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INFO SAMAG
ATAXIA INFORMATION
MEET SOME FAMILIES
DISCUSSION BOARD
SAMAG REGISTRATION
RESOURCES
SAMAG Online Membership Registry
Membership open to anyone who wish to be a SAMAG Member/Volunteer.
Note
:
If patients are unable to register online on their own, their family members/guardians/
relatives or friends can register them with their consent.
Name:
Age:
Sex:
MALE
FEMALE
Qualification:
Occupation:
E-mail address:
Phone no:
(OR) Moblie no:
Address for
Communication:
Country:
Zip Code:
State:
Do you have any Ataxia:
Yes
No
If Yes, select the type
Select type of Ataxia
Charcot-Marie-Tooth Disorder (CMT)
episodic ataxia
Gluten Ataxia
Hereditary Spastic Paraplegia (HSP)
Marie's Ataxia
Olivopontocerebellar Atrophy (OPCA)
Paraneoplastic Cerebellar Degeneration (PCD)
Post-Infectious Ataxia
Friedreich’s ataxia
Spinocerebellar Ataxias (SCA's) (type 1
Spinocerebellar Ataxias (SCA's) (type 2
Spinocerebellar Ataxias (SCA's) (type 3
Spinocerebellar Ataxias (SCA's) (type 4
Spinocerebellar Ataxias (SCA's) (type 5
Spinocerebellar Ataxias (SCA's) (type 6
Spinocerebellar Ataxias (SCA's) (type 7
Spinocerebellar Ataxias (SCA's) (type 8
Spinocerebellar Ataxias (SCA's) (type 9
Spinocerebellar Ataxias (SCA's) (type 10
Spinocerebellar Ataxias (SCA's) (type 11
Spinocerebellar Ataxias (SCA's) (type 12
Spinocerebellar Ataxias (SCA's) (type 13
Spinocerebellar Ataxias (SCA's) (type 14
Spinocerebellar Ataxias (SCA's) (type 15
Spinocerebellar Ataxias (SCA's) (type 15
Spinocerebellar Ataxias (SCA's) (type 16
Spinocerebellar Ataxias (SCA's) (type 17
Spinocerebellar Ataxias (SCA's) (type 18
Spinocerebellar Ataxias (SCA's) (type 19
Mitochondrial ataxia
Vestibular ataxia
Ataxia Telangiectasia (A-T)
Muscular dystrophies
Other ataxias
Do you have any
Muscular Disorder:
Yes
No
Select type of Neuro Muscular Disease
If Yes, select the type
Congenital Muscular Dystrophy
Distal Muscular Dystrophy
Duchenne Muscular Dystrophy
Emery-Dreifuss Muscular Dystrophy
Facioscapulohumeral Muscular Dystrophy
Limb-Girdle Muscular Dystrophy
Myotonic Muscular Dystrophy
Congenital Myotonic Muscular Dystrophy
Oculopharyngeal Muscular Dystrophy
Amyotrophic Lateral Sclerosis
Spinal Bulbar Muscular Atrophy
Spinal Muscular Atrophy Type 1
Spinal Muscular Atrophy Type 2
Spinal Muscular Atrophy Type 3
Congenital Myasthenic Syndrome
Lambert-Eaton Syndrome
Myasthenia Gravis
Hyperthyroid Myopathy
Hypothyroid Myopathy
Dermatomyositis
Non-MDA Diseases
General
Periodic Paralysis
Myotubular Myopathz
Nemaline Myopathy
Central Core Disease
Paramyotonia Congenita
Myotonia Congenita
Mitochondrial Myopathy - MERRF
Metabolic Diseases
Carnitine Deficiency
Carnitine Palmityl Transferase Deficiency
Inclusion-Body Myositis
Polymyositis
Debrancher Enzyme Deficiency
Lactate Dehydrogenase Deficiency
Myoadenylate Deaminase Deficiency
Phosphorylase Deficiency
Phosphofructokinase Deficiency
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Mitochondrial Myopathy - MNGIE
Mitochondrial Myopathy - MILS
Mitochondrial Myopathy - NARP
Mitochondrial Myopathy - PEO
Mitochondrial Myopathy - CPEO
Pearson Syndrome
Mitochondrial Myopathies
Muscular Dystrophies
Motor Neuron Diseases
Inflammatory Myopathies
Neuromuscular Junction Diseases
Endocrine Myopathies
Peripheral Neuropathies
Other Myopathies
"If you would like to report more information in brief like Patient’s symptoms/ Onset of disease/ Present condition, etc., provide it in the box below.
Membership desired as:
Ataxia patient (or) Patient's associate
Volunteer
SAMAG Representative
What kind of support would you like to extend:
Social (Volunteer)
Medical Advice
Any Other
You can write to us with your past experience as a social worker in any field or what interested you to support SAMAG cause. (sam_ataxiaindia@yahoo.com)
.
Applicant’s signature: (typing your name is accepted as your signature)
I authorize SAMAG to Accept my details furnished in the registry form. Therefore all details furnished in the registry form is upto the best of my knowledge and consent, thereby understanding the terms of SAMAG.
ALL INFORMATION SUBMITTED WILL BE KEPT CONFIDENTIAL
CHECK FAQ ON SAMAG REGISTRATION
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