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Raise Awareness of the Reality of Rare Disorders

Posted by | 2:52am on Friday, February 6, 2009
Rare Disease Day

By designating a day to the awareness of rare diseases, we are giving a voice to many who feel isolated and alone. 

This is a cross post from “e-patients.net“.

One in ten Americans is living with a rare disorder, but they are often overlooked in the media, in research circles, and in their local communities. The 2nd Annual Rare Disease Day on Feb. 28, 2009, is an opportunity to change that.

Typically, rare-disorder patients form their own small advocacy group but find it difficult to be heard. These patient communities may be the primary source of information about the disease and treatment options. Many of these patients have never met anyone else in person that has the same disorder, so finding ways to connect and share experiences and support is especially powerful. NORD, the National Organization for Rare Disorders, is an important umbrella group dedicated to helping these communities collaborate and impact public policy through programs of education, advocacy, research, and service.

To raise awareness of rare diseases and the need for safe, effective treatments, people around the world will join together to observe the 2nd Annual Rare Disease Day on the last day of February (Feb. 28, 2009). NORD is asking all organizations, companies, and individuals working with and/or interested in rare diseases to become a Rare Disease Day partner.

Actions you can take include:

Here are some facts about the prevalence of rare diseases:

  • A rare disease is defined as one that does not afflict more than 200,000 people in the United States.
  • 10% of Americans (about 25 million people) have some kind of rare disease
  • There are close to 7,000 known rare diseases
  • The National Disease Research Interchange reports that research on rare diseases often leads to a better understanding of more common diseases.
  • By designating a day to the awareness of rare diseases, we are giving a voice to many who feel isolated and alone. Rare diseases are really a public health issue, especially since rare diseases affect so many people, directly or indirectly.

About Wendy White

Since founding Siren Interactive in 1999, Wendy has been recognized as a thought leader at the intersection of niche pharma brands, patient empowerment and online marketing. Her vision for how the internet can facilitate interactions and provide crucial information that patients, caregivers and their healthcare providers previously struggled to find has propelled Siren to the forefront of relationship marketing for rare disorder therapies.

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