MOMS NIGHT OUT!

Thank you to Adrienne for the invite!

If you know any ds mommas out there that would like a night out then pass this along!

DSAGSL ANNUAL FAMILY PICNIC! MAY 14, 2011!

Click here to get more info!

Are you planning on going?

YOUR HELP IS NEEDED!

Act Now to Help Increase Funding for Down Syndrome Research Dear  DSAGSL Members and Friends, The DSAGSL is joining with the National Down Syndrome Congress and the Global Down Syndrome Foundation (GDSF) to strongly encourage you to take action now to help increase funding for DS research. The National Institutes for Health has issued a Request for Information regarding a national Down syndrome registry, research database and biobank.  Every e-mail counts!  A large, clear response is likely to lead to funding for these important projects. The deadline to respond is April 1st! What can I do? Take a look at GDSF's recommendations at the bottom of this note.  If you agree, send an original message, or cut-and-paste into the message provided below, and send your response to dsrdrfi@mail.nih.gov by April 1st. Use the Subject header:  "RESPONSE TO NIH DOWN SYNDROME RESEARCH DATABASE & BIOBANK RFI" Please cc: the GDSF at nihresponse@globaldownsyndrome.org, so they can keep track of the responses. What if I need additional information? View one of Global Down Syndrome Foundation's upcoming 30 minute webinars on responding to this RFI:    Tuesday, March 29, 12:00pm MST Wednesday, March 30, 5:00pm MST  Sample Letter/Key Points Below is a sample letter of support, and below that some key points to consider: To Whom It May Concern: It is morally, economically and scientifically important that the National Institutes of Health increase funding for people with Down syndrome.  We are pleased that the Linda Crnic Institute for Down Syndrome and the Global Down Syndrome Foundation have taken the lead with the NIH in this regard.  We support and agree with the Linda Crnic Institute's assessment of what the parameters should be for our future centralized Down syndrome patient registry, database and biobank.  Please continue to work towards this end. We appreciate NIH's renewed interest in Down syndrome research and we appreciate NIH addressing the historical and alarming disparity of funding for research that would improve the lives of people with Down syndrome. Sincerely, (name) Key points to consider (provided by the Global Down Syndrome Foundation): ·        People with Down syndrome deserve The best medical care to reach their potential The best educational supports, tools and curriculum to reach their potential The best scientists working on long-term medical and cognitive issues that increase a healthy lifespan and potentially allow for increased safety ·        Without research There is no body of evidence to provide to the doctor's office, the teachers and school systems, the therapists or others who interact with people with Down syndrome ·        Examples to consider Sleep apnea Early onset of Alzheimer's Autoimmune disorders, increased risk for infection Average lifespan of a Caucasian with Down syndrome is +/- 60; for an African American with Down syndrome it's 36 Significantly higher risk of sexual and other abuse Evidence-base for best practices  Our Down syndrome community needs a national, centralized registry, research database and biobank in order to Connect people with Down syndrome and their families interested in participating in research to reliable and ethical research projects Manage meaningful clinical trials that have enough numbers in a study to have a conclusion Manage information resulting in clinical trials to the participants when appropriate Have economy of scale and quality control - back-up storage systems, alarms and remote paging, responsible personnel on call at all times, sources of funding Have research that leads to breakthroughs for people with Down syndrome medically and developmentally Attract the best and brightest researchers to dedicate their lives to people with Down syndrome Must exist to benefit people with Down syndrome Must protect the participants  ·        Ownership Samples and information are owned by the participants Hosted, but not owned, by a group managing the registry A Research Review board will Have oversight of the registry, research database and biobank Ensure the researcher has approvals, funding, and a sound plan prior to accessing the registry Have the power to grant/deny a researcher access to the registry Ensure researchers provide results to participants, care providers and post publication of their data Consist of participants (people with DS and their families), medical care providers, researchers, representatives from funding agencies

FREE PODCAST FROM THE NACD!

The National Association for Child Development - Download free podcast episodes by NACD - The Nation

I was able to listen in on this last night and there was so much great information!

I would recommend listening to the free podcast. I am going to listen again and take better notes.

Thank you Ria!

STEP UP FOR DOWN SYNDROME ~ SUNDAY JUNE 5th!!!

Step Up for Down Syndrome is SUNDAY, JUNE 5! Read information about the event

LOSE THE TRAINING WHEELS!

Space is Limited and Moving Fast Lose the Training Wheels™ Bike Camp June 6-10, 2011 Deer Creek Center 3238 Laclede Station Road St. Louis, MO  63143        The Down Syndrome Association of Greater St. Louis and Pujols Family Foundation are teaming up again to bring Lose the Training Wheels to St. Louis.  The mission of Lose the Training Wheels™ is to teach individuals with disabilities to ride a conventional two wheel bicycle and become lifelong independent riders. This achievement, in turn, creates a gateway of opportunity, helping them gain assurance and self-reliance in many other aspects of their lives.  For more information, visit our website or click here for an application form.     The bike camp fee is $150 per rider and there are only 40 participant slots.  If you are interested, send your application to the DSAGSL office today.   To learn more about Lose the Training Wheels program, please visit www.losethetrainingwheels.org/.

GATEWAY CENTER for the ARTS NEEDS OUR HELP!

204 Elm Street Washington MO 

636-239-8939

You have probably heard that the Gateway Center for the Arts building was
damaged during Sunday's storm.  You may not have heard how extensive the damage
was.  Part of the roof blew off in the storm, letting rainwater inside.  Gym
mats & pieces of equipment are ruined, the walls where the water ran down are
soaked, and the floors are damaged from standing water.

Gateway serves our community in a very unique way, offering dance, tumbling,
art, etc, as well as much-needed special needs classes.  It is a place where
typically developing and challenged kids alike can find things they love and
help them grow.  So many special needs families in particular count on
Gateway's support to help their children flourish. 

Volunteer times:

Tues March 8th  12pm-4pm

Wed March 9th  12pm-4pm

Thurs  March 10th  9am-11am  & 12pm-4pm

Friday March 11th  9am-3pm

http://www.gatewaycenterarts.org/

If you are not able to stay all day then just stay for an hour or so! 

Any help is appreciated!!!

(Thank you Ria & Kristin!)