Guest guest Posted August 11, 2008 Report Share Posted August 11, 2008 From: news@... Sent: Monday, August 11, 2008 10:31 AM To: Liz Subject: Research says 1 in 200 people may be born with mitochondrial disease NEWS FROM UMDF Dear Liz , RESEARCH PARTIALLY FUNDED BY UMDF SHOWS ONE in 200 PEOPLE ARE BORN WITH DNA MUTATION We are truly excited to announce to you revolutionary study results by Dr. Chinnery of the University of Newscastle in the UK. UMDF partially funded Dr. Chinnery’s study, titled “Pathogenic Mitochondrial DNA mutations are common in general populations†published in the August 8, 2008 issue of the American Journal of Human Genetics. Dr. Chinnery’s research clearly determined that mitochondrial mutations are not rare. Dr. Chinnery studied 3000 samples of cord blood from newborns in the U.K. His team found that one in every 200 people have a mtDNA mutation that could cause a mitochondrial disease in the children of women who carry the mutation. If you would like to read the UMDF news release, visit www.umdf.org and look for it under out 'NEWS' heading. We congratulate Dr. Chinnery and his team! This research confirms for us that mitochondrial diseases are not rare diseases. We also want to congratulate our members and supporters. Your hard work across the country in having awareness walks, brew’s at the zoo, coins for a cure (and the list goes on) makes it possible for the UMDF to be the largest non-governmental funder of mitochondrial disease research. It is research like this that benefits all mitochondrial disease patients. Dr. Chinney’s research results makes us wonder what other new discoveries stemming from UMDF grants may be on the horizon. LETS USE THIS AS AN OPPORTUNITY TO CALL FOR MORE FEDERAL FUNDING FOR MITOCHONDRIAL DISEASE RESEARCH We need to educate our elected officials about this study and call for an increase in federal funding for mitochondrial disease research. Send a letter to your U.S. House and Senate representatives. you can dowlnoad and save a template by clicking here . To find the name and address of your U.S. Congress member or U.S. Senator click here. If you are a Canadian resident, you can find your Member of Parliment here. You may also send a letter to the editor of your local newspaper. Feel free to use this template and add your own, personalized information. Once you have sent your letters, tell us about your results. Send us an email at news@.... The UMDF has an " Advocacy Toolkit " that describes the action items all members can take leading up to our symposium in 2009. If you haven’t reviewed our advocacy tool kit, please click here. Member of the House and Senate are back in their home districts and states throughout the month of August. Now would be a great time for you to schedule a meeting with your representaive and call for the need for additional research funding. Your meeting or letter is the first step as we prepare for our symposium in Washington, D.C. next summer. Please plan to join us June 24- 27, 2009 at the Sheraton Premiere Hotel, Tysons Corner, Virginia! 8085 Saltsburg Road, Suite 201 | Pittsburgh, PA 15239 | Toll-Free 1-888-317-UMDF | P | F | info@... Copyright 2008 © The United Mitochondrial Disease Foundation. All rights reserved. This and all UMDF e-mail communications are intended for informational purposes only and The UMDF assumes no liability for information provided herein. It is strongly recommended that you discuss any diagnoses, treatment or medications with your physician. Remove yourself from this mailing. Remove yourself from all mailings from United Mitochondrial Disease Foundation. No virus found in this incoming message. Checked by AVG - http://www.avg.com Version: 8.0.138 / Virus Database: 270.6.0/1603 - Release Date: 8/10/2008 6:13 PM Quote Link to comment Share on other sites More sharing options...
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