Become a Patient

Get a Prescription

Ready to find relief with medical marijuana? In Texas, you must have a prescription from a physician that is registered in the Compassionate Use Program. Texas Original makes this process easy! 

  1. To get started, fill out the form. Texas Original will send you a text and email confirming your submission.
  2. You will be contacted same-day by a partnering cannabis clinic (please note: you may be contacted the following business day if the form is submitted after business hours).
  3. The cannabis clinic will provide further instruction on setting your appointment.
  4. After your appointment, call, chat or sign up on our Patient Portal to begin your journey to relief with medical cannabis, grown for Texans by Texans.

Call or text us: (512) 614-0343



Open the conversation with your current doctor or let us help you find one.

1. Get a Prescription

In Texas, you must have a prescription from a physician that is registered in the Compassionate Use Program. Texas Original makes the process of getting a prescription easy! To get started, click the link below and fill out the form. Texas Original will send you a text and email confirming your submission. You will be scheduled for a virtual appointment with a cannabis clinic that can prescribe you. 

GET A PRESCRIPTION >

Medical marijuana dispensaries must be notified the prescription has been entered in electronically

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 request a refill through our online Patient Portal to process your prescription fulfillment.

FILL A PRESCRIPTION >

Welcome to the family. Relief is coming your way from right here in Texas

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 eight locations throughout the great state of Texas, we could not be happier to have you and your family be a part of ours. Plus, take advantage of our first-time patient discount and get 20% off your first order and buy one, get one 50% off your second order.

FREQUENTLY ASKED QUESTIONS >

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

Cancer

Cerebral Palsy

Epilepsy

And other seizure disorders

Huntington’s Disease

MS

(Multiple Sclerosis)

Parkinson's Disease

Peripheral Neuropathies

PTSD

Spasticity

SEE MORE CONDITIONS

 

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

A

  • Adenylosuccinate synthase Deficiency
  • Alpers-Huttenlocher syndrome
  • ALS (Amyotrophic Lateral Sclerosis)
  • Alzheimer's Disease and other dementias
  • Argyrophilic Grain Disease
  • Aromatic L-amino acid decarboxylase deficiency
  • Ataxia neuropathy spectrum
  • Autism and other spectrum disorders

B

  • Bidirectional enzyme deficiency

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
  • Creatine Transporter Defect, also known as SLC 6A8
  • CTE (Chronic Traumatic Encephalopathy)

D

  • Deoxyguanisine kinase deficiency
  • Dihydropirimidinase Deficiency
  • Dihydropteridine reductase
  • Dihydropyrimidine dehydrogenase Deficiency
  • Duchenne Muscular Dystrophy

E

F

  • Facioscapulohumeral Muscular Dystrophy
  • Familial or Sporadic Fatal Insomnia
  • Familial Spastic Paraplegia
  • Frontotemporal dementia and parkinsonism linked to chromosome 17 caused by mutations in MAPT gene
  • Frontotemporal Lobar Degeneration

G

  • Gerstmann-Straussler-Scheinker Disease
  • Glycine encephalopathy, also known as non-ketotic hyperglycinemia
  • Glycogen Storage-Lysosomal: Pompe Disease
  • 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

L

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

M

  • Manosidosis alpha and beta
  • Metachromatic leukodystrophy
  • Methylenetetrahydrofolate reductase deficiency severe variant
  • Mitochondrial Depletion syndromes types 1 through 14
  • Mitochondrial Encephalopathy Lactic Acidosis Stroke
  • Mitochondrial Encephalopathy Ragged Red Fiber
  • Mitochondrial neurogastrointestinal encephalopathy
  • Monoamine oxidase deficiency
  • Mucolipidoses Type II, also known as Inclusion Cell disease
  • Mucolipidoses Type III, also known as pseudo-Hurler polydystrophy
  • 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
  • Myoclonic epilepsy myopathy sensory ataxia

N

  • 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

O

P

  • Pantothenate Kinase Associated Neurodegeneration
  • Pelizaeus-Merzbacher disease
  • Peripheral neuropathy types 1 through 4
  • Peroxisomal biosynthesis defects
  • Polymerase G Related Disorders
  • 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
  • Spinal-bulbar muscular atrophy
  • Subacute necrotizing encephalopathy, also known as Leigh syndrome
  • SUCLG1-related mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria

T

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

V

W

X

  • X-linked adrenoleukodystrophy

Z

SUCCESS STORIES

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