Category Archives: Dysautonomia International

Rare Diseases… Not So Rare

RDD_whiteDysautonomia International is pleased to partner with the National Organization for Rare Disorders (NORD) to celebrate Rare Disease Day today.  Did you know that overall, rare diseases are not that rare?

1 in 10 Americans has a rare disease.  That’s over 30 MILLION people, and there are even more people with rare diseases around the world.  Two thirds of people with rare diseases are children.  There are over 7,000 identified rare diseases and new diseases are discovered every year.

What is a “rare” disease?
In the United States, a disease is considered rare if it
is believed to affect fewer than 200,000 Americans.
The European Union considers rare diseases to be
those that impact Screen shot 2014-02-28 at 1.38.48 PMfewer than 1 in 2000 individuals.  Other countries have similar definitions.

What are some examples of rare diseases?
Rare diseases are present across the spectrum of medical conditions.  Most types of cancer are rare diseases. There are also rare neurological and neuromuscular diseases, metabolic diseases, chromosomal disorders, skin diseases, bone and skeletal disorders, and rare diseases affecting the heart, blood, lungs, kidneys, and other body organs and systems.

Within the realm of autonomic disorders there are several rare diseases such as Autoimmune Autonomic Ganglionopathy, Multiple System Atrophy, Pure Autonomic Failure, Familial Dysautonomia, and Dopamine Beta Hydroxylase Deficiency.

What are some of the problems experienced by people who have rare diseases?

  • Difficulty in obtaining an accurate diagnosis
  • Limited treatment options
  • Little or no research being done on the disease
  • Difficulty finding physicians or treatment centers with experience in treating a particular rare disease
  • Treatments that are generally more expensive than those for common diseases
  • Reimbursement issues related to private insurance, Medicare, and Medicaid
  • Difficulty accessing medical, social, or financial services or assistance because those making the decisions are not familiar with the disease
  • Feelings of isolation and of having been abandoned or “orphaned” by our healthcare system

What can you do to help?
Share this blog post on social media or e-mail today.  For a list of other easy ideas to help spread the word about Rare Disease Day, you can visit the following websites:
U.S. Rare Disease Day website
Global Rare Disease Day website

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Thanks For The Memories 2013, Hello 2014!

2013 Recap
2013 was a year of tremendous growth and many firsts for Dysautonomia International. With the help of hundreds of amazing volunteers and generous donors, we held our first Dysautonomia Lobby Day on Capitol Hill (and a second lobby day), hosted our first national conference, battled insurance companies that are denying coverage for autonomic testing, launched the first POTS Research Registry, helped researchers recruit patients for groundbreaking dysautonomia research projects, presented a patient friendly research update from the 24th Symposium on the Autonomic Nervous System, and gave out our first four research grants.  Our volunteers also organized the second annual Dysautonomia Awareness Month in October, held the second annual Dysautonomia Awareness Tweet-A-Thon, increased press coverage on dysautonomia, obtained proclamations from state and local governments, distributed newly diagnosed patient brochures to medical offices, and held fundraisers, large and small, all year long.  Of course, we continued to provide patients and caregivers with educational resources, videos, resources, and connections to support groups that can help make life with dysautonomia a little bit more manageable.

A New Blog for a New Year
What better way to kick off the New Year than with another first – our first blog post on our new blog!  Through this blog, we’ll be bringing you the latest dysautonomia news, events, and research, as well as guests posts from physicians, researchers and other experts.

When we have a new blog post, we will announce it on our Facebook and Twitter pages, so be sure to follow us on one or both of those sites.  The blog will allow us to bring you more in-depth information that just a simple Facebook or Twitter post.

Our blog team is excited to offer “Dysautonomia Q&A” posts.  A few times per year, we will reach out to our network of dysautonomia savvy physicians, physical therapists, psychologists, school social workers, lawyers and other experts to answer 10 questions submitted by patients and caregivers.  The questions can be on any topic related to dysautonomia.  If you would like to submit a question, please send your question to blog@dysautonomiainternational.org.   We will select 10 questions that are applicable to a broad audience of patients, find an expert to answer each question, and publish their response on this blog .   If your question is selected, your name and e-mail will not be published.

Dysautonomia International wishes you all a Happy Healthy New Year!  We’re looking forward to new adventures in dysautonomia awareness, advocacy, and research in 2014.

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