Father weighs in on the quality of medical care for disabled children in Japan

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    Craig Morrey, the American father featured in the recent CNN story, has left a comment on Japan Probe providing details that were not included in Kyung Lah’s report. Here is what he has to say about the quality of medical care available for his disabled son:

    I appreciate the attention and passion this one line has created, but perhaps you should try to walk a mile in my shoes- so to speak. Kyung Lah’s comment about the care was directly related to what I told her. It has nothing to do with being foreign. I don’t think it was even intended as a slight.

    I readily admit some aspects of the Japanese system are better (ex all car companies have separate line of handicapped cars – for the elderly), but on the whole the conditions could be much, much better.

    Yes, we get a subsidy to offset some costs, but money can’t buy something that is not available.

    Consider a few facts:

    National insurance covers 3 home nurse visits per week (1.5 hrs)- if there are sufficient providers available- there are not. Most will not allow the parent to leave the house for shopping, etc.

    One of the few handicapped school/ hospital/ care facilities in Aichi has exactly 1 pediatrician on staff for 2000+ patients. The average caseload for a PT is 200+ . There are virtually no private therapists for children as it is not economically viable compared to the elderly.

    There is no “day care” available for medically fragile children, ie. requiring a nurse’s care. Other prefectures might have more, but most places require the parent accompany the child at all time. The legal definition is also an obstacle.

    The closest facility for a short stay (another Prefecture) has 4 beds being used by 70+ parents. Reservations must be made 3-4 months in advance. There is 1 other facility in Nagoya which is in danger of being closed or downsized for financial reasons.

    Most prefectures don’t even have a dedicated children’s hospital. Should a spot in a long-term facility be available (personally not an option), it could be anywhere in Japan.

    There are few support/advocacy/ NPO groups. Organizations like United Cerebral Palsy do not exist

    There are less than 10 specialists in swallowing therapy for children in all of Japan. Virtually all lodging facilities have one.

    We were never once approached by a counselor, nor was it even suggested by another doctor.

    The list goes on. It is the same for Japanese people.

    Unfortunately, the news media needs to streamline stories and stay on message. Investigative journalism has gone the way of the dinosaurs- especially TV.

    Yes, there are some minor mistakes, but nothing egregious. Our case is so complex I get confused.
    I would have preferred not to be linked to the Savoie situation because it is completely different. As sad as it seems, our story would probably not have been considered newsworthy without it though.

    It shouldn’t detract from the failings of the system for Japanese and foreigners and the need for an international standard (not necessarily the Hague). Forest for the trees.

    I am grateful to Kyung Lah as she was trying to help.

    P.S. I will be trying to get the “whole” story out on our website http://www.ForeverYourFather.com. Please pass it along. Spencer’s Dad

    Morrey is taking online donations through his website, so please give money if you want to support his cause.

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