I got to do a
very brief interview with KITV4 6 o'clock News last week Wednesday, August 10, 2005. I only received the phone call about 2 hours prior to the interview, but I didn't want to give up this opportunity. I was hoping that they could do a more "in-depth" story on what moyamoya actually is and interview my neurologist to answer any direct medical questions; however, I believe this interview was just to promote my recent fundraiser event coming up so they wanted to basically hear my story.... Our interview lasted about 30 minutes, but the segment that "aired" was no more than about a minute and a half to two minutes....way too short to explain what MM is and how it affects individuals....
Nonetheless, I've received responses from others here in the Islands that also have this rare disease.
I hope to be able to organize a Hawaii Moyamoya Ohana Support Group where we can meet once or twice a month. ("Ohana" means "family" in Hawaiian...) I'm also directing them to visit this site if they haven't already been here.....to post/look for questions & answers, concerns and most importantly, support from all of you!
Slowly but surely, we will all work together to raise MM awareness.
Aloha,
Shan
http://www.thehawaiichannel.com/news/4836773/detail.html
http://www.thehawaiichannel.com/news/1298194/detail.html
p.s. Hillary, please PM me if you can send me a copy of your interview. ;