Guest guest Posted October 31, 2005 Report Share Posted October 31, 2005 Yes.. My son started wearing the corrective shoes at 14 months. And now (at 2 1/2 yrs) has just been fitted with the bar. We're having struggles. Yes at night is apparently the most important time to wear it. H wrote: I want to introduce myself to the group. My name is Holly and we are currently adopting a wonderful baby from China. We requested special needs and she has a right club foot (not sure of the correct term but pointing downward and inward). We hope to bring her home when she is about 16-18 months old. We are so in love with her and can't wait to hold her! Does anyone have experience treating their child as a toddler or older (beginning treatment)? We have emailed Dr. Ponseti and he has been wonderful. We are definately considering going to Iowa for treatment. Also, in all of the brace photos I see a bar between the two shoes. Is this what our daughter will wear when she sleeps even though only one foot is affected? Thanks for your help. We are trying to learn as much as possible and look forward to learning from you! Holly Blessed Mom to Caroline from China -age 6 from Guatemala - age 3 Mia from China- age 1 --------------------------------- Yahoo! FareChase - Search multiple travel sites in one click. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2005 Report Share Posted October 31, 2005 Congratulations on your new baby. They are such blessings. My daughter, Kelsey, was 10 months old when she began Ponseti method treatment. She was 12 months when she had the tenotomy and then almost 13 months when she went into the FAB(the shoes with the bar) for 3 months at 23 hours daily. She has done great. Your daughter will wear the FAB as well even with only one foot affected. Kelsey only has a left clubfoot. She now sleeps in the brace at night. I am so grateful that we chose the Ponseti method even if we chose it late. If it is possible for you to go to Iowa for treatment, I am sure that you will not be sorry. No one knows more about all of this than he does. Jenni --- H wrote: > I want to introduce myself to the group. My name is > Holly and we are currently adopting a > wonderful baby from China. We requested special > needs and she has a right club foot (not sure of the > correct term but pointing downward and inward). We > hope to bring her home when she is about 16-18 > months old. We are so in love with her and can't > wait to hold her! > > Does anyone have experience treating their child as > a toddler or older (beginning treatment)? We have > emailed Dr. Ponseti and he has been wonderful. We > are definately considering going to Iowa for > treatment. > > Also, in all of the brace photos I see a bar between > the two shoes. Is this what our daughter will wear > when she sleeps even though only one foot is > affected? > > Thanks for your help. We are trying to learn as > much as possible and look forward to learning from > you! > > Holly > Blessed Mom to > Caroline from China -age 6 > from Guatemala - age 3 > Mia from China- age 1 > > > > --------------------------------- > Yahoo! FareChase - Search multiple travel sites in > one click. > > [Non-text portions of this message have been > removed] > > Jenni- Mom to (10/31/01) and Kelsey (11/7/03)happy girl in DBB nights only for left clubfoot. __________________________________ Yahoo! Mail - PC Magazine Editors' Choice 2005 http://mail.yahoo.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2005 Report Share Posted October 31, 2005 HI Holly and welcome to the group. What a gift you will receive from adopting this special child. Though my experience is with an infant, a friend of mine and a member of this group, Joyce, adopted a child from China as well. is her name and she suffered from very severe BL CF and is undergoing treatment with Dr. Ponseti. Dr. Ponseti is an amazing man as we have been to him as well. I wish you all the best and please email Joyce. She will be thrilled to hear from you. She has been very busy with , practically living at the Mc House for months while Dr. Ponseti treats who had already learned to walk on her BL CF. It is an amazing story that I am sure she will share with you. Here is her email:childrenloveall@... B. Mom to (6-11-05) corrected BL CF - Ponseti/M 22/7 H wrote: I want to introduce myself to the group. My name is Holly and we are currently adopting a wonderful baby from China. We requested special needs and she has a right club foot (not sure of the correct term but pointing downward and inward). We hope to bring her home when she is about 16-18 months old. We are so in love with her and can't wait to hold her! Does anyone have experience treating their child as a toddler or older (beginning treatment)? We have emailed Dr. Ponseti and he has been wonderful. We are definately considering going to Iowa for treatment. Also, in all of the brace photos I see a bar between the two shoes. Is this what our daughter will wear when she sleeps even though only one foot is affected? Thanks for your help. We are trying to learn as much as possible and look forward to learning from you! Holly Blessed Mom to Caroline from China -age 6 from Guatemala - age 3 Mia from China- age 1 --------------------------------- Yahoo! FareChase - Search multiple travel sites in one click. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2005 Report Share Posted October 31, 2005 Was he casted since 14mo's up till now? What prompted the bar and shoes just now if not? Non-surgical cluboot treatment involves 4-7 weekly castings (9 being the max) and then immediately into the shoes and bar for 3 mo's full time, then gradually decreasing over the next year. Night time wear alone is ONLY indicated after the child has been through the longer hours over the first year in the brace, although older children are often given an accelerated decreasing because of age. They still must wear the brace full time for at least 6w (more like 8 or even 12 depending on severity) and then still gradually decreasing over the next few months. 12-14hr/d (nights only) is the last phase of the treatment process, and comes to walkers who have worn the brace longer hours for a while (most often 12-16mo's in age assuming treatment started in infancy). By then these children are so used to the brace they do not complain much if at all (mine can't hardly sleep without hers actually) which is one of the advantages to having done the longer hours previously. Can you tell us more about his treatment thus far and where you're located (what doc are you seeing?)? With the information you've posted, it sounds like something is very amiss with his treatment and I would recommend that you get a second opinion from a Ponseti trained doc immediately. If you've just been fitted for the FAB (shoes and bar) without proper full correction attained, no wonder he's having struggles wearing it. Uncorrected feet cannot wear this brace well if at all, and most tolerance issues are a result of uncorrected feet prematurely fitted for the FAB. It should not be a struggle at all and absolutely should have been done a long time ago. However it is not too late to get him to a good doc who knows how to treat older children, there has been great success lately with older children so do not despair. Unfortunately not all docs are created equal with this method, and I fear your child may have been a victim of this if indeed he has just started wearing the FAB after this long just in corrective shoes. If I am assuming incorrectly, I apologize. If not however, we can help you to know what should be happening and help you to find someone who can truly fix your son's feet. I am looking forward to hearing more about you and your son. You are not alone with this, many other parents have been in your same shoes only to come out of it with happy little feet. Just let us know a little more about what's going on and we can help you figure it all out. Welcome! Kori At 11:53 AM 10/31/2005, you wrote: >Yes.. My son started wearing the corrective shoes at 14 months. And >now (at 2 1/2 yrs) has just been fitted with the bar. We're having struggles. > Yes at night is apparently the most important time to wear it. > >H wrote: >I want to introduce myself to the group. My name is Holly and >we are currently adopting a wonderful baby from China. We >requested special needs and she has a right club foot (not sure of >the correct term but pointing downward and inward). We hope to >bring her home when she is about 16-18 months old. We are so in >love with her and can't wait to hold her! > >Does anyone have experience treating their child as a toddler or >older (beginning treatment)? We have emailed Dr. Ponseti and he >has been wonderful. We are definately considering going to Iowa for treatment. > >Also, in all of the brace photos I see a bar between the two >shoes. Is this what our daughter will wear when she sleeps even >though only one foot is affected? > >Thanks for your help. We are trying to learn as much as possible >and look forward to learning from you! > >Holly >Blessed Mom to >Caroline from China -age 6 > from Guatemala - age 3 >Mia from China- age 1 > > > >--------------------------------- >Yahoo! FareChase - Search multiple travel sites in one click. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 2, 2005 Report Share Posted November 2, 2005 Welcome to the group Holly. My son was almost 10 months old when we started the Ponseti method. We had a non-Ponseti doctor who was going to operate on 's feet, but luckily I found this group and Dr. Ponseti's website. I believe it's possible to correct feet up to the age of 2 with the Ponseti method. Your daughter will wear the shoes and bar just like children with bilateral clubfeet, but her non-clubfoot will not be rotated as far out. Good luck to you and let us know how things go. and 11/10/03 bilateral cf dbb 14/7 > > I want to introduce myself to the group. My name is Holly and we are currently adopting a wonderful baby from China. We requested special needs and she has a right club foot (not sure of the correct term but pointing downward and inward). We hope to bring her home when she is about 16-18 months old. We are so in love with her and can't wait to hold her! > > Does anyone have experience treating their child as a toddler or older (beginning treatment)? We have emailed Dr. Ponseti and he has been wonderful. We are definately considering going to Iowa for treatment. > > Also, in all of the brace photos I see a bar between the two shoes. Is this what our daughter will wear when she sleeps even though only one foot is affected? > > Thanks for your help. We are trying to learn as much as possible and look forward to learning from you! > > Holly > Blessed Mom to > Caroline from China -age 6 > from Guatemala - age 3 > Mia from China- age 1 > > > > --------------------------------- > Yahoo! FareChase - Search multiple travel sites in one click. > > Quote Link to comment Share on other sites More sharing options...
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