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Awareness Calendar for Cancer & Other Causes | Personalized Cause

Personalized Cause's 2019 cause awareness events calendar features medical, cancer, psychological and social causes. Causes listed by awareness months, weeks and days.

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Rare Disease Day

Rare Disease Day

Rare Disease Day is observed on the last day of February each year. This very important day seeks to raise awareness in the general public and with key decision-makers about rare diseases and their impact on patients’ lives. On Rare Disease Day, rare disease patients and families, patient organizations, politicians, caregivers, medical professionals, researchers and industry rasie awareness of rare diseases through thousands of events all over the world.

The issue of research is key on Rare Disease Day. It brings hope to the millions of people, and their families, across the world living with a rare disease.

Rare Disease Day is therefore an opportunity to call upon researchers, universities, students, companies, policy makers and clinicians to do more research for the rare disease community.

"When you hear hoofbeats, think of horses not zebras".
Sometimes, however, physicians are confronted with rare diseases (the zebras).
FindZebra is a tool for helping diagnosis of rare diseases.
To learn more, visit

The image for Rare Diseases and Rare Disease Awareness is Zebra.

Personalized Cause supports Rare Disease Day with:

Zebra Custom Awareness Ribbon for Rare Disease Awareness, click here.

Zebra Awareness Ribbon for Rare Disease Awareness, click here.

These Rare Diseases that can be represented by the Zebra awareness ribbon:
Adrenal Insufficiency
Alcardi Syndrome
Alagille Syndrome
Apert Syndrome
Autoimmune Autonomic Ganglionopathy
Avascular Necrosis
Bardet-Biedl Syndrome
Beckwith-Wiedemann Syndrome
Behcet's Disease
Bohring-Opitz Syndrome
Brown-Vialetto-Van Laere Syndrome
Canavan Disease
Cardiofaciocutaneous Syndrome
Charcot-Marie-Tooth Disease
CHARGE Syndrome
Chromosone 12, Microdeletion
CLOVES Syndrome
Coffin-Siris Syndrome
Common Variable Immune Deficiency
Congenital Adrenal Hyperplasia
Congenital Central Hypoventilation Syndrome
Congenital Diaphragmatic Hernia
Congenital Generalized Lipodystrophy
Conradi-Hunermann Syndrome
Costello Syndrome
Crouzon Syndrome
CSF Leak (Spinal)
Cyclic Vomiting Syndrome
Dercum's Disease (Adiposis Dolorosa)
Dermatomyositis (Juvenile)
Dravet Syndrome
Duchenne Muscular Dystrophy
Dup 15q Syndrome
Eosinophilic Esophagitis
Eosinophilic Fasciitis
Epidermolysis Bullosa
Familial Adenomatous Polyposis
Fetal Alcohol Spectrum Disorder
Food Protein-Induced Enterocolitis Syndrome (FPIES)
Fragile X Syndrome
Gaucher Disease
Generalized Gangliosidoses
Glutaric Acidemia
GM1 Gangliosidosis
Granulomatosis with Polyangiitis (GPA)
Helsmoortel-Van Der Aa Syndrome
Hemicrania Continua
Hemiplegic Migraine
Heterotaxy Syndrome
Hirschsprung's Disease
Hunter Syndrome
Huler Syndrome
Hutchinson-Gilford Progeria Syndrome
Idic 15
Intercranial Hypertension
Ivemark Syndrome
Joubert Syndrome
Kabuki Syndrome
Klippel-Feil Syndrome
Krabbe Disease
L1 Syndrome
Langerhans Cell Histiocytosis
Lennox-Gastaut Syndrome
Marfan Syndrome
Mast Cell Activation Disorder
McCune-Albright Syndrome
Melkersson-Rosenthal Syndrome
Meniere's Disease
Menkes Disease
Mitochondrial Disease
Moebius Syndrome
Multiple Chemical Sensitivity
Multiple Endocrine Neoplasia Type 2
Myeloproliferative Neoplasms
Nemaline Myopathy
Neurofibromatosis Type 1
NGLY1 Deficiency
Occipital Neuralgia
Osteogenesis Imperfecta
Parkes Weber Syndrome
Pelizaeus-Merzbacher Disease
Periodic Paralysis
Pitt-Hopkins Syndrome
Prader-Willi Syndrome
Primary Immunodeficiency
Propionic Acidemia
Relapsing Polychondritis
Ring 22 Syndrome
Rubinstein-Taybi Syndrome
Saethre-Chotzen Syndrome
Schwartz-Jampel Syndrome
Scimitar Syndrome
Septo-Optic Dysplasia
Short Bowel Syndrome
Smith-Magenis Syndrome
Snyder-Robinson Syndrome
Sotos Syndrome
Stiff-Person Syndrome
Sturge-Weber Syndrome
Systemic Sclerosis
Takayasu's Arteritis
Tay-Sachs Disease
Tethered Spinal Cord Syndrome
Transverse Myelitis
Trigeminal Neuralgia
Trimethylaminuria (Fish Odor Syndrome)
Trisomy 18/Edwards' Syndrome Trisomy 5q
Tuberous Sclerosis Complex
Type I, II, and III Autoimmune Polyglandular Syndromes
Urea Cycle Disorder
von Hippel-Lindau Syndrome (VHL)
Warburg Micro Syndrome
Williams Syndrome

Earlier Event: February 28
International STAND UP to Bullying Day
Later Event: March 1
Trisomy Awareness Month