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Updated:
7-29-10
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Our
Mission
 To
provide support to parents/caregivers and act as a reference source for
information, financial resources, used equipment exchanges, research and
clinical studies, support groups, web links, etc. This will be done in
the form of creating an interactive website, and monthly newsletters.
 To
try to consolidate, and then disseminate, all the available information
tools available to caregivers, from sources such as the internet,
newsletters, parenting organizations, support groups, etc. There is a
lot of information out there, but it takes so much time to search for it
that most caregivers just don’t have the time to spare to look for
needed assistance on their own. We would like to put together a
newsletter that would be a source of information for parents/caregivers
to help
them
help their children.
To
make small individual grants (products & services only) to parents/caregivers of special children
for travel expenses to attend medical conferences that they would not
otherwise be able to afford to attend. No parent/caregiver, or their
family for that matter, should have to “bleed” in order to give their
child the opportunity to be evaluated by experts, and to seek the
support of other families in the same situation.
To
make small individual grants
(products
& services only) to
parents/caregivers of special children, for things like positional
seating, adaptive car seats, durable medical equipment not covered by
Medicaid, vehicle modifications, respite services,
and other non-covered items that would make caring for these children
easier on the parent/caregiver and help to improve their quality of life.
Our primary goal right now is to
aggressively seek corporate sponsors, large donors and dedicated
volunteers in order to become a viable organization, make valuable
connections & tap resources in our community, and raise funds in order
to provide the goals of
The
M.O.R.G.A.N.
Project.
Please ....
won't you consider helping?
 
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