In Re Nikolas E.

1998 ME 243, 720 A.2d 562, 1998 Me. LEXIS 264
CourtSupreme Judicial Court of Maine
DecidedNovember 19, 1998
StatusPublished
Cited by7 cases

This text of 1998 ME 243 (In Re Nikolas E.) is published on Counsel Stack Legal Research, covering Supreme Judicial Court of Maine primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Nikolas E., 1998 ME 243, 720 A.2d 562, 1998 Me. LEXIS 264 (Me. 1998).

Opinion

WATHEN, Chief Justice.

[¶ 1] The guardian ad litem of Nikolas E. appeals from a judgment entered in the District Court (Newport, Clapp, J.) denying the *563 child protection petition brought by the Department of Human Services (hereinafter referred to as the “State”). The State sought custody of Nikolas for the limited purpose of approving medical treatment for his HIV condition. 1 The guardian argues on appeal that the court applied an incorrect legal standard and that its factual findings are contrary to the weight of the evidence. Finding no error of law, and concluding that the evidence falls short of compelling a finding in favor of the State, we affirm the judgment.

[¶ 2] The facts presented at trial may be briefly summarized as follows: Nikolas is a four-year-old boy who is HIV positive. Ni-kolas’s mother and father, who are also HIV positive, are divorced and Nikolas lives with his mother who has sole responsibility for his medical care. In January of 1997, Nikolas’s sister died at the age of four from complications with AIDS. Nikolas and his mother are under the care of their family physician, Jean Benson, M.D. After learning of a clinical trial program for children with HIV, Dr. Benson referred Nikolas and his mother to a specialist in pediatric infectious diseases, Dr. John Milliken of Bangor. Both the mother and Nikolas’s deceased sister had been treated in the past by Dr. Milliken.

[¶ 3] In September of 1997, Dr. Milliken examined Nikolas and met with his mother. He recommended a drug therapy known as highly aggressive anti-retroviral therapy (HAART). Based upon developments in her own illness and her experience with the drug therapy that accompanied the tragic and painful death of her daughter, the mother expressed her distrust of the drug therapy and declined to permit her son to participate at that time. Dr. Milliken, weighing in his mind whether the mother’s refusal to provide the therapy to Nikolas constituted neglect, waited for nearly two months before writing his recommendations to Dr. Benson. In November, with updated medical information recommending that all children with HIV infection should be treated for that disease, Dr. Milliken sent a report to Dr. Benson and provided a copy to the State. In the report he explained his recommendations for treatment and his concern about the mother’s decision to forego treatment within the context of her own disease. He suggested that the mother could be offered “a voluntary release of parental rights with residential custody for her,” and that medical decisions could be removed from her.

[¶ 4] As a result of Dr. Milliken’s report, the State met with the mother and discussed her treatment plans for Nikolas. Because of differing opinions offered by Dr. Benson and Dr. Milliken, the State arranged for the mother and Nikolas to consult with Dr. Kenneth McIntosh, Chief of the Division of Infectious Diseases at Children’s Hospital in Boston, Massachusetts. Dr McIntosh is head of the AIDS program at tie hospital and professor of pediatrics at Harvard Medical School. He provided the mother with information regarding treatment and suggested that Nikolas would benefit from HAART therapy. Specifically, the therapy would involve giving Nikolas daily dosages of three different kinds of drugs — two nucleoside analogue reverse transcriptase inhibitors, in this case, d4T and 3TC, and one protease inhibitor, in this case, nelfinavir, for an extended period of time, possibly for his lifetime. Dr. McIntosh saw no irrationality on the part of the mother, and he confirmed that he had never reported parents to child protective agencies for failing to accept his recommendations regarding therapy.

[¶ 5] Later, the mother returned to Dr. McIntosh on her own to discuss the risks and long term effects of the proposed therapy. The District Court summarized the information she obtained on this visit as follows:

Dr. McIntosh gave her all the information currently available from the limited experience the medical community has had in this treatment for children and could not give her any definitive information concerning long term effects. This drug *564 treatment regimen is still in the evolving stages. Because of stepped-up FDA approval of drugs and programs in this area due to public and political pressure nationwide, all ongoing AIDS treatment programs (especially for children), when compared to traditional methods of approving medical drugs and treatment protocols, are experimental. In effect, treatment is being provided to sufferers of this illness at the same time as statistics and efficacy studies are being conducted. The various regimens are changing constantly, and it is expected that new and more effective drugs and treatment protocols will emerge each year, if not sooner. It can be fairly said that the HAART regimen was still in experimental stages when [the mother] first consulted with Dr. Milliken. The CDC published its guidelines for children’s HIV treatment over six months later, making this regimen conventional state of the art.
Dr. McIntosh’s [sic] feels that because Ni-kolas’s blood tests (viral load count and CD4 cell count) meet the CDC guidelines qualifying him for aggressive drug therapy, the child may well benefit from such treatment. However, this benefit cannot be quantified. No good estimation can be given either on whether or how much longer Nikolas will survive solely because he participates. Dr. McIntosh is of the opinion that no child should be started on this program unless his parents are fully accepting and in support of the treatment.

[¶ 6] The court concluded that the long term effects of the drug therapy were essentially unknown and observed that the mother, although she had not agreed to the therapy at the time of hearing, stated clearly that her mind was not closed on the issue. The court stated that “[although she would rather spare Nikolas the effects and risks of this treatment, if his health begins to deteriorate significantly, she will reconsider and would now, if ordered, comply with treatment.”

[¶ 7] Against this factual background, the State in May of 1998, filed a petition for a child protection order, seeking custody of Nikolas so he could receive the treatment recommended by Dr. McIntosh. A guardian ad litem was appointed pursuant to 22 M.R.S.A. § 4005 (1992 & Supp.1997), amended by P.L.1997, ch. 715, §§ A-1, A-2 (effective June 30, 1998), and a hearing was held on the petition in September. The court denied the petition and the matter is now before us on an expedited appeal. 2

I. Standing

[¶ 8] As a preliminary matter, the mother argues that the guardian lacks standing to prosecute an appeal in a child protection action. She contends that the guardian’s rights and duties are limited to those delineated in 22 M.R.S.A. § 4005 and that appealing the court’s judgment is not included in the list of rights and duties. The mother also argues that appeal is controlled by 22 M.R.S.A. § 4006, that only an “aggrieved party” may bring an appeal under section 4006, and that neither Nikolas nor his guardian is a party to the child protection hearing.

[¶ 9] The right to appeal from a child protection order is set forth in 22 M.R.S.A. § 4006 as follows:

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Bluebook (online)
1998 ME 243, 720 A.2d 562, 1998 Me. LEXIS 264, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-nikolas-e-me-1998.