Guest guest Posted August 4, 2004 Report Share Posted August 4, 2004 Hello Jagjit, Congratulations on the birth of your son! The doctors were right, there is no reason to worry. Clubfeet, as they are also called, are very fixable! You are on the right board if you are interested in the Ponseti Method! Our daughter was born in February with one clubfoot which has been now corrected using the Ponseti Method. She wears the Foot Abduction Brace to maintain the correction and will do so until she is 3-4 years old. The treatment that they are suggesting you start with is not how the Ponseti Method works. Here is a brief summary of the steps. Casting of the feet should begin ASAP, our daughter received her first cast at 8 days old. It was changed weekly for five casts (it is an above the knee cast, can be from 5-9 casts). Each one rotated the foot out further. The Dr. then performed a tenotomy to release the achilles tendon. Clubfoot children's tendon is often short or tight. This is more of a procedure than a surgery, it allows the foot to have more dorsiflexion (when you flex your foot up). It took 20 minutes and can be done either in the dr. office or in the O.R., different doctors have different preferences. She then had a cast for 3 weeks while the tendon healed. She will now wear a Foot Abduction Brace (FAB) until she is 3-4 years old. At first it is worn 23 hours/day for 3 months. Then time is reduced to 16-18 hours/day until they crawl and then it is nap and night until they walk, then last, bed time until 3-4 years old. The FAB keeps the correction of the foot. It is two shoes with a bar attached to the bottom and the shoes are rotated out. Our daughter is 5 months old and is doing the things that she should, starting to sit up, rolling over, bringing her knees up to get ready to crawl, etc. I have read wonderful stories about their active children doing all the sports, dancing, running and playing that children without clubfeet do. There is a difference in the genetic makeup of the lower leg and foot, so the foot may be smaller and the calves may be thinner, but I have also read stories about how you can't tell the difference between the two feet and legs. If you haven't been to Dr. Ponseti's webite, here is the link. http://www.vh.org/pediatric/patient/orthopaedics/clubfeet/index.html There is a gentleman on this board named Egbert who has knowledge about doctors in India who practice the method, he will likely comment on specifics for you. Best of luck in your decision making! Keep us posted on how things go and if you have any questions, ask away! Louisa 6-27-99 Zoe 2-22-04 Right Unilateral Clubfoot -- In nosurgery4clubfoot , " Jagjit Singh " wrote: > My wife delivered a Baby Boy last week who's born with Billateral > Talipes. We are based in Mumbai. Having consulted with a few > doctors, who assured me that there is nothing to get worried about > and the fact that this is 100% curable, i thought it will be better > off to find some more information on the condition & related > treatments on the internet. > > I came across the Ponseti method. Though I am in no position (with > my limited knowledge) to decide whats the best treatment for the > baby. > > At the moment doctors have suggested for some foot exercise to be > performed 200-250 times a day for next 1.5 months and then they > propose to put a casting / plaster (5 of them to be changed every 2 > weeks). This according to the doctors would cure the disorder / > condition upto 90% and if required a surgery. > > I would appreciate your advice & assistance on the same. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2004 Report Share Posted August 4, 2004 Hello Jagjit, Congratulations on the birth of your son! The doctors were right, there is no reason to worry. Clubfeet, as they are also called, are very fixable! You are on the right board if you are interested in the Ponseti Method! Our daughter was born in February with one clubfoot which has been now corrected using the Ponseti Method. She wears the Foot Abduction Brace to maintain the correction and will do so until she is 3-4 years old. The treatment that they are suggesting you start with is not how the Ponseti Method works. Here is a brief summary of the steps. Casting of the feet should begin ASAP, our daughter received her first cast at 8 days old. It was changed weekly for five casts (it is an above the knee cast, can be from 5-9 casts). Each one rotated the foot out further. The Dr. then performed a tenotomy to release the achilles tendon. Clubfoot children's tendon is often short or tight. This is more of a procedure than a surgery, it allows the foot to have more dorsiflexion (when you flex your foot up). It took 20 minutes and can be done either in the dr. office or in the O.R., different doctors have different preferences. She then had a cast for 3 weeks while the tendon healed. She will now wear a Foot Abduction Brace (FAB) until she is 3-4 years old. At first it is worn 23 hours/day for 3 months. Then time is reduced to 16-18 hours/day until they crawl and then it is nap and night until they walk, then last, bed time until 3-4 years old. The FAB keeps the correction of the foot. It is two shoes with a bar attached to the bottom and the shoes are rotated out. Our daughter is 5 months old and is doing the things that she should, starting to sit up, rolling over, bringing her knees up to get ready to crawl, etc. I have read wonderful stories about their active children doing all the sports, dancing, running and playing that children without clubfeet do. There is a difference in the genetic makeup of the lower leg and foot, so the foot may be smaller and the calves may be thinner, but I have also read stories about how you can't tell the difference between the two feet and legs. If you haven't been to Dr. Ponseti's webite, here is the link. http://www.vh.org/pediatric/patient/orthopaedics/clubfeet/index.html There is a gentleman on this board named Egbert who has knowledge about doctors in India who practice the method, he will likely comment on specifics for you. Best of luck in your decision making! Keep us posted on how things go and if you have any questions, ask away! Louisa 6-27-99 Zoe 2-22-04 Right Unilateral Clubfoot -- In nosurgery4clubfoot , " Jagjit Singh " wrote: > My wife delivered a Baby Boy last week who's born with Billateral > Talipes. We are based in Mumbai. Having consulted with a few > doctors, who assured me that there is nothing to get worried about > and the fact that this is 100% curable, i thought it will be better > off to find some more information on the condition & related > treatments on the internet. > > I came across the Ponseti method. Though I am in no position (with > my limited knowledge) to decide whats the best treatment for the > baby. > > At the moment doctors have suggested for some foot exercise to be > performed 200-250 times a day for next 1.5 months and then they > propose to put a casting / plaster (5 of them to be changed every 2 > weeks). This according to the doctors would cure the disorder / > condition upto 90% and if required a surgery. > > I would appreciate your advice & assistance on the same. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2004 Report Share Posted August 4, 2004 Hello Jagjit, Congratulations on the birth of your son! The doctors were right, there is no reason to worry. Clubfeet, as they are also called, are very fixable! You are on the right board if you are interested in the Ponseti Method! Our daughter was born in February with one clubfoot which has been now corrected using the Ponseti Method. She wears the Foot Abduction Brace to maintain the correction and will do so until she is 3-4 years old. The treatment that they are suggesting you start with is not how the Ponseti Method works. Here is a brief summary of the steps. Casting of the feet should begin ASAP, our daughter received her first cast at 8 days old. It was changed weekly for five casts (it is an above the knee cast, can be from 5-9 casts). Each one rotated the foot out further. The Dr. then performed a tenotomy to release the achilles tendon. Clubfoot children's tendon is often short or tight. This is more of a procedure than a surgery, it allows the foot to have more dorsiflexion (when you flex your foot up). It took 20 minutes and can be done either in the dr. office or in the O.R., different doctors have different preferences. She then had a cast for 3 weeks while the tendon healed. She will now wear a Foot Abduction Brace (FAB) until she is 3-4 years old. At first it is worn 23 hours/day for 3 months. Then time is reduced to 16-18 hours/day until they crawl and then it is nap and night until they walk, then last, bed time until 3-4 years old. The FAB keeps the correction of the foot. It is two shoes with a bar attached to the bottom and the shoes are rotated out. Our daughter is 5 months old and is doing the things that she should, starting to sit up, rolling over, bringing her knees up to get ready to crawl, etc. I have read wonderful stories about their active children doing all the sports, dancing, running and playing that children without clubfeet do. There is a difference in the genetic makeup of the lower leg and foot, so the foot may be smaller and the calves may be thinner, but I have also read stories about how you can't tell the difference between the two feet and legs. If you haven't been to Dr. Ponseti's webite, here is the link. http://www.vh.org/pediatric/patient/orthopaedics/clubfeet/index.html There is a gentleman on this board named Egbert who has knowledge about doctors in India who practice the method, he will likely comment on specifics for you. Best of luck in your decision making! Keep us posted on how things go and if you have any questions, ask away! Louisa 6-27-99 Zoe 2-22-04 Right Unilateral Clubfoot -- In nosurgery4clubfoot , " Jagjit Singh " wrote: > My wife delivered a Baby Boy last week who's born with Billateral > Talipes. We are based in Mumbai. Having consulted with a few > doctors, who assured me that there is nothing to get worried about > and the fact that this is 100% curable, i thought it will be better > off to find some more information on the condition & related > treatments on the internet. > > I came across the Ponseti method. Though I am in no position (with > my limited knowledge) to decide whats the best treatment for the > baby. > > At the moment doctors have suggested for some foot exercise to be > performed 200-250 times a day for next 1.5 months and then they > propose to put a casting / plaster (5 of them to be changed every 2 > weeks). This according to the doctors would cure the disorder / > condition upto 90% and if required a surgery. > > I would appreciate your advice & assistance on the same. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2004 Report Share Posted August 4, 2004 Jagjit, Here is a listing of doctors in India on Dr. Ponseti's web site who are approved in the use of his method. There may also be others in India who are using the method as well. The description that you have given of a month of physiotherapy does not sound like the Ponseti method, but if they indicated that they avoid the surgery 90% of the time, that sounds like the Ponseti method. If you have any questions, I encourage you to e-mail some of the following doctors. Ponseti method doctors in India. Milind Chaudhary, M.D. Chaudhary Trust Hospital Civil Lines Akola, India 444001 akl_milind7 @ sancharnet.in Dr. Dhiren Ganjwala 302, Anshi Avenue, Gulbai Tekra Ahmedabad, Gujarat, India 380 015 Tel: 91 982500 25600 Email Dr. Ganjwala gangwala @ icenet.net Dr. Varghese New Delhi, India Email Dr. Varghese ssh @ vsnl.com Dr. Joy Patankar Bombay, India Email Dr. Patankar joypatankar @ yahoo.com and (born 3-17-99) > My wife delivered a Baby Boy last week who's born with Billateral > Talipes. We are based in Mumbai. Having consulted with a few > doctors, who assured me that there is nothing to get worried about > and the fact that this is 100% curable, i thought it will be better > off to find some more information on the condition & related > treatments on the internet. > > I came across the Ponseti method. Though I am in no position (with > my limited knowledge) to decide whats the best treatment for the > baby. > > At the moment doctors have suggested for some foot exercise to be > performed 200-250 times a day for next 1.5 months and then they > propose to put a casting / plaster (5 of them to be changed every 2 > weeks). This according to the doctors would cure the disorder / > condition upto 90% and if required a surgery. > > I would appreciate your advice & assistance on the same. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2004 Report Share Posted August 4, 2004 Hi, Congratulations on the birth of your baby boy! I remember none of our doctors was very concerned about her foot being bent. It wasn't until we saw the specialist that we heard the words " clubfoot " . I had read everything I could get my hands on about pregnancy and childbirth, and I'm still amazed that there wasn't any information anywhere about the most common birth defect! Then I had to go home and do a google search on clubfoot to find out what it was. We were lucky. Our second doctor was just starting with the method...but was making modifications. Fortunately, we found this website, educated ourselves, and made the decision to switch to a more qualified doctor. Although we understood the importance of our child being a " guinea pig " in order for a new doctor to learn the method, we were only going to go so far once we saw the changes our doctor was making to the ponseti method. If you would like to learn about our experience with the Ponseti method, please check out our website: www.geocities.com/joannewalton2003/clubfootstory.html I do think the word is slowly getting out. When I mentioned our experience to one of my daughter's pediatricians, he was happy to report that there had been a special local meeting of pediatricians specifically about the " new " method of treating clubfoot. There is an organization in the US working with the Indian government and a Canadian doctor to try and train more doctors in India. It's called A Leg to Stand On. The website is www.altso.org. Best to you. Look forward to reading about your progress. Joanne Walton, mom to Zoe (3-25-01, right clubfoot) Message: 11 Date: Wed, 04 Aug 2004 15:35:18 -0000 Subject: Baby with Billateral Talipes My wife delivered a Baby Boy last week who's born with Billateral Talipes. We are based in Mumbai. Having consulted with a few doctors, who assured me that there is nothing to get worried about and the fact that this is 100% curable, i thought it will be better off to find some more information on the condition & related treatments on the internet. I came across the Ponseti method. Though I am in no position (with my limited knowledge) to decide whats the best treatment for the baby. At the moment doctors have suggested for some foot exercise to be performed 200-250 times a day for next 1.5 months and then they propose to put a casting / plaster (5 of them to be changed every 2 weeks). This according to the doctors would cure the disorder / condition upto 90% and if required a surgery. I would appreciate your advice & assistance on the same. _________________________________________________________________ Overwhelmed by debt? Find out how to ‘Dig Yourself Out of Debt’ from MSN Money. http://special.msn.com/money/0407debt.armx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2004 Report Share Posted August 4, 2004 Dear Jagjit, I am from Hyderabad. The following are contact numbers of Doctors in Mumbai and Ahmedabad. Dr. Dhiren Ganjwala 302, Anshi Avenue, Gulbai Tekra Ahmedabad, Gujarat, India 380 015 982500 25600 ganjwala@... Dr. Joy Patankar Bombay, India 9820076126 I tried the conventional way of what you said in your mail. I am not happy with the correction, so I am planning to take my son to Ahmedabad next week. If you need any info, please feel free to contact me. Satyendra 09849377818 > My wife delivered a Baby Boy last week who's born with Billateral > Talipes. We are based in Mumbai. Having consulted with a few > doctors, who assured me that there is nothing to get worried about > and the fact that this is 100% curable, i thought it will be better > off to find some more information on the condition & related > treatments on the internet. > > I came across the Ponseti method. Though I am in no position (with > my limited knowledge) to decide whats the best treatment for the > baby. > > At the moment doctors have suggested for some foot exercise to be > performed 200-250 times a day for next 1.5 months and then they > propose to put a casting / plaster (5 of them to be changed every 2 > weeks). This according to the doctors would cure the disorder / > condition upto 90% and if required a surgery. > > I would appreciate your advice & assistance on the same. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.