UNHAPPY CI USERS NEED TO REPORT TO MEDWATCH!
There is a government program where anyone who have issues can report to them for regulation and modification.
Thursday, January 17, 2008
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3 comments:
What is the MedWatch website and email address and phone number, please?
I truly appreciate your past efforts as an advocate to steamroll the widespread use of CI.
Let's work together along with Jack Barr, Aidan Mack and other deaf individuals?
We ought to make the documentary film about the real horrors of CI as a rebuttal to the "Sound of Fury" biased film.
Let's do it and make $$ out of our documentary film to fund the powerful constitutency group to fight against the CI's!
Time for Real Action, Not "Huff and Puff"!
Robert L. Mason (RLM)
RLMDEAF blog
Hello, I am grateful cause my mom did not push me into cochlear implant. She asked me if I wanted to have cochlear implant when I was teenager. I said no. She said why? I said "I am happy with who I am". My mom said ok and dropped it.
Also, I am not sure if this really happened to a woman who I know from college. She had cochlear implant which she made this choice on her own. I think she was about 25 yrs old, not sure the age. After receiving cochlear implant, she had lot of problem with it. Dr found out that she had lukemina and she died shortly after receiving cochlear implant. Someone said that cochlear implant caused this. True or not???? I will never know but it was sad that she had to die.
I have always believed the systematic process of inserting cocklear implants in deaf childrens' heads is a form of crime against humanity being committed by the international medical and hearing community.
There should be some way we can bring them to the Humans Rights Commission.
Regards,
Oneninefive
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