WELCOME TO OUR PARKINSON'S PLACE!

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

Thursday, April 10, 2014

It’s Parkinson’s Awareness Month!

It’s Parkinson’s Awareness Month! How can you make a difference? Get advice from the PD pros and double your difference through the The Light of Day Foundation $100,000 Matching Gift Challenge!
Parkinson's Disease Foundation LogoPD Helpline (800) 457-6676
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Share: Greg Paints the Town … with Posters!
What’s a powerful way to raise awareness of Parkinson’s? Show your support, on a tree, on a bulletin board … or on you! That’s what PDF Research Advocate Greg Hardoby is doing in Rahway, NJ. He is putting PDF’s free awareness posters around town, including in his local library. And he’s topped it off by wearing a PDF hat. How can you do the same? Order free posters from our e-store and see tips on where to post them.
 See Tips
 Order Your Free Poster
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Learn: Partner with Professionals like Maria
Do you know dedicated professionals who care for people with Parkinson’s? Are you one of them?  Ask to speak to hospital staff members, physical therapists or future professionals, for example, nursing students, about life with PD. That’s what Maria De Leon, M.D., did a few months ago at Stephen F. Austin Medical School in Nacogdoches, TX. Dr. De Leon, a PD specialist and a person living with PD, did a “show and tell” to educate students about Parkinson’s disease.
 See Tips
 Order Free Materials for Professionals
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Support: Double Your Donations like Emily Alice
Did you know that this month only, The Light of Day Foundation will match your donation to PD research for up to $100,000? PDF Champions like Emily Alice, who is donating a portion of proceeds from her jewelry sales to PDF, are taking advantage of the challenge by fundraising in April. Every dollar she raises will be doubled! Get your donation doubled by donating by Wednesday, April 30.
 Donate & See Challenge Progress
 Learn More About Emily Alice
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Question of the Week
How are others raising awareness?
 Click for the Answer
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Thanks to our low administrative costs, 80% of our budget goes directly to Parkinson’s research, education and advocacy. Make a donation today to support our mission.Thank you for your generosity.
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If you have or believe you have Parkinson’s disease, then promptly consult a physician and follow your physician’s advice. This email is not a substitute for a physician’s diagnosis of Parkinson’s disease or for a physician’s prescription of drugs, treatment or operations for Parkinson’s.

Tuesday, April 8, 2014

PARKINSON'S DISEASE FACTS COPIED FROM SHERRI WOODBRIDGE ( http://parkinsonsjourney.com/author/Sherri)

 

Blogs on Parkinson’s SHERRI WOODBRIDGE


By  The following is an extensive list of currently active (unless otherwise noted) blogs pertaining to Parkinson’s disease. It is intended to provide information for those seeking encouragement, inspiration, information, support and more on their journey with PD and are written by those who understand and are walking the same path.

If you know of a blog or author a blog about PD (caregiving, personal journey with PD, etc) that is not listed below and would like to be a part of this network, please feel free to let me know at parkinsonsjourney@gmail.com. 

BLOGS ON PARKINSON’S DISEASE
Currently active as of March 2014
A diagnosis with Parkinson’s Disease in September 2009 at age 80 gave life a new focus and challenge for John Schappi. Finding ways to meet this challenge helped make 2010 the best year of his life. The hope for this blog is that it will be a place where he can connect with others who also are dealing with aging and its afflictions and attractions so that together you can share your “experiences, strengths and hopes.”
This blog is published by the APDA (American Parkinson’s Disease Foundation) Massachusetts Chapter. It is meant to be a series of articles on items of interest to the PD community and posts and do not necessarily reflect the official position of the APDA . Some really good posts.

Making the best of a life with PD

Reflections of an early onset Parkinson’s patient.

A personal perspective on Young Onset Parkinson’s disease, written by Zalamanda who lives in Hampshire, England. She is a mother, a writer, a scientist and an artist.
In the autumn of 2009, she was diagnosed with Young Onset Parkinson’s Disease. Almost a year later, she started this blog.

Although this blog appears to be inactive (as of 4/2014), it still hast seven years of great posts of a Midwestern retiree with Parkinson’s disease.

The decidedly non-frivolous musings of a battle-clever Dystonia damsel – less in distress – seeking a bit of comic relief as she airs her “neurological dirty laundry”.

“Today With PokieToo and Parkinson’s and Acute RA Disease”: A daily journal of my fighting not only Parkinson’s Disease but Acute Rheumatoid Arthritis with My Lord on one side and Patientslikeme.com on the other….with a sense of fun and friendship all around.

Diagnosed with Parkinson’s Disease and Peripheral Neuropathy in 2006, her symptoms seemed to take a turn in a different direction in late 2007. The current diagnosis is ESSENTIAL MYOCLONUS. Share her journey – coping with the testing, the medicines, nutrition, digestion problems, exercise, the emotions, uncertain diagnoses and no telling what else!



Dragonflies and Driftwood is the story of two government workers and how they got their wings… Featuring teenagers, titillation, trials, tribulations, and the miracle of love.

From Pekin, Illinois, this blogger was diagnosed with YOPD in January 2011 and determined to not let the disease have the upper hand..

A Pastry Chef’s journey with early onset Parkinson’s, diagnosed at age 26

Writing poetry and stories since she was a child, Elaine has a passion for writing. While the rest of the world snug in their beds, you will find her immersed in words as sleep eludes her due to the effects of having Parkinson’s disease.

An evolution of art. A journey through life with Parkinson’s

An ordinary girl, blessed with an extraordinary life while living with Young Onset Parkinson’s disease.

Living creatively with Parkinson’s Disease using Creativity, Courage and Comedy by Peggy van Hulsteyn



Karyn is from Australia and was diagnosed with PD at age 44. A world traveler, she has ridden through Vietnam, raising funds and awareness for PD.

[INACTIVE] Chronicles of my sometimes funny, sometimes sad, but always enlightening journey of a woman whose husband is diagnosed with Parkinson’s Disease.

Yoga for Parkinson’s disease and Movement Disorders

Living alone with Parkinson’s for over 20 years, this blogger has learned through research, trial and error what works for them. (Alternative approaches)

Peter Dunlap-Shohl authors this blog from Alaska drawing from personal experience and using wit, humor and comics. Great information.

How one Christian woman deals with life living with PD.

Life with Early Onset Parkinson’s and Pain

Parkinsonsecrets.com blog is the Official Website for the book: Parkinson’s Treatment: 10 Secrets to a Happier Life by Dr. Michael Okun, the National Medical Director for the National Parkinson Foundation, as well as the author of several books including Ask the Expert about Parkinson’s Disease, Lessons from the Bedside, and his latest book Parkinson’s Treatment: 10 Secrets to a Happier life due out in 2013.
The purpose of this blog is to create a simple forum for Parkinson’s disease patients to learn and exchange the secrets that can help them to live a happier life

One blogger’s personal experience with PD

Bev Ribaudo, aka ‘Yuma Bev’, shares her optimistic attitude about life with PD, regardless of what’s happening, good or bad. You can also read about Bev’s DBS experience here.

Offers encouragement, inspiration, and support to people with PD and their caregivers. By a person with PD. Good  resources.

PD PLAN FOR LIFE – Living well with Parkinson’s Disease
Hope springs from refusing to give up. “Once you choose hope, anything is possible,” said the late Christopher Reeve. Instead of allowing Parkinson’s to limit and define her, Sheryl has found new purpose for her life, done things she never dreamed she’d do, and made friends she would not otherwise have met.
Meet Sheryl and her friend Jean Burns as they share their challenges, triumphs, humorous perspective, and coping strategies to empower others to live well with Parkinson’s.

A Canadian visual artist, radio broadcaster, and writer with PD.

[IRREGULAR POSTINGS]
Diagnosed with Parkinson’s disease before her 33rd birthday, Angie shares her story running, trying to race awareness and funds in hopes of finding a cure for PD.

An insider’s view of Parkinson’s Disease and DBS

“Shaky Paws Grampa” is Kirk Hall, author of Carson And His Shaky Paws Grampa and patient perspective Parkinson’s advocate. His personal experience as a PWP includes support group meetings, two visits to the National Institute of Health’s National Institute of Neurological Disease & Stroke to participate in clinical research studies, participation in workshops at the Southeast Parkinson’s Conference, participation in clinical research studies, and joint presentations with movement disorder specialists to support groups sponsored by the Parkinson Association of the Rockies (PAR) and University of Colorado Hospital. Kirk has been a guest speaker at the Muhammad Ali Parkinson Center in Phoenix and other events in the Denver area. He and his wife of 43 years, Linda, are PDF Clinical Research Advocates.

Andy Daly tries to avoid the subject of life with Parkinson’s disease by trying to reflect on life without Parkinson’s Disease.

One man’s personal experience living with PD

Terri Reinhart, a former kindergarten teacher of 18 years, now enjoys spending time making brooms, felting, knitting, bookbinding, painting, and filling up the house with various craft supplies. She is probably the only woman who has ever asked her husband for 50 pounds of broomcorn for her birthday. She also enjoys writing because, as she says, “It helps me to process all the crazy wonderful things in life without screaming or hitting anything.” Join her on her PD path as she enjoys life to the fullest.

[IRREGULAR POSTINGS (but very good ones)]
Corey King shares his journey of having been diagnosed with YOPD at the age of 47.

The adventures of one family as they homeschool, travel, and explore their way through life… which is made more scenic by the additions of Asperger’s, Early-Onset Parkinson’s, and Gluten Intolerance.

Stan has Parkinson’s Disease (PD) and is a gardener, however he claims he is not an expert in neither. This blog is a little bit about PD and a little bit about gardening. Stan lives in Ottawa, Ontario, Canada


Allison is a “thirty-something girl” who has been a medical anomaly since age 13. She wanted to help people… to really make a difference. So she went to graduate school to become a Psychotherapist and during her second year, she was diagnosed with Parkinson’s disease. The only thing that made sense to her was to give back. She launched a program called “Parkinson’s in Balance” in 2010 with the goal to help her community. Her program offers fitness classes, support groups and social events. You can also follow her advocacy work through her blog. “Don’t underestimate the power of sharing what you do,” she says, as “you might just give inspiration to someone in need of a boost.”
A young woman’s journey as she provides support for her husband with YOPD. [Irregular posting but inspiring.]





Marian shares her life and times dealing with Parkinson’s Disease and everything else, including her art. Marian was also chosen as the winning finalist in the PDF T-shirt contest in 2011.

Written by four authors, WearingOff has helpful information about adjusting to life with Parkinson’s Disease
Bryn’s website is for people looking for information on Parkinson’s Disease and particularly for information on living well with Parkinson’s Disease. The people who blog on this site are advocates of using Laughter, Hope and a Positive Attitude towards managing your condition.
[IRREGULAR POSTINGS]
“Life is either a daring adventure of nothing at all.” Join Bev as she shares her story.
A yogini with a PhD and a passion to help people live well with Parkinson’s disease, Her grandfather diagnosed with PD, Kaitlyn made it her passion to improve the daily lives of people affected by neurological disorders.
With a PhD in Health & Exercise Sciences (specifically, daily physical function in persons with Parkinson’s), she is a Kripalu yoga instructor (Trinity Yoga Centre, Kelowna BC) and value yoga for its ability to improve physical and mental well-being, stress, energy and mood… in ALL people!
Here you’ll find Parkinson’s disease information, yoga inspirations and some of her daily adventures.
Diagnosed with Parkinson’s Disease in 2006 at age 34, this young father is still working full time and raising a young family with him and his wife.
Andrew was diagnosed with Young Onset Parkinson’s Disease at 35 years old. Since then his disease has progressed rapidly, and he has been forced to make major changes to he and his family’s lives as a result.
He is fortunate to be supported by a group of amazing mates and their families, his own extended family and of course his wonderful, patient, loving, supportive, funny, caring and beautiful wife Lynn and their two awesome kids. 

Monday, April 7, 2014

Day 5: What Parkinson’s Does…

What a person with Parkinson’s disease may to deal with on a daily basis…
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Day 4: Did You Know?

Flying foxes… Heard of them? They are a species of bats that can grow to a whopping six feet across. Ugh! How'd you like those hanging around the attic? Don't worry – unless you live in Guam and have been fixing them for supper, which some have and in turn? Well, becase the 'foxes' eat cycad seeds and becasue those cycad seeds contain a neurotoxing, many of those fox eating Guam feasters have developed PD.
Did you know that in 1875, there was a French neurologist by the name of Henri Huchard? Did you know Henri had a patient that had all of the symptoms of Parkinson's Disease? Did you know that patient was a mere three years old? Oui oui – yes- it's true.
And did you know that Nicolas Culpepper, an English botanist, herbalist, physician, and astrologer claimed that worms were useful in the treatment of PD symptoms? Anyone want to try a little Alfredo sauce with their worms?
And – speaking of physicians and such, in medieval Damascus in the 9th century there was a Syriac Christian physician named Yahya Ibn Sarafyun, who collect and put together in an abridged form the opinions of the Greek and Arabic physicians concerning diseases and their treatment. One of these opinions was his, which was that he believed that a formulation that he himself had devised would treat PD. The formulation? Frankincense, myrrh and – you guessed it – gold frogs!
And then there's James Parkinson, the man who Parkinson's disease is named after – but he never knew it.
PD is labeled an 'old' person's disease – a disease whose chances of getting hold of you as you age are greater – but did you know that those who live longest (namely those in the 110+ yrs.) almost wholly escape this monster? Crazy!
The 'Evil Eye' is known as a 'sickness' transmitted by a child of Bombay's Parsi people, who is jealous, envious, or covetous. It is 'treated' by burning poisonous Aspand seeds. Which is worse? A child's jealousy or the ritual to treat said condition, which in turn can produce PD in those breathing in the toxin of tyranny?

Day 3: Why A Tulip?

The James Parkinson Tulip
If you were to see a yellow ribbon logo, you'd think of supporting our troops. Likewise, a pink ribbon being in support/advocating for breast cancer awareness. But a tulip?
Ah, the tulip. Red, at that. Unlike the red rose, the red tulip doesn't symbolize love, but is a symbol adopted by the Parkinson's community worldwide to bring awareness to Parkinson's disease.
On April 11, 2005, the red tulip with a fringe of white was launched as the official symbol of PD at the 9th World Parkinson's disease Day Conference in Luxembourg (even though the red tulip had been associated with Parkinson's awareness since the early 1980's).
The tulip is described in detail as the exterior being a glowing cardinal red, small feathered white edge, the outer base whitish; the inside, a currant-red to turkey-red, broad feathered white edge, anthers pale yellow”.
Developed by Dutch horticulturist and Parkinson's disease patient J.W.S. Van der Wereld, the new tulip was named after Dr. James Parkinson, the doctor who discovered Parkinson's disease. Not only did the tulip receive the Award of Merit that year from the Royal Horticultural Society in England, but it also was the recipient of the Trial Garden Award from the Royal General Bulb Growers of Holland.
There are several different variations of the PD tulip symbol, which include the following:

The PDF (Parkinson'd Disease Foundation) specifically uses a yellow tulip to denote optimism and hope. The three petals are used to denote their three-pronged mission: Hope through research, education and advocacy.

The European Parkinson's Disease Association chose this tulip as the symbol for its logo in 1996.
This tulip, recognized by many was designed by early-onset Parkinson's patient, Karen Painter.


The tulip design for the NINDS (National Institute of Neurological Diseases and Stroke) Parkinson's Disease Biomarkers Program captures the red and white tulip enfolded by leaves in the shape of hands that symbolize the overarching goal of the PDBP initiative in bringing together the PD community to build resources and develop technologies that will lead to PD biomarker discovery and innovation.

This tulip logo hails from Europe, specifically, The Eurobodalla Parkinson’s Support Group in the Eurobodalla Shire. The Shire includes amongst others the towns of Batemans Bay, Moruya and Narooma on the South Coast of New South Wales. There are approximately 80,000 people in Australia living with Parkinson’s, and quite a few of these live in the Eurobodalla Shire. None of them are hobbits.
And this one represents Canada…



Which is your favorite or, would you have chosen a different logo altogether? Inquiring minds want to know.

Sunday, April 6, 2014

ISRADIPINE BEING TESTED FOR PARKINSON'S DISEASE

2nd April 2014 - New clinical trial

After proving safe in a study funded by The Michael J.Fox Foundation, Isradipine is moving
to Phase III testing of its effect on Parkinson’s Disease thanks to a $23 million grant from the
National Institutes of Health. They hope to enrol more than 300 participants at 56 clinical
sites throughout North America. For more information go to the Michael J.Fox Foundation :
https://www.michaeljfox.org/foundation/news-detail.php?podcast-drug-that-may-slow-parkinson-progression-granted-23-million-from-nih-for-phase-iii
Isradipine is a calcium channel blocker that is marketed as
Dynacirc. Dynacirc is a drug that is prescribed to treat high blood
pressure. For more information concerning Dynacirc go to
Medline Plus :
http://www.nlm.nih.gov/medlineplus/druginfo/meds/a693048.html
The basis for the clinical trial is that data from large studies found
that there was a lower incidence of Parkinson's Disease among
those people who took Isradipine.
However, when Isradipine was tested in Phase II clinical trials in people who had Parkinson's
Disease Isradipine caused side effects. The most common adverse events were peripheral
edema and dizziness. Isradipine also failed to have any significant effect on Parkinson's
Disease symptoms. For more information go to the Phase II clinical trial outcome :
https://www.michaeljfox.org/foundation/grant-detail.php?grant_id=486

In order to treat Parkinson's Disease effectively dopamine formation must be increased but,
even in theory, calcium channel blockers can not do that.