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From: FireShot Capture 008 - WebMD - Better information. Better health. - www.webmd.com

COVID-19: What People With Parkinson’s Should Know

By Robert Preidt
HealthDay Reporter

 

WEDNESDAY, March 25, 2020 (HealthDay News) — The new coronavirus poses a significant risk to people with Parkinson’s disease, and experts say they and their caregivers need to take precautions.

“People living with Parkinson’s disease are at high risk if they contract COVID-19, whether they are above age 50 or if they have young-onset Parkinson’s disease, which occurs in people younger than 50,” said Dr. Frederick Southwick, an infectious disease expert at the University of Florida in Gainesville.Southwick was part of a Parkinson’s Foundation panel that held a live Facebook forum to answer questions about COVID-19’s effect on people with Parkinson’s.Parkinson’s is a neurodegenerative disorder that causes tremor, rigidity and problems with balance and gait.

“While people with Parkinson’s disease don’t have compromised immune systems by nature of the Parkinson’s disease diagnosis, the respiratory tract is where the danger is,” Southwick said in a foundation news release. “Issues with the respiratory system muscles can make it difficult for people with Parkinson’s disease to take deep breaths and get enough oxygen into the lungs.”

He urged family members of people with Parkinson’s disease to stay home and avoid contact with others as much as possible to avoid COVID-19 exposure.

Loved ones living in group facilities should remain there, if possible, to take advantage of 24-hour resources, the foundation advised. Family members should try to ensure that facility employees are following safety guidelines, including hand-washing and social distancing. Use phone calls and video chats to stay in touch.

Some families may have the resources and support to bring a loved one with Parkinson’s home, but the COVID-19 pandemic may last several months. Before making a decision, talk to your medical team and ensure you have the right gear, medication and support, the foundation advised.

People with Parkinson’s should get seasonal flu and pneumonia shots, if they haven’t already received them. The vaccines aren’t effective against COVID-19, but can prevent or lessen infections from those diseases — and preventing pneumonia in people with Parkinson’s is crucial.

Dr. Michael Okun is the foundation’s national medical director. He said that decisions about medical appointments for Parkinson’s patients to manage their disease “should be a discussion between you and your medical team. Regular checkups and even appointments for urgent concerns may be able to be conducted virtually, so check with your doctor to see if that is an option.”

Okun suggested that “people with Parkinson’s disease — and their care partners — should postpone elective or preventative doctors’ appointments.”The foundation noted that the combination of low mood, depression and anxiety has the greatest impact on the health of people with Parkinson’s, even more than the movement problems associated with the disease.Therefore, it’s critical for people with Parkinson’s to combat loneliness and anxiety caused by self-isolation. Use social media to connect with others multiple times a day, or call people on the phone for a chat, the foundation suggested.

WebMD News from HealthDay

Sources

SOURCE: Parkinson’s Foundation, news release, March 2020

Copyright © 2013-2018 HealthDay. All rights reserved.

 

 

 

 

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As the world confronts the corona virus pandemic, we ask how the societal impact of the disease – and the virus itself – could affect people living with Parkinson’s

The coronavirus disease (COVID-19) – a respiratory virus, which affects the lungs and airways – has now been reported in more than 100 countries around the world.

Symptoms include a fever and a continuous cough – and can take up to 14 days to appear following exposure to the virus. While many people with the illness will have milder symptoms, similar to a cold, others can experience more severe symptoms and disease-related complications. The World Health Organisation declared a pandemic on 11 March 2020.

So, what does this mean for people with Parkinson’s? Because the disease is new and has only affected humans since the end of last year, scientists don’t know exactly how it affects people with the condition.

The UK government has published a list of those at higher risk of severe illness from COVID-19 which includes all people over the age of 70, and people under 70 with a chronic neurological condition such as Parkinson’s. This means people with the condition are considered at a higher risk of having severe symptoms or complications if they are infected by the virus.

Russell Patten, secretary general of the European Parkinson’s Disease Association (EPDA), said: “These are challenging, worrying and frustrating times for everyone in the world – particularly European people with Parkinson’s and their families as the continent is seemingly at the centre of the coronavirus crisis. Borders are closing down at furious speed and movement everywhere is restricted.

“In such difficult circumstances, we must stay strong and grow resilient as a community. Parkinson’s organisations and individuals around the globe are offering support and hope to the masses, mostly online via extra free resources and information to help us stay fit, energised and strong (mentally and physically) while we stay indoors and as safe as possible. We at the EPDA are busily preparing some exciting home-based exercise resources that we’ll share in the next week or so, so watch this space.

“Now is not the time to retreat inwardly; we must tackle anxiety and isolation at home by communicating in new ways.”

The Parkinson’s community is being affected by worldwide cancellations, including that of the Parkinson’s Vision 2020 conference, which was due to take place on 17 and 18 April in Leicester, UK.

The Conference Volunteer Team said: “Although we are bitterly disappointed that the conference is not going ahead as planned, the momentum behind highlighting the issues for those of us living with YOPD has been driven forward by the support of this conference through social media, media and other channels.”

Parkinson’s UK is advising the organisers of local Parkinson’s groups to stop local activities as a precautionary measure. Parkinson Canada said that in-person support meetings had been cancelled until further notice, and US charity, Parkinson’s Foundation, has announced that all in-person events until the end of May will be postponed, although they will continue to run online webinars.

The Michael J Fox Foundation introduced a topic change for a planned webinar on 19March, to provide ‘Information on Coronavirus for the Parkinson’s Community’.

On 11 March the Foundation posted an interview with movement disorder specialist Susan Bressman, MD, who said information on the virus is changing daily: “We’re learning more about it – how it spreads, the odds of getting it, how we can treat it – but we still need more information.”

For up-to-date information about COVID-19 please get in touch with your healthcare authorities and check updates provided by reliable Parkinson’s organisations.


 

Professor Simon Lewis calls it as he sees it

35

check out Simon’s own YT Channel here <

If you’re thinking he’s about to talk about “laser beams”, you’re not far off..


 


 


 

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World Parkinson Congress 2019 Bloggers: Heather Kennedy PERSPECTIVES Author: Heather Kennedy Published: 7 March 2018

 

 

 

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