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Atypical clubfeet

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Hey , thanks for the info. All of this is so confusing.

Trying to get things set up through our insurance and contacting the

Shriners to see if they can help us at all. If you don't mind me

asking, how did you take care of the financial aspect of seeing Dr

Ponseti? I'm so afraid that we are going to incur(?) so much

financially that it's going to be difficult for us to do this trip

out to Iowa. If anyone has info please let me know.

Mia

> My daughter has bilateral nontypical atypical clubfeet (Dr

Ponseti's

> words). What ever that is. We ended up taking her to Dr Ponseti

> also. His website has information for the Mc house.

> They were very nice and I was able to get in for all of the days I

> needed to, but I ended up staying with my aunt anyway.

> You will probably go into the shoes when treatment is

done.

> Those shoes are not covered by insurance but he takes payments

also.

> http://www.mdorthopaedics.org/default.html I would try to get to

see

> as soon as you get to Iowa so you can get your shoes

on

> order. It takes him awhile to get them made. Make sure they

measure

> her feet before they put the first cast on. I am sure they will

take

> care of all of that stuff for you though. They did for me. Bring

> pictures of your daughters feet at birth. Dr Ponseti was very

> intersted in them.

> Good luck.

>

> Tori 1/30/04 bilateral atypical cf brace 18 hrs

> 12/7/01 non cf

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