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The Oregon Lyme Disease Network, Inc is a 501(c)3 170(a)(b)
organization.
In accordance with the governing laws of the State of Oregon and the Federal
IRS laws this location will contain links to important Charitable
information regarding the Oregon Lyme Disease Network.
Mission Statement:
Oregon Lyme Disease Network is a 501(3)C non profit organization
established to assist Oregon patients in understanding lyme disease, and
educating state officials, physicians and others on current trends in Lyme
Disease diagnosis and treatments. Our goals are to increase access of
care to all Oregon patients and to maintain open communications with specialty
physicians and local medical professions.
Annual Reports: 2004-2005
http://oregonlyme.org/200405Tax/annual.bmp
2005-2006
not in web system yet
2006-2007 reinstatement :
http://oregonlyme.org/200607Tax/2007annual1.jpg
annual report :
http://oregonlyme.org/200607Tax/2007annual2.jpg
990 EZ Filing (PDF files)
2004-2005
pg 1(bmp files)
http://oregonlyme.org/200405Tax/990a.bmp
2004-2005 pg 1(bmp files)
http://oregonlyme.org/200405Tax/990b.bmp
2005-2006 (PDF files)
http://oregonlyme.org/200506Tax/tax06.pdf
2006-2007
(PDF files)
http://oregonlyme.org/200607Tax/tax07pdf
Program Service Accomplishments:
2004-05- Received our 501(3) C status
2005 - 06
- Ashley Denham's Children's Fund aided four children in receiving proper
testing and medical care through physicians affiliated and with ILADS.
- Two separate support groups were started through help from Oregon Lyme
Disease Network
- Lyme disease information website and forum were created for patient
support
- Media Goals were met
- Preliminary survey and compilation of preliminary results regarding
access to care issues.
- Network of out of state physicians and local support physicians has been
started and will continue to grow in 2006
- Children Kick off began in December. Schools we have made contact
with : Hood River, Salem/Keizer, Bend, Some of the Portland Schools,
Wilsonville Schools. More schools to be targeted during 2007 for Lyme
disease Awareness.
2006-07
- Worked with physicians across the state to increase awareness and assist
in joining with ILADS.
- Supported 3 sets of children to see physicians and gain testing.
- Meeting with state AG regarding access of care
- Kick off new support group in Hood River
- Kick off new support group in Bend, OR
- Kick off new support group in Idaho
Current Roster: Officers and Board
Most Recent finance information:
Past 12 months overview:
Beginning balance
$84.46
Total Revenues:
$ 489.25
Salaries/Compensation
( $ 0)
Professional Fees
($ 339.50)
Rents for meetings
($ 0)
Printing and postage
($ 0)
Other (awareness campaignes)
($ 224.14)
Balance
$ 10.07
Proposed Budget 2007:
Income
General Account
Previous Balance (2007)
$ 10.07
General Donations expected (2008) $1,000.00
Fund Raising Goal (other projects) $3,000.00
Fund Raising Goal Kari's Project
$ $1,000.00
Grant requests Tick Study $1,000.00
Total General
Income
$6010.07
Children's Fund
Previous Childs Fund Balance (2007)
$ 9.00
WE RECEIVED NO DONATIONS LAST YEAR FOR THIS FUND. WE HAD 339.00 go out of
this fund to support children, and we had 600.00 in requests for support for
children whose parents are also ill.
Total
Childrens Fund
$ The children need your help!
Expense
General Account
Tick Testing
($2,000.00)
Reimbursements (tick test travel) ($1,500.00)
Education physician (2 OR phys) ($2,500.00)
Education Patients (pamphlets, DVD) ($1,200.00)
Misc Office Expenses- ($1,200.00)
mailing, fees,website, etc
Total projected
expenses $(9,400.00)
Children's
Fund
Projected Children Support $ (1,200.00)
Most recent CT-12 Oregon DOJ Filing (Oregon Charitable Activities , Oregon DOJ)
Oregon Lyme Disease Network Privacy Policy:
The policy of OLDN has been and continues to be that our organization is for
the sole purpose of being able to assist patients with access to care issues,
and to aid in access to education for physicians and legislators in tick borne
illness specific issues.
Patients names and information will be gathered for the soul purpose of being
able to contact the patient with new information on lyme disease, to assist
patients in receiving access to care and to validate surveys.
No information will be made available to third parties, or sold or given to a
third party without the explicit consent from the patient.
Online payment receipt:
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