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About me:
I live in southwestern PA and work part time as an environmental consultant.
About my family:
I'm married to Miles, and we have two sons, Quinton and Connor.
Name(s) of child(ren)/individual(s) with Duchenne:
Age(s) of child(ren)/individual(s) with Duchenne:
Irwin PA

Comment Wall (7 comments)

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At 12:14am on February 17, 2012, Gail D. McVicker said…

Hi Susan,


I live in Pottstown, PA and have two grandsons (ages 5 and 8) with Duchenne. I am reaching out to get more Pennsylvanian constituent activity when PPMD advocates in two weeks. If you know of any other families in PA could you please share?

I am sending out the following reminder to maximize constituent activity for PPMD's Advocacy effort coming up in two weeks. We will increase our chances to get government support for our boys by sharing how Duchenne has touched our lives. You won’t even have to leave your home.
If you can't attend PPMD’s 2012 Advocacy conference in Washington, DC, there other ways to to advocate and help get government support for DUCHENNE. To date, we only have 2 or Pennsylvania’s 19 Congressional districts backed up by actual Duchenne constituents.  Those of us that are there will pick up other PA districts that are not ours. We need to have input (personal stories) from 17 more Congressional Districts in Pennsylvania to help our boys as effectively as possible.


The goal this year is called 50 STATE CHALLENGE . This means we hope for Duchenne advocacy input from constituents from all 50 states and, hopefully, all congressional district. Pennsylvania, so far, needs input from 17 of its 19 districts. Here's how to do this without traveling to Washington – or anywhere. WE STILL HAVE TIME TO DO THIS.    (Scroll down and read Options #2 and #3.)

You can sign-up for the Packet Drop Off (link provided above and below) where you can also fill out a quick survey (include a photo if you wish) regarding your situation.  This information will be included in the packet delivered to your Congress rep.

You can also get free help to create a more in-depth one-page flyer about your situation that can be included in the Drop Off Packets and delivered to your representatives by those who do go to Washington. The flyer telling your story can be duplicated for additional copies, easily sent as an email attachment, and can be easily edited for other Duchenne-related awareness and fund-raising purposes.  Visit link below to see a sample flyer.

SHARING OUR PERSONAL STORIES raises awareness, raises concern and makes others want to join in the fight against Duchenne.    (Scroll down and read Options #2 and #3.)

Thanks for reading this.



Personal Stories so Congress will help boys with Duchenne

At 10:50am on October 13, 2008, Stacy Anderson said…
Sean has a good personality and can be the sweetest child at times. He takes prednisolone on the weekends and then I can tell a change in his attitude. He gets angry easy and yells alot. I just try to deal with it and realize that the medicine affects him. I raise Sean as if he were a so called "normal" child because I don't want him to feel different or become uncontrollable. He has a 14 year old half brother who has lived with us for the last 6 sixs, so I try to treat them the same. Of course everything can't be handled the same but I don't want Sean to feel bad about himself or depressed. Duchenne's MD has also affected Sean mentally so he is delayed some and doesn't quite understand things fully. He is 10 but has the mind of a 5 year old. He understands that his muscles are weak and that he's not the only one affected with this type of disease. I teach him to love Jesus and know that he will never turn his back on him. Sean smiles all the time and is very loving. He hurts sometimes but still remains happy. I'm thankful that God has truly blessed his spirit!
At 2:42pm on October 12, 2008, Stacy Anderson said…
Hi, Susan
I am new to this website and am just trying to meet new people who share a son like mine. Your son looks like a happy, handsome young man. I'm sure he is a blessing to your family like my son has been to mine. I hope to hear back from you. God bless and cherish every day!
At 4:03am on October 9, 2008, Jasmine Stringer said…
I am also worried about the short stature and the roundness of the face. I am so sad to see that my son will be transformed. My son has only been on deflazacort for 9 months, he is 5.
But looking on this site i can see that the boys all have this similar look. Being on deflazacort has also changed his demeanour, he is aggressive and difficult. It's been such a big adjustment. I am having a hard time accepting all this.
At 7:13pm on September 24, 2008, Kari said…

I am not a good source since Jared is not taking any supplements or drugs yet. We see Dr. Wong in November and will take it from there. There is a lot of good discussions about this so check out info there regarding steroids. There are lots of people currently discussing this now.
At 3:48pm on September 24, 2008, Jacobs Mommom said…
Hi Susan:
I'm the MomMom of Jacob, 8 years old with DMD. I live in Doylestown, PA and and Jacob, my daughter and the rest of her family live in Lansdale.

Hopefully the PA members can arrange a meeting for the spring.
At 11:34am on September 23, 2008, Kari said…
Welcome, Susan to PPMD Community.

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