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Moyamoya Related Topics >> Surgeons with Bypass Experience >> Johns Hopkins Moyamoya center http://www.moyamoya.com/cgi-bin/yabb2/YaBB.pl?num=1217006105 Message started by tkrut86 on Jul 25th, 2008 at 1:15pm |
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Title: Johns Hopkins Moyamoya center Post by tkrut86 on Jul 25th, 2008 at 1:15pm
Has anyone been recently treated at Johns Hopkins for Moyamoya surgery? My sister is a patient who is going through a presurgical angiogram today and plans to have surgery with Dr Huang. Any thoughts or experiences with Johns Hopkin lately? My sister was to have surgery at U of Penn but they were not medically advanced regarding this very intricate disease and our family felt that a second opinion was warranted. Thanks for any input... :D
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Title: Re: Johns Hopkins Moyamoya center Post by moody on Jul 25th, 2008 at 4:19pm
Hi
I'm sorry that your sister have to go through this, but glad that you found this web site, welcome to moyamoya family. I had surgeries at Johns Hopkins on April and November of 2006, my neurosurgeon is Dr. Tamargo, he is the Board director of neuro department, he had good experienced of moyamoya disease, people come to him from the all over the world, I love his team,and the nurse staff is wonderful. You could send me a PM so we can talk. Your sister and family is in my thoughts and prayers, I hope to hear from you soon. Take care Kieu |
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