Dreama Whitlock
  • Female
  • West Virginia
  • United States
Share on Facebook
Share

Dreama Whitlock's Friends

  • dr ibrahim mohammed abd el azeem
  • Thomas Hoel
  • PPMD
 

Dreama Whitlock's Page

Profile Information

About me:
I have been married to my husband for 13 years. I was a medical assistant for 14 years and currently not working. I have had my own karaoke business for several years now, but I rent the equipment. I enjoy scrapbooking, singing, american idol, and camping and anything nature related. I like to paint and remodel homes. Now my greatest passion is fighting for Duchenne and my grandson.
About my family:
Between my husband and I, we have 2 daughters and a son. We have five grandchildren now, our newest addition Jareth is due in April. My oldest grandson Aydon passed away at 6 weeks due to heart conditions. Riley whom is my daughters second born, Aydon's brother, was diagnosed with Duchenne in October 2011. Then their is my son's daughter Jaelynn and my daughters youngest Corey.
Name(s) of child(ren)/individual(s) with Duchenne:
Riley Cole Lucas-Vickers
Age(s) of child(ren)/individual(s) with Duchenne:
4-6
City:
huntington

Dreama Whitlock's Photos

  • Add Photos
  • View All

Dreama Whitlock's Blog

Our first official donation to our event!

Posted on April 1, 2012 at 11:46pm 2 Comments

Terrific news on a donation for the event that we are proposing to Camden Park! Riley's World and Parent Project Muscular Dystrophy A Celebration Of Life! I just received an email from Sleepy Hollow Chalets in response to my letter explaining our proposal and what we are doing: here is their letter:



Hi Dreama,



Thanks for contacting us. We are definitely interested in supporting this cause. We will most likely donate a couples only, two-night romantic getaway. We can send a… Continue

Planning an Event to promote research and awareness is very difficult, but worth it.

Posted on March 25, 2012 at 11:03am 0 Comments

So, I have been thinking about the type of event that I would be interested in hosting. I kept racking my brain for months, I want an event that also promotes Family Time...Quality family time.



Then the other day, an idea hit me. We have a local amusement park that doesn't get as many daily visitors as when I was a child. So, I am getting all my event details worked out, before pitching the idea to the park management. I have started sending out emails to other local venues asking… Continue

Great eye checkup today!

Posted on March 22, 2012 at 2:02pm 0 Comments

Riley had is appt with the eye doctor today and he is doing great. he passed with flying colors. I have my appt with the doctor tomorrow to find out if I am a carrier. Duchenne is the most difficult thing to understand, I can't imagine that I would be a carrier and pass it to my daughter to pass to her children, yet I didn't pass it to my own son. Just mind-boggling.

Life now, living with Duchenne

Posted on March 19, 2012 at 10:40pm 2 Comments

October 17th, the second time in my life that I heard the most agonizing words...my grandson Riley has Duchenne. Riley's older brother Aydon was my first born grandchild and passed away at 6 weeks of age from heart defects. When Riley was born, I thought will God take him too. It was hard to let myself love him completely, I was scared, but Riley broke that wall of fear right down and took my heart in his hands.



Knowing that Riley has Duchenne's is very difficult for all of us. Riley… Continue

Comment Wall (2 comments)

You need to be a member of PPMD Community to add comments!

Join PPMD Community

At 9:43pm on September 25, 2017, Kim Watters said…

 HI  dreama KImmy my  fb  not working,  l like  to  still   keep  in  touch /

At 10:20am on March 26, 2012,
Staff
PPMD
said…

Welcome Dreama! 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.

 
 
 

Need help using this community site? Visit Ning's Help Page.

Members

Events

© 2019   Created by PPMD.   Powered by

Badges  |  Report an Issue  |  Privacy Policy  |  Terms of Service