Buna,imi pare rau pentru situatia ta,pt baietelul tau care are soarta asta crunta,la fel sunt si eu,distrusa pt ca am sperat ca macar al doilea copil al meu sa fie sanatos,din pacate am doi copii bolnavi ,unul de 2 anisori iar celalalt de 6,te inteleg perfect pt ca numai cine nu trece prin asta nu crede,sparam ca Dumnezeu va face o minune pt toate aceste sufletele nevinovate.iar sotul tau daca a fugit cand ai avut cea mai mare nevoie de el,nu te merita.fii puternica.de unde anume esti.din ce oras din Romania??
Welcome Cercek! 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 & families 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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Buna,imi pare rau pentru situatia ta,pt baietelul tau care are soarta asta crunta,la fel sunt si eu,distrusa pt ca am sperat ca macar al doilea copil al meu sa fie sanatos,din pacate am doi copii bolnavi ,unul de 2 anisori iar celalalt de 6,te inteleg perfect pt ca numai cine nu trece prin asta nu crede,sparam ca Dumnezeu va face o minune pt toate aceste sufletele nevinovate.iar sotul tau daca a fugit cand ai avut cea mai mare nevoie de el,nu te merita.fii puternica.de unde anume esti.din ce oras din Romania??
StaffPPMD said…
Welcome Cercek! 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 & families of boys with Duchenne, e-newsletters, additional web-based research reports, and other information specifically targeted for members of the community.