Hyperemesis Education and Research Foundation

The HER Foundation is the world's largest network of HG survivors and the leading resource for HG information. In 2003, HER became...En savoir plus

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Hugh Darwin collecte des fonds
Hugh Runs For HER
Hello there,

On Sunday 16th March 2025, I will be donning my 15kg weight vest and running the Bath Half Marathon to raise money for Hyperemesis Education and Research (HER) Foundation.

Hyperemesis Gravidarum (HG) is a potentially life-threatening pregnancy disease that may cause weight loss, malnutrition, dehydration, debility due to severe nausea and/or vomiting, further pregnancy complications, and long-term health issues for mother and baby(ies). In many cases, HG can have a major negative impact to mental health through PTSD, anxiety and depression; financial strain and job loss/difficulties; and even pregnancy loss, including TFMR (termination for medical reasons).

Like so many areas of women’s reproductive health, HG is under-researched and underfunded, despite affecting up to 11% of pregnancies, with 20% of these resulting in TFMR.

The HER Foundation is the global voice of HG progress, providing support, groundbreaking research, advocacy, and education on hyperemesis. HER is dedicated to helping those suffering HG and those who have survived it. Since 2000, they have helped 2.2 million people across the globe.

Thank you in advance for your contribution to this important cause.

Hugh
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55 soutiens
Rivka Kolman collecte des fonds
Help women with HG get the care they need
Dear Friends and Family,

Those of you who know me know HG.

HG Is a debilitating pregnancy illness where women suffer from severe nausea and vomiting oftentimes leading to dehydration , malnutrition, and a host of medical problems.

The HER Foundation has done extensive research over the past few years and has come up with a medical regimen that's helping to alleviate the symptoms of HG. The OBs and DRs are completely uneducated and are unwilling to prescribe these medications thus women are suffering needlessly.

As I'm dealing with severe HG I begged 2 DRs to prescribe the meds but being that they are lacking the education were unwilling to prescribe. As I landed in the hospital I was very blessed to meet a very experienced high risk Dr that willingly prescribed one of the meds that the HER foundation recommends. I can say that this new medication helps more Than others I've been taking till now. But there's a lot more out there. The HER foundation has put together a curriculum that with your help will become mandatory for all OBs to learn thus enabling women with HG to get the care they so desperately need.

If you can please find a place in your heart to donate to this cause that is very near and dear to me, I'll forever be grateful.

Thanks In advance

Rivka R kolman
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91 soutiens

À propos de l'association Hyperemesis Education and Research Foundation

The HER Foundation is the world's largest network of HG survivors and the leading resource for HG information. In 2003, HER became the global voice of hope and understanding for women with HG. Our mission is to find a cure through research, to provide education and support for those seeking effective management strategies, and to provide them with clinical resources. Goals: 1. Minimize suffering & complications. 2. Eradicate morbidity & mortality. 3. Improve outcomes. 4. Promote a universal protocol. 5. Raise public awareness & improve policies. 6. Educate practitioners & caregivers. 7. Expand clinician education & awareness. 8. Publish clinically relevant research. 9. Fundraise for research, awareness, and educational projects. 10. Develop tools to improve diagnosis & management.

10117 SE Sunnyside RdClackamas, OR 97015

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Causes

Education, Diseases and conditions

Établi

2018

NIF

71-0912435

Code NTEE

Alliance/Advocacy Organizations

Hyperemesis Education and Research Foundation est un organisme caritatif public de type 501(c)(3), EIN : 71-0912435. Les dons sont déductibles des impôts. Le contenu sélectionné est fourni par GuideStar.

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