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Accessia Health Patient Programs

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Accessia Health Patient Programs

Our patient programs are all board-approved and eligible individuals may utilize their assistance to pay for one or more of the following: medication and provider copays, coinsurance, health insurance premiums, approved medical expenses, and travel. * denotes programs that are active

Chronic Conditions

Ongoing conditions requiring sustained management

Alzheimer's Disease

Amyotrophic Lateral Sclerosis

Asthma*

Cardiomyopathy

Chronic Kidney Disease

Chronic Obstructive Pulmonary Disease

Circadian Rhythm Disorders*

Cystinosis

Diabetes

Epilepsy

Heart Disease

Heart Failure*

Hepatitis C

HIV Prevention and Support

Huntington's Disease

Inflammatory Bowel Disease

Interstitial Lung Disease

Kidney Stones*

Lipodystrophy

Lupus

Multiple Sclerosis*

Myasthenia Gravis*

Obesity

Parkinson's Disease

Progressive Familial Intrahepatic Cholestasis

Pulmonary Fibrosis*

Pulmonary Hypertension

Rheumatoid Arthritis

Sarcoidosis

Schizophrenia and Schizoaffective Disorders

Sickle Cell Disease

Stroke

Urea Cycle Disorder

Rare Diseases

Rare and genetic conditions, including lysosomal storage and immune disorders

Acromegaly

Activated PI3K Delta Syndrome

Alpha Mannosidosis

Alpha-1*

Atypical Hemolytic Uremic

Syndrome

Batten Disease

Chronic Inflammatory

Demyelinating Polyneuropathy*

Common Variable Immune Deficiency

Cystic Fibrosis

Duchenne Muscular Dystrophy

Eosinophilic Esophagitis

Eosinophilic Granulomatosis with Polyangiitis

Epidermolysis Bullosa

Fabry Disease*

Facioscapulohumeral Muscular Dystrophy

Fibrodysplasia Ossificans Progressiva

Gangliosidosis

Gaucher Disease*

Graft-Versus-Host Disease

Guillain-Barré Syndrome

Hereditary Angioedema*

Hypoparathyroidism*

Immune Thrombocytopenic Purpura

Inherited and Acquired Factor Deficiencies*

Inherited Retinal Diseases

Krabbe Disease

Lambert-Eaton Myasthenic Syndrome

Limb-Girdle Muscular Dystrophy

Lysosomal Acid Lipase Deficiency

Metachromatic Leukodystrophy

MPS I (Hurler Syndrome/Scheie Syndrome)*

MPS II (Hunter Syndrome)

MPS III (Sanfilippo Syndrome)

MPS IV (Morquio Syndrome)

MPS VI (Maroteaux-Lamy Syndrome)

MPS VII (Sly Syndrome)

Multifocal Motor Neuropathy

Myotonic Dystrophy

Neuromyelitis Optica Disorder

Niemann-Pick Disease

Oculopharyngeal Muscular Dystrophy

Paroxysmal Nocturnal Hemoglobinuria

Phenylketonuria

Plasminogen Deficiency*

Pompe Disease*

Primary Immune Deficiency*

Severe Combined Immunodeficiency

Spinal Muscular Atrophy

Thrombotic Thrombocytopenic Purpura*

Thyroid Eye Disease

Wiskott-Aldrich Syndrome

X-linked Agammaglobulinemia

Oncology

Cancers and related blood disorders

Acute Lymphoblastic Leukemia

B-Cell Lymphoma

Basal and Squamous Cell Skin Cancers

Beta Thalassemia

Bone Sarcomas

Breast Cancer

Burkitt Lymphoma

Cervical Cancer

Chronic Lymphocytic Leukemia

Chronic Myeloid Leukemia*

Colorectal Cancer

Diffuse Large B-Cell Lymphoma

Follicular Lymphoma

Gastrointestinal Cancers

Gastrointestinal Stromal Tumor*

Hairy Cell Leukemia

Mantle Cell Lymphoma

Marginal Zone Lymphoma

Multiple Myeloma

Myelodysplastic Syndromes

Non-Small Cell Lung Cancer*

Ovarian Cancer

Pancreatic Cancer

Prostate Cancer

Soft Tissue Sarcomas

Tenosynovial Giant Cell Tumor

Waldenstrom Macroglobulinemia

Support Programs

Assistance that spans every diagnosis

Clinical Trial Travel Assistance

Diagnostic Testing Funds

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