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Sunday, May 25, 2014

Dementia in Hindi : "Is dementia something new?"

Article by Swapna Kishore in Hindi : "Is dementia something new?"

link: http://dementiahindi.wordpress.com/2014/05/24/is-dementia-new-%E0%A4%95%E0%A5%8D%E0%A4%AF%E0%A4%BE-%E0%A4%A1%E0%A4%BF%E0%A4%AE%E0%A5%87%E0%A4%82%E0%A4%B6%E0%A4%BF%E0%A4%AF%E0%A4%BE-%E0%A4%A8%E0%A4%AF%E0%A4%BE-%E0%A4%B0%E0%A5%8B%E0%A4%97/

Friday, May 23, 2014

KERALA PERSPECTIVE ON DEMENTIA

From Ardsi Kkm Kerala : KERALA PERSPECTIVE ON DEMENTIA

Joining hands with Kerala Govt., ARDSI is heading towards framing Kerala Perspective on Dementia. As a first step, we will be conducting a One-day Workshop with Dementia Experts in the second Week of June. Those dementia experts interested to be part of this initiative, please write to us rdc@ardsi.org

Wednesday, May 7, 2014

Dementia and caregiving in India : A national priority ?

From Swapna Writes Blog: ... " In a country like India, struggling with multiple basic problems in areas like health, education, law and order, infrastructure, etcetera, I have no basis to expect that dementia will be made a “national priority”.
Surely child mortality, primary health care, basic sanitation, farmer support, poverty eradication, reducing school drop outs, and many, many basic causes are already contending for, and deserve more national attention, funds, and priority." [ ...]
"We forget how much foundational work needs to be done in India before we can afford lofty dreams. We forget that, in India, we have yet to establish a foundational understanding of dementia, and our overall quality of life and social support and welfare schemes is not good. 

How can we justify aiming for a quality of life of dementia-affected families that is grander than what is normally found around us?" [...]
"Awareness is so poor that there is no way to tap the bulk of actual, hands-on caregivers. Besides, caregivers come in various stripes; the ones who most need help are not visible, not tapped, not participating in most dialogues. 
Patients who need the most help are the ones locked up in houses because of social stigma, or who remain undiagnosed or are labelled as crazy and shunned. 
So where are their voices, their concerns, their perspectives on what they need most and fastest? Where can we find persons diagnosed early enough to have insight into their dementia who may share their realities so that we can know what “friendliness” means to someone who actually has dementia? 
Don’t their opinions matter?"...