Guest guest Posted January 12, 2005 Report Share Posted January 12, 2005 Joanne, Over the past 4 years or so I have written 2 letters and made couple of phone calls to the March of Dimes. I have sent them information, backup from studies, etc. just asking them to include information about the Ponseti method in addition to the surgical route so that any parents reading their web site would be able to know the Ponseti method existed. At that time, they weren't really very receptive to the idea. Hopefully they may be more responsive now. > Hi All, > > If you have a chance, check out the March of Dimes Clubfoot Fact Sheet: > http://search.marchofdimes.com/cgi-bin/MsmGo.exe? grab_id=354&page_id=5964032&query=clubfoot&hiword=clubfoot+ > > (since the link is so long, you may have to copy and paste it into a new > browser window) > > Unfortunately, the March of Dimes is educating people that surgery as the > only option!! > > I was directed to contact the March of Dimes by the local hospital where > I've been trying to start a support group. As you can imagine, I'll be > calling my local chapter today!! > > In addition, I will be writing a letter to the national organization. I hope > you will join me in educating the March of Dimes about the existence of the > Ponseti method! Perhaps we should also ask our doctors to write a letter as > well? > > Best, Joanne W. mom to Zoe, 3-25-01, right clubfoot Quote Link to comment Share on other sites More sharing options...
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