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NRSF and Dick Van Dyke Go To The SAG Awards!

In 1987, Dick Van Dyke lost his granddaughter, Jessica Van Dyke, to Reye’s Syndrome.  Like so many others, Dick’s dickvandyke1relatives and friends had never heard of Reye’s Syndrome prior to Jessica’s death. When Dick found out about the lack of general knowledge on this childhood killer, he pledged his full support in bringing the awareness of Reye’s Syndrome to the public by volunteering to become the Honorary National Chairman for the National Reye’s Syndrome Foundation.

He donated his time and services to create a series of television and radio commercials for the National Reye’s Syndrome Foundation to raise public awareness about Reye’s Syndrome and the danger aspirin posed to children.  That same year, he became the official spokesperson for the National Reye’s Syndrome Foundation.

 Dick Van Dyke Warns about Reye’s Syndrome

  During that time, he also promoted Reye’s Syndrome awareness by appearing on the Phil Donahue Show and Hour Magazine co-hosted by Gary Collins. Dick participated in the Annual Jaime Beth Slavin Celebrity Golf Tournaments in support of NRSF’s Reye’s Syndrome research.

At the age of 86 he shows no signs of slowing down. This year, the Screen Actors Guild will award Dick its highest honor; The Life Achievement Award.

Screen Actors Guild & American Federation of Television and Radio Artists co-president Ken Howard called Van Dyke “an enormously talented performer whose work has crossed nearly every major category of entertainment.”

The 86-year-old entertainer will receive the honor at the annual Screen Actors Guild Awards ceremony in January. His humanitarian work on behalf of the NRSF will be highlighted in a special segment.

Born December 13, 1925, in West Plains, Missouri, to Loren and Hazel Van Dyke, he grew up in Danville, Illinois. He is the father of Barry Van Dyke, and older brother of actor Jerry Van Dyke, who is best known for his role on the TV series Coach. His grandson, Shane Van Dyke, is also an actor and directed Titanic II. Dick’s career spans six decades.

Dick starred in the films Bye Bye Birdie, Mary Poppins and Chitty Chitty Bang Bang and in the TV series The Dick Van Dyke Show and Diagnosis: Murder. He has a star on the Hollywood Walk of Fame on Hollywood Boulevard, and he has already won a Tony, a Grammy and five Emmy awards.

Dick will be presented the performers union’s most prestigious accolade, given annually to an actor who fosters the “finest ideals of the acting profession,” at the 19th Annual Screen Actors Guild Awards®, which premieres live on TNT and TBS on Sunday, Jan. 27, 2013, at 8 p.m. ET, 7 p.m. CT, 6 p.m. MT and 5 p.m. PT.  The work he has done with the NRSF will also be showcased.

Thanks for all you do, Dick! We’ll be cheering with you!  Chim, Chim, Cherri! 

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2012 Gratitude Report

2012 Gratitude Report

EDUCATION:

school nurseEvery year for the past 38 Years the National Reye’s Syndrome Foundation has provided life-saving Reye’s Syndrome information to the families of students in more than 136,000 schools across the United States and its Territories.

School Nurses and Administrators send a Reye’s Syndrome  packet of information home with each student at the beginning of every school year.  This packet includes Reye’s Syndrome Symptoms literature, bookmarks with NRSF contact information, wallet size ‘ingredients to avoid’ cards for Over-The-Counter children’s medications, a Reye’s Syndrome brochure, and a list of medicines that contain aspirin.

We know that this huge, educational initiative saves the lives of children all across the U.S. and we thank all school administrators and nurses for promoting Reye’s Syndrome Awareness!

VOLUNTEERS:

With the guidance of volunteer leaders from across the United States on our Board,  our RS survivors, and our caring community volunteers, the National Reye’s Syndrome Foundation  has stayed on mission for 38 years, educating and promoting awareness and saving lives.

We truly cherish your investment of time and money, and we count on your trust in our mission to eradicate the incidence of Reye’s Syndrome. The work we do at the NRSF is built on a solid foundation of financial accountability, transparency, and ethics.

And there is one more critically important element to our continued success. You. You are here to show us that there is a community of people who keep the mission of the National Reye’s Syndrome Foundation in their hearts each and every day.

bodNRSF’s All Volunteer Board of Directors

ACCOMPLISHMENTS:

A major milestone was achieved this year when talks between the NRSF, the FDA, and Bayer Consumer Health Care resulted in all aspirin manufacturers removing the words “baby aspirin” from all packaging and marketing.  For 37 years we fought for this life saving agreement and it finally came to fruition.  We know that this change will save many lives and we thank the FDA and the aspirin manufacturers for recognizing and acting upon this most serious issue.

This year, we have developed more technology to support our Awareness efforts; Android Apps, and E-books, promoting Reye’s Syndrome Awareness.  Our new apps; Aspirin Sense and Sensitivity, and A Guide to Chickenpox are both available in the google play store.

Our Reye’s Syndrome website is used by more than 150,000 people across the globe each month.  Visits always increase at the beginning of the school year, and during flu season. We are proud, and pleased to provide this quality information.

With the help of Transfer Me To DVD, located at www.TransferMeToDvd.com, all films and videos spanning our 38 year history have now been transferred to DVD for additional preservation.  We Thank them for donating so much of the work and supplies!

WITH YOUR SUPPORT:babyheart_right

  • 6,500 Emails answered this year.
  • 6,200 Phone Calls answered this year.
  • 136,000 Families Educated this year.
  • 1500 Reye’s Syndrome School Projects this year.

Several Major Dreams Came True this year:

  • Bayer removed all ‘baby’ aspirin packaging
  • NRSF goes to the SAG Awards
  • Millions of Young Lives Saved!

We invite you to join us in our work.  We invite you to donate toward our Awareness and Education programs.  We invite you to join the NRSF as a Member.

Thank You!

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Fall 2012

Fall 2012 Message From The NRSF President

johnWe have spent a lot of time this year, as always, on Reye’s Syndrome Awareness projects. We had several Reye’s cases reported, both here in the United States and from other countries. Several cases, are several too many! All we can do is continue to spread awareness and work hard at educating as many people as we can in an effort to save lives.

Spreading awareness and educating new parents, caregivers, and medical professionals not only requires a lot of time, it also requires support.

Issues that are rising include:

  • Parents are not immunizing their children, and this can potentially
    create an epidemic of viral infections like measles, chickenpox,
    and whooping cough returning to plague our youngsters. Viral
    infections that were once almost wiped out are coming back
    around because new parents and caregivers are confused about
    immunizations.
  • H1N1 flu, and new mutating flu strains, are evolving and circling
    the globe. We are not immune, and neither are our children.
    Bird Flu found its way to the North American Continent this
    summer, and Mexico killed millions of chickens and other fowl to
    attempt to contain the virus. The question lingers, did they
    contain the virus?
  • The Internet, with all its wonderful data, also perpetuates a host
    of incorrect information and a lot of it is about Aspirin and
    Aspirin use! There are facial mask recipes made of crushed
    aspirin tablets for teen-agers, and even people who challenge the
    existence of Reye’s Syndrome!
  • Chickenpox Parties! Of all the things to subject a child to, one
    who has no choice in the matter—another child’s germs and
    body fluids! This one should make us all ill just thinking about it!

In all instances, the possibility of Reye’s Syndrome lurks in the background and many parents and caregivers still don’t know about this deadly monster.

So we educate, we provide awareness, and we attempt to reach as many as we possibly can. We hope you are doing the same thing. Our message, your message, can save a little one’s life! Speak Up, and Speak Out—Remind parents about Reye’s Syndrome!

We also congratulate NRSF spokesperson Dick Van Dyke on his Screen Actors Guild selection to receive the coveted dickvandyke1Life Achievement Award. Dick will accept the award January 27 during the SAG Awards. His work with the NRSF and for Reye’s Syndrome will be highlighted during the presentation.

We also thank you, and hope you will continue to support the work that we do. We need your voice, and we need your membership. It all counts, and it all makes a huge difference!

Thank You for Caring.

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Spring 2012

Spring 2012: Message From The NRSF President

johnAlready, this year is shaping up to be a busy year as we extend our Reye’s Syndrome education and awareness outreach.

This year, we are asking families to come together in support of Reye’s Syndrome awareness.  We are asking the older generations to impart their knowledge to the younger generations, and we invite those younger generations to become active in supporting Reye’s Syndrome education and awareness.  Until we find a cure for Reye’s Syndrome, we must continue putting the message out; Kids and aspirin products don’t mix!  We must hand Reye’s Syndrome awareness down from generation to generation until we find a cure!

The uniqueness of the National Reye’s Syndrome Foundation is that all involved  are family.  My wife, Terri, and I have met most of you, and your families, at annual meetings, at hospital bedsides, at chapter gatherings, and at various fund raising events over the years.  The Foundation itself is one big family, with one single goal in mind; the eradication of a monstrous disease!  We don’t have hundreds of thousands of members, or donors.  We know each of you by name, and the name of your loved one attacked by Reye’s Syndrome.  You are not a stranger, you are family.

In today’s electronic world, it is easier than ever to stay in touch, and it is easier than ever to create support for Reye’s Syndrome education and awareness.

How simple it is to ask your boss if every  Friday, or every third Friday of the month be designated a Reye’s Syndrome Awareness Friday, and perhaps a ‘dress down day’, or potluck can be held with proceeds donated to the NRSF in support of educational programs.  Or maybe one sports game at school each year can be dedicated to Reye’s Syndrome Awareness and ticket proceeds  donated to the NRSF for educational programs.  And, for all those who have ‘friends’ on Facebook and other social media sites, creating a Birthday Wish Cause, or Memorial, with the NRSF as recipient of the gift, is a wonderful and so easy way to support Reye’s Syndrome Awareness.  It also helps the NRSF family grow stronger in outreach programs.

We are in this together, you and I.  We are partners in a common cause.   baby1

We are guardians of children past, present and future, and we shall not let them down.

Join the NRSF family in this most important cause.

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