Destiny or Fate!
November 15th 2006 01:11
http://www.medra.com/
I have been searching for more than a year for a doctor to treat me with stem cell and I believe hard work has paid off. I found the doctor’s information in an internet ad by Google, few weeks ago, when I was updating my blogs, I saw the ad and I clicked, I saw your clinic and Dr. Rader video about your baby story which I called a miracle.
My story is a little complicated because I have 6 misdiagnosis. In 1992, I started falling until May 1993 my condition got so worst that I lose rapidly all my strength and ability to breathe and moved in my native country Puerto Rico. At first, the doctors thought that I had a brain tumor dream due a MRI and almost sent me to a hospital for treatment. Secondly, the doctors thought that I had MS and even treatment me with steroids. Thirdly, I got diagnosed with a malformation of a vein in the cervical area in the spine.
My condition got worst and the doctors asked my mother to transport me to the United States for help. At that time the prognosis was ALS which was the final conclusion at that time after been admitted for a month at the Columbia Presbyterian Hospital in New York and every test negative.
Once again the doctor failed because I did die after six years and I was breaking the world the record of ALS without deterioration. Once again, they review my records and came out with the new diagnose which was, PLS.
Years later I did the text for Lyme disease which can positive with numbers very high. I was treating for a year and an half with antibiotics.
I breath well although, I suffer with of Dysarthria which I have learned to understand it with speech therapy. My range of motion is excellent because I have been extensively doing physical and occupational therapy for 10 years. I walk with a little with assistance, I'm married, doing a bachelor degree in sociology, and wrote this letter to you with assistive technology.
I am willing to visit Dr. Rader for an evaluation and in regards of the money. I am willing write for grants, fundraisings, etc. Because I believe that $25,000 is nothing, if I will be able to regain some movement or more. If any of you have any information about this matter, I will truly appreciate it.
Maddy
I have been searching for more than a year for a doctor to treat me with stem cell and I believe hard work has paid off. I found the doctor’s information in an internet ad by Google, few weeks ago, when I was updating my blogs, I saw the ad and I clicked, I saw your clinic and Dr. Rader video about your baby story which I called a miracle.
My story is a little complicated because I have 6 misdiagnosis. In 1992, I started falling until May 1993 my condition got so worst that I lose rapidly all my strength and ability to breathe and moved in my native country Puerto Rico. At first, the doctors thought that I had a brain tumor dream due a MRI and almost sent me to a hospital for treatment. Secondly, the doctors thought that I had MS and even treatment me with steroids. Thirdly, I got diagnosed with a malformation of a vein in the cervical area in the spine.
My condition got worst and the doctors asked my mother to transport me to the United States for help. At that time the prognosis was ALS which was the final conclusion at that time after been admitted for a month at the Columbia Presbyterian Hospital in New York and every test negative.
Once again the doctor failed because I did die after six years and I was breaking the world the record of ALS without deterioration. Once again, they review my records and came out with the new diagnose which was, PLS.
Years later I did the text for Lyme disease which can positive with numbers very high. I was treating for a year and an half with antibiotics.
I breath well although, I suffer with of Dysarthria which I have learned to understand it with speech therapy. My range of motion is excellent because I have been extensively doing physical and occupational therapy for 10 years. I walk with a little with assistance, I'm married, doing a bachelor degree in sociology, and wrote this letter to you with assistive technology.
I am willing to visit Dr. Rader for an evaluation and in regards of the money. I am willing write for grants, fundraisings, etc. Because I believe that $25,000 is nothing, if I will be able to regain some movement or more. If any of you have any information about this matter, I will truly appreciate it.
Maddy
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