Cognitive Impairment Websites
Celebrate Aging! | ELDR.com
ELDR seeks to inspire people over 60 to celebrate the joys and navigate the challenges of aging. ELDR provides resources on retirement, aging, drugs, travel, being an elder, insurance, financial services, special products, real estate, games, housing and services for seniors.
8,785,656
$
8.95
Chemo brain? Lose the fog/regain your focus! Get the book!
Your Brain After Chemo is the definitive book on the cognitive effects of cancer treatment: problems with memory, concentration, word retrieval + multitasking
24,339,174
$
8.95
The NeuroCognitive Institute NJ | Alzheimer's, ADHD, Autism, Dementia
The NeuroCognitive Institute (NCI) | Integrating Science with Practice
2,519,232
$
480.00
Alzheimer Research Finding a cure for Alzheimer disease
Alzheimer Research Finding a cure for Alzheimer disease
Not Applicable
$
8.95
STXBP1 Disorders | Encephalopathy, STXBP1 Mutations, Rare Epilepsy
STXBP1 encephalopathy is a rare form of genetic epilepsy. Increasing awareness through family advocacy, support, funding research. Patient registry, genetic
Not Applicable
$
8.95
STXBP1 Disorders | Encephalopathy, STXBP1 Mutations, Rare Epilepsy
STXBP1 encephalopathy is a rare form of genetic epilepsy. Increasing awareness through family advocacy, support, funding research. Patient registry, genetic
Not Applicable
$
8.95
STXBP1 Disorders | Encephalopathy, STXBP1 Mutations, Rare Epilepsy
STXBP1 encephalopathy is a rare form of genetic epilepsy. Increasing awareness through family advocacy, support, funding research. Patient registry, genetic
Not Applicable
$
8.95
STXBP1 Disorders | Encephalopathy, STXBP1 Mutations, Rare Epilepsy
STXBP1 encephalopathy is a rare form of genetic epilepsy. Increasing awareness through family advocacy, support, funding research. Patient registry, genetic
Not Applicable
$
8.95
STXBP1 Disorders | Encephalopathy, STXBP1 Mutations, Rare Epilepsy
STXBP1 encephalopathy is a rare form of genetic epilepsy. Increasing awareness through family advocacy, support, funding research. Patient registry, genetic
Not Applicable
$
8.95
STXBP1 Disorders | Encephalopathy, STXBP1 Mutations, Rare Epilepsy
STXBP1 encephalopathy is a rare form of genetic epilepsy. Increasing awareness through family advocacy, support, funding research. Patient registry, genetic
Not Applicable
$
8.95
CVL Dallas » Center for Vital Longevity
CVL Dallas - Center for Vital Longevity
8,028
$
1,924,560.00
We2Link-We2Link is dedicated to helping people with Traumatic Brain In
We2Link is dedicated to helping people with Traumatic Brain Injury (TBI), Alzheimer's Disease, Dementia, and other cognitive impairments live healthier and happier lives. We support both the person with the cognitive impairment and the caregiver. We are also dedicated to enhancing support to medical providers and resea
Not Applicable
$
8.95
BoCA| Home
Boston Cognitive Assessment (BoCA) is a self-administered online test intended for longitudinal cognitive monitoring.
Not Applicable
$
8.95
