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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