Guest guest Posted May 15, 2010 Report Share Posted May 15, 2010 , There is almost an entirely different treatment plan for young kids with congenital scoliosis than for those with no spine malformations. There is a group for families dealing with congenital scoliosis, if you find out you need us. CongenitalScoliosisSupport/Hope you don't, but if you do, there are great experiences to hear about.CarmellMom to Kara, idiopathic scoliosis and hypothyroidism, Blake 19, GERD, and Braydon 14, VACTERL-congenital scoliosis (fusion surgery 5/96), VEPTR patient #137 (implant 8/01), Thoracic Insufficiency Syndrome (TIS), rib anomalies, missing coccyx, fatty filum/TC (released 4/99 & 12/06), anal stenosis, chronic constipation, horseshoe (cross-fused) kidney, dbl ureter in left kidney, ureterocele (excized 6/95), kidney reflux (reimplant surgery 1/97), neurogenic bladder, dysplastic right leg w/right clubfoot with 8 toes (repaired 2/96, 3/96, 1/97, 3/04), tibial torsion, 4cm length discrepancy-wears 3cm lift, valgus deformity, GERD, Gastroparesis, SUA, etc. http://carmellb-ivil.tripod.com/myfamily/Congenital scoliosis support groupCongenitalScoliosisSupport/ Quote Link to comment Share on other sites More sharing options...
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