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Phone - 949-533-4977

Email - PersonalizedCause.Awareness@gmail.com

Sales & Orders - Sarah.PersonalizedCause@gmail.com

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 - I | Personalized Cause

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

RARE DISEASES AND DISORDERS - I


I cell disease
IBIDS syndrome
ICF syndrome
Ichthyosiform erythroderma corneal involvement deafness
Ichthyosiform erythroderma nonbullous congenital
Ichthyosis alopecia eclabion ectropion mental retardation
Ichthyosis and male hypogonadism
Ichthyosis bullosa of Siemens
Ichthyosis cheek eyebrow syndrome
Ichthyosis congenita biliary atresia
Ichthyosis deafness mental retardation skeletal anomaly
Ichthyosis follicularis atrichia photophobia syndrome
Ichthyosis hepatosplenomegaly cerebellar degeneration
Ichthyosis hystrix gravior
Ichthyosis hystrix Curth Macklin type
Ichthyosis lamellar 1
Ichthyosis lamellar 2
Ichthyosis lamellar 3
Ichthyosis lamellar autosomal dominant
Ichthyosis linearis circumflexa
Ichthyosis mental retardation dwarfism renal impairment
Ichthyosis prematurity syndrome
Ichthyosis tapered fingers midline groove up
Ichthyosis vulgaris
Ichthyosis with hypotrichosis autosomal recessive
Ichthyosis acquired
Ichthyosis erythrokeratolysis hemalis
Ichthyosis follicular
Ichthyosis leukocyte vacuoles alopecia and sclerosing cholangitis
Ichthyosis mental retardation dwarfism and renal impairment
Ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin
Idiopathic acute eosinophilic pneumonia
Idiopathic adolescent scoliosis
Idiopathic alveolar hypoventilation syndrome
Idiopathic basal ganglia calcification childhood-onset
Idiopathic diffuse interstitial fibrosis
Idiopathic dilatation of the pulmonary artery
Idiopathic dilated cardiomyopathy
Idiopathic double athetosis
Idiopathic eosinophilic chronic pneumopathy
Idiopathic hypersomnia
Idiopathic juxtafoveal retinal telangiectasia
Idiopathic myopathy
Idiopathic pulmonary fibrosis
Idiopathic pulmonary hemosiderosis
Idiopathic pulmonary hypertension
Idiopathic subglottic tracheal stenosis
Idiopathic thrombocytopenic purpura
Iida Kannari syndrome
IgM deficiency
Illum syndrome
Imaizumi Kuroki syndrome
Imerslund-Grasbeck syndrome
Iminoglycinuria
Immotile cilia syndrome due to defective radial spokes
Immune defect due to absence of thymus
Immune deficiency familial variable
Immune dysfunction with T-cell inactivation due to calcium entry defect 1
Immune dysfunction with T-cell inactivation due to calcium entry defect 2
Immune thrombocytopenia
Immunodeficiency with hyper IgM type 1
Immunodeficiency with hyper IgM type 2
Immunodeficiency with hyper IgM type 3
Immunodeficiency with hyper IgM type 4
Immunodeficiency with hyper IgM type 5
Immunodeficiency without anhidrotic ectodermal dysplasia
Immunodeficiency microcephaly with normal intelligence
Immunodysregulation polyendocrinopathy and enteropathy X-linked
Immunoglobulin A deficiency 2
Impairment of oral perception
Imperforate anus
Imperforate oropharynx costo vetebral anomalies
Impossible syndrome
Inappropriate Sinus Tachycardia
Inborn amino acid metabolism disorder
Inborn renal aminoaciduria
Inclusion body myopathy 2
Inclusion body myopathy 3
Inclusion body myositis
Inclusion conjunctivitis
Incontinentia pigmenti
Indolent B cell lymphoma
Indomethacin antenatal infection
Infant epilepsy with migrant focal crisis
Infantile apnea
Infantile axonal neuropathy
Infantile convulsions and paroxysmal choreoathetosis familial
Infantile digital fibromatosis
Infantile histiocytoid cardiomyopathy
Infantile multisystem inflammatory disease
Infantile myofibromatosis
Infantile onset spinocerebellar ataxia
Infantile Parkinsonism-dystonia
Infantile recurrent chronic multifocal osteomyolitis
Infantile scoliosis
Infantile sialic acid storage disorder
Infantile spasms broad thumbs
Infantile striato thalamic degeneration
Infantile-onset ascending hereditary spastic paralysis
Infectious arthritis
Infectious myocarditis
Infective endocarditis
Infective myositis
Inflammatory breast cancer
Inflammatory linear verrucous epidermal nevus
Inflammatory myofibroblastic tumor
Infundibulopelvic dysgenesis
Inherited hypoprothrombinemia
Inherited peripheral neuropathy
Iniencephaly
Insensitivity to pain congenital with anhidrosis
Insulin autoimmune syndrome
Insulin-like growth factor 1 resistance to
Insulin-like growth factor I deficiency
Insulin-resistance type B
Insulin-resistant acanthosis nigricans type A
Insulinoma
Intellectual deficit Buenos-Aires type
Intercellular cholesterol esterification disease
Interferon gamma receptor 1 deficiency
Internal carotid agenesis
Intervertebral disc disease
Intestinal atresia multiple
Intestinal neuronal displaysia
Intestinal pseudo-obstruction
Intestinal pseudoobstruction neuronal chronic idiopathic X-linked
Intracranial aneurysms multiple congenital anomaly
Intracranial arteriovenous malformation
Intracranial Hypertension
Intractable hiccups
Intrahepatic cholangiocarcinoma
Intraocular melanoma
Intrathoracic kidney vertebral fusion
Intrauterine growth retardation mandibular malar hypoplasia
Intrauterine growth retardation with increased mitomycin C sensitivity
Intrauterine infections
Intravascular papillary endothelial hyperplasia
Intravenous leiomyomatosis
Intrinsic factor congenital deficiency of
Iodine antenatal infection
IRAK4 deficiency
Iridocorneal endothelial syndrome
Iridogoniodysgenesis and skeletal anomalies
Iridogoniodysgenesis type1
Iridogoniodysgenesis dominant type
Iris coloboma with ptosis hypertelorism and mental retardation
Iris dysplasia hypertelorism deafness
Iris hypoplasia and glaucoma
Irons Bhan syndrome
Isaac's syndrome
Ischiadic hypoplasia renal dysfunction immunodeficiency
Ischiopatellar dysplasia
Isobutyryl-CoA dehydrogenase deficiency
Isolated growth hormone deficiency type 1A
Isolated growth hormone deficiency type 1B
Isolated growth hormone deficiency type 2
Isolated growth hormone deficiency type 3
Isosporiasis
Isotretinoin embryopathy like syndrome
Isovaleric acidemia
Isthmian coarctation
ITCH E3 ubiquitin ligase deficiency
Ivemark syndrome
IVIC syndrome