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Angie Evans and cercel alexandra silvia are now friends

Feb 23

cercel alexandra silvia favorited Angie Evans's photo

Sean and Ellie

Feb 22

cercel alexandra silvia favorited Angie Evans's photo

Sean all tuckered out

Feb 22

cercel alexandra silvia commented on Angie Evans's blog post Life on Wheels

"ps :i have to say theat my husbend left uss when the doctors give uss the diagnosi ...........theat why..........."

Feb 22

cercel alexandra silvia commented on Angie Evans's blog post Life on Wheels

"i understend you perfectly......your words are my byble i foth the same thing every day ,every night.every moment of my life... i can't stop to wander myself why i'm healthi and he is'n why did jesus christ don't give me…"

Feb 22

cercel alexandra silvia shared Angie Evans's blog post on Facebook

Life on Wheels

Feb 22

cercel alexandra silvia shared Angie Evans's blog post on Facebook

Life on Wheels

Feb 22

cercel alexandra silvia favorited Angie Evans's blog post Life on Wheels

Feb 22

cercel alexandra silvia and lisa burke are now friends

Feb 22

StaffPPMD left a comment for cercel alexandra silvia

"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,…"

Feb 22

cercel alexandra silvia is now a member of PPMD Community

Feb 22

Welcome Them!

Profile Information

About me:: 26 years devorces,roumanian,mother of an 2 years old son named mateo whit dmd ,mateo is my life,t my hart i feel like in hell

About my family:: i live whith my boyfriend(italyan)theat isn't my son dad and mateo in italy,a country theat is foreighn for me .i don't have anibody but them .....

Age(s) of child(ren)/individual(s) with Duchenne:: 0-3

City and State:: roma

Country:: italy

Comment Wall (1 comment)

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At 4:57pm on February 22, 2012, 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.