hi angela my name is kimmy watters, i h ave been part of ppmd for about four years. this is the best place for you get your support. my best friends son has duchenne and been on the band wagon to rase money to find a cure. kimmy
Welcome Angela! We hope using the community site to connect with families all over the world to share stories, news, and information about Duchenne is empowering for you and your family.
Please don't hesitate to contact us by phone, email, or message if you ever need anything -- 800-714-5437 - community@parentprojectmd.org
And if you haven't already, we hope you consider registering on PPMD's main website. Registering allows us to send you information tailored to parents of boys with Duchenne, e-newsletters, additional web-based research reports, and other information specifically targeted for members of the community.
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hi angela my name is kimmy watters, i h ave been part of ppmd for about four years. this is the best place for you get your support. my best friends son has duchenne and been on the band wagon to rase money to find a cure. kimmy
StaffPPMD said…
Welcome Angela! We hope using the community site to connect with families all over the world to share stories, news, and information about Duchenne is empowering for you and your family.
Please don't hesitate to contact us by phone, email, or message if you ever need anything -- 800-714-5437 - community@parentprojectmd.org
And if you haven't already, we hope you consider registering on PPMD's main website. Registering allows us to send you information tailored to parents of boys with Duchenne, e-newsletters, additional web-based research reports, and other information specifically targeted for members of the community.