Guest guest Posted September 16, 2004 Report Share Posted September 16, 2004 Meg! I had no idea that you are expecting a second angel! Congratulations to you and your family! Dr. Cambell and Dr. are brilliant human beings..I was very impressed with these docs. I am so glad that you can put some worry aside, for now...Especially, since you are expecting another babe. That must be tough sometimes. Hang in there. Atleast now, you are moving in a direction that could give some definate answers. I'll be thinking of you and Darryl, so please update us upon your return. Good Luck! HRH Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2004 Report Share Posted September 16, 2004 Meg, that is fabulous news! I will keep Darryl in my prayers. gail > > From: " Meg Wirantono " <mdco@...> > Date: 2004/09/16 Thu AM 05:13:03 GMT > <infantile scoliosis treatment > > Subject: Hi from Meg & Darryl > > Hi everyone, > First of all I want to thank you for this wonderful site, H. and > all great parents here. Because of your valuable information, we just > received good news from Texas, after waiting for several months, > finally Darryl's turn is coming for the Titanium Rib Project's > evaluation by Dr. in San , TX. Yesterday, we got a call > from our insurance that Darryl's evaluation has been approved and we can > go. Thanks God. We will be leaving Colorado on Sep 21 - 25. The actual > evaluation dates are Sep 22, 23. I am so excited as well as so nervous, > I don't know what will happen there especially because my husband could > not go with us and I am expecting our second angel, I will be going with > our friend so she can be with Darryl during the test in the X-ray room. > I am doing my reading and preparing some questions to ask at the meeting > with doctors on the second day of evaluation. In case if any of you have > any suggestion or advice. I would appreciate that. > For new members, Darryl is 2.5 years old with congenital scoliosis. He > has hemivertebra at T12, butterfly at T8, fusion on C4 & C5. his curve > is around 55-58 degree, no change for the last 3 months. We are still > doing 'wait and see', hopefully after come back from TX , we will have > the answer of what to do. > Thanks, Meg. > > > > > Gail *********************************** Mom to , 11/28/98 , 02/02/02 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2004 Report Share Posted September 17, 2004 Meg, It is so great to have you back. I have been wondering how you and Daryll were. Thanks again for your visit to me and Moriah while we were in Denver. I'm so excited to hear about your evaluation with Texas. They are wonderful people. We are still in contact with them about Moriah. She's still in her halo -4 months now. Her curves were 120 scoli 120 kyphosis and now she is 66scoli and 75 kyphosis. We are hoping it is enough of an improvement for Dr. to asess her again and consider the Rib. We also found out she has hemivertebrae too. I will be praying for you and Daryll on this trip. It must be difficult going without your husband and expecting a new little one. I'm glad you have a close friend to go with you and be of help. You will love Texas. They are honest and will answer your questions. Let us know how it turns out. Tell Daryll Moriah say hi. Shellie and MoriahMeg Wirantono <mdco@...> wrote: Hi everyone, First of all I want to thank you for this wonderful site, H. and all great parents here. Because of your valuable information, we just received good news from Texas, after waiting for several months, finally Darryl’s turn is coming for the Titanium Rib Project’s evaluation by Dr. in San , TX. Yesterday, we got a call from our insurance that Darryl’s evaluation has been approved and we can go. Thanks God. We will be leaving Colorado on Sep 21 – 25. The actual evaluation dates are Sep 22, 23. I am so excited as well as so nervous, I don’t know what will happen there especially because my husband could not go with us and I am expecting our second angel, I will be going with our friend so she can be with Darryl during the test in the X-ray room. I am doing my reading and preparing some questions to ask at the meeting with doctors on the second day of evaluation. In case if any of you have any suggestion or advice. I would appreciate that. For new members, Darryl is 2.5 years old with congenital scoliosis. He has hemivertebra at T12, butterfly at T8, fusion on C4 & C5. his curve is around 55-58 degree, no change for the last 3 months. We are still doing ‘wait and see’, hopefully after come back from TX , we will have the answer of what to do. Thanks, Meg. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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