Become a Patient

WHAT CONDITIONS QUALIFY?

Browse for information on qualifying conditions, or search for your condition or symptom.

ALS

(Amyotrophic Lateral Sclerosis)

Alzheimer’s Disease

And other dementias

Autism

And other spectrum disorders

Cerebral Palsy

CTE

(Chronic Traumatic Encephalopathy)

Epilepsy

And other seizure disorders

Huntington’s Disease

MS

(Multiple Sclerosis)

Parkinson's Disease

Peripheral Neuropathies

Spasticity

Terminal Cancer

SEE MORE CONDITIONS
  • 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
  • 5-aminoimidazole-4-carboxamide ribonucleotide transformylase deficiency

A

  • Adenylosuccinate synthase Deficiency
  • Alexander disease
  • Alpers-Huttenlocher syndrome
  • Argyrophilic Grain Disease
  • Aromatic L-amino acid decarboxylase deficiency
  • Asparylglucosaminuria
  • Ataxia neuropathy spectrum

B

  • Bidirectional enzyme deficiency
  • Biopterin Defects

C

  • Cerebral Autosomal Dominant Arteriopathy with Sub-cortical Infarcts and Leukoencephalopathy
  • Charcot Marie Tooth and related hereditary neuropathies
  • Childhood Myocerebrohepatopathy spectrum
  • Congenital Disorders of Glycosylation
  • Corticobasal Degeneration
  • Creatine Disorders
  • Creatine Transporter Defect, also known as SLC 6A8
  • Creutzfeldt-Jakob Disease

D

  • Dementia with Lewy Bodies
  • Deoxyguanisine kinase deficiency
  • Dihydropirimidinase Deficiency
  • Dihydropteridine reductase
  • Dihydropyrimidine dehydrogenase Deficiency
  • Duchenne Muscular Dystrophy

F

  • Facioscapulohumeral Muscular Dystrophy
  • Familial or Sporadic Fatal Insomnia
  • Familial Spastic Paraplegia
  • Fatty Acid Oxidation
  • Freidreich’s Ataxia
  • Frontotemporal dementia and parkinsonism linked to chromosome 17 caused by mutations in MAPT gene
  • Frontotemporal Lobar Degeneration

G

  • Galactosialidosis
  • Gaucher Type 2 and Type 3
  • Gerstmann-Straussler-Scheinker Disease
  • Globular Glial Tauopathy
  • Glutaric acidemia type 1
  • Glycine encephalopathy, also known as non-ketotic hyperglycinemia
  • Glycogen Storage-Lysosomal: Pompe Disease
  • GM1 gangliosidosis
  • GM2 gangliosidosis also known as Tay-sachs and Sandhoff Disease
  • Guanidinoacetate methytransferase deficiency
  • Guanosine triphosphate cyclohydrolase deficiency

H

  • Homocysteine re-methylation defects
  • Hypoxanthine-guanine phosophoribosyltransferase Deficiency also known as Lesch-Nyhan disease

K

  • Kearn Sayers Syndrome

L

  • L-2-hydroxyglutaric aciduria
  • L-Arginine/glycine amidinotransferase deficiency
  • Lewy Body Disorders
  • Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency
  • Lysosomal Storage Diseases

M

  • Manosidosis alpha and beta
  • Maple Syrup Urine Disease
  • Metachromatic leukodystrophy
  • Metal Metabolism
  • Methylenetetrahydrofolate reductase deficiency severe variant
  • Mitochondrial Conditions
  • Mitochondrial Depletion syndromes types 1 through 14
  • Mitochondrial Encephalopathy Lactic Acidosis Stroke
  • Mitochondrial Encephalopathy Ragged Red Fiber
  • Mitochondrial neurogastrointestinal encephalopathy
  • Monoamine oxidase deficiency
  • Motor Neuron Disease
  • Mucolipidoses Type II, also known as Inclusion Cell disease
  • Mucolipidoses Type III, also known as pseudo-Hurler polydystrophy
  • Mucopolysaccaridosis
  • Mucopolysaccharidosis Type I, also known as Hurler Syndrome or Scheie Syndrome
  • Mucopolysaccharidosis Type II, also known as Hunter Syndrome
  • Mucopolysaccharidosis Type III, also known as Sanfilippo A and B
  • Mucopolysaccharidosis Type IV, also known as Maroteaux-Lamy
  • Mucopolysaccharidosis Type VII, also known as Sly
  • Multiple Sulfatase deficiency
  • Multiple System Atrophy
  • Muscular Dystrophies
  • Myoclonic epilepsy myopathy sensory ataxia

N

  • Neimann Pick Type A and B
  • Neimann Pick Type C
  • Neonatal Adrenoleukodystrophy
  • Neurodegeneration with brain iron accumulation
  • Neurofibrillary Tangle dementia, also known as Primary Age-related Tauopathy
  • Neuronal ceroid lipofuscinosis types 1-10 including Batten Disease
  • Neuropathy, Ataxia, and Retinitis Pigmentosa
  • Neurotransmitter defects

O

  • Oligosaccharidoses

P

  • Pantothenate Kinase Associated Neurodegeneration
  • Pelizaeus-Merzbacher disease
  • Peripheral neuropathy types 1 through 4
  • Peroxisomal biosynthesis defects
  • Peroxisomal Disorders
  • Polymerase G Related Disorders
  • Polyol disorders
  • Primary Lateral Sclerosis
  • Progressive Choreas
  • Progressive dystonias DYT genes 1 through 20
  • Progressive Muscular Atrophy
  • Progressive Supranuclear Palsy
  • Pterin-4-carbinolamine dehydratase
  • Purine and Pyrimidine Defects
  • Pyruvate Carboxylase Deficiency
  • Pyruvate Dehydrogenase Deficiency
  • Pyruvoyl-tetahydropterin synthase

R

  • Respiratory chain disorders complex 1 through 4 defects: Co Q biosynthesis defects
  • RRM2B-related mitochondrial disease

S

  • Segawa Diease, also known as Dopamine Responsive Dystonia
  • Sepiapterin reductase
  • Sphingolipidoses
  • Spinal Muscular Atrophy
  • Spinal-bulbar muscular atrophy
  • Spinocerebellar ataxia
  • Subacute necrotizing encephalopathy, also known as Leigh syndrome
  • SUCLG1-related mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
  • Synucleinopathies

T

  • Thymidine Kinase
  • Transactive response DNA-binding protein-43 (TDP-43) Proteinopathies
  • Trifunctional protein deficiency

V

  • Vascular dementia

W

X

  • X-linked adrenoleukodystrophy

Z

  • Zellweger syndrome

1. Talk to a doctor

Open the conversation with your current doctor or let us help you find one. Doctors must be registered to prescribe in the Compassionate Use Program. If you qualify and are ready to start on the road to relief, fill out our Find a Doctor form. Our team will reach out to you by phone and email so be sure to check your spam if you do not receive a message from us within 24 hours.

FIND A DOCTOR >

2. Fill Your Prescription

Unlike traditional pharmacies, medical marijuana dispensaries must be notified by the patient that their prescriber has put their prescription in electronically. You will not receive a handwritten prescription. Our dispensary team is always ready to fill your prescription. After your appointment, call, message or fill out the request to fill form to process your prescription fulfillment.

FILL A PRESCRIPTION >

3. Welcome to the family

You did it! Relief is coming your way from right here in Texas at our facility in Southwest Austin. Whether you scheduled a delivery or pick-up at one of our four locations throughout the great state of Texas, we could not be happier to have you and your family be a part of ours.

FREQUENTLY ASKED QUESTIONS >

Need help FINDing A PREscribing doctor?

Finding the right doctor to cover your needs can be frustrating. Let us take out the guesswork by connecting you with our network of physicians, registered to prescribe medical cannabis.

Whether you’re looking for a Neurologist in El Paso, a Family Doctor in Dallas or an Oncologist in Houston, our doctor network covers a wide range of specialists and locations across the great state of Texas.

CALL US: (512) 614-0343

TEXT US: (512) 817-3656

Dispenary Hours: Monday-Friday 9-5, Saturdays 9-3


 

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