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Questions for Dr. Kennedy
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chronic inflammatory demyelinating polyneuropathy
Posted by: Susan
Date: July 16, 2001 10:19 AM

I was told I have CIDP in 1997. It has been a long, hard road for me. I see a doctor every six months. I never get told anything, just see you in six months. The doctors here know nothing about CIDP They act like they want to know more, but just don't. I have had every treatment under the sun, but nothing has worked. In 1999, I was put in a wheelchair and I am still there. Please don't take me wrong, I am a verry happy person, but I want to get better. I thank God every day that I wake up, another day with my children. I have three children, my first is a young woman, 20 years old, married and a baby boy on the way. She and my son-in-law live in Charleston, South Carolina. My middle child is a 17 year old young man, still at home with me. Last but not least, my baby girl, she is 13 years old and yes, still home with me. I am a 35 year old woman who needs answers. I keep going down hill. What will the end be like? Am I going to die a young woman? I know at this time I will never get to hold my grandchildren because I will drop them. I can't hold anything.

RE: chronic inflammatory demyelinating polyneuropa
Posted by: Ron Kennedy, M.D.
Date: July 16, 2001 3:12 PM

Of course you have a hard to treat illness, one which mainstream medicine has little to offer. In my experience the best approach is through diet, detoxification and treatment with the SanPharma remedies. Also, hormonal evaluation and treatmeat usually yields benefits. You could start by clicking the blue button above: Basis of Physical Health.

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