26 great life experiences

Posted by on Jul 25 2016 | 26 great life experiences, Facial Pain/Trigeminal Neuralgia, MS

Oysters on Cortes Island 2004

Oysters on Cortes Island 2004

When I first started the idea of writing about great life experiences, I was not feeling well and figured I’d never feel great again as MS is a terrible disease. I wanted to leave some evidence that I was HERE and I LIVED a life. The best I could hope for was not to get worse and that’s why I started the drug treatment. Little did I know that some of the people and ideas I encountered along the way would provide me with much more hope and some actual healing. I got to the point where I thought I might be one of the lucky ones who figured out how to stop attacks.

Now that I am suffering another brain stem attack so similar in many ways to the one in 2011, I realize I was wrong. Did I do something wrong? Exposure to gluten or dairy? Stress? Surgeries? Exposure to toxins? Re-stenosis of my jugular veins? I was tolerating the drug well but the only things that really made a difference to how I felt were the TVAM/CCSVI procedure in California in February 2014, and the change in my diet following the example of Dr. Terry Wahls. After the TVAM/CCSVI, my energy improved, my blood pressure and pulse normalized, my hands and feet got warmer. I tolerated heat better and actually began to sweat.  With changes in my diet, I had quite a remarkable two years, ate food and enjoyed so many things in my life again that I thought were long gone, including exercise, swimming, riding my bike and hosting dinner parties with friends! I even had a glass of wine once or twice on very special occasions. Yet these times were interspersed with episodes of recurring trigeminal neuralgia, pain, stress and trips to Winnipeg for surgery.

Last summer, I recall saying to Daniel that it almost felt like the MS was gone. I was doing a lot of fun and interesting things. I felt mentally sharp. My feet felt normal and the feeling was coming back to my face as the rhizotomy healed. The only thing that persisted was a bit of tingling in my hands from the C5-6 spinal stenosis. But it wasn’t getting worse and actually had shown some signs of improvement with the annual MS MRI scans, plus I was seeing my chiropractor regularly and physiotherapist occasionally.

As I may not have time to go through all of the great experiences and scan photos, I’ll list them in the next post.


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