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A non-Profit 501c3 organization focusing on quality of life issues. |
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Share our dream...share our vision! |
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Legend: All text in RED is hyperlinked.
First, a warm welcome from Brenda and Nan, the founders of this website, and the members of PLWP. Whether you have Parkinson’s disease yourself, are a care partner, a child, a friend, or are interested in the disease for other reasons, there is something here for you. We are glad that you have joined us and hope that you will find information and connections that are right for you here. If you have not officially joined PLWP, Inc., simply click HERE and complete the registration form.
It is imperative that you join PLWP's Yahoo Group by the name of plwp2. Not only do we use this group site for our chat room and message board, we also use the email function exclusively to communicate with our membership. If you did not join plwp2 when you completed the registration form, just go to plwp2 and join.
Note: When you join plwp2 Yahoo Group, the default for email is to receive an email of every individual post to the message board. This could become a burden. To alleviate that potential problem, simply click on Edit Membership on the home page of plwp2 and then under the topic of Message Delivery, chose your preference. We ask that you NOT select No Email as this is the tool used by the administration of PLWP, Inc. for mass mailings to its members.
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PLWP was created to:
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PLWP Website Highlights:
All of these interactions can easily be accessed on our COMMUNICATIONS CENTER
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PLWP - The Organization: As an international organization that is based solely on the internet, 99% of our membership is people who have been diagnosed with Parkinson's. We do not collect dues. We have no paid staff. We do things in a determined, well thought out manner. We've spent 3 1/2 years building a foundation and understanding how to manage such an organization as we have here. PLWP is determined to make a
difference. We have a cord blood donation for research program
called Baby Jack's Cord Blood Project working hand in hand with Harvard
Medical. We have a Patients as Providers Program where we
invite individuals from the medical community to meet with people who have
Parkinson's to interact and share information. Three out of the past
four years, we have gone to New York City for the annual Parkinson's Unity
Walk averaging approximately 50 team members. |
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PLWP - Is it for you?
If you have Parkinson's...if you are a relative or a friend of a person diagnosed with Parkinson's...if you simply care about those with Parkinson's...the answer is YES! If you want to volunteer your services with people who want to make a difference, the answer is YES! If you only want to find others like yourself and share from time to time, the answer is YES! If you are still "in the
closet" so to speak, not wanting your employer or your clients to know you
have PD but needing to talk to others for moral support if nothing
else...you require to remain anonymous, the answer is YES! |
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YOU are invited....
Come on in and check us out. Join us and participate at the level you want. Sure we need volunteers...sure we need fundraisers...sure we need YOU! But more importantly, we need each other. No one should have to go on this journey alone. With PLWP, no one has to! |
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