clinic

WeCare Neurology - Riverside, California

5 Stars (11 Reviews)

WeCare Neurology is a clinic in Riverside, CA offering Concierge Neurology, with 1 physician on staff.

1 Doctor | Website
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About WeCare Neurology

"Our approach to patient care is based on the notion that all aspects of people’s lives (physical, emotional, psychological, and social) should be taken into account and seen as a whole with respect to managing health. This means practicing conventional western medicine using a mind-body-spirit approach to diagnosing and treating neurological disease."

Address

6833 Indiana Avenue Ste 102, Riverside,
CA 92506

Modes of Payment

Card | Cash

Providers
Dhrupad Joshi - 6833 Indiana Avenue, Riverside, California, 92506
Dhrupad Joshi, DO
WeCare Neurology
Concierge Neurology
(11)
Fee $25 - $100
Max no. of Patients: 500
Accepting New Patients: NA
6833 Indiana Avenue, Ste 102, Riverside, CA 92506
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Reviews
Posted by FMDD User
January 22, 2025
Guided me in choosing the best treatment option.

Review For Dhrupad Joshi

Posted by FMDD User
January 15, 2025
Very professional care and consult.

Review For Dhrupad Joshi

Conditions Treated
  • Hiv
  • Encephalitis
  • Meningitis
  • Addiction (alcohol)
  • Angelman syndrome
  • Trigeminal neuralgia
  • Torticollis
  • Amyotrophic lateral sclerosis
  • Scoliosis
  • Tension headache
  • Sleep paralysis
  • Lewy body dementia
  • Paraplegia
  • Huntington's disease
  • Hydrocephalus
  • Absence seizure
  • Migraine
  • Neck pain
  • Sleep apnea
  • Multiple sclerosis
  • Alzheimer's disease
  • Seizures
  • Stroke
  • Atrial fibrillation
  • Heart attack
  • Vertigo
  • Tinnitus
  • Whiplash
  • Dementia
  • Concussion
  • Insomnia
  • Myasthenia gravis
  • Parkinson's disease
  • Epilepsy
  • Narcolepsy
  • Tardive dyskinesia
  • Cluster headache
  • Peripheral neuropathy
  • Cerebral palsy
  • Carpal tunnel syndrome
  • Brain aneurysm
  • Ptosis
  • Headache
  • Guillain-barre syndrome
  • Spinal stenosis
  • Radiculopathy
  • Glioblastoma
  • Neuropathy
  • Restless legs syndrome
  • Decerebrate posture
  • Essential tremor
  • Postural orthostatic tachycardia syndrome
  • Cervical dysplasia
  • Thoracic outlet syndrome
  • Cerebrovascular disease
  • Fainting
  • Orthostatic hypotension
  • Acoustic neuroma
  • Agnosia
  • Alcoholic neuropathy
  • Amaurosis fugax
  • Anosmia
  • Aphantasia
  • Apraxia
  • Arachnoid cysts
  • Arachnoiditis
  • Arteriovenous malformation
  • Autonomic dysreflexia
  • Bacterial meningitis
  • Blurry vision
  • Brown sequard syndrome
  • Cerebellar hypoplasia
  • Cerebrospinal fluid leak
  • Cervical myelopathy
  • Cervical radiculopathy
  • Cervical spondylosis
  • Charcot marie tooth disease
  • Chiari malformation type 1
  • Chorea
  • Chronic headache
  • Complex regional pain syndrome
  • Creutzfeldt jakob disease
  • Crps
  • Cubital tunnel syndrome
  • Dandy walker syndrome
  • Decorticate posture
  • Deep brain stimulation
  • Delirium
  • Delirium tremens
  • Diabetic neuropathy
  • Diplopia
  • Dravet syndrome
  • Drowsiness
  • Duchenne muscular dystrophy
  • Dysarthria
  • Dysgraphia
  • Epidural hematoma
  • Erb's palsy
  • Erythromelalgia
  • Eyestrain
  • Fatal familial insomnia
  • Foot drop
  • Fragile x syndrome
  • Friedreich ataxia
  • Frontotemporal dementia
  • Glioma
  • Hemiplegia
  • Hemorrhagic stroke
  • Holoprosencephaly
  • Horner syndrome
  • Hydranencephaly
  • Hyperhidrosis
  • Hypopituitarism
  • Inclusion body myositis
  • Labyrinthitis
  • Lennox gastaut syndrome
  • Lissencephaly
  • Medulloblastoma
  • Memory loss
  • Meningioma
  • Microcephaly
  • Moebius syndrome
  • Moyamoya disease
  • Multiple system atrophy
  • Muscle atrophy
  • Myelitis
  • Myelomeningocele
  • Myotonic dystrophy
  • Myotonic dystrophy type 2
  • Neuralgia
  • Neurofibromatosis
  • Neurofibromatosis type 1
  • Neurogenic bladder
  • Neurosyphilis
  • New daily persistent headache
  • Normal pressure hydrocephalus
  • Notalgia paresthetica
  • Obsessive compulsive disorder
  • Optic neuritis
  • Papilledema
  • Periodic limb movement disorder
  • Pituitary tumor
  • Poliomyelitis
  • Polymyositis
  • Pompe disease
  • Progressive supranuclear palsy
  • Prolactinoma
  • Pseudobulbar affect
  • Rett syndrome
  • Schwannoma
  • Sleep disorders
  • Spasticity
  • Spinal cord injury
  • Spinal muscular atrophy
  • Status epilepticus
  • Sturge weber syndrome
  • Subarachnoid hemorrhage
  • Syringomyelia
  • Tarsal tunnel syndrome
  • Tethered cord syndrome
  • Transient global amnesia
  • Transient ischemic attack
  • Transverse myelitis
  • Traumatic brain injury
  • Tuberous sclerosis
  • Wernicke korsakoff syndrome
  • Acute flaccid myelitis
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Alexander disease
  • Alien hand syndrome
  • Hypotonia
  • Myositis
  • Diabetic peripheral neuropathy
  • Empty sella syndrome
  • Cysticercosis
  • Encephalitis lethargica
  • Familial dysautonomia
  • Emery dreifuss muscular dystrophy
  • Facioscapulohumeral muscular dystrophy
  • Familial hemiplegic migraine
  • Fetal hydantoin syndrome
  • Foxg1 syndrome
  • Fumarase deficiency
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Hereditary spastic paraparesis
  • Hyperkalemic periodic paralysis
  • Hypokalemic periodic paralysis
  • Hypothalamic hamartomas
  • Joubert syndrome
  • Lafora disease
  • Leigh syndrome
  • Limb girdle muscular dystrophy
  • Melas syndrome
  • Metachromatic leukodystrophy
  • Myotonia congenita
  • Nemaline myopathy
  • Neurofibromatosis type 2
  • Neuronal ceroid lipofuscinoses
  • Niemann pick disease
  • Oculopharyngeal muscular dystrophy
  • Ependymoma
  • Excessive daytime sleepiness
  • Facial paralysis
  • Focal dystonia
  • Ganglioglioma
  • Generalized tonic clonic seizure
  • Gerstmann syndrome
  • Gliosarcoma
  • Glossodynia
  • Glossopharyngeal neuralgia
  • Hemimegalencephaly
  • Herpes simplex encephalitis
  • Herpes zoster oticus
  • Increased intracranial pressure
  • Infant botulism
  • Isaacs syndrome
  • Japanese encephalitis
  • Juvenile myoclonic epilepsy
  • Kleine levin syndrome
  • Kluver bucy syndrome
  • Lambert eaton syndrome
  • Landau kleffner syndrome
  • Mal de debarquement syndrome
  • Meige syndrome
  • Miller fisher syndrome
  • Mononeuritis multiplex
  • Melkersson rosenthal syndrome
  • Alstrom syndrome
  • Anton syndrome
  • Ataxia telangiectasia
  • Athetosis
  • Auditory neuropathy spectrum disorder
  • Becker muscular dystrophy
  • Benign essential blepharospasm
  • Benign rolandic epilepsy
  • Bilateral perisylvian polymicrogyria
  • Brachial plexopathy
  • Brain abscess
  • Brain herniation
  • Bulging fontanelles
  • Canavan disease
  • Carotid stenosis
  • Cavernous sinus thrombosis
  • Central pain syndrome
  • Cerebellar degeneration
  • Cerebral amyloid angiopathy
  • Cerebral cavernous malformation
  • Cerebral hypoxia
  • Chiari malformation type 2
  • Childhood disintegrative disorder
  • Choroid plexus cyst
  • Choroid plexus papilloma
  • Chronic subdural hematoma
  • Coffin lowry syndrome
  • Coloboma of optic nerve
  • Congenital myasthenic syndrome
  • Cortical dysplasia
  • Corticobasal degeneration
  • Cramp fasciculation syndrome
  • Multifocal motor neuropathy
  • Myoclonic epilepsy
  • Myoclonus dystonia
  • Nerve compression
  • Nerve injury
  • Neurogenic bowel
  • Neuromyelitis optica
  • Neurosarcoidosis
  • Neurotrophic keratitis
  • Opisthotonos
  • Optic glioma
  • Osmotic demyelination syndrome
  • Palatal myoclonus
  • Hypothalamic tumor
  • Periventricular leukomalacia
  • Photosensitive epilepsy
  • Pneumococcal meningitis
  • Poems syndrome
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Post polio syndrome
  • Primary lateral sclerosis
  • Primary progressive aphasia
  • Progressive multifocal leukoencephalopathy
  • Pudendal neuralgia
  • Rasmussen encephalitis
  • Schwannomatosis
  • Septo optic dysplasia
  • Spasmodic dysphonia
  • Spasmus nutans
  • Spastic paraparesis
  • Spinal muscular atrophy type 1
  • Spinal shock
  • Spinal tumor
  • Subacute combined degeneration
  • Adult polyglucosan body disease
  • Subacute sclerosing panencephalitis
  • Subependymoma
  • Susac syndrome
  • Tabes dorsalis
  • Tick paralysis
  • Tolosa hunt syndrome
  • Transient cerebral ischemia
  • Tuberculous meningitis
  • Vertebral artery dissection
  • Vocal cord paralysis
  • Wallerian degeneration
  • West syndrome
  • Acute cerebellar ataxia
  • Adie syndrome
  • Aids dementia complex
  • Angiostrongyliasis
  • Bilirubin encephalopathy
  • Brain and nerves
  • Cerebral arteriovenous malformation
  • Common peroneal nerve dysfunction
  • Congenital mirror movement disorder
  • Diencephalic syndrome
  • Diffuse midline glioma h3 k27m mutant
  • Door syndrome
  • Dopa responsive dystonia
  • Meige disease
  • Drug induced dyskinesia
  • Early infantile epileptic encephalopathy
  • Femoral nerve dysfunction
  • Fourth cranial nerve palsy
  • Gliomatosis cerebri
  • Hepatocerebral degeneration
  • Neurocutaneous melanosis
  • Multiple mononeuropathy
  • Pelizaeus merzbacher disease
  • Refsum disease
  • Sandhoff disease
  • Schizencephaly
  • Spinocerebellar ataxia
  • Tuberous sclerosis complex
  • Walker warburg syndrome
  • Acrocallosal syndrome
  • Adenylosuccinate lyase deficiency
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Andermann syndrome
  • Andersen tawil syndrome
  • Autosomal dominant nocturnal frontal lobe epilepsy
  • Cdkl5 deficiency disorder
  • Central core disease
  • Centronuclear myopathy
  • Cerebellar agenesis
  • Cerebrotendinous xanthomatosis
  • Chorea acanthocytosis
  • Cln2 disease
  • Coach syndrome
  • Cytochrome c oxidase deficiency
  • Dentatorubral pallidoluysian atrophy
  • Dihydrolipoamide dehydrogenase deficiency
  • Dysferlinopathy
  • Dystrophinopathy
  • Familial periodic paralysis
  • Gerstmann straussler scheinker syndrome
  • Giant axonal neuropathy
  • Glycine encephalopathy
  • Gomez lopez hernandez syndrome
  • Hallervorden spatz disease
  • Hereditary ataxia
  • Hereditary neuralgic amyotrophy
  • Hyperprolinemia
  • L1 syndrome
  • Limb girdle muscular dystrophy type 2a
  • Marden walker syndrome
  • Mitochondrial complex 1 deficiency
  • Miyoshi myopathy
  • Multiple sulfatase deficiency
  • Myofibrillar myopathy
  • Pantothenate kinase associated neurodegeneration
  • Paramyotonia congenita
  • Peho syndrome
  • Perrault syndrome
  • Progressive external ophthalmoplegia
  • Intracranial injury
  • Intraventricular hemorrhage of the newborn
  • Jumping frenchmen of maine
  • Marchiafava bignami disease
  • Marcus gunn phenomenon
  • Meningoencephalocele
  • Migraine and headache
  • Migraine with brainstem aura
  • Monomelic amyotrophy
  • Neural crest tumor
  • Neuroretinitis
  • Olivopontocerebellar atrophy
  • Opsoclonus myoclonus syndrome
  • Paraneoplastic cerebellar degeneration
  • Peripheral nerve disorders
  • Periventricular heterotopia
  • Petrositis
  • Pineocytoma
  • Post traumatic epilepsy
  • Posterior fossa tumor
  • Primary amebic meningoencephalitis
  • Primary lymphoma of the brain
  • Relapsing multiple sclerosis
  • Thyrotoxic periodic paralysis
  • Pseudotumor cerebri syndrome
  • Radial nerve dysfunction
  • Satoyoshi syndrome
  • Sensorimotor polyneuropathy
  • Spinal cord abscess
  • Secondary parkinsonism
  • Spinal trauma
  • Sporadic hemiplegic migraine
  • Staphylococcal meningitis
  • Stormorken syndrome
  • Subdural effusion
  • Supranuclear ophthalmoplegia
  • Syringobulbia
  • Tubular aggregate myopathy
  • Tumefactive multiple sclerosis
  • Western equine encephalitis
  • Wyburn mason syndrome
  • Accessory deep peroneal nerve
  • Axillary nerve dysfunction
  • Cerebellar multiple system atrophy
  • Collagen vi related myopathy
  • Congenital fiber type disproportion
  • Congenital muscular dystrophy type 1a
  • Contracture deformity
  • Cytoplasmic body myopathy
  • Distal median nerve dysfunction
  • Epilepsy with myoclonic atonic seizures
  • Horizontal gaze palsy with progressive scoliosis
  • Htlv 1 associated myelopathy
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Infantile onset spinocerebellar ataxia
  • Internal carotid agenesis
  • Irregular sleep wake syndrome
  • Mcleod neuroacanthocytosis syndrome
  • Mitochondrial neurogastrointestinal encephalopathy disease
  • Myelin oligodendrocyte glycoprotein antibody associated disease
  • Nerve laceration
  • Neuroepithelioma
  • Neurotoxicity syndromes
  • Oculocerebrocutaneous syndrome
  • Oppenheim dystonia
  • Optic atrophy type 1
  • Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
  • Radiation induced meningioma
  • Retinal vasculopathy with cerebral leukodystrophy
  • Rigid spine syndrome
  • Shapiro syndrome
  • Dizziness and falls
  • Progressive myoclonic epilepsy
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Pyruvate dehydrogenase deficiency
  • Renpenning syndrome
  • Schindler disease
  • Sialidosis
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal and bulbar muscular atrophy
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spinocerebellar ataxia type 1
  • Spinocerebellar ataxia type 2
  • Spinocerebellar ataxia type 6
  • Spinocerebellar ataxia type 7
  • Subcortical band heterotopia
  • Succinic semialdehyde dehydrogenase deficiency
  • Sulfite oxidase deficiency
  • Troyer syndrome
  • Wieacker wolff syndrome
  • Wildervanck syndrome
  • X linked myotubular myopathy
  • Adenosine monophosphate deaminase deficiency
  • Alg1 cdg
  • Alg3 cdg
  • Alg6 cdg
  • Amyotonia congenita
  • Ataxia pancytopenia syndrome
  • Autosomal dominant partial epilepsy with auditory features
  • Autosomal recessive primary microcephaly
  • Benign familial neonatal seizures
  • Beta propeller protein associated neurodegeneration
  • Boucher neuhauser syndrome
  • Cach syndrome
  • Capos syndrome
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial transthyretin amyloidosis
  • Fragile xe syndrome
  • Genetic epilepsy with febrile seizures plus
  • Glucose transporter deficiency
  • Glutamate decarboxylase deficiency
  • Guanidinoacetate methyltransferase deficiency
  • Harding ataxia
  • Hereditary cerebral amyloid angiopathy
  • Hereditary hyperekplexia
  • Hereditary sensory and autonomic neuropathy type 2
  • Hereditary sensory neuropathy type 1
  • Inclusion body myopathy 2
  • Infantile axonal neuropathy
  • Infantile refsum disease
  • Lateral meningocele syndrome
  • Limb girdle muscular dystrophy type 1a
  • Limb girdle muscular dystrophy type 1b
  • Limb girdle muscular dystrophy type 2c
  • Limb girdle muscular dystrophy type 2i
  • Maternally inherited leigh syndrome
  • Megalencephalic leukoencephalopathy with subcortical cysts
  • Mitochondrial complex 2 deficiency
  • Mitochondrial complex 3 deficiency
  • Mitochondrial complex v deficiency
  • Mitochondrial trifunctional protein deficiency
  • Neuronal intranuclear inclusion disease
  • Pena shokeir syndrome type 2
  • Phosphoglycerate mutase deficiency
  • Potassium aggravated myotonia
  • Primary familial brain calcification
  • Pyruvate decarboxylase deficiency
  • Riboflavin transporter deficiency neuronopathy
  • Sengers syndrome
  • Sialic acid storage disease
  • Sialuria
  • Subacute cerebellar degeneration
  • Subependymal nodular heterotopia
  • Supranuclear ocular palsy
  • Syphilitic aseptic meningitis
  • Ulnar nerve dysfunction
  • Spastic paraplegia type 11
  • Spastic paraplegia type 2
  • Spastic paraplegia type 4
  • Spastic paraplegia type 7
  • Spinocerebellar ataxia type 10
  • Spinocerebellar ataxia type 11
  • Spinocerebellar ataxia type 12
  • Spinocerebellar ataxia type 13
  • Spinocerebellar ataxia type 14
  • Spinocerebellar ataxia type 15
  • Spinocerebellar ataxia type 17
  • Spinocerebellar ataxia type 27
  • Spinocerebellar ataxia type 28
  • Spinocerebellar ataxia type 29
  • Spinocerebellar ataxia type 4
  • Spinocerebellar ataxia type 5
  • Spinocerebellar ataxia type 8
  • Tomaculous neuropathy
  • Unverricht lundborg syndrome
  • Woodhouse sakati syndrome
  • X linked creatine deficiency
  • X linked dystonia parkinsonism
  • X linked infantile spinal muscular atrophy
  • Neurohypophyseal diabetes insipidus
  • Pinched nerves
  • Stiff person syndrome
  • Tarlov cysts
  • Vascular dementia
  • Viral meningitis
  • Wilson disease
  • Cockayne syndrome
  • Frey's syndrome
  • Primary orthostatic tremor
  • Granulomatous hypophysitis
  • Leukodystrophy
  • Behr syndrome
  • Gaba transaminase deficiency
  • Partial seizure
  • Laryngeal nerve damage
  • Lhermitte duclos disease
  • Congenital insensitivity to pain with anhidrosis
  • Progressive hemifacial atrophy
  • Alternating hemiplegia of childhood
  • Anti nmda receptor encephalitis
  • Carpenter syndrome
  • Chronic inflammatory demyelinating polyneuropathy
  • Marinesco sjogren syndrome
  • Corpus callosum agenesis
  • Spinocerebellar ataxia type 3
  • Aromatic l amino acid decarboxylase deficiency
  • Familial porencephaly
  • L 2 hydroxyglutaric aciduria
  • Limb girdle muscular dystrophy type 2b
  • Spastic ataxia charlevoix saguenay type
  • Vldlr associated cerebellar hypoplasia
  • Bell's palsy
  • Head injury
  • Tourette syndrome
  • Brain injury
  • Autonomic neuropathy
  • Ischemic stroke
more..
Treatments & Procedures
  • Eeg
  • Neuromodulation
  • Emg
  • Lumbar puncture
  • Electromyogram
  • Electroencephalogram
  • Diagnostic medial branch block
  • Peripheral nerve stimulation
  • Brain aneurysm repair
  • Tms transcranial magnetic stimulation
  • Concussion management
  • Occupational therapy evaluation
  • Neuroma

Frequently Asked Questions

Where is WeCare Neurology located?

WeCare Neurology is located in 6833 Indiana Avenue Ste 102, Riverside, CA 92506.

What are the various modes of payment does WeCare Neurology Accept?

WeCare Neurology accepts Card | Cash.

What are the doctors who practice in WeCare Neurology specialize in?

Currently there are around 1 providers practice in WeCare Neurology who specialise in Concierge Neurology, etc

How can I make appointments with doctors in WeCare Neurology?

You can take appointments for doctors who practice in WeCare Neurology online on their website or by calling them.

Location