Do you love to go out to eat? Do you want to help fundraise, but don't have the time? Then this is the event for you!! You can participate whenever you visit a new restaurant without doing extra work! It's fast and easy!!
Dine Out for Duchenne is a week-long, online event where people can…Continue
Added by Danielle Garrigan on March 12, 2012 at 4:30pm — No Comments
PPMD President Pat Furlong and Colorado FACES Coordinator Ivy Scherbarth discuss the bravery of their sons, and all young men fighting Duchenne. Please, share your thoughts after reading this month’s co-blog.
Weakness. A familiar word in the context of…Continue
By now we hope you have heard that Parent Project Muscular Dystrophy will be hosting our first West Coast Connect Meeting, April 13-15, 2012 in San Diego, CA at the…Continue
Added by PPMD on March 7, 2012 at 10:00am — No Comments
Everyone gives something to somebody for something. Whether through acts of kindness, services, or hard-earned money, everyone has the opportunity to make the world a better place. No energy required.
Literally from the comfort of our couch, we are able to reach across the world to support others in need. 250,000 boys/young men have Duchenne. They live everywhere,…Continue
Added by Pat Furlong on February 22, 2012 at 3:00pm — No Comments
As you know, ensuring appropriate federal funding for Duchenne research has been a cornerstone of PPMD’s advocacy agenda over the past decade. Our persistence – your persistent and collective voice - has paid off with over $250 million directed to Duchenne research.
Today we now find ourselves at a pivotal moment with multiple potential therapies for Duchenne in various stages of the development process. We must now, once again, look forward to what is next for Duchenne.…
Added by PPMD on February 21, 2012 at 10:00am — No Comments
I don’t know about you, but when I am in DC or receive government related information, I am always about 3 acronyms behind in the conversation. PDUFA – this is one acronym you want to put in your memory bank for 2012. PDUFA – Prescription Drug User Fee Act.
This legislation is all about FDA, about what biotech’s/pharmaceuticals have to pay for the process, about rare disorders and incentives to develop drugs for rare conditions, and about the process of…Continue
West Coast Connect Meeting
First, PPMD is excited to host our first West Coast Connect Meeting, April 13-15, 2012 in San Diego, CA. This will be a great opportunity to get…
Added by PPMD on February 13, 2012 at 4:30pm — No Comments
PPMD continues to bring you the most up-to-date care resources, so that you and your family and everyone who helps care for your son, has the information they need at their fingertips. Here are some recent updates we wanted you to be aware of:
Added by Holly Peay on February 13, 2012 at 11:00am — No Comments
I am so excited to announce a new sporting fundraiser we have this year called Ice Duchenne!
PPMD has partnered with the Central Collegiate Hockey Association Coaches (CCHA) this weekend, February 10th and 11th. The coaching staffs of all 11 teams will band together to help raise awareness for Duchenne and wear pins with the…Continue
Added by Danielle Garrigan on February 9, 2012 at 11:30am — No Comments
Biochemist Gunter Scheuerbrandt has been following exon skipping for the international Duchenne community for years. Read the latest update from one of this community’s greatest allies.
Added by PPMD on February 8, 2012 at 11:30am — No Comments
PPMD President Pat Furlong and Colorado FACES Coordinator Ivy Scherbarth co-blog about vulnerability and what you risk when you open your heart to people. One the one hand, we risk fraud – a subject Ivy has been dealing with intensely with her family, as of late. But at the same time, our vulnerability allows us to love and be loved. Pat and Ivy explore two perspectives on a similar idea.
Added by Pat Furlong on February 7, 2012 at 10:30am — No Comments
PPMD welcomes Dr. Padraig Wright from GlaxoSmithKline as our guest for a webinar on February 22, 2012 at 1pm eastern.
GSK2402968 is an antisense oligonucleotide…Continue
Added by PPMD on February 6, 2012 at 4:30pm — No Comments
Our Featured Voice for February 2012 is 18-year-old Jonathan Piacentino, a second semester freshman at Nazareth College. PPMD’s Advocacy Conference, held in the first quarter of each…Continue
Added by Will Nolan on February 3, 2012 at 4:00pm — No Comments
Currently there is no newborn screening for Duchenne in the United States. However, groundbreaking work from Jerry Mendell’s lab at The Ohio State University may have a hand in changing this.
Mendell’s recent pilot study was funded by the Centers for Disease Control (CDC) and…Continue
Was your son in the placebo group in the PTC ataluren trial?
PPMD has partnered with researchers at the National Institutes of Health (NIH) for an interview study. The purpose of this study is to describe the experiences of people involved in phase II clinical trials of ataluren for Duchenne muscular dystrophy. We are interested in learning about motivations for being in the clinical trial, expectations of the trial, the experience of the trial, and interactions between families…Continue
Added by PPMD on February 1, 2012 at 2:00pm — No Comments
PPMD is proud to be chosen by the Webkinz Foundation as a featured charity, which includes a donation from the Caring Valley! (Read the Release)
Webkinz is a great toy brand that your kids probably already love. And for the month of February, you can purchase…Continue
Added by Will Nolan on February 1, 2012 at 10:00am — No Comments
Seems like a long time ago, Kimberly and I went to the Starting point of the Disney Marathon. I had no idea what to expect, having never watched a marathon and absolutely no desire to run a city block let alone 26.2 miles. One mom had called Kimberly to talk…Continue
Added by Pat Furlong on January 30, 2012 at 2:30pm — No Comments
PPMD President Pat Furlong and Colorado FACES Coordinator Ivy Scherbarth co-blog about the older patients in the Duchenne community, and what we can learn from the journeys they have been on. They are the real Duchenne experts. We hope that after you read these entries, you'll post your own thoughts on the topic.
Listen & Learn…Continue
With deficit reduction remaining a top priority in Congress and a $1.2 trillion spending reduction on the horizon, 2012 will be a critical year to protect Duchenne research and public health priorities. For this to happen, we need your voice on Capitol Hill now more than ever before. Whether that be by joining us in Washington at the Annual Advocacy Conference or advocating from home by contacting…Continue
Added by Ryan Fischer on January 5, 2012 at 2:00pm — No Comments