Qualifying Conditions for Medical Cannabis in Texas
Medical Marijuana is legal, low-THC medicine that is prescribed by board-certified, registered physicians (like myself)to treat the symptoms of the qualifying conditions in the Compassionate Use Program. In Texas, medical marijuana can contain up to 1% THC by weight. All medical marijuana products in Texas must undergo rigorous testing and analysis to ensure that products are consistent, purely extracted, correctly formulated and dosed, and are free of any toxins or heavy metals.
While there is no age minimum for medical marijuana in Texas, you must meet a few requirements to access it:
- Muscle cramping and stiffness
- Pain
- Mobility
- Insomnia
- Anxiety
- Depression
- Appetite loss and weight loss
- Cognitive impairment
- Memory loss
- Neuroinflammation
- Neurodegeneration
- Pain
- Insomnia
- Agitation and behavioral changes
- Difficulty with social interaction
- Difficulty with speech or communication
- Obsessive or repeated behaviors
- Depression
- Seizures
- Restlessness
- Aggression or disruptive behavior
- Insomnia
- Pain
- Anxiety
- Nausea and vomiting
- Decreased appe
- ADENYLOSUCCINATE SYNTHASE DEFICIENCY
- ALEXANDER DISEASEAMYLOIDOSES
- ARGYROPHILIC GRAIN DISEASE
- ASPARYLGLUCOSAMINURIA
- ATAXIA NEUROPATHY SPECTRUM
- BIDIRECTIONAL ENZYME DEFICIENCY
- BIOPTERIN DEFECTS
- CANAVAN DISEASE
- CENTRAL CORE
- CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY
- 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
- DEMENTIA WITH LEWY BODIES
- DEOXYGUANISINE KINASE DEFICIENCY
- DIHYDROPIRIMIDINASE DEFICIENCY
- DIHYDROPTERIDINE REDUCTASE
- DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY
- DUCHENNE MUSCULAR DYSTROPHY
- FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY
- FAMILIAL OR SPORADIC FATAL INSOMNIA
- FAMILIAL SPASTIC PARAPLEGIA
- FARBER DISEASE
- FATTY ACID OXIDATION
- FREIDREICH’S ATAXIA
- FRONTOTEMPORAL DEMENTIA AND PARKINSONISM
- LINKED TO CHROMOSOME 17 CAUSED BY MUTATIONS IN MAPT GENE
- FRONTOTEMPORAL LOBAR DEGENERATION
- GALACTOSEMIA
- GALACTOSIALIDOSIS
- GAUCHER TYPE 2 AND TYPE 3
- GLOBULAR GLIAL TAUOPATHY
- GLUTARIC ACIDEMIA TYPE 1
- GLYCINE ENCEPHALOPATHY
- ALSO KNOWN AS GM1 GANGLIOSIDOSIS AND SANDHOFF DISEASE
- GUANIDINOACETATE METHYTRANSFERASE DEFICIENCY
- GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE DEFICIENCY
- HUNTINGTON’S DISEASE
- KEARN SAYERS SYNDROME
- KRABBE
- KURU
- LEUKODYSTROPHY
- LEWY BODY DISORDERS
- LYSOSOMAL STORAGE DISEASES
- MANNOSIDOSIS
- 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
- Dyskinesia
- Bradykinesia
- Muscle spasms
- Rigidity
- Insomnia
- Anxiety
- Pain
Chronic Traumatic Encephalopathy (CTE) is a neurodegenerative disease that causes irreparable brain damage triggered by repeated head traumas. This rare degenerative disease is also one of the many conditions eligible for medical marijuana in Texas. As the disease progresses, patients may experience changes in their mood and behavior, memory loss, confusion, impaired judgment, depression, aggression, insomnia and eventually progressive dementia.
CTE Symptoms Medical Marijuana Can Relieve:- MUCOLIPIDOSES TYPE III, ALSO KNOWN AS MUCOPOLYSACCARIDOSIS
- MUCOPOLYSACCHARIDOSIS TYPE I
- 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
- NEIMANN PICK TYPE A AND B
- NEIMANN PICK TYPE C
- NEONATAL ADRENOLEUKODYSTROPHY
- NEURODEGENERATION WITH BRAIN IRON ACCUMULATION
- NEUROFIBRILLARY TANGLE DEMENTIA,
- ALSO KNOWN BATTEN DISEASE
- NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA
- NEUROTRANSMITTER DEFECTS
- LIGOSACCHARIDOSES
- PANTOTHENATE KINASE ASSOCIATED NEURODEGENERATION
- PARKINSON’S DISEASE
- PERIPHERAL NEUROPATHY TYPES 1 THROUGH 4
- PEROXISOMAL BIOSYNTHESIS DEFECTS
- PEROXISOMAL DISORDERS
- PICK DISEASE
- POLYMERASE G RELATED DISORDERS
- POLYOL DISORDERS
- PRIMARY LATERAL SCLEROSIS
- PRION DISEASES
- PROGRESSIVE CHOREAS
- DYSTONIAS DYT GENES 1 THROUGH 20
- PROGRESSIVE MUSCULAR ATROPHY
- PROGRESSIVE SUPRANUCLEAR PALSY
- PURINE AND PYRIMIDINE DEFECTS
- PYRUVATE CARBOXYLASE DEFICIENCY
- PYRUVATE DEHYDROGENASE DEFICIENCY
- REFSUM DISEASE
- RESPIRATORY CHAIN DISORDERS COMPLEX 1 THROUGH 4 DEFECTS: COQ BIOSYNTHESIS DEFECTS
- SALIDOSIS
- SCHINDLER
- SEGAWA DISEASE
- ALSO KNOWN AS DOPAMINE RESPONSIVE DYSTONIA
- SEPIAPTERIN REDUCTASE
- SIALIDOSIS
- SPHINGOLIPIDOSES
- SPINAL MUSCULAR ATROPHY
- SPINOCEREBELLAR ATAXIA
- SUBACUTE NECROTIZING ENCEPHALOPATHY,
- ALSO KNOWN AS LEIGH SYNDROME
- ENCEPHALOMYOPATHIC FORM WITH METHYLMALONIC ACIDURIA SYNUCLEINOPATHIES
- TAUOPATHIES
- THYMIDINE KINASE
- PROTEINOPATHIES
- TRIFUNCTIONAL PROTEIN DEFICIENCY
- NEUROTRANSMITTER DEFECTS VASCULAR DEMENTIA
- NEUROTRANSMITTER DEFECTS WILSON DISEASE
- NEUROTRANSMITTER DEFECTS ZELLWEGER SYNDROME
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