Guest guest Posted August 1, 2011 Report Share Posted August 1, 2011 Hello, I am not sure what the EDG is, perhaps in my recesses I do, but today I am brain dead. I am guessing it is either Botox or a stretch. Regardless, whatever it relates to seems exorbitant by any means on a child. My son was 14 when we discovered he had Achalasia. You however are saying your child was diagnosed at the age of 10??? Often times a doctor who does not know what the " latest technologies or discoveries " are will use the method most often recommended for a situation. Unfortunately, it sometimes causes more damage to the area. This is the biggest reason most in this group recommend starting at the TOP of the specialist pile and getting the BEST help, no matter what, right from the start. From this point forward, it is well worth your time to pursue a specialist who is WELL-VERSED in all aspects of achalasia. The Heller has saved many lives... by giving those affected the ability to get nutrition into their systems to live. When the LES closes, it effectively creates a STARVING to death scenario. Below is a specialist in the Dallas area that is very well published. I could not locate his email but the phone is there. If you can locate the email, most doctors respond immediately, especially if in the subj. line you have child achalasia desperate.. Good luck .. if you need more help support or advice.. don't hesitate.. people will respond. Carolyn mom of Cameron fundo'd and myo'd in 2005Dallas: Specialist, teaching professor, well documented and published. Name: Stuart Jon Spechler, M.D. Telephone: 214-374-7799 Endowed Title: Berta M. and Cecil O. Chair in Gastroenterology Academic Title: Professor Administrative Title: Chief of Gastroenterology, Veterans Affairs Medical Center, and Vice Chief, Division of Digestive and Liver Diseases, UT Southwestern Primary Appointment: Internal Medicine - Digestive and Liver Diseases School: Southwestern Medical School Department Website: Internal Medicine - Digestive and Liver Diseases Address: UT Southwestern Medical Center at Dallas 5323 Harry Hines Blvd, Dallas, Texas 75390-VAMC Good morning how is everyone? I am fairly new to the support group, I joined last month but I just now decided to narrow the group down to my area. I live in the Dallas/Ft. Worth area and I am looking for a really good doctor for my son who has achalasia. He is 15 years old and was diagnosed 5 years ago and so far no real success that I am happy about. He has had 16 EDG's over the past 5 years which means he has the procedure every 3-6 months as needed. The physician at Children's in Dallas has hit a brick wall with treatment options due to his age and he doesnt want to take any risk just to keep repeating the same thing over and over. I have researched the Heller Myotomy, Does anyone think it would be helpful for my son? Quote Link to comment Share on other sites More sharing options...
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