Committed to Awareness, Education and Support
for Ehlers-danlos syndromes and other Rare Diseases

NH EDS Coalition is a nonprofit organization established and operated by volunteers with a personal connection to Ehlers-Danlos syndromes (EDS). The goal is to change the culture surrounding EDS so that affected individuals will gain earlier recognition and better care in New Hampshire.

Ehlers-Danlos syndromes (EDS) are a group of genetic collagen disorders, each with different presentations. Collagen provides support and structure to the body. In EDS the collagen is deficient and easily damaged. Loose tendons and ligaments allow the joints to move past the normal range of motion and cause joint instability leading to widespread musculoskeletal pain. Many people may have similar presentations yet fail to meet the new strict diagnostic criteria for EDS. These individuals may be given the diagnosis of hypermobility spectrum disorder (HSD). EDS and HSD likely have similar underlying etiologies and may benefit from the same treatment approaches. Since collagen is found in all major body systems people can have a broad range of symptoms such as digestive problems, fatigue, headaches, dizziness and fainting. Due to the systemic nature and symptoms that seem unrelated, it can take years, decades, and generations from the time of symptom onset to diagnosis.


The 2018 New England Connective Tissue Disorders Symposium
Saturday, September 22, 2018
Manchester, New Hampshire

This Symposium is intended for people living with a connective tissue disorder, family members, caregivers, and healthcare providers. Topics covered include Ehlers-Danlos syndromes, Marfan syndrome, Loeys-Dietz syndrome and related disorders. 


Why the Zebra? 

Medical students are taught to think horses (common illnesses), not zebras (rare illnesses), when they hear hoofbeats (symptoms). The result is that folks with rare diseases are frequently undiagnosed or misdiagnosed because physicians are looking for the most common cause of symptoms. This leads to further pain and disability during the years it takes for an accurate diagnosis. The peculiar thing is that EDS are likely not rare, but rarely diagnosed.


About

Find out about our organization, mission, vision, and meet our Directors/Board Members.

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SUPPORT

NH EDS Support Group was created in October 2015 to connect people whom are diagnosed with EDS/HSD in New Hampshire, and surrounding states (VT, ME, MA), to each other. It is a forum to discuss the symptoms and peculiarities of EDS/HSD and to offer support to those living with it, their families and loved ones.

Join NH EDS Support Group 


RECENT RESEARCH

The most recent, March 2017, EDS research articles are available to everyone in the American Journal of Medical Genetics!

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GIVE

Donate your time or money to help make progress for Ehlers-Danlos syndromes.

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