan =
