Application of George

625 S.W.2d 151, 1981 Mo. App. LEXIS 3281
CourtMissouri Court of Appeals
DecidedAugust 25, 1981
DocketWD 32822
StatusPublished
Cited by3 cases

This text of 625 S.W.2d 151 (Application of George) is published on Counsel Stack Legal Research, covering Missouri Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Application of George, 625 S.W.2d 151, 1981 Mo. App. LEXIS 3281 (Mo. Ct. App. 1981).

Opinion

DIXON, Judge.

James G. George appeals from an order of the Juvenile Court of Jackson County denying his application for an order to open the records of his adoption pursuant to § 453.120 RSMo 1978. The controlling and dispositive issue is whether or not the trial court properly followed the procedures for release of such information outlined in Application of Maples, 563 S.W.2d 760 (Mo. banc 1978), and Application of Gilbert, 563 S.W.2d 768 (Mo. banc 1978).

The applicant, James G. George, was born August 18, 1947, and was adopted shortly thereafter. The adoption occurred in the Juvenile Court of Jackson County, Missouri. In September, 1980, he first initiated an inquiry by letter to the court requesting information about his adoption records. The Juvenile Judge responded to that letter of inquiry pointing out that he was unable to release such information absent a proper application and a showing of good cause. Thereafter, George filed a written application seeking the release of the names of his natural parents. The court, acting pursuant to the directive of Maples, supra, contacted the natural mother and requested certain information from her and appointed for her a guardian ad litem, likewise suggested by the decision in Maples. The natural mother refused to consent to the release of her name to the applicant and further asserted to the juvenile judge that applicant’s natural father did not know of her pregnancy resulting in the applicant’s birth and if identified he would probably deny paternity.

These facts were communicated to the applicant and his attorney and an open evi-dentiary hearing was conducted.

The record in this case consists almost entirely of medical testimony. Because of the circumstances, the medical testimony is of necessity largely theoretical. The fundamental issue of necessity, however, rests upon the medical evidence.

The applicant is 33 years old and was born at a maternity center in Kansas City, Missouri. He was adopted shortly after his birth by a couple whose surname he bears. His adoptive father is deceased, and the file contains a verified consent from his adoptive mother to release any information concerning his natural parents.

Sometime in 1980, the applicant came under the care of a Dr. Rosen in Florida *153 where the applicant now lives. Dr. Rosen diagnosed the applicant’s medical problem as chronic myelocytic leukemia which is a term synonymous with chronic granulocytic leukemia. This is a malignant disease of the bone marrow. The disease is diagnosed upon appearance of the factors of anemia and high white cell count in the blood and by physical changes in the bone marrow. The physical changes in the bone marrow are an alteration of the bone marrow from a composition of half fat and half blood producing cells to a state where no fat is present and the bone marrow consists entirely of blood producing cells. Characteristically, the balance of cells producing white cells and red cells for the blood is altered and an excessive number of white cells is produced with an excessive number of immature white cells. There are usually present in a higher than normal number white cells referred to as granulocytes. The chronic granulocytic leukemia is distinguished from acute leukemia by the presence or absence of any mature white cells. In acute leukemia, there are larger accumulations of immature white cells. Both acute leukemia and chronic granulocytic leukemia typically present an overproliferation of blood cells, but in chronic granulocytic leukemia some of the blood cells are mature and can perform a normal function while in acute leukemia few if any mature cells appear.

Chronic granulocytic leukemia is a progressive disease and ultimately will cause the death of the patient. The progression of the disease is not uniform, either time-wise or in type. One half of the patients survive less than forty months; one half survive more than forty months. The progression of chronic granulocytic leukemia is most usually to acute leukemia in three-fourths of the cases, but it sometimes progresses to other acute forms or types. The evidence speaks of a “transformation” of chronic granulocytic leukemia to some other form of bone marrow disease, usually acute leukemia in which there is an absence of normal bone marrow function in the supply of normal mature white cells, the absence of which causes the death of the patient from bleeding or infection. When the disease has “transformed,” death occurs within months or weeks.

Chronic granulocytic leukemia in the stage present in the applicant is treated with drugs, busulfan or hydroxyurea, which tend to make the blood counts normal or near normal and symptoms absent. Such chemotherapy is continued “until it no longer works,” which may be “weeks, months, or years.”

The applicant has been treated with bu-sulfan and at the time of the hearing was not receiving such treatment. The applicant was being regularly checked for the progression of the disease and his explanation for the suspension of the treatment was that it becomes progressively less effective and that once a remission is achieved, its use is suspended until the white count again reaches an unreasonable level. The medical testimony was that various other types of therapy had been utilized and that once the disease had become “refractory” or “failed on standard therapy” no increase or different treatment by way of chemotherapy would check the ultimate course of the disease.

Most of the medical testimony centered upon the technique of bone marrow transplant which has been developed in the last four or five years. In that procedure, the bone marrow of the patient is eliminated by radiation and the patient is sustained by blood transfusions since the elimination of the bone marrow has eliminated the body’s capacity to generate blood. Bone marrow from a donor is then injected into the blood stream of the patient and, if successful, will result in the regeneration of the patient’s bone marrow. If the transplant fails, the patient dies. The procedure presents a high risk of failure with somewhat over half of the patients surviving the transplant and its complications when it has been done between full blooded siblings. When the procedure has been utilized between identical twins, the results are dramatically better with an 80 percent survival rate.

*154 The medical testimony was based on twenty cases of identical twins and approximately fifty other cases of persons who were not identical twins. The total number of such transplants in all categories is less than one hundred. Only one case of a transplant in a patient with chronic granu-locytic leukemia was within the personal knowledge of the medical witness, and it had been performed six months before the hearing. All other cases known to the witness had been performed after the disease had become “refractory” or transformed. The procedure is characterized as “experimental.”

The success of the procedure depends upon the acceptance by the patient’s body of the transplanted marrow and that, in turn, apparently depends upon the degree of matching between the donor and the donee in what is referred to as the blood antigens.

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Related

In re the Adoption of Infant Sherman
48 V.I. 221 (Superior Court of The Virgin Islands, 2007)
In Re Assalone
512 A.2d 1383 (Supreme Court of Rhode Island, 1986)
Application of George
630 S.W.2d 614 (Missouri Court of Appeals, 1982)

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Bluebook (online)
625 S.W.2d 151, 1981 Mo. App. LEXIS 3281, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-george-moctapp-1981.