The Andrea Foundation For EDS

Fighting The Pain You Can't See

These days, there are people who have been suffering from Ehlers-Danlos Syndrome (EDS) without receiving the best health care services from other professionals. That is why The Andrea FoundationFor EDSwas created to provide support. We want to educate and spread awareness among many individuals and in different parts of the world about the said hereditary disease. We want to make affected patients familiar on what their syndrome really is and how to face their problem with optimism.

As a non-profit organization, we have a team of committed staffs who are willing and dedicated to help many individuals. We cannot see people suffering from EDS without making an action that makes us very eager to provide awareness. Even though our mission may sound hard, giving affected patients an idea on EDS makes us feel fulfilled. We consider raising awareness as a vocation. That is why hard things become easy and simple. Nevertheless, we cannot do our mission without your help. We need donations to reach all people who need us. With any support you can give, you can make them aware and positive towards the syndrome.

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We support cost-effective initiatives that provide everyday basics – such as early diagnosis for all 6 types of EDS, medical equipment, health care, education – and promote cutting-edge research to find the best solutions to help prevent the cause of chronic pain in children and adults.

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