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Awareness Calendar for Cancer & Other Causes | Personalized Cause

Personalized Cause's 2017 cause awareness events calendar features medical, cancer, psychological and social causes. Causes listed by awareness months, weeks and days.

Rare Disease Day


Rare Disease Day

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

Research is key. It brings hope to the millions of people, and their families, across the world living with a rare disease.

Rare Disease Day 2017 is therefore an opportunity to call upon researchers, universities, students, companies, policy makers and clinicians to do more research for the rare disease community.

Rare Diseases:
Achondroplasia
Adrenal Insufficiency
Alcardi Syndrome
Alagille Syndrome
Albinism
Apert Syndrome
Autoimmune Autonomic Ganglionopathy
Avascular Necrosis
Babesiosis
Bardet-Biedl Syndrome
Beckwith-Wiedemann Syndrome
Behcet's Disease
Bohring-Opitz Syndrome
Bronchiectasis
Brown-Vialetto-Van Laere Syndrome
Canavan Disease
Cardiofaciocutaneous Syndrome
Charcot-Marie-Tooth Disease
CHARGE Syndrome
Chromosone 12, Microdeletion
Citrullinemia
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
Craniosynostosis
Crouzon Syndrome
CSF Leak (Spinal)
Cyclic Vomiting Syndrome
Cystinosis
Dercum's Disease (Adiposis Dolorosa)
Dermatomyositis
Dermatomyositis (Juvenile)
Dravet Syndrome
Duchenne Muscular Dystrophy
Dup 15q Syndrome
Dwarfism
Eosinophilic Esophagitis
Eosinophilic Fasciitis
Epidermolysis Bullosa
Erythromelalgia
Familial Adenomatous Polyposis
Fetal Alcohol Spectrum Disorder
Food Protein-Induced Enterocolitis Syndrome (FPIES)
Fragile X Syndrome
Gastroschisis
Gaucher Disease
Generalized Gangliosidoses
Glutaric Acidemia
GM1 Gangliosidosis
Granulomatosis with Polyangiitis (GPA)
GRIN2B
Helsmoortel-Van Der Aa Syndrome
Hemangioma
Hemicrania Continua
Hemiplegic Migraine
Heterotaxy Syndrome
Hirschsprung's Disease
Hunter Syndrome
Huler Syndrome
Hutchinson-Gilford Progeria Syndrome
Hydrocephalus
Hypersomnia
Hypophosphatasia
Idic 15
Intercranial Hypertension
Ivemark Syndrome
Joubert Syndrome
Kabuki Syndrome
Klippel-Feil Syndrome
Krabbe Disease
L1 Syndrome
Langerhans Cell Histiocytosis
Lennox-Gastaut Syndrome
Leukodystrophy
Lissencephaly
Marfan Syndrome
Mast Cell Activation Disorder
McCune-Albright Syndrome
Melkersson-Rosenthal Syndrome
Meniere's Disease
Menkes Disease
Microcephaly
Misophonia
Mitochondrial Disease
Moebius Syndrome
Mucopolysaccharidoses
Multiple Chemical Sensitivity
Multiple Endocrine Neoplasia Type 2
Myeloproliferative Neoplasms
Nemaline Myopathy
Neurofibromatosis
Neurofibromatosis Type 1
NGLY1 Deficiency
Occipital Neuralgia
Osteogenesis Imperfecta
Panhypopituitarism
Parkes Weber Syndrome
Pelizaeus-Merzbacher Disease
Periodic Paralysis
Pitt-Hopkins Syndrome
PMM2-CDG
Polymicrogyria
Prader-Willi Syndrome
Primary Immunodeficiency
Progeria
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
Syringomyelia
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
VACTERL
von Hippel-Lindau Syndrome (VHL)
Warburg Micro Syndrome
Williams Syndrome