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Tracey Snyder
- Female
- Moorhead, MN
- United States
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Latest Activity
Marian Lamberson left a comment for Tracey Snyder"HI there, I saw you had made a comment about same deletion, yet progress differently. I just had a talk with my neurologist (I live in Ottawa Canada, and both of my boys have DMD as well) about this. Although my situation is different,…"
Tracey Snyder commented on PPMD's group Duchenne Parents"In response to Rebecca, i have two boys with DMD. Dylan is 19 and Zachary is 12. They have the exact same deletions (2-18). Their development has been completely different. Dylan was slower to walk and talk, but he walked until he was 13 and Zachary…"
StaffPPMD left a comment for Tracey Snyder
"Welcome Tracey! 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…"
Profile Information
- About me:
- I live in Minnesota and am a homemaker.
- About my family:
- I have 4 children, two girls and two boys. Both of my boys have DMD.
- Name(s) of child(ren)/individual(s) with Duchenne:
- Dylan and Zachary
- Age(s) of child(ren)/individual(s) with Duchenne:
- 7-12, 19 or older
- City and State:
- Moorhead MN
- Country:
- USA
Comment Wall (2 comments)
- At 2:31pm on January 30, 2012, Marian Lamberson said…
HI there, I saw you had made a comment about same deletion, yet progress differently. I just had a talk with my neurologist (I live in Ottawa Canada, and both of my boys have DMD as well) about this. Although my situation is different, that my boys have different dads, therefore different sets of Y chromosomes. My youngest (5) is doing things that my oldest (10) at that age was not doing. My oldest took easy to riding a bike, where as my youngest just can't get his bearings. Anyway, hope you are good, and that the boys are well. Marian
- At 1:16pm on October 27, 2011,
StaffPPMD said… Welcome Tracey! 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.
Need help using this community site? Visit Ning's Help Page.
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Events
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Paint for Peyton to end Duchenne
June 8, 2012 from 6:30pm to 7:30pm – Spirited Art
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