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http://www.moyamoya.com/cgi-bin/yabb2/YaBB.pl Moyamoya Related Topics >> Moyamoya Related Information and Support >> Moyamoya in Philippines http://www.moyamoya.com/cgi-bin/yabb2/YaBB.pl?num=1383916296 Message started by Mom_to_Kyle on Nov 8^th, 2013 at 8:11am

Title: Moyamoya in Philippines
Post by Mom_to_Kyle on Nov 8^th, 2013 at 8:11am

I'm from Manila, mom to Kyle now 5 years old. He was diagnosed with MM when he was 2. Wondering if anyone else in Philippines have MM or with relative who has MM. I only know doctors so it would be great to have someone near who are in the same boat as me.

Title: Re: Moyamoya in Philippines
Post by hrsridermom on Nov 8^th, 2013 at 6:09pm

If you have facebook another place to connect with some one from the Philipines is World Moyamoya Day - May 6th. This site and the facebook page are both great places for info and friends.

I hope you are staying safe in the storm.

Title: Re: Moyamoya in Philippines
Post by Ross on Dec 30^th, 2015 at 7:17pm

Hi, I'm a Filipino, how was your child doing? My wife was diagnosed with MM and successfully underwent surgery at left / right side of brain at Stanford Hospital in California, USA. The Dr's name is Gary Steinberg. If you need more information, I'm just a mail away. Just curious, is MM can be treated in PH? What hospital and the name of Dr's? Thank you Ross