by Norma


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.



Posted on Jan 16, 2004, 4:26 PM

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

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