Everyone has a birthday, and October 1st is ours! We are celebrating 16 years as a 501(c)3 nonprofit! But what’s a birthday without gifts? We begin the celebration unwrapping gifts from our community…to our community.
Our amazing partners in Copenhagen, CanopyLAB, have been working with us since June to prepare FREE online HG courses for you and your family. This is a dream come true for many of us: HG courses available for all. HER’s knowledge and CanopyLAB’s talent and platform come together to bring you four courses!! Create your login and take the courses.
Introduction to HG: Hyperemesis Gravidarum
HG: a survival guide for expecting moms
HG: tips, support, and resources
The ABC of HG for friends and family
Special birthday cheers and lots of love to #HGsister, Sahra-Josephine, CEO, and Yamanda, eLearning Designer, for making this happen. We are grateful!
16% and Giveaway
OCTOBER 1st ONLY, Your Little Dove is donating 16% of all sales to the HER Foundation! When we say, 16% of sales, we mean 16% of ALL sales. We are so thankful for this generous gift from #HGsister, Cindy, and how it will help to continue progress in education, research, and support. So go shopping for the holidays! Learn about how Cindy started this online heirloom toy company after the loss of her second little one.
In addition, Cindy is sponsoring a giveaway for YOU! Between October 1st and October 22nd, the three largest donors to the HER Foundation will receive store credits from Your Little Dove and be able to choose from the beautiful selection of items: these three lucky people will receive a gift of either $100, $50, or $25. Thank you Cindy!
Courses, 16% donations, and a giveaway are only the part of the celebration. Each Sunday in October will be something special for you!
- HER’s HG experts are launching a new HG management tool, 10/6. HER HG Algorithm
- Hyperemesis Sisterhood is hosting a Q&A with HER on Instagram, 10/13.
- The three donors with the highest recurring, new donations will receive a tougHGirl t-shirt (minimum $25/month), 10/20.
- We will announce the winners of the Your Little Dove giveaway, 10/27.
- And ALL month, members of our community will tell their stories and many more will be featured in HER social media graphics.
- Show us your selfies: #WeAreHER! Print the linked flier or hand write your own signs! Be sure to tag the HER Foundation when you share: I am HER! You are HER! We are HER! Together WE are the HER Foundation.
Thank you: Together, we are making HG Progress
We are thankful for our generous partners adding a lot of excitement and kindness to our 16th celebration. But we cannot do what we do without our wonderful community: YOU! Please help us reach our fundraising goal of $16,000 for HG Progress. We are excited to celebrate with you.
I am HER!
You are HER!
We are HER!
Together, we are an unstoppable
force for healthy moms and babies.
The International HG Awareness Movement began in 2012 when the HER Foundation held the first HG Awareness Day on May 15th.
On May 17, 2012, the Governor of North Dakota, Dennis Daugaard, issued an Official Executive Proclamation for the HER Foundation naming May 15th to be HG Awareness Day! “We want to thank Governor Daugaard for being the first Governor to recognize HG Awareness Day, and we are encouraged by his recognition of the need for awareness for HG women in his state. We hope it will inspire state lawmakers to follow in his footsteps for future Awareness Days. This is a huge step in raising awareness, education, and research. We are truly grateful,” said Ann Marie King, Co-Founder of the HER Foundation.
Since the first HGAD with the theme of “Pregnant and Starving for Answers,” the international movement has grown to include organizations and people from around the world. The HER Foundation is proud to be the global leader in awareness, research, education, advocacy, and support for the HG community.
HER has achieved many firsts including over two dozen ground-breaking research studies including those identifying the first genes associated with HG, developing HG assessment tools and protocols, and creating the first HG Care app to improve tracking and reporting of symptoms and treatment. HER continues to be the voice of hope and help for HG.
Support the work of HER to ensure continued progress for the next generation!
After three years of hard work by HER Foundation and UCLA Health, we celebrate the official public release of the first HG Care iOS app! Now women can track their symptoms and treatments to find out what’s working. Plus they can easily share insights into their progress with family and health professionals. The app is free. Remember if it makes you ill to use your phone, just have family input your data.
DOWNLOAD the app: https://itunes.apple.com/us/app/hg-care/id1148105670?mt=8
We’re starting the next chapter at HER as we kick off our 15th Anniversary!! From scientists to business experts, health professionals and digital health specialists, HER has assembled a team vast expertise! We launched our formal Board of Directors with an awesome meeting that discussed many ways to support families during/after HG, improve treatment by educating health professionals and launching the next version of the app, changing treatment protocols and public policy, and reaching more of the international community. Watch for many new opportunities to be part the next decade of HG progress!
HER Foundation helps UCLA, USC and 23&Me link debilitating pregnancy illness to two genes
FINALLY A BREAKTHROUGH FOR women suffering from the severe pregnancy illness, hyperemesis gravidarum (HG). Many people remember Princess Kate Middleton being hospitalized during her first pregnancy due to the severity of the disorder. However, other women affected by the pregnancy illness have limited family size, quit their jobs or sadly felt so desperate due to the debilitating illness that they terminated wanted pregnancies. Many HG women describe the illness as something no one can truly understand unless they have endured it themselves. Instead of the joy every pregnancy should bring, HG women spend most of the 9 months suffering in silence unable to eat or simply keep water down.
The HER Foundation, researchers at UCLA and USC, and 23andMe, Inc. conducted the first genome-wide analysis of Hyperemesis Gravidarum (HG) and identified two genes associated with HG, which was published this week in Nature Communications. (https://www.nature.com/articles/s41467-018-03258-0). Continue reading
A study published by UCLA and supported, in part, by the Hyperemesis Education and Research Foundation found no evidence linking Zofran to birth defects.
“What was really significant to me was that women with extreme morning sickness who took Zofran reported fewer miscarriages and terminations and experienced higher live birth rates,” Fejzo said. “Taking this medication helped them get through their pregnancies and gave them their desired outcome, a live birth.”
Marlena Fejzo, PhD
Source: UCLA Health
Read the full study or HER Foundation collaborative research. Continue reading