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Join the National CMV Foundation in raising awareness for congenital cytomegalovirus this June during CMV awareness month. This event will be completely virtual and held on June 26th. We can't all be together physically, but we can still make a difference apart!
HOW DOES THIS WORK?
Since this event is virtual, you choose your own starting line, starting time, and route. Your challenge is to walk, run, or roll for 5k (3.1 miles) on June 26th, and if you feel up for it, post your accomplishment on social media with the hashtags #stopcmv, #screen4cmv, and #strides4cmv so we can see how well you did!
IS THERE A FUNDRAISING REQUIREMENT?
No, there is not, but it is appreciated. All funds raised (including registration fees) will be donated to the National CMV Foundation in support of our mission to prevent pregnancy loss, childhood death, and disability due to congenital CMV. If you're interested, we suggest using Facebook to fundraise for the event! https://help.runsignup.com/support/solutions/articles/17000091661-how-to-create-a-facebook-fundraiser-from-your-existing-fundraising-page
WHAT IS CMV?
Congenital Cytomegalovirus (sy·toe·MEG·a·low·vy·rus), or CMV, is the most common viral infection, and the leading non-genetic cause of hearing loss, that infants are born with in the United States. Every pregnant woman is at risk of acquiring CMV. And only 9% of women know about it.
CMV is common, serious, and preventable.
CMV is a member of the herpes virus family. Coming into contact with the CMV virus is a common occurrence, typically harmless to the general population. A CMV infection causes cold-like symptoms, such as a sore throat, fever, fatigue, and swollen glands. These mild cytomegalovirus symptoms last for only a few short weeks and are rarely a cause for concern for healthy kids or adults.
The CMV virus can also cause severe disease in babies who were infected with CMV before birth (referred to as congenital CMV infection).
According to the Centers for Disease Control and Prevention (CDC), between 50 and 80 percent of people in the United States have had a CMV infection by the time they are 40 years old.
WHERE CAN I FIND OUT MORE ABOUT CMV?
We suggest visiting the National CMV Foundation's website for more information about all things CMV including signs & symptoms, prevention tips, screening, outcomes, and much more. https://www.nationalcmv.org
Please let us know if you have any questions at any time by reaching out via email, or messaging us directly, and thank you for your interest in the Strides 4 CMV virtual event! ❤️
At the National CMV Foundation, we work to inform and educate others on specific prevention measures to protect against the risk of CMV infection. Congenital CMV is the most common viral infection that infants are born with in the United States, occurring in about 1 in 200 births. Because CMV is a silent disease – meaning most people who are infected have no signs of symptoms (asymptomatic) – the mother is likely unaware she has CMV during her pregnancy. Find out more about the National CMV Foundation below.
Our sweet, beautiful Abby was born on June 12, 2020 and was immediately a bright light in this world! After multiple failed hearing tests and a referral to Children's Hospital, we found out that Abby has bilateral moderate hearing loss (hearing loss in both ears) that was caused from Congenital CMV. Our first call with Infectious Diseases was on July 10th, where we learned the severity of this virus and that hearing loss is only one of the health problems associated with cCMV. Anxiety and fear of the unknown seemed to take over our lives. For months, Abby took medicine twice a day, had regular blood draws, scans, phone calls, appointments, physical therapy, and occupational therapy, but she never let that get her down! Through all of the testing, we found out that along with Abby's hearing loss, she also has brain abnormalities that can possibly affect her development over time. When we got Abby's diagnosis, I remember thinking to myself, "how have I not heard of this virus before?" Our family had never heard of congenital CMV. Our friends had never heard of Congenital CMV. A virus that has changed our lives forever, and we had never heard of it. Our family will continue to share our sweet Abby's story to raise awareness and help educate families about the severity of this virus. Abby is the most joyful, beautiful, adventurous, resilient, goofiest little girl with the biggest heart and smile and we could not be more proud of her!
Ellie was diagnosed with CMV at three days old after baffling doctors - she was a healthy, although petite baby, who had low platelets and failed her newborn hearing screen. While everyone assured us her hearing would be normal, she did suffer hearing loss eventually leading to a cochlear implant in her left ear. Today, Ellie is a feisty, loving 20-month old who keeps her family on their toes. We’re so grateful for her cochlear implant on one side and her normal hearing on her right side. Thanks to the doctors, therapists, and teachers along the way, Ellie is thriving. CMV won’t stop Ellie!
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