Rare Disease Day is the official international awareness-raising campaign for rare diseases. Rare Disease Day takes place on the last day of February each year. The main objective of the campaign is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients' lives.
GladGirl continues its support for Rare Disease Day in 2024 with 10% of all sales on Thursday 29th February to be donated to the organization.
A disease or disorder is defined as rare in Europe when it affects fewer than 1 in 2000.
A disease or disorder is defined as rare in the USA when it affects fewer than 200,000 Americans at any given time.
One rare disease may affect only a handful of patients in the EU (European Union), and another may touch as many as 245,000. In the EU, as many as 30 million people may be affected by one of over 6000 existing rare diseases.
- 80% of rare diseases have identified genetic origins whilst others are the result of infections (bacterial or viral), allergies and environmental causes, or are degenerative and proliferative.
- 50% of rare diseases affect children.
Beta-propeller protein-associated neurodegeneration (BPAN) is a disorder that damages the nervous system and is progressive, which means that it gradually gets worse.
In addition to GladGirl's support of Rare Disease Day, you can also donate directly to both Rare Disease Day and BPAN. Thank you, as always, for your support, Lash Lovers.
Lashing out since 1981, GladGirl brings over 40 years experience to the beauty industry. The Eyelash Extensions Blog is our contribution to the advancement of professional skills and industry standards. Here you will find salon business articles, training resources, beauty tips and general health and wellness content.
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Today is Rare Disease Day—2025! At GladGirl, we’re proud to stand alongside families affected by rare disorders, raising awareness and supporting critical research. This year, we’re donating 10% of all sales today to the NBIA Disorders Association, helping to fund research, provide support, and raise awareness for ultra-rare conditions like BPAN.
