Guest guest Posted September 19, 2005 Report Share Posted September 19, 2005 - How do I go about joining the CF pic site? Is there a link? thnx, Stacie wrote: Hi Stacey, Our daughter also has right unilateral. Glad that Jordan's foot looks so good! Everything about Jordan's treatment sounds right except usually the 23/7 wear is for 3 months give or take a bit (Grace was no where near pulling up when her hours were reduced - she was 4.5 mos). Not a biggie, you have already gotten past that and I am sure that longer is better than a shorter time at 23/7. You must have been sooo happy when his time was reduced!! 6 months is a long time at 23/7! Jordan will get really good at pulling up, crawling and cruising in his shoes!! Even if he dosen't have them on a lot when he is up he will probably be doing it in his crib. Have you guys joined the CFpics site? Would love to see a pic of him and his little right foot! tc & Grace > Hi Stacie, > > I am curious, how long in total did he wear the shoes 23/7? I thought > that the protocol for Ponseti trained doctor's was to prescribe 23/7 > brace wear for 3 months unless the foot was atypical or otherwise a > challenge to treat. > > & Grace > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > until he could pull himself up to a stand w/ the shoes on... that was > at about 9 months old. I would check on that w/ Ponseti. > > Good Luck! > > Stacie > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 19, 2005 Report Share Posted September 19, 2005 - How do I go about joining the CF pic site? Is there a link? thnx, Stacie wrote: Hi Stacey, Our daughter also has right unilateral. Glad that Jordan's foot looks so good! Everything about Jordan's treatment sounds right except usually the 23/7 wear is for 3 months give or take a bit (Grace was no where near pulling up when her hours were reduced - she was 4.5 mos). Not a biggie, you have already gotten past that and I am sure that longer is better than a shorter time at 23/7. You must have been sooo happy when his time was reduced!! 6 months is a long time at 23/7! Jordan will get really good at pulling up, crawling and cruising in his shoes!! Even if he dosen't have them on a lot when he is up he will probably be doing it in his crib. Have you guys joined the CFpics site? Would love to see a pic of him and his little right foot! tc & Grace > Hi Stacie, > > I am curious, how long in total did he wear the shoes 23/7? I thought > that the protocol for Ponseti trained doctor's was to prescribe 23/7 > brace wear for 3 months unless the foot was atypical or otherwise a > challenge to treat. > > & Grace > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > until he could pull himself up to a stand w/ the shoes on... that was > at about 9 months old. I would check on that w/ Ponseti. > > Good Luck! > > Stacie > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 19, 2005 Report Share Posted September 19, 2005 http://health.groups.yahoo.com/group/CFPics/ Check the email addy you used to sign up with as there will be a file sent to you with information about the list, and in that file you will find a little survey to fill out. Reply to that email, copy the survey section into the body of the email, answer the really easy and simple questions (asks about you - very general but it weeds out the wackos) and send it back to me. I'll get you approved as soon as I see the survey which will then be forwarded to the list to introduce and welcome you. Make sure you're on individual emails if you want to see the pictures people send You will not be able to look at previous attachments on the website, yahoo does not archive attachments anymore. This is why you'll need to be on individual emails for this list. If you want to see a particular picture that was sent before you joined, email the original poster and ask them to send you copies of the photos directly. If you want to send a picture, just send an email with your photo embedded or attached right to the list as a post. Just like this list, but the CFPics list accepts attachments. There is a photo section on the website that we use for our photo library but we don't have personal folders there. All the pictures are sent to the list in emails so we can keep the library freed up for educational photos. Yahoo only allows so much space for photos and files and when it's filled... no one can access the photos until a moderator deletes some. It ends up being a mess with not knowing if it's ok to delete something or whatever... so we just don't post photos there and leave it as a reference library for parents. I need to update the library big time I know... will try to work on that someday soon. Everyone is welcome of course as long as you're not a wacko, but PLEASE fill out the survey. I don't approve people without that, sorry. The wacko factor is too real with this list so we've had to be strict with that rule. I know I've missed a lot of people who wanted to join but I don't have enough time to police the requests and remind people to send the survey back. After 14 days your subscription request expires so please, if you want to join this list make sure you read the file that is sent to you and send back the survey. Thanks and I hope to see some new subs soon! Oh, we love pictures of feet... but we ADORE pictures of faces and families! Fun list to be a part of if you like to see who you're talking about/to online. Lots of babies of course but we also have the occasional mom or brother/sister, pet, tattoo... :-D Kori CFPics Owner and Mama 'o Darb At 08:45 PM 9/19/2005, you wrote: >- >How do I go about joining the CF pic site? Is there a link? >thnx, >Stacie > > wrote: >Hi Stacey, > >Our daughter also has right unilateral. Glad that Jordan's foot looks >so good! Everything about Jordan's treatment sounds right except >usually the 23/7 wear is for 3 months give or take a bit (Grace was >no where near pulling up when her hours were reduced - she was 4.5 >mos). Not a biggie, you have already gotten past that and I am sure >that longer is better than a shorter time at 23/7. > >You must have been sooo happy when his time was reduced!! 6 months is >a long time at 23/7! Jordan will get really good at pulling up, >crawling and cruising in his shoes!! Even if he dosen't have them on >a lot when he is up he will probably be doing it in his crib. > >Have you guys joined the CFpics site? Would love to see a pic of him >and his little right foot! > >tc > & Grace > > > > Hi Stacie, > > > > I am curious, how long in total did he wear the shoes 23/7? I >thought > > that the protocol for Ponseti trained doctor's was to prescribe >23/7 > > brace wear for 3 months unless the foot was atypical or otherwise a > > challenge to treat. > > > > & Grace > > > > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > > until he could pull himself up to a stand w/ the shoes on... that >was > > at about 9 months old. I would check on that w/ Ponseti. > > > Good Luck! > > > Stacie > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 19, 2005 Report Share Posted September 19, 2005 http://health.groups.yahoo.com/group/CFPics/ Check the email addy you used to sign up with as there will be a file sent to you with information about the list, and in that file you will find a little survey to fill out. Reply to that email, copy the survey section into the body of the email, answer the really easy and simple questions (asks about you - very general but it weeds out the wackos) and send it back to me. I'll get you approved as soon as I see the survey which will then be forwarded to the list to introduce and welcome you. Make sure you're on individual emails if you want to see the pictures people send You will not be able to look at previous attachments on the website, yahoo does not archive attachments anymore. This is why you'll need to be on individual emails for this list. If you want to see a particular picture that was sent before you joined, email the original poster and ask them to send you copies of the photos directly. If you want to send a picture, just send an email with your photo embedded or attached right to the list as a post. Just like this list, but the CFPics list accepts attachments. There is a photo section on the website that we use for our photo library but we don't have personal folders there. All the pictures are sent to the list in emails so we can keep the library freed up for educational photos. Yahoo only allows so much space for photos and files and when it's filled... no one can access the photos until a moderator deletes some. It ends up being a mess with not knowing if it's ok to delete something or whatever... so we just don't post photos there and leave it as a reference library for parents. I need to update the library big time I know... will try to work on that someday soon. Everyone is welcome of course as long as you're not a wacko, but PLEASE fill out the survey. I don't approve people without that, sorry. The wacko factor is too real with this list so we've had to be strict with that rule. I know I've missed a lot of people who wanted to join but I don't have enough time to police the requests and remind people to send the survey back. After 14 days your subscription request expires so please, if you want to join this list make sure you read the file that is sent to you and send back the survey. Thanks and I hope to see some new subs soon! Oh, we love pictures of feet... but we ADORE pictures of faces and families! Fun list to be a part of if you like to see who you're talking about/to online. Lots of babies of course but we also have the occasional mom or brother/sister, pet, tattoo... :-D Kori CFPics Owner and Mama 'o Darb At 08:45 PM 9/19/2005, you wrote: >- >How do I go about joining the CF pic site? Is there a link? >thnx, >Stacie > > wrote: >Hi Stacey, > >Our daughter also has right unilateral. Glad that Jordan's foot looks >so good! Everything about Jordan's treatment sounds right except >usually the 23/7 wear is for 3 months give or take a bit (Grace was >no where near pulling up when her hours were reduced - she was 4.5 >mos). Not a biggie, you have already gotten past that and I am sure >that longer is better than a shorter time at 23/7. > >You must have been sooo happy when his time was reduced!! 6 months is >a long time at 23/7! Jordan will get really good at pulling up, >crawling and cruising in his shoes!! Even if he dosen't have them on >a lot when he is up he will probably be doing it in his crib. > >Have you guys joined the CFpics site? Would love to see a pic of him >and his little right foot! > >tc > & Grace > > > > Hi Stacie, > > > > I am curious, how long in total did he wear the shoes 23/7? I >thought > > that the protocol for Ponseti trained doctor's was to prescribe >23/7 > > brace wear for 3 months unless the foot was atypical or otherwise a > > challenge to treat. > > > > & Grace > > > > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > > until he could pull himself up to a stand w/ the shoes on... that >was > > at about 9 months old. I would check on that w/ Ponseti. > > > Good Luck! > > > Stacie > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2005 Report Share Posted September 21, 2005 I know this is a little late in coming but we just came back from a visit with Dr. ponseti on 9/19. Our son Eli is almost 5 months old and he was just reduced to 12 hours a day! I was rather surprised but this is coming from THE Doctor himself. Eli started casting (once a week for 5 weeks) at the end of May. Had the heel cord release after the 4th cast, wore the 5th one for 3 weeks, we took that off ourselves (as per Dr. P's instructions) and started the shoes23/7 on July 11. We then went to see Dr. Ponseti on Aug 1 and were reduced to 16-18/7. Now on the 19th we are down to 12/7. It all seemed a lot quicker than I have read on all the postings, we are very happy but I guess there are variations here and there on brace protocol even coming directly from Dr. Ponseti. Leah frogabog wrote: http://health.groups.yahoo.com/group/CFPics/ Check the email addy you used to sign up with as there will be a file sent to you with information about the list, and in that file you will find a little survey to fill out. Reply to that email, copy the survey section into the body of the email, answer the really easy and simple questions (asks about you - very general but it weeds out the wackos) and send it back to me. I'll get you approved as soon as I see the survey which will then be forwarded to the list to introduce and welcome you. Make sure you're on individual emails if you want to see the pictures people send You will not be able to look at previous attachments on the website, yahoo does not archive attachments anymore. This is why you'll need to be on individual emails for this list. If you want to see a particular picture that was sent before you joined, email the original poster and ask them to send you copies of the photos directly. If you want to send a picture, just send an email with your photo embedded or attached right to the list as a post. Just like this list, but the CFPics list accepts attachments. There is a photo section on the website that we use for our photo library but we don't have personal folders there. All the pictures are sent to the list in emails so we can keep the library freed up for educational photos. Yahoo only allows so much space for photos and files and when it's filled... no one can access the photos until a moderator deletes some. It ends up being a mess with not knowing if it's ok to delete something or whatever... so we just don't post photos there and leave it as a reference library for parents. I need to update the library big time I know... will try to work on that someday soon. Everyone is welcome of course as long as you're not a wacko, but PLEASE fill out the survey. I don't approve people without that, sorry. The wacko factor is too real with this list so we've had to be strict with that rule. I know I've missed a lot of people who wanted to join but I don't have enough time to police the requests and remind people to send the survey back. After 14 days your subscription request expires so please, if you want to join this list make sure you read the file that is sent to you and send back the survey. Thanks and I hope to see some new subs soon! Oh, we love pictures of feet... but we ADORE pictures of faces and families! Fun list to be a part of if you like to see who you're talking about/to online. Lots of babies of course but we also have the occasional mom or brother/sister, pet, tattoo... :-D Kori CFPics Owner and Mama 'o Darb At 08:45 PM 9/19/2005, you wrote: >- >How do I go about joining the CF pic site? Is there a link? >thnx, >Stacie > > wrote: >Hi Stacey, > >Our daughter also has right unilateral. Glad that Jordan's foot looks >so good! Everything about Jordan's treatment sounds right except >usually the 23/7 wear is for 3 months give or take a bit (Grace was >no where near pulling up when her hours were reduced - she was 4.5 >mos). Not a biggie, you have already gotten past that and I am sure >that longer is better than a shorter time at 23/7. > >You must have been sooo happy when his time was reduced!! 6 months is >a long time at 23/7! Jordan will get really good at pulling up, >crawling and cruising in his shoes!! Even if he dosen't have them on >a lot when he is up he will probably be doing it in his crib. > >Have you guys joined the CFpics site? Would love to see a pic of him >and his little right foot! > >tc > & Grace > > > > Hi Stacie, > > > > I am curious, how long in total did he wear the shoes 23/7? I >thought > > that the protocol for Ponseti trained doctor's was to prescribe >23/7 > > brace wear for 3 months unless the foot was atypical or otherwise a > > challenge to treat. > > > > & Grace > > > > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > > until he could pull himself up to a stand w/ the shoes on... that >was > > at about 9 months old. I would check on that w/ Ponseti. > > > Good Luck! > > > Stacie > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2005 Report Share Posted September 21, 2005 I know this is a little late in coming but we just came back from a visit with Dr. ponseti on 9/19. Our son Eli is almost 5 months old and he was just reduced to 12 hours a day! I was rather surprised but this is coming from THE Doctor himself. Eli started casting (once a week for 5 weeks) at the end of May. Had the heel cord release after the 4th cast, wore the 5th one for 3 weeks, we took that off ourselves (as per Dr. P's instructions) and started the shoes23/7 on July 11. We then went to see Dr. Ponseti on Aug 1 and were reduced to 16-18/7. Now on the 19th we are down to 12/7. It all seemed a lot quicker than I have read on all the postings, we are very happy but I guess there are variations here and there on brace protocol even coming directly from Dr. Ponseti. Leah frogabog wrote: http://health.groups.yahoo.com/group/CFPics/ Check the email addy you used to sign up with as there will be a file sent to you with information about the list, and in that file you will find a little survey to fill out. Reply to that email, copy the survey section into the body of the email, answer the really easy and simple questions (asks about you - very general but it weeds out the wackos) and send it back to me. I'll get you approved as soon as I see the survey which will then be forwarded to the list to introduce and welcome you. Make sure you're on individual emails if you want to see the pictures people send You will not be able to look at previous attachments on the website, yahoo does not archive attachments anymore. This is why you'll need to be on individual emails for this list. If you want to see a particular picture that was sent before you joined, email the original poster and ask them to send you copies of the photos directly. If you want to send a picture, just send an email with your photo embedded or attached right to the list as a post. Just like this list, but the CFPics list accepts attachments. There is a photo section on the website that we use for our photo library but we don't have personal folders there. All the pictures are sent to the list in emails so we can keep the library freed up for educational photos. Yahoo only allows so much space for photos and files and when it's filled... no one can access the photos until a moderator deletes some. It ends up being a mess with not knowing if it's ok to delete something or whatever... so we just don't post photos there and leave it as a reference library for parents. I need to update the library big time I know... will try to work on that someday soon. Everyone is welcome of course as long as you're not a wacko, but PLEASE fill out the survey. I don't approve people without that, sorry. The wacko factor is too real with this list so we've had to be strict with that rule. I know I've missed a lot of people who wanted to join but I don't have enough time to police the requests and remind people to send the survey back. After 14 days your subscription request expires so please, if you want to join this list make sure you read the file that is sent to you and send back the survey. Thanks and I hope to see some new subs soon! Oh, we love pictures of feet... but we ADORE pictures of faces and families! Fun list to be a part of if you like to see who you're talking about/to online. Lots of babies of course but we also have the occasional mom or brother/sister, pet, tattoo... :-D Kori CFPics Owner and Mama 'o Darb At 08:45 PM 9/19/2005, you wrote: >- >How do I go about joining the CF pic site? Is there a link? >thnx, >Stacie > > wrote: >Hi Stacey, > >Our daughter also has right unilateral. Glad that Jordan's foot looks >so good! Everything about Jordan's treatment sounds right except >usually the 23/7 wear is for 3 months give or take a bit (Grace was >no where near pulling up when her hours were reduced - she was 4.5 >mos). Not a biggie, you have already gotten past that and I am sure >that longer is better than a shorter time at 23/7. > >You must have been sooo happy when his time was reduced!! 6 months is >a long time at 23/7! Jordan will get really good at pulling up, >crawling and cruising in his shoes!! Even if he dosen't have them on >a lot when he is up he will probably be doing it in his crib. > >Have you guys joined the CFpics site? Would love to see a pic of him >and his little right foot! > >tc > & Grace > > > > Hi Stacie, > > > > I am curious, how long in total did he wear the shoes 23/7? I >thought > > that the protocol for Ponseti trained doctor's was to prescribe >23/7 > > brace wear for 3 months unless the foot was atypical or otherwise a > > challenge to treat. > > > > & Grace > > > > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > > until he could pull himself up to a stand w/ the shoes on... that >was > > at about 9 months old. I would check on that w/ Ponseti. > > > Good Luck! > > > Stacie > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2005 Report Share Posted September 22, 2005 Our dr. did this as well, so we called Dr. Ponseti, and basically were told the same thing. He said 12-14 hours. Re: Re: **brace protocol** ?'s I know this is a little late in coming but we just came back from a visit with Dr. ponseti on 9/19. Our son Eli is almost 5 months old and he was just reduced to 12 hours a day! I was rather surprised but this is coming from THE Doctor himself. Eli started casting (once a week for 5 weeks) at the end of May. Had the heel cord release after the 4th cast, wore the 5th one for 3 weeks, we took that off ourselves (as per Dr. P's instructions) and started the shoes23/7 on July 11. We then went to see Dr. Ponseti on Aug 1 and were reduced to 16-18/7. Now on the 19th we are down to 12/7. It all seemed a lot quicker than I have read on all the postings, we are very happy but I guess there are variations here and there on brace protocol even coming directly from Dr. Ponseti. Leah frogabog wrote: http://health.groups.yahoo.com/group/CFPics/ Check the email addy you used to sign up with as there will be a file sent to you with information about the list, and in that file you will find a little survey to fill out. Reply to that email, copy the survey section into the body of the email, answer the really easy and simple questions (asks about you - very general but it weeds out the wackos) and send it back to me. I'll get you approved as soon as I see the survey which will then be forwarded to the list to introduce and welcome you. Make sure you're on individual emails if you want to see the pictures people send You will not be able to look at previous attachments on the website, yahoo does not archive attachments anymore. This is why you'll need to be on individual emails for this list. If you want to see a particular picture that was sent before you joined, email the original poster and ask them to send you copies of the photos directly. If you want to send a picture, just send an email with your photo embedded or attached right to the list as a post. Just like this list, but the CFPics list accepts attachments. There is a photo section on the website that we use for our photo library but we don't have personal folders there. All the pictures are sent to the list in emails so we can keep the library freed up for educational photos. Yahoo only allows so much space for photos and files and when it's filled... no one can access the photos until a moderator deletes some. It ends up being a mess with not knowing if it's ok to delete something or whatever... so we just don't post photos there and leave it as a reference library for parents. I need to update the library big time I know... will try to work on that someday soon. Everyone is welcome of course as long as you're not a wacko, but PLEASE fill out the survey. I don't approve people without that, sorry. The wacko factor is too real with this list so we've had to be strict with that rule. I know I've missed a lot of people who wanted to join but I don't have enough time to police the requests and remind people to send the survey back. After 14 days your subscription request expires so please, if you want to join this list make sure you read the file that is sent to you and send back the survey. Thanks and I hope to see some new subs soon! Oh, we love pictures of feet... but we ADORE pictures of faces and families! Fun list to be a part of if you like to see who you're talking about/to online. Lots of babies of course but we also have the occasional mom or brother/sister, pet, tattoo... :-D Kori CFPics Owner and Mama 'o Darb At 08:45 PM 9/19/2005, you wrote: >- >How do I go about joining the CF pic site? Is there a link? >thnx, >Stacie > > wrote: >Hi Stacey, > >Our daughter also has right unilateral. Glad that Jordan's foot looks >so good! Everything about Jordan's treatment sounds right except >usually the 23/7 wear is for 3 months give or take a bit (Grace was >no where near pulling up when her hours were reduced - she was 4.5 >mos). Not a biggie, you have already gotten past that and I am sure >that longer is better than a shorter time at 23/7. > >You must have been sooo happy when his time was reduced!! 6 months is >a long time at 23/7! Jordan will get really good at pulling up, >crawling and cruising in his shoes!! Even if he dosen't have them on >a lot when he is up he will probably be doing it in his crib. > >Have you guys joined the CFpics site? Would love to see a pic of him >and his little right foot! > >tc > & Grace > > > > Hi Stacie, > > > > I am curious, how long in total did he wear the shoes 23/7? I >thought > > that the protocol for Ponseti trained doctor's was to prescribe >23/7 > > brace wear for 3 months unless the foot was atypical or otherwise a > > challenge to treat. > > > > & Grace > > > > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > > until he could pull himself up to a stand w/ the shoes on... that >was > > at about 9 months old. I would check on that w/ Ponseti. > > > Good Luck! > > > Stacie > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2005 Report Share Posted September 22, 2005 Our dr. did this as well, so we called Dr. Ponseti, and basically were told the same thing. He said 12-14 hours. Re: Re: **brace protocol** ?'s I know this is a little late in coming but we just came back from a visit with Dr. ponseti on 9/19. Our son Eli is almost 5 months old and he was just reduced to 12 hours a day! I was rather surprised but this is coming from THE Doctor himself. Eli started casting (once a week for 5 weeks) at the end of May. Had the heel cord release after the 4th cast, wore the 5th one for 3 weeks, we took that off ourselves (as per Dr. P's instructions) and started the shoes23/7 on July 11. We then went to see Dr. Ponseti on Aug 1 and were reduced to 16-18/7. Now on the 19th we are down to 12/7. It all seemed a lot quicker than I have read on all the postings, we are very happy but I guess there are variations here and there on brace protocol even coming directly from Dr. Ponseti. Leah frogabog wrote: http://health.groups.yahoo.com/group/CFPics/ Check the email addy you used to sign up with as there will be a file sent to you with information about the list, and in that file you will find a little survey to fill out. Reply to that email, copy the survey section into the body of the email, answer the really easy and simple questions (asks about you - very general but it weeds out the wackos) and send it back to me. I'll get you approved as soon as I see the survey which will then be forwarded to the list to introduce and welcome you. Make sure you're on individual emails if you want to see the pictures people send You will not be able to look at previous attachments on the website, yahoo does not archive attachments anymore. This is why you'll need to be on individual emails for this list. If you want to see a particular picture that was sent before you joined, email the original poster and ask them to send you copies of the photos directly. If you want to send a picture, just send an email with your photo embedded or attached right to the list as a post. Just like this list, but the CFPics list accepts attachments. There is a photo section on the website that we use for our photo library but we don't have personal folders there. All the pictures are sent to the list in emails so we can keep the library freed up for educational photos. Yahoo only allows so much space for photos and files and when it's filled... no one can access the photos until a moderator deletes some. It ends up being a mess with not knowing if it's ok to delete something or whatever... so we just don't post photos there and leave it as a reference library for parents. I need to update the library big time I know... will try to work on that someday soon. Everyone is welcome of course as long as you're not a wacko, but PLEASE fill out the survey. I don't approve people without that, sorry. The wacko factor is too real with this list so we've had to be strict with that rule. I know I've missed a lot of people who wanted to join but I don't have enough time to police the requests and remind people to send the survey back. After 14 days your subscription request expires so please, if you want to join this list make sure you read the file that is sent to you and send back the survey. Thanks and I hope to see some new subs soon! Oh, we love pictures of feet... but we ADORE pictures of faces and families! Fun list to be a part of if you like to see who you're talking about/to online. Lots of babies of course but we also have the occasional mom or brother/sister, pet, tattoo... :-D Kori CFPics Owner and Mama 'o Darb At 08:45 PM 9/19/2005, you wrote: >- >How do I go about joining the CF pic site? Is there a link? >thnx, >Stacie > > wrote: >Hi Stacey, > >Our daughter also has right unilateral. Glad that Jordan's foot looks >so good! Everything about Jordan's treatment sounds right except >usually the 23/7 wear is for 3 months give or take a bit (Grace was >no where near pulling up when her hours were reduced - she was 4.5 >mos). Not a biggie, you have already gotten past that and I am sure >that longer is better than a shorter time at 23/7. > >You must have been sooo happy when his time was reduced!! 6 months is >a long time at 23/7! Jordan will get really good at pulling up, >crawling and cruising in his shoes!! Even if he dosen't have them on >a lot when he is up he will probably be doing it in his crib. > >Have you guys joined the CFpics site? Would love to see a pic of him >and his little right foot! > >tc > & Grace > > > > Hi Stacie, > > > > I am curious, how long in total did he wear the shoes 23/7? I >thought > > that the protocol for Ponseti trained doctor's was to prescribe >23/7 > > brace wear for 3 months unless the foot was atypical or otherwise a > > challenge to treat. > > > > & Grace > > > > > > > Wow- Our Dr. (Ponseti approved) had our son wear his shoes 23/hrs > > until he could pull himself up to a stand w/ the shoes on... that >was > > at about 9 months old. I would check on that w/ Ponseti. > > > Good Luck! > > > Stacie > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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