Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 In case anyone is interested.... May 6, 2005 The pictures show Olivia's feet are short and chubby but they are probably not atypical. She does have limitation of dorsiflexion on the left and that is probably why she does not stay in the shoes. These feet should be braced with the brace. Dr. Mosca is acquainted with this brace and he can make arrangements to obtain one for Olivia. In my opinion she should wear the brace at least 16 hours a day and wait before anything more is done to her feet. They tend to improve in time. However, if Dr. Mosca uses physical therapy to increase dorsiflexion, it might help. I.V. Ponseti, M.D. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 Darby, I am about close to getting Shriners here in Portland to get me a P/M brace for Darbi. In fact, I'm pretty sure they're going to do it. It's all set up, I just need to figure out if they are sending the impression kits or if I am. I've talked to the orthotists, the care coordinator and Dr. Sussman. I am sure it'll go through. Here's my thought, if you can't get insurance to cover the brace you may want to have Dr. Mosca refer you to Shriners here and come on down to see Dr. Sussman and ask for this brace too. I know it's a long drive, and right now I'm the only one who is pushing it here but I know when they see it that they'll love it. They have to. And maybe you can get Shriners to provide the brace for you. I know you're frustrated, I would be too. But if Dr. Mosca contacts Dr. Sussman and explains the situation, perhaps they'll help you out? They do just *accept* clubfoot patients here, it took a whole 5 min on the phone to get Darbi in to be seen. I know it'll seem weird but maybe if you don't tell them it was me who suggested it, and if Dr. Mosca calls Dr. Sussman personally asking if Livi can be seen here and get the brace through them it'll further push that this brace is needed for many patients and they really need to look into using it more. You are in need, and Shriners here has patients all over the NW, including Alaska. In fact, the orthotists are up there in Anchorage right now doing a clinic. So you're not out of the coverage area and they should accept you just fine. LMK if you want the contact info, but I think Dr. Mosca would make the best case for Livi and the P/M brace if he called himself. Keep me out of it! lol! (kidding, I don't care a bit if you mention me, I'm their thorn in the rear and I like it that way!) Can't wait to hear about ! Keep your chin up, it'll all work out in the end. Big hugs! Kori At 09:42 AM 5/6/2005, you wrote: >In case anyone is interested.... > >May 6, 2005 > >The pictures show Olivia's feet are short and chubby but they are >probably not atypical. She does have limitation of dorsiflexion on the >left and that is probably why she does not stay in the shoes. These >feet should be braced with the brace. Dr. Mosca is >acquainted with this brace and he can make arrangements to obtain one >for Olivia. In my opinion she should wear the brace at least 16 hours >a day and wait before anything more is done to her feet. They tend to >improve in time. However, if Dr. Mosca uses physical therapy to >increase dorsiflexion, it might help. > >I.V. Ponseti, M.D. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 Darby. That is good news. I would also print Dr. P's reply and turn it in to insurance. How can they turn it down when Dr. Ponseti himself recommended them? Shook Retail Operations Manager/Baking Instructor Vie de France Yamazaki, Inc. 2070 Chain Bridge Rd. Suite 500 Vienna, VA 22182 x374 x374 fax Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 Thanks Kori! I have so many ideas right now about getting these shoes paid for - one way or another, you are right, it will all work out. I spoke to the nurse at Children's this am and passed on some ideas people here gave about getting insurance to pay for these... I know one of the parents here mentioned submitting them using the AFO code, which the nurse thought was a great idea, and I also suggested having their orthotics dept order them for me so it would be a preferred orthotics provider w/ aetna. We get full financial aid from Children's hospital, so if I can get these through them, my insurance will pay their share and the financial aid will take up the rest. I won't need to pay anything. I'm VERY encouraged and super excited - this may just work out perfectly after all - we'll see. I'm about to call the orthotics people and convince them to do this... If that doesn't work I may take your suggestion and go to Shriners - and then maybe I can help out your case and all the other patients there as well. Get everyone on the bandwagon. But I would like to avoid the Portland drive if possible... with a new baby that would be a test of patience to say the least! I think I'm becoming the thorn in the side of Dr. Schmale, too. I don't really care. I am blessed with having Olivia - she has taught me so much about asserting myself and being persistant! Darby > >In case anyone is interested.... > > > >May 6, 2005 > > > >The pictures show Olivia's feet are short and chubby but they are > >probably not atypical. She does have limitation of dorsiflexion on the > >left and that is probably why she does not stay in the shoes. These > >feet should be braced with the brace. Dr. Mosca is > >acquainted with this brace and he can make arrangements to obtain one > >for Olivia. In my opinion she should wear the brace at least 16 hours > >a day and wait before anything more is done to her feet. They tend to > >improve in time. However, if Dr. Mosca uses physical therapy to > >increase dorsiflexion, it might help. > > > >I.V. Ponseti, M.D. > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 told me that he actually did something to the shoes that qualifies them as AFO's. I wonder if it's not the insole? So there's some kind of change from the first models, or something special about them making them qualify as AFO's now. I may be wrong, but that's what I got from what he said to me. At 12:10 PM 5/6/2005, you wrote: >Thanks Kori! > >I have so many ideas right now about getting these shoes paid for - >one way or another, you are right, it will all work out. > >I spoke to the nurse at Children's this am and passed on some ideas >people here gave about getting insurance to pay for these... I know >one of the parents here mentioned submitting them using the AFO code, >which the nurse thought was a great idea, and I also suggested having >their orthotics dept order them for me so it would be a preferred >orthotics provider w/ aetna. We get full financial aid from >Children's hospital, so if I can get these through them, my insurance >will pay their share and the financial aid will take up the rest. I >won't need to pay anything. I'm VERY encouraged and super excited - >this may just work out perfectly after all - we'll see. I'm about to >call the orthotics people and convince them to do this... > >If that doesn't work I may take your suggestion and go to Shriners - >and then maybe I can help out your case and all the other patients >there as well. Get everyone on the bandwagon. But I would like to >avoid the Portland drive if possible... with a new baby that would be >a test of patience to say the least! > >I think I'm becoming the thorn in the side of Dr. Schmale, too. I >don't really care. I am blessed with having Olivia - she has taught >me so much about asserting myself and being persistant! > >Darby > > > > > >In case anyone is interested.... > > > > > >May 6, 2005 > > > > > >The pictures show Olivia's feet are short and chubby but they are > > >probably not atypical. She does have limitation of dorsiflexion >on the > > >left and that is probably why she does not stay in the shoes. >These > > >feet should be braced with the brace. Dr. Mosca is > > >acquainted with this brace and he can make arrangements to obtain >one > > >for Olivia. In my opinion she should wear the brace at least 16 >hours > > >a day and wait before anything more is done to her feet. They >tend to > > >improve in time. However, if Dr. Mosca uses physical therapy to > > >increase dorsiflexion, it might help. > > > > > >I.V. Ponseti, M.D. > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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