The Michael J. Fox Foundation (MJFF), the National Institutes of Health (NIH) and five life sciences companies announced a public-private partnership to advance understanding, measurement and treatment of Parkinson’s disease. The latest focus of the NIH Accelerating Medicines Partnership (AMP) model, this new AMP PD project will apply cutting-edge technologies to tease apart microscopic differences in the cells of people with Parkinson’s disease (PD).
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Apomorphine (MOVAPO) has received a positive recommendation by CADTH, the Canadian Agency for Drugs and Technologies in Health.
A positive recommendation means CADTH is recommending that the provinces offer public coverage for the cost of the drug for patients (with conditions):
Here’s the full recommendation report from CADTH: https://cadth.ca/sites/default/files/cdr/complete/SR0527_Movapo_complete-Jan-25-18.pdf
The President of The Cure Parkinson’s Trust, Tom Isaacs, passed away unexpectedly on May 31st, at age 49. He was a trailblazer in the Parkinson’s community, and was diagnosed with the disease at 26 years old. His core and personal understanding of the disease, as well as his determination and advocacy, made him an incredible leader in the field.
He pushed several significant components crucial to Parkinson’s research that the Quebec Parkinson Network shares, such as the importance of clinical trial participation, and awareness initiatives.
The QPN offer our condolences to Tom’s family and The Cure Parkinson’s Trust team.
Posted on the Micheal J. Fox Foundation Blog, by author Stephen Bergenholtz.
Stephen Bergenholtz talks about how he adjusted his lifestyle and mindset to overcome the loss of motivation associated with his Parkinson’s, through a list he called the “8 Disciplines of a Parkinson’s Patient”. He writes about how his substitute for loss of motivation is simply discipline, or regular repetition of an activity until it eventually becomes comfortable.
I will meet regularly with my doctor, follow his or her advice and find a new doctor if he or she becomes unavailable.
I will take my prescribed medications, track my medication supplies and discuss any side effects with my doctor.
I will follow a personalized exercise program in consultation with medical and fitness professionals.
I will make good sleep habits a priority and reduce factors which inhibit me from getting a good night’s rest.
I will foster an attitude of optimism and well-being and strive to alleviate stress through fun and healthy activities.
I will remain engaged with my family, friends, caregivers and others, resisting the tendency to withdraw socially.
I will read about maintaining a positive outlook grounded in my faith beliefs or my spiritual development.
I will contribute to the Parkinson’s community by giving my time, talents, money, or by participating in medical trials.
A new article posted in Nature, Journal of Science suggests that Parkinson’s could be an autoimmune disorder, in which the immune system mistakenly attacks parts of the body. David Sulzer and his team at Columbia University studied brain tissue samples postmortem, and discovered that dopamine-producing neurons do display antigens.
The prevailing thought in Parkinson’s research has been that the disease begins with clumping of a protein called synuclein in the brain, which causes neighbouring dopamine-producing neurons to die—the result of this being tremors and difficulty moving associated with Parkinson’s.
This appears to be the first evidence that the immune system plays a major pathological role in Parkinson’s. However despite the findings by Sulzer, they are still looking into whether the neuron death is caused by immune response, or if it is a side effect of the disease.
Either way, the research found could lead to new ways to treat the illness.
—Source: Nature, Journal of Science (https://tinyurl.com/y9z47lhj)
A new technique developed by researchers in University College London (UCL), involves in depth examination of the eye which allows doctors to see individual nerve cell death in the back of the eye. Initially clinical trials were carried out on glaucoma patients, but nerve cell death is also associated with neurodegenerative diseases like Parkinson’s, and so the hope is through the technique, earlier detection of Parkinson’s symptoms will become common.
The technique is called DARC, or the Detection of Apoptosing Retinal Cells. It uses a fluorescent marker that attaches to cell proteins when injected into patients, and this allows more visibility and clearer detection of the retinal nerve cell situation.
The Weston Brain Institute awards over $30 million nationally for high-risk, high-reward translational research projects to help speed up the development of treatments for neurodegenerative diseases of aging. The Institute is Canada’s largest privately funded national initiative aimed at accelerating breakthrough discoveries for the treatment of neurodegenerative diseases of aging, including Alzheimer’s, Parkinson’s and frontotemporal dementia.
Of the researchers that received funding, there is Dr. Marta Kaminska (Assistant Professor, Department of Medicine/ RI-MUHC), who focuses on respiratory issues, particularly sleep-related breathing disorders, in neurological diseases such as Parkinson’s disease (PD). With the funding from the Weston Institute, she will be examining the effects of long-acting levodopa (a chemical precursor of dopamine and a standard PD treatment) on obstructive sleep apnea in PD patients in a pilot proof-of-concept trial.
Congratulations and best of luck to all the recipients!
Exercise is one of the most effective ways to manage Parkinson’s disease and to lessen the magnitude of its symptoms.
This new Ask the MD video from the Michael J Fox Foundation outlines the ways in which exercise can help anyone at any stage of Parkinson’s disease.
Dr Dolhun explains that dance can help with coordination issues, and yoga and tai chi are great for postural instability and loss of balance. She adds that whether it’s cycling, golfing, swimming, boxing, or anything else, if you enjoy it and feel safe while doing it, you’re more likely to stick to it and see a greater improvement in your quality of life. The best plan is to work with your doctor and a physical therapist to devise an exercise routine that works for you.
To read more about exercise and Parkinson’s, click on the links below: