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