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Fanconi Anemia – Bone Marrow Drive

Scott and Nancy Finnegan learned last year that both their 17-year-old son, Blaise, and 13-year-old daughter, Madeline, have Fanconi anemia. They will eventually need bone marrow transplants to survive.
Madeline and Blaise also have aplastic anemia, meaning they have lost some bone marrow, and is being treated by a Minneapolis doctor who specializes in Fanconi anemia.
On October 31st, a bone marrow/blood drive sponsored by Life South will be held at Hampton Cove Middle School in hopes of finding a donor for Blaise and Madeline. Siblings are usually the best bone marrow donors, but the Finnegans’ youngest child, 8-year-old Trinity, is not a match.

The ordeal began in March 2007, when Madeline, now in her final year at Hampton Cove Middle School, went to the doctor because of stomach pain and vomiting. Her pediatrician suspected appendicitis, but tests showed problems with her red blood cells, white blood cells and platelets.
Eventually, Madeline developed sores in her mouth and throat and was sent to St. Jude for a bone marrow biopsy; she was diagnosed with Fanconi anemia a few days later.
Fanconi anemia is a genetic blood disorder that causes bone marrow failure and often leads to acute myelogenous leukemia. Even after bone marrow transplants, Fanconi patients have an increased risk of developing cancer and other serious health problems.
Blaise, a Huntsville High senior who plays bass guitar and golf, was diagnosed while being tested for a bone marrow match for his sister. Neither child appears sick, but must be careful to observe signs related to Fanconi anemia.
Madeline and Blaise will eventually need a match if their bone marrow continues to fail. Nancy is Mexican, so there may be an increased chance to find a match within the Hispanic ethnicity; but we encourage all to support the effort in finding a positive bone marrow match.
We are asking for your support at the bone marrow/blood drive on October 31st at Hampton Cove Middle School from 7a.m.-7 p.m. Bone marrow testing is a painless swab of the check with a Q-Tip.

For more information, please contact
Chanda W. Davis at 256-755-4600 or Stacy Copeland at 256-428-8380

Short URL: http://chandadavis.net/?p=642

7 Comments for “Fanconi Anemia – Bone Marrow Drive”

  1. Nice post I belief that we need to be more carefully with our heath but I need information about migraine

  2. gabrielle covey 5 period

    Blaise and Madeline will need a blood transplant so they can live. They have Fanconi anemia. They have lost some blood marrow ang go to a doctor who specializes in Fanconi anemia. At Hampton Cove Middle School they were having a blood transplant for the two childern. Most of the time siblings are a match, but there youngest chld was not a match.

  3. gabrielle covey 5 period

    Blaise and Madeline will need a blood transplant so they can live. They have Fanconi anemia. They have lost some blood marrow and go to a doctor who specializes in Fanconi anemia. At Hampton Cove Middle School they were having a blood transplant for the two children. Most of the time siblings are a match, but there youngest child was not a match.

  4. to people have fancoi anemia

    they will need bone marrow to survive

    they only have aplastic anima

    october 31 they had a blood drive sponcerd by life south

    test showed she had problems with red blood cells wight blood cells and platlets

  5. yo

  6. Both Finnegan kids have Fanconi Anemia.
    They will need a blood transplant so they can live.
    Their bodies don’t have enough bone marrow.
    This means they can’t make as much blood as some people.
    In October there was a blood drive for them.

  7. Cars and houses are expensive and not everybody is able to buy it. However, business loans was created to aid people in such situations.

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