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Re: STEPS-US?

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Joanne,

Yes, I think that we should be in touch with STEPS and Sue Banton. I

believe that Sue's son born in 1980 had clubfoot and that from that

experience that she felt a desire to try to help other parents. But

in the 1980's they set up their system prior to the internet and so

had to work out the logistics of printing pamphets, getting

information into hospitals, fund raising and Public Relations to help

get out their message.

Plus, Sue and STEPS have had the experience of organizing and helping

to fund 2 training clinics that addressed the use of the Ponseti

method.

We on the internet groups may have more experience in one to one

internet information but we haven't dealt with the physical

organization issues that will need to be dealt with if we are to help

make this possible for all of the children of the world.

and (3-17-99)

> Hi ,

>

> Wow, I finally had a chance to check out the STEPS website. What an

amazing

> organization! I agree. This would be a great model for what could

be done in

> the US. Would it be a good idea to contact Sue Banton to discuss

the

> possibility of starting a STEPS here in the US? Since she's been

doing this

> type of thing for 20 years, perhaps we should learn from what she

has done

> already?

>

> What a useful organization this is...It would have been so helpful

to have

> had this type of organization when my daughter was born...

>

> Thanks for bringing it to my attention.

> Joanne W. mom to Zoe (3-25-01) right clubfoot

>

>

>

> _________________________________________________________________

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