Guest guest Posted October 20, 2003 Report Share Posted October 20, 2003 Hi , my 2 year old son Collin had surgery at 8 weeks old at AI Dupont in Wilmingon, DE with Dr. Jay. I know I told that to someone recently so it could of been you, sorry if I'm repeating myself. We stopped seeing Dr. Jay around the time Collin started to walk, we started seeing Dr. Herzenberg this month and it was the best decsion that I have made so far. Dr. H said Collin's foot is stiff from the surgery he had at 8 weeks old, and he avoids that way of doing things. Dupont was about a 45 min drive for me Dr. H is about a 2 hour drive for me and that extra hour is so worth it!!! Also Collin just started to relapse recently, and DR. H has just put him into a corrective cast, Dr. Jay only used long leg casts on Collin after his surgery, he had Collin in a few short leg casts before the surgery, and in no casts for a few weeks before the surgery, I trusted him because he had 20 + years of clubfoot treatment experience, but I don't think he even tried to treat Collin with just corrective casts, I think he planned on doing the suregery at 8 weeks old from the day we met him. I didn't know anything about clubfoot at the time, and was rushing to do research, etc. I can't change the past but if I could, I would of held off on the surgery and tried to find someone that used a ponsieti method, and tried to treat his feet with casting before quickly jumping to surgery. I hope this helps, also ask Dr. Jay how many of the babies he treats relapse by a few years old, because now you deffienaly know of one. Maybe the relapse rate will be less with Dr. H, I don 't know but it would be a good question to ask both of them. I am a very involved parent and have done everything like all of the dr.'s have instructed me, so I know the relapse isn't because I didn't put his DBB on him on anything like that, I did everything exactly as they all told me. Dr. H did tell me that Dr. Jay attended one of his recent seminars so maybe Dr. Jay is thinking about switching methods, or second guessing what he has been doing. I use to ask him if he was doing the ponsieti method, and he never quite told me no, but he was deffianlty just doing his own variation of it from what I know and understand now. I even asked some med students a few times, and they never told me either that it was just him own vatiation of the method. I hope it doesn't seem like I'm bashing him because he is a very smart man with a lot of experience, and everyone at the hopital was very nice and it was clean, had indoor & outdoor playgrounds, etc there but alls I'm trying to say, is if I could go back in time I would not have seen him, I would of seen Dr. H and used Dr. Jay as a backup plan if I didn't like the treatment Dr. H was given, etc. Michele Collin 8-24-01 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 23, 2003 Report Share Posted October 23, 2003 Hello! My wife and I (more my wife) gave birth to our first daughter 3 weeks ago. We found out that our daughter may have clubbed feet at an ultrasound around 7 months. The doctor requested that we revisit to confirm but, after much discussion, we decided against it because it would do us no good to revisit so we prayed and awaited the birth. As soon as the our daughter was born, my eyes shot toward her feet and, to my surprise, she had bilateral clubbed feet. While saddened, I was more determined than anything else and spent the next few days investigating possible treatments. It was then that I came accross this board and spent hours reading. Luckily, we have a physician 2 miles from our small town in land who specialized in the Ponsetti method (Dr. Tuck). We made our first appointment 4 days after her birth and she was casted. Dr. Tuck stated that her feet responded well to massaging and started her at level 3 casts. We have since gone back twice and our daughter was able to go from level 3 to level 6 casts within 2 weeks. On Monday her casts were removed and we ordered the DBB shoes. Shoes arrived today and Dr. Tuck put them on. This is the first time our daughter has been fussy as she is still getting used to them. We continue to pray and would like to thank everybody who contributes to this board. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2004 Report Share Posted January 3, 2004 Hi christina welcome to the group,we see Dr.Dobbs also. My daughter Isabella was born october 6,2002 bilateral clubbed feet. She was corrected by Dr.Bonar but we had to move because of my husbands new job so now we see Dr.Dobbs. Even though he wasn't the doctor who corrected Isabella he now sees her and I am very pleased with him. I am so glad we are able to see him now. I feel very confident that he will treat my daughters feet correctly. It sounds like you have been through alot. I feel you are in great hands. Just follow Dr.Dobbs instructions and do as he says and everything will be fine. I don't know what to tell you about the head deformity. My first daughter would always hold her head to the right and the doctor made me lay her on her belly so her neck would get stronger. I did that and in a few months she was just fine. I don't know if that was what you were refering to on your son favoring the right side. As for my clubbed foot child. Isabella is doing great. She is 15 months old and is running around like crazy. She started walking at 12 months. Her left clubbed foot was alot stiffer than her right foot but since she has been walking Dr.Dobbs was amazed that her left foot is alot looser now. He said the more walking she does the better so we have her walk everywhere. Well good luck. If you need anything just email me at lemikha@... We go back to Dr.Dobbs on March 4th maybe we will see you one day there. It would be great to meet parents who are going through the same thing as I. (Isabella 10-12-02 bilateral cf) > Hi my name is Kramer I am from Belleville, IL. My son has > congenital bilateral Clubfoot. He was born 7 weeks prematue. He sees > Dr. Dobbs at Shriner's in St. Louis, MO. I think that he is a > wonderful DR. He has put my son first. He won't cast him until his > feet are big enough. What I mean by that is that only weigh > 3lbs. 8oz. at birth. He was casted three times while he was in the > NICU. When he went to see DR.DOBBS he wouldn't recast him until he > thinks that his feet is big enough for the shoes. > > So please anyone who's child has seen Dr. Dobbs I would like some > info. Who's child has had a positional head deformity. My son really > favors his R side. > > He is 3 months old now and is hopefully getting casted Jan.15, 2004. > > Kramer Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2004 Report Share Posted January 3, 2004 Hi , Jordan was born 4-9-00 with bilateral clubfoot and his head tilted slightly to one side. This was a serious problem when breastfeeding him. He screamed bloody murder whenever I tried to feed him on my right side. I assumed it was because the shortened tendon in his neck (?) hurt when trying to bend into me. I can't remember how long it was before he stopped favoring that side. Probably when he was six months old it ceased to be an issue. Neither of his doctors (original hospital orthopedic surgeon, and then Ponseti Method Dr. we saw when he was four months old) seemed to think it was related to clubfoot. I had a cousin born with a similar tilt though. Thanks to Dr. Colburn Jordan's feet are perfect. Again, nothing was done to address his tilted head. It disappeared as he matured. Hope this helps a bit. Congrats on your baby boy! Eddie and Jordan new member Hi my name is Kramer I am from Belleville, IL. My son has congenital bilateral Clubfoot. He was born 7 weeks prematue. He sees Dr. Dobbs at Shriner's in St. Louis, MO. I think that he is a wonderful DR. He has put my son first. He won't cast him until his feet are big enough. What I mean by that is that only weigh 3lbs. 8oz. at birth. He was casted three times while he was in the NICU. When he went to see DR.DOBBS he wouldn't recast him until he thinks that his feet is big enough for the shoes. So please anyone who's child has seen Dr. Dobbs I would like some info. Who's child has had a positional head deformity. My son really favors his R side. He is 3 months old now and is hopefully getting casted Jan.15, 2004. Kramer Quote Link to comment Share on other sites More sharing options...
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