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Moyamoya.com Forum › Moyamoya Related Topics › Surgeons with Bypass Experience › Johns Hopkins Moyamoya center

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Johns Hopkins Moyamoya center (Read 4537 times)

tkrut86

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nurse and proud sister
of MM patient

Posts: 1
Belvidere, USA, usa, 357, 117, IL, Illinois
Gender: female

Johns Hopkins Moyamoya center
Jul 25^th, 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... Cheesy

« Last Edit: Jul 25^th, 2008 at 6:36pm by tkrut86 »

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moody

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In all the thing I lost
I miss my mind the most.

Posts: 207
richmond, USA, VA, Virginia
Gender: female

Re: Johns Hopkins Moyamoya center
Reply #1 - Jul 25^th, 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

Yesterday is past, tomorrow is future, today is the gift, that why we call it present.

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