Purple Day 2024: Raising Awareness for Rare Epilepsies

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Suzanne H.

Sales and Marketing

Each year on March 26th, epilepsy advocates in more than 80 countries celebrate Purple Day. Starting as an annual event in 2008, participants are asked to wear purple to bring awareness to this group of chronic neurological disorders characterized by repeated seizures. Currently, only Canada recognizes Purple Day as an official holiday, but epilepsy ambassadors embrace the holiday around the globe.

Most patients diagnosed with epilepsy will require medical treatment throughout their lives and support from family and loved ones along the way. Although epilepsy is one of the most common diseases of the central nervous system, some argue it is one of the least understood.

How you can help promote #PurpleDay and Epilepsy within your community?

  • Contact your local association and ask to volunteer
  • Hold a fundraising event to support your local agency
  • Share Purple Day information and Epilepsy facts on your social media accounts
  • Donate your Facebook Status to your local agency
  • Organize a local walk or run in support of Purple Day and Epilepsy
  • Talk about epilepsy and/or Purple Day in your blog or vlog

Epilepsy affects over 50 million people worldwide, with an estimated 2% of all children presenting with the disease. With 1 in 100 people diagnosed with epilepsy during their lifetime, there is a great chance we all know at least one person fighting this condition.

There are four main types of epilepsy: Generalized, Focal, Generalized and Focal, and Unknown if Generalized or Focal. Under these four disease headings fall dozens of individual seizure disorders, each with slight differences in how they present.

In the United States, a rare disease is defined as one affecting less than 200,000 people. While seizure disorders as a whole do not fall under the rare disease category, over 20 rare forms of the condition exist to date.

Angelman Syndrome (AS)

This hereditary form of epilepsy results from the absence of genes on chromosome 15 from the maternal side. It is characterized by jerky movements, speech impairments, and mental disability. With support, patients with Angelman syndrome can live to average life expectancy. The Angelman Syndrome Foundation has been assisting patients and their caregivers since 1992.

CDKL5 Deficiency Disorder (CDKL5)

First discovered in 2004, this genetic form of epilepsy is caused by mutations in the CDKL5 gene. Seizures usually begin in infancy, followed by fine and gross motor skill delays and intellectual disability issues. Because this type of epilepsy is relatively new, insufficient data is available on these patients’ life expectancy. Again, a great deal of support is necessary for these patients throughout their lives. Created in 2017, the CDKL5 Alliance supports those living with the disorder and those who care for them.

Rett Syndrome (RTT)

This genetic form of epilepsy occurs due to a mutation of the MECP2 gene. Diagnosed almost exclusively in females, this type of epilepsy is progressive, causing severe and debilitating disorders in multiple body systems. Common symptoms include loss of speech, control over body functions, and breathing issues. These patients are characterized by near-constant repetitive hand movements and are typically diagnosed by 18 months of age. Rett syndrome patients live an average of 24 years and often need round-the-clock attention and medical care from doctors from many areas of medicine. The International Rett Syndrome Foundation (IRSF) was established in 2007 and offers support and services to patients and families affected by Rett syndrome

Learn More

View this link for a more detailed listing and description of rare epilepsies.

Personalized Support Services for Patients with Epilepsy

Patients with epilepsy often live with the uncertainty of not knowing exactly when their subsequent seizure may occur or the severity of that next seizure. Those with rare forms of the disorder will need to see multiple specialists to address the various medical issues caused by the disease. Many patients will require additional care from family and friends.

Rare epileptic patients who elect to be in clinical trials for their disorder will require expanded support services to enroll in and remain in their study throughout completion. They are paired one-on-one with a patient coordinator who understands the many logistical challenges each patient and their caregiver will face throughout the study. Many participants will need wheelchair-accessible vehicle transportation, medical equipment rentals, and Americans with Disabilities Act (ADA) compliant hotel rooms.

Pharmaceutical sponsors who partner with a patient concierge services company provide their participants with a coordinator who understands the patient’s language, cultural nuances, and the many intricacies of their specific disease. This support enables both the rare disease patient and their caregiver to feel unprecedented support. This personal relationship with their coordinator and the heightened level of support the patient receives allows participants to remain in the trial through completion, leading to more complete data collection for the study sponsor.

On #PurpleDay2024, show your support for those with epilepsy by wearing the color purple. Help raise awareness of the causes of the many forms of epilepsy, as well as current treatment therapies and research opportunities. 

Learn how Clincierge's Patient Concierge Services Support your Rare Disease Clinical Trial Participants and Their Caregivers.

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