BAHA

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My daughter is now fifteen (15) years old in a single-parent family home. She and I are very much hoping that someday she will be able to wear a BAHA. But with my financial situation, I cannot afford to pay for the device. Private medical insurance, Medicaid and Child Care Connection do not cover it. I am interested in knowing where I can go for this kind support.

I also want to know where my daughter and I can attend a support group for people with treacher collins syndrome.

Thank you for your attention and response to my post.

Please e-mail me.

Sincerely,

Norma



Posted on Jan 16, 2004, 4:26 PM

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  1. To pay for the BaHa. , Mar 21, 2004
    1. Just wondering. , May 30, 2005
      1. hello. , Jun 8, 2005
        1. info?. , Nov 23, 2005
          1. Re: info?. , Dec 2, 2005

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