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Brandi Cammarata
  • Male
  • Flowery Branch, GA
  • United States
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Brandi Cammarata's Discussions

Hello

Started this discussion. Last reply by Nida Zuberi Apr 16, 2016. 3 Replies

Hello everyone! I am excited to join you all in the PPMD community. Forgive me if I'm not writing this in the correct area. I'm new and learning. Our son, Beck was diagnosed with DMD in January. It…Continue

 

Brandi Cammarata's Page

Latest Activity

Kim Watters left a comment for Brandi Cammarata
" hi  brandi     did  you get my message   fb     kick  me off,     have  new   email    account   so hope allow me  back  on kimmy"
Sep 20
Vanita favorited Brandi Cammarata's discussion Hello
Apr 29, 2016
Vanita favorited Brandi Cammarata's discussion Hello
Apr 29, 2016
Vanita favorited Brandi Cammarata's discussion Hello
Apr 29, 2016
Alpa Khushalani left a comment for Brandi Cammarata
"Hi Brandi, Its extremely hard to go through the initial diagnosis days and lots of hugs and prayers for your son and family. I can tell you from our experience about a year and half back when we got our diagnosis that joining this group and most of…"
Apr 21, 2016
Nida Zuberi replied to Brandi Cammarata's discussion Hello
"Hi Brandy, My 5 year old son was just diagnosed this Thursday. I'm in shock! Never heard of it, none in my family have it. Pretty much lost right now. Just stayed up all night and researched. Really tired. Can't believe it."
Apr 16, 2016
Limca Jhaveri replied to Brandi Cammarata's discussion Hello
"Hi Brandi, My son Jaylen was 3.5 years old in August 2015 when he was diagnosed.  Its tough getting the diagnosis, but we are trying to learn as much as possible about it.  I am also not a carrier of the disease and no one in our family…"
Mar 14, 2016
Shelly favorited Brandi Cammarata's discussion Hello
Mar 11, 2016
Jay Griffin replied to Brandi Cammarata's discussion Hello
"Brandi, we were recently diagnosed as well. Glad that you reached out to this group. If you need to talk, I am here. It helps me daily"
Mar 10, 2016
Brandi Cammarata posted a discussion

Hello

Hello everyone! I am excited to join you all in the PPMD community. Forgive me if I'm not writing this in the correct area. I'm new and learning. Our son, Beck was diagnosed with DMD in January. It did come back as genetic HOWEVER we have never had a family member diagnosed with any type of MD so needless to say, the news was very shocking! I am ready to fight for our boys and ready to find a cure! I just wanted to thank you all for accepting me into such a wonderful group!
Mar 10, 2016
Brandi Cammarata is now a member of PPMD Community
Mar 10, 2016

Profile Information

About me:
I am a mother of two beautiful teenage daughters and a 5 year old son. They are my life.
Name(s) of child(ren)/individual(s) with Duchenne:
Beck Cammarata
Age(s) of child(ren)/individual(s) with Duchenne:
4-6
City:
Flowery Branch
State:
Georgia

Comment Wall (2 comments)

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At 3:32pm on September 20, 2017, Kim Watters said…

 hi  brandi     did  you get my message   fb     kick  me off,     have  new   email    account   so hope allow me  back  on

kimmy

At 12:43am on April 21, 2016, Alpa Khushalani said…

Hi Brandi,

Its extremely hard to go through the initial diagnosis days and lots of hugs and prayers for your son and family. I can tell you from our experience about a year and half back when we got our diagnosis that joining this group and most of all going to the PPMD annual connect conference gave us a lot of information, connections, strength and hope. There are a lot of trials in pipeline and based on Beck's mutation, you might have more than one choice. Take one day at a time and stay strong as Beck needs to see you that way. 

 
 
 

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