gotchlorine
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Our daughter, Tara, lives with MM
Posts: 776
San Jose, USA, usa, 24, 158, CA, California
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Hi Cheryl, and welcome to our family! I am sorry circumstances led you here, but am very glad you found us!
This post won't be long, as it's time for the big game, but there are a whole bunch of people on this site who have had surgery by Dr. Scott. You will hear from them (or their parents) soon, I'm sure! He's one of the "experts" we're always advising people to go to. As you continue to read, you will see that it is extremely important for treatment to be given by a doctor who sees this disease on a daily basis. Dr. Scott definitely falls in this category, so your son will be in very good hands! The more education you have also, the better you'll be able to advocate for him. So, please don't hesitate to ask whatever questions come to your mind. There is a wonderful, supportive group of people here . . . all who have walked this road in one way or another. (By the way, I am the mom of a 19 year old daughter who had 2 MM surgeries at Stanford just 20 months ago. She is doing very well, and you'd never even know she'd had surgeries.)
The prospect of surgery is frightening, but know that you're on the right track. There should be every reason for YuYu's surgery to be successful with the wonderful care he'll get. Hang in there, and we'll be here for you!
Hugs from California, Jill
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