Thanks, Be interesting to hear what he says. I've got Type 2 Diabetes as well but there does not seem to be a definite link between the two or I can't find any papers on a link.

Frank

--- On Thu, 18/6/09, Gregory Nail <g.nail@...> wrote:

From: Gregory Nail <g.nail@...>
Subject: RE: [Cervical_Spondylosis] New to the group but not to the disease
To: Cervical_Spondylosis@yahoogroups.com
Date: Thursday, 18 June, 2009, 3:26 PM

Hi Frank,

 

I think you may be correct about some people producing more calcium than others.  I’ve always produced extra calcium in my teeth.  I now have osteopenia and am taking calcium and vitamin D which surely cannot help my spinal issues.  I take it largely because I cannot do enough “ground pounding” exercise (due to my spinal issues).  I have to strengthen and lay down calcium on my hips but I don’t want to be causing problems in other areas by taking lots of calcium & vitamin D.  I will discuss this issue with my endocrinologist.  I will let you know what he says.

 

Best regards,

Greg

 

---

From: Cervical_Spondylosi s@yahoogroups. com [mailto: Cervical_Spondylosi s@yahoogroups. com ] On Behalf Of Antstig
Sent: Wednesday, June 17, 2009 7:58 AM
To: Cervical_Spondylosi s@yahoogroups. com
Subject: RE: [Cervical_Spondylos is] New to the group but not to the disease

 

Hi Greg, thanks for that. My neurologist said that it's a spur between c5 and c6 which was not a problem until I started to shrink as I was getting older. I thought oh charming not only this but to be told it's due to advancing old age loll.   This interests me as I had capsulitis a couple of years before. From what I gather the body lays down calcium deposits due to joint inflammation. I'm not convinced and wonder if some people have higher levels of calcium than others.   Frank --- On Tue, 16/6/09, Gregory Nail <g.nail@sbcglobal. net> wrote: From: Gregory Nail <g.nail@sbcglobal. net> Subject: RE: [Cervical_Spondylos is] New to the group but not to the disease To: Cervical_Spondylosi s@yahoogroups. com Date: Tuesday, 16 June, 2009, 6:34 PM Dear DM,   Thank you.  That is very kind of you.  You are very caring…again thanks.    I take Neurontin (it also helps prevent my seizures) and Baclofen to decrease my spasticity which allows me to walk, not have arm spasms/tremors, etc.    Thanks to my oncologist, who was my only physician willing to manage my pain; I wear a Duragesic pain patch and use Percocet when needed.  He was “pissed” my neurologist was not willing to manage my pain when without it my body is absolutely racked with pain.   Thank you for caring.  Thank goodness for doctors who care greatly about their patients.   I wish you and your loved ones good health and happiness. Greg   From: Cervical_Spondylosi s@yahoogroups. com [mailto:Cervical_ Spondylosis@ yahoogroups. com] On Behalf Of Teddyberen@Aol. com Sent: Monday, June 15, 2009 10:32 PM To: Cervical_Spondylosi s@yahoogroups. com Subject: Re: [Cervical_Spondylos is] New to the group but not to the disease   Greg... Welcome to the group.    I want to wish you well and for you to have some pain free days.  Thank you for sharing your experiences. DM In a message dated 6/15/2009 11:08:38 P.M. Eastern Daylight Time, g.nail@sbcglobal. net writes:   Hello All. My name is Greg. I was diagnosed with Cervical Myelopathy, myelomalacia, cervical stenosis, spondylosis, hypertrophy facet disease, degenerative disc disease, etc. I have been battling the symptoms and dealing with the effects of the disease and the surgeries since 1999. I've had 4 cervical spinal surgeries, but I have pain and problems throughout my entire spine. Like most I began having tingling in my fingers, I began dragging my right side & hunching over like Quasi Moto dragging my right leg. The more tired my body was the worse I dragged around. My legs felt heavy. I lumbered around like Frankenstein. At the time it was unknown to me but cervical stenosis at the C3-C6 level had gotten so bad it permanently damaged the signals sent & received between my feet and brain. What that did was make me fall when the grade of the sidewalk leaned to the side, forward or back. I would lose balance and stumble, often times unable to get my footing back before I fell. I was seen by several neurosurgeons and even 2 of the surgeons suggested a particular surgeon for this job. Both said and my neurologist agreed that he is the best in the area for this type of surgery. I went forward with him and had an ACDF (anterior disectomy & fusion) of C3 - C6 which worked great for about 6 months. My symptoms were all returning. By month 8 my neurosurgeon was suggesting a second surgery to C7 and to clean up osteophytes that had grown back in the C3-C6 area. His suggested method was to do it from the backside, a laminectomy. I told him the solution was not to have a surgery every 8 months. After postponing a several months, due to several reasons, I became as bad as or worse than I was originally. During this delay time the neurosurgeon identified that C7 was severely herniated. To make this story a little shorter, the surgeon failed to correct C7. I got worse and worse. The surgeon did everything in his power to avoid letting me know that C7 had NOT fixed. My next choice surgeon leveled with me what had happened by requesting and studying an MRI. He requested a myelogram but the stenosis at C7 had gotten so bad that the contrast could not even get past the area. I now had proof and he admitted only working on C3-C6 but now denied C7 needed any attention (although previous MRIs said differently) . He told me there was nothing else he could do for me. I did not want to sue I just wanted to get fixed. I contacted 4 neurological groups around the country known for fixing "botched" surgeries. I was told I had 60 to 90 days to live due to my situation which now included the vertebrae tearing apart. Only 1 group of surgeon would accept my case. They were and are awesome. They did the final 2 corrective surgeries back to back on Sept 9 & 10, 2002. Once again I am beginning to have my problems return but at least they saved my life and bought me 7 years with relatively stable conditions. Now I am beginning to have problems to the point I am having MRIs taken and sent to them. I wish all of you hope and help. If I can be your friend or a sounding block I will. I certainly understand how difficult it can be as I have been at every stage from feeling fine to unable to hold things without dropping them, walking upright to walking with cane, in a wheelchair, walking upright again to using Loftstrand crutches to keep from falling again, etc. I hope everyone's tests and procedures come out well. I wish you luck and great doctors. Your friend, Greg   Download the AOL Classifieds Toolbar for local deals at your fingertips.