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Phone - 949-533-4977

Email - PersonalizedCause.Awareness@gmail.com

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Fundraising and large quantity orders

Personalized Cause offers specialty pricing for Fundraising Events and Large Quantity Orders. Please give us a call at (949) 533-4977 or fill out the form to the right to request pricing. We offer reduced pricing on all Awareness Ribbon Pins and Personalized Awareness Ribbon Pins. Let us know how we can help. 

Awareness Bracelets and Car Magnets available in quantities of 25+.

949-533-4977

YOUR source for SINGLE custom awareness ribbons. Personalized awareness ribbons engraved with name, date, logo. Large selection of cancer ribbons.

Rare Diseases and Disorders Awareness Ribbons - E | Personalized Cause

Blue Jeans rare diseases awareness ribbons for rare diseases and disorders that begin with the letter E. Source: Global Genes®.

RARE DISEASES AND DISORDERS - E


EAF
Eagle syndrome
Eales disease
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia
Eastern equine encephalitis
Ebola virus disease
Ebstein's anomaly
Eccentrochondrodysplasia
Eccrine acrospiroma
Eccrine mucinous carcinoma
Eclampsia
Ectodermal dysplasia
Ectodermal dysplasia 2 hidrotic
Ectodermal dysplasia adrenal cyst
Ectodermal dysplasia alopecia preaxial polydactyly
Ectodermal dysplasia anhidrotic
Ectodermal dysplasia arthrogryposis diabetes mellitus
Ectodermal dysplasia Bartalos type
Ectodermal dysplasia Berlin type
Ectodermal dysplasia blindness
Ectodermal dysplasia hypohidrotic with hypothyroidism and ciliary dyskinesia
Ectodermal dysplasia Margarita type
Ectodermal dysplasia mental retardation CNS malformation
Ectodermal dysplasia mental retardation syndactyly
Ectodermal dysplasia neurosensory deafness
Ectodermal dysplasia osteosclerosis
Ectodermal dysplasia skin fragility syndrome
Ectodermal dysplasia trichoodontoonychial type
Ectodermal dysplasia with natal teeth Turnpenny type
Ectodermal dysplasia hidrotic Christianson-Fourie type
Ectodermal dysplasia sensorineural hearing loss and distinctive facial features
Ectopia lentis isolated autosomal recessive
Ectopia pupillae
Ectopic ossification familial type
Ectopic pregnancy
Ectrodactyly and ectodermal dysplasia without cleft lip/palate
Ectrodactyly cardiopathy dysmorphism
Ectrodactyly cleft palate syndrome
Ectrodactyly polydactyly
Ectropion inferior cleft lip and or palate
Edinburgh malformation syndrome
Edwards Patton Dilly syndrome
Edwards syndrome
EEC syndrome
EEM syndrome
Egg shaped pupils
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome arthrochalasia type
Ehlers-Danlos syndrome Beasley Cohen type
Ehlers-Danlos syndrome dermatosparaxis type
Ehlers-Danlos syndrome dysfibronectinemic type
Ehlers-Danlos syndrome hypermobility type
Ehlers-Danlos syndrome kyphoscoliotic type
Ehlers-Danlos syndrome progeroid type
Ehlers-Danlos syndrome type 5
Ehlers-Danlos syndrome vascular type
Ehlers-Danlos syndrome classic type
Ehlers-Danlos-like syndrome due to tenascin-X deficiency
Ehrlichiosis
Eisenmenger syndrome
Elastosis perforans serpiginosa
Elective mutism
Elliott Ludman Teebi syndrome
Ellis Yale Winter syndrome
Ellis-Van Creveld syndrome
Emanuel syndrome
Embryonal carcinoma
Embryonal sarcoma
Emerinopathy
Emery Nelson syndrome
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy dominant type
Emery-Dreifuss muscular dystrophy X-linked
Emphysema congenital lobar
Empty sella syndrome
Enamel hypoplasia cataract hydrocephaly
Encephalitis lethargica
Encephalocele
Encephalocele anencephaly
Encephalocraniocutaneous lipomatosis
Encephalomyopathy
Encephalopathy intracranial calcification growth hormone deficiency microcephaly retinal degeneration
Encephalopathy progressive optic atrophy
Encephalopathy recurrent of childhood
Encephalopathy-basal ganglia-calcification
Enchondroma
Enchondromatosis dwarfism deafness
Endemic Kaposi sarcoma
Endocardial fibroelastosis
Endolymphatic sac tumors (ELST's) in Von Hippel Lindau (VHL) disease
Endometrial stromal sarcoma
Endomyocardial fibroelastosis
Endomyocardial fibrosis
Eng Strom syndrome
Engelhard Yatziv syndrome
Enlarged vestibular aqueduct syndrome
Enolase deficiency type 1
Enolase deficiency type 2
Enolase deficiency type 3
Enolase deficiency type 4
Enterobiasis
Enteropathica
Enteropathy-associated T-cell lymphoma
Enterovirus antenatal infection
Envenomization by bothrops lanceolatus
Eosinophilia-myalgia syndrome
Eosinophilic cryptitis
Eosinophilic cystitis
Eosinophilic enteropathy
Eosinophilic esophagitis
Eosinophilic fasciitis
Eosinophilic pustular folliculitis
Ependymoblastoma
Ependymoma
Epidermal nevus vitamin D resistant rickets
Epidermodysplasia verruciformis
Epidermolysa bullosa simplex with muscular dystrophy
Epidermolysis bullosa
Epidermolysis bullosa acquisita
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex Dowling-Meara type
Epidermolysis bullosa simplex generalized
Epidermolysis bullosa simplex localized
Epidermolysis bullosa simplex Ogna type
Epidermolysis bullosa late-onset localized junctional with mental retardation
Epidermolysis bullosa lethal acantholytic
Epidermolysis bullosa pretibial
Epilepsy benign neonatal dominant form
Epilepsy benign neonatal recessive form
Epilepsy juvenile absence
Epilepsy mental deterioration Finnish type
Epilepsy microcephaly skeletal dysplasia
Epilepsy occipital calcifications
Epilepsy progressive myoclonic type 3
Epilepsy telangiectasia
Epilepsy with myoclono-astatic crisis
Epilepsy benign occipital
Epilepsy female restricted with mental retardation
Epilepsy nocturnal frontal lobe type
Epilepsy partial familial
Epilepsy rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epileptic encephalopathy Lennox-Gastaut type
Epimerase deficiency
Epimetaphyseal dysplasia cataract
Epimetaphyseal skeletal dysplasia
Epiphyseal dysplasia dysmorphism camptodactyly
Epiphyseal dysplasia hearing loss dysmorphism
Epiphyseal dysplasia multiple with early-onset diabetes mellitus
Episodic ataxia
Episodic ataxia with nystagmus
Epithelial basement membrane corneal dystrophy
Epithelial-myoepithelial carcinoma
Epithelioid sarcoma
Epitheliopathy acute posterior multifocal placoid pigment
Erdheim-Chester disease
Ermine phenotype
Eronen Somer Gustafsson syndrome
Erosive pustular dermatosis of the scalp
Erysipelas
Erythema elevatum diutinum
Erythema multiforme
Erythema nodosum familial
Erythema nodosum idiopathic
Erythroderma desquamativa of Leiner
Erythroderma lethal congenital
Erythrokeratodermia ataxia
Erythrokeratodermia progressive symmetrica ichthyosis
Erythrokeratodermia symmetrica progressiva
Erythrokeratodermia variabilis ichthyosis
Erythrokeratodermia variabilis Mendes da Costa type
Erythrokeratodermia with ataxia
Erythromelalgia primary
Erythroplakia
Erythropoietic protoporphyria
Escher Hirt syndrome
Escobar syndrome type B
Esophageal atresia
Esophageal atresia associated anomalies
Esophageal atresia coloboma talipes
Esophageal cancer
Esophageal cancer childhood
Esophageal duodenal atresia abnormalities of hands
Esophageal varices
Esotropia
Essential thrombocythemia
Esthesioneuroblastoma
Ethylmalonic encephalopathy
Eunuchoidism familial hypogonadotropic
Evans syndrome
Ewing's family of tumors
Ewing's sarcoma
Exencephaly
Exercise induced anaphylaxis
Exercise-induced hyperinsulinemic hypoglycemia
Exertional headache
Exfoliative dermatitis
Exogenous lipoid pneumonia
Exogenous ochronosis
Exostoses anetodermia brachydactyly type E
Exostoses multiple type 1
Exostoses multiple type 2
Exostoses multiple type 3
Exstrophy of the bladder
Exstrophy of the bladder-epispadias
Exsudative retinopathy familial autosomal dominant
Exsudative retinopathy familial autosomal recessive
Exsudative retinopathy familial X-linked recessive
Exsudative retinopathy familial
Extracranial germ cell tumor childhood
Extragonadal germ cell tumor
Extrasystoles short stature hyperpigmentation microcephaly
Eyebrows duplication of with stretchable skin and syndactyly