ACTIVITY OF TRUST -
Dhanvantari Charitable Trust was formed in 1999 with dedicated towards the welfare and twin objective of Care & Control of Sickle Cell Anaemia affected at Gujarat State.
Dr.Kavita Desai and Dr.Atul Desai have degree of Bachelor of Ayurveda and practicing at Vyara since 1989. During these years they came across many complicated patients of SCA. For better life of SCA affected tribal people Dhanvantari Charitable Trust design a programmed. There motivations are Painless life -Better life.
Six Step Program are implemented for SCA awareness and treatment
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Common Registry |
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Clinical Evaluation |
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Laboratory Evaluation |
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Management |
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Counseling |
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Mass Education |
The program started with training of the trainers where training workshops were conducted for laboratory investigative method and awareness campaign for the relatives of the patients and general population at the interiors part of Vyara ,Songhadh and Dang territory. People of this area have socio-economical backwardness and need to be aware about genetic disorders SCA. Sickle screening and other hematological information delivered by experts. Trust provides services to the door steps.
Organize screening camps at village places for the target population of marriageable youth and pregnant mothers, in schools, colleges and town places.
Trust having first clinic in India, who provide only sickle cell Anaemia related services at Balpur.Here they provide information about Ayurvedic living standards,which helps to be provide them a quality of life .T-AYU-HM™ an Ayurvedic Herbo-Mineral anti sickling medicine have good results on SCA patients. It reduces painful conditions and given painless life-better life to the sickler.
Mass Education - Awareness camps, informative material in vernacular languages, street plays, rallies, poster competitions, slogans competition are few of the many activities of the centre.
Aim
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To serve all affected patients of Sickle Cell Anaemia.. |
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To create a great level of awareness regarding the disease amongst public. |
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To help affected families keep in touch with each other, to encourage for regular treatment, follow-up etc. |
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To carry out genetic survey program to detect Sickle Cell and sufferers |
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To find out undiagnosed Sickle Cell patients. |
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To enlighten patients and parents about the correct scientific method to treat Sickle Cell patients. |
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To provide genetic and marriage counseling. |
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To help the blood bank by organizing / helping blood donation camps. |
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To provide diagnostic facilities for Sickle Cell Anaemia |
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To provide Health education |
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To educate the parents and patients of Sickle Cell Anaemia |
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