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Terri Mauro

Neurofibromatosis on 'NCIS'

By October 25, 2012

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TelevisionA subplot on this past Tuesday's episode of NCIS dealt with neurofibromatosis -- specifically, a child with neurofibromatosis whose helicopter-pilot father was mysteriously missing and then more mysteriously dead. The inclusion of NF in the plot, particularly the little bit of exposition about the condition given by the child's mother, made it seem as though perhaps someone involved in the show wanted to spread some NF awareness. And indeed, according to a Facebook post by Washington State Neurofibromatosis Families, Chris Waild, who wrote the episode and is an NCIS co-producer, "is a friend and supporter of Leah Manth, a 12 year old from the Buffalo, NY area with NF2. In an effort to raise awareness, he has written an episode that includes a sub-plot about a child with NF2." The touching story told by the mother in the episode, about surgery for tumor removal robbing the little boy of his smile, comes directly from Leah's own experience, as told by her father in a video from Neurofibromatis Inc. Northeast. (Leah's obviously a fan of the show, judging from her Abby-themed Halloween costume last year.)

It's great to see such a popular show work in information on a disability that doesn't have a high media profile. From a more general special-needs perspective, though, I cheered at the way the show refuted the idea that a man whose son has a serious medical condition could naturally be expected to kill himself -- first by his wife insisting that "you don't give up on a kid like this" and later by the investigators figuring out why he was murdered. The mom was depicted as strong and determined in what could have been a depressing "how will I ever handle this horrible double tragedy" situation. Kudos to Waild, the actors, and the show for playing some different notes. Did you catch the episode? What did you think? If you missed it, the episode, entitled "Lost at Sea," is currently up for watching on the CBS site. You can share your feelings about it on that video page, on Waild's blog page, on NCIS's Facebook page, or right here in the comments.

Photo by Terri Mauro

Comments
October 26, 2012 at 12:05 pm
(1) PJ says:

I watched this episode of NCIS and was thrilled at how the family was portrayed and how the diagnosis was treated. Kudos indeed to this show which never ceases to entertain me and now educate me.

October 26, 2012 at 7:24 pm
(2) JOANNE MALAFARINA says:

I am on a committee that raises money for research for Fibromatosis. A friend’s son had a 6 pound tumor on his hamstring when he was 10 years old. He is still being treated, these nasty things don’t give up.
See a link on DTRF’s website.

April 17, 2013 at 12:20 pm
(3) Ana McCool says:

I was watching the show with my husband and Wow! That was great.
Small, but great for being in such a popular show. Hooray to NCIS!

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