tag:blogger.com,1999:blog-6645130.post8095528509310305067..comments2023-07-02T11:59:05.334-07:00Comments on Jenelle's Journey: Genetics and Visiting Med Student!Kellyhttp://www.blogger.com/profile/17256371707801041596noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-6645130.post-4399871524192286742007-01-11T16:23:00.000-08:002007-01-11T16:23:00.000-08:00hello. I just wanted to say my prayers will be wi...hello. I just wanted to say my prayers will be with you as you await the results of the Atypical Rett Syndrome blood test. My daughter was diagnosed with typical Rett Syndrome a year ago. <br /><br />Also, very well said about the Ashley Treatment. We feel similar here. Our Caitlyn does walk, but due to her loss of hand use, is dependant on us for every aspect of her daily life. It's never easy to make the medical decisions for your child!Rebeccahttps://www.blogger.com/profile/07083975974025991852noreply@blogger.comtag:blogger.com,1999:blog-6645130.post-3776651660983010482007-01-09T03:29:00.000-08:002007-01-09T03:29:00.000-08:00I don't think I have commented on your blog before...I don't think I have commented on your blog before, but I have passed by before. Good news from your Dr. I took Sheena off Zantac, and it was not a bother. I am hoping to reduce her Epilim dose in the morning, as she is also more active in the afternoon/evening. She has been really good for about 1 1/2 months - not 100% sure seizure free as her seizures are very subtle. I am still in the stage that I am just happy that she is smiling and happy at last.jotcr2https://www.blogger.com/profile/01366448629677893285noreply@blogger.com