Hi Denise,
I am glad you came here in spite of the beware online sources warnings. You will learn more about thalassemia here than many doctors know. In fact, many doctors from throughout the world access this site for information. Some have even joined, including one doctor from the top bone marrow transplant center on earth. We do our best to guide people here.
The first thing you should do is contact Eileen Scott at CAF. Getting registered with CAF is important as they can direct you in many ways. Eileen can help you find a thal familiar doctor in your area. She will also most likely direct you to one of the US Centers of Excellence for thalassemia care. Her contact info is
Cooley's Anemia Foundation
330 Seventh Avenue, #900
New York, NY 10001
(800)522-7222
Fax: 212-279-5999
Patient Services Manager
Eileen Scott
eileen.s@cooleysanemia.org
I cannot overstress how important it is for your child to be under a treatment program directed by one of these centers. Closest to you is Dr Cohen at Children’s Hospital of Philadelphia. A complete evaluation is necessary as soon as possible. Hearing loss is not common in thalassemia outside of those whose hearing loss is directly caused by chelators. It is well known that desferal can cause hearing loss, but less known is that Exjade has also been shown to cause hearing loss in a small minority of users, so the true cause should be investigated. The difference between the Centers of Excellence and hospitals with no connection to these centers is night and day. All patients in the US should be seen at one of these centers or one of their satellite centers, at least once per year for an evaluation of the patient's progress and revisions to their treatment program, if needed. They design treatment programs specifically for each patient based on the needs of that patient. I can give you mountains of information and advice but nothing I can tell you is as important as call Children’s Hospital of Philadelphia and set up an appointment with Dr Cohen.
Children’s Hospital of Philadelphia
Appointments, consultations and referrals Contact: Marie Martin, 215-590-2197
Philadelphia, Pennsylvania
Director: Alan Cohen, MD
http://www.chop.edu/consumer/jsp/division/meet_the_team.jsp?sid=26685Physician Referral Service 1-800-TRY CHOP (1-800-879-2467)
The source of your thal gene may be a mystery but thal carriers are found all over the earth and not just in the typically considered areas. It could be that some ancestor long ago traveled as a merchant or sailor and brought back home a wife from the Mediterranean area. We do often hear from people of Northern European descent who are carriers, so it is not quite as unusual as many believe.
I would like to add that there are many parents in this group who have similar stories and experience as you, who will share what they have learned with you about the day to day reality of raising a child with thalassemia. There are things you just won't hear from doctors, because they don't live it. The parents and patients do, and there are many things that only experience teaches. Please feel at home here and ask anything at all. This is a truly unique online site with a wonderful group of people from all over the world. We are here to help.