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I HAVE PARKINSON'S DISEASES AND THOUGHT IT WOULD BE NICE TO HAVE A PLACE WHERE THE CONTENTS OF UPDATED NEWS IS FOUND IN ONE PLACE. THAT IS WHY I BEGAN THIS BLOG.

I COPY NEWS ARTICLES PERTAINING TO RESEARCH, NEWS AND INFORMATION FOR PARKINSON'S DISEASE, DEMENTIA, THE BRAIN, DEPRESSION AND PARKINSON'S WITH DYSTONIA. I ALSO POST ABOUT FUNDRAISING FOR PARKINSON'S DISEASE AND EVENTS. I TRY TO BE UP-TO-DATE AS POSSIBLE.

I AM NOT RESPONSIBLE FOR IT'S CONTENTS. I AM JUST A COPIER OF INFORMATION SEARCHED ON THE COMPUTER. PLEASE UNDERSTAND THE COPIES ARE JUST THAT, COPIES AND AT TIMES, I AM UNABLE TO ENLARGE THE WORDING OR KEEP IT UNIFORMED AS I WISH. IT IS IMPORTANT TO UNDERSTAND I AM A PERSON WITH PARKINSON'S DISEASE. I HAVE NO MEDICAL EDUCATION,

I JUST WANT TO SHARE WITH YOU WHAT I READ ON THE INTERNET. IT IS UP TO YOU TO DECIDE WHETHER TO READ IT AND TALK IT OVER WITH YOUR DOCTOR. I AM JUST THE COPIER OF DOCUMENTS FROM THE COMPUTER. I DO NOT HAVE PROOF OF FACT OR FICTION OF THE ARTICLE. I ALSO TRY TO PLACE A LINK AT THE BOTTOM OF EACH ARTICLE TO SHOW WHERE I RECEIVED THE INFORMATION SO THAT YOU MAY WANT TO VISIT THEIR SITE.

THIS IS FOR YOU TO READ AND TO ALWAYS KEEP AN OPEN MIND.

PLEASE DISCUSS THIS WITH YOUR DOCTOR, SHOULD YOU HAVE ANY QUESTIONS, OR CONCERNS. NEVER DO ANYTHING WITHOUT TALKING TO YOUR DOCTOR FIRST..

I DO NOT MAKE ANY MONEY FROM THIS WEBSITE. I VOLUNTEER MY TIME TO HELP ALL OF US TO BE INFORMED.

I WILL NOT ACCEPT ANY ADVERTISEMENT OR HEALING POWERS, HEALING FROM HERBS AND ETC. UNLESS IT HAS GONE THROUGH TRIALS AND APPROVED BY FDA. IT WILL GO INTO SPAM.

THIS IS A FREE SITE FOR ALL WITH NO ADVERTISEMENTS

THANK YOU FOR VISITING! TOGETHER WE CAN MAKE A DIFFERENCE!

TRANSLATE

Tuesday, September 2, 2014

Partners in Parkinson's


partnersinPD
When asked to be an ambassador for a new health initiative co-sponsored by the Michael J. Fox Foundation (MJFF) and Abbvie — I jumped at the opportunity to be part of this groundbreaking effort, which promises to provide new educational tools and resources to help ensure optimal care for patients at every stage in PD progression.
Success is dependent on patients making greater use of Movement Disorders Specialists (MDS) — neurologists with advanced training in PD and up to date knowledge of cutting edge PD treatments and clinical trials. Currently, less than one-third of those diagnosed with PD see a MDS, meaning the majority likely are not receiving the best care available to them.
Explore the new “Partners in Parkinson’s” web site (http://www.partnersinparkinsons.org) to find new tools to help you locate a MDS near your home and empower you in the overall treatment process. Register to receive ongoing updates, information on events (including clinical trials) in your area, and access to new tools and resources as they become available.
Those who have long advocated for patients to have a seat and a voice at the table where decisions are made about our healthcare needs, should appreciate that this initiative is patient-centered, designed with patient input to benefit patients. Grab a seat before the music stops.
Once again, MJFF has stepped up to the plate and shown its willingness and ability to lead in research and beyond. As patients and care partners we must publicly recognize this and continue to urge all the national orgs to combine into one community working towards one common set of goals.
Small but mighty, the Parkinson’s community is bound together by a common thread — a progressive, incurable “designer disease” that affects no two of us the exact same way. Sidelined way too young, and feeling marginalized, many of us seek opportunities that will allow us to apply our experience, skills, and knowledge to leave the Parkinson’s community a better place than we found it.Partners in Parkinson’s may just be our best opportunity yet.

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