By Helen Russon
Food is never a boring subject for most of us. Nor is the idea that certain foods might actually help in fighting MS.
That was the topic at our January meeting of the Providence MS Support Group. We focused on an excellent 2008 article in Momentum Magazine by Judy Hassan. The title of the article was, “Is there an MS Diet?” And while she concluded that there probably was not, she still suggested some ways to eat better and stay healthier – which cannot help but be useful in coping with our MS.
Introducing Sheila Mawsdley, one of our 2015 I Ride with MS ambassadors
By Amy Harris
Amy: Sheila, thank you so much for taking the time to speak with us today. Can you tell us a little about yourself?
Sheila: I’d be happy to! I live in Bend, Oregon, with my wonderful husband, Mike and my two step-children Ethan and Katelyn. I love spending time with my pup, Piper, who just got certified as a therapy dog. I like to think of myself as a happy, compassionate, tenacious person who loves to cheer on others.
Amy: What’s your job?
Sheila: I work as a certified life coach. It’s an extraordinary opportunity to join people on their journey as they get outside their comfort zones into something really fulfilling and invigorating. This year, I’m ready to start working with people with MS. I look forward to being of service to others who want to live a full life with MS as a consideration, not a limitation.
by Helen Russon
It has been a promising year on the MS front, and this was highlighted in the Oregon Chapter’s annual meeting December 6, 2014.
Attendees started the day with a healthy and plentiful brunch, with plenty of time to connect with each other. Chapter President Lisa Roth then gave a quick rundown of where our efforts and funds have been going. She detailed an array of research, programs, new equipment and events, and invited everyone to contact the National MS Society, Oregon Chapter with ideas for other projects.
Hi Volunteer Army!
As the year comes to a close, I think back on the memories we shared at Walk MS, Bike MS, A Night in the Park (remember David Osmond singing “Sacred Emotion”?), working together in our office, and so much more.
And that makes me grateful for YOU. Because your talent, your time, and your BIG heart helped make all of these events and our Chapter’s work so AWESOME — and led to one of the most successful years in our Chapter’s history. Isn’t that cool?
by Nan Devlin
When Kevin was a cadet at West Point, he overheard Brigadier General Robert Foley tell a story to a group of visitors about the mental, physical and emotional tenacity of brave soldiers. The general said that even in relentless onslaughts of overwhelming enemy forces, military leaders never stop; they never quit.
Kevin was no ordinary soldier. The mental conditioning, physical strength and readiness training gained at West Point made him an Apache attack helicopter pilot and earned him a command of 140 troops in South Korea. He was at the top of his game—young, fit and healthy. Then came a day in 1999.
He was elected for four terms and led the country through some of the most frightening times we have ever known — including the attack on Pearl Harbor, 73 years ago this December 7.
by Helen Russon
In the late 19th and early 20th centuries, there were laws on the books – known as the Ugly Laws – that actually prohibited people from presenting themselves in public if they had disfiguring disabilities. But it was during this era of disability phobia that the United States elected a president who could not walk.
A recap of October’s Providence MS Center Support Group
By Helen Russon
Just like last month, we barely got through our introductions before the support group time was up. Everyone attending this month’s Providence Multiple Sclerosis support group seemed to feel like talking about – and listening to – how MS has changed our lives and how we cope with the “new normal.”
This is the kind of group where you don’t have to make excuses about not having read the book, nor do you have to get on a scale in front of everyone. All you need is to have a connection to MS – through yourself, a friend or a family member.
by Helen Russon
In June on this blog we covered the new requirements for parking with a disabled placard in Portland (see “Parking Rules are Changing for People with Disabilities”). Those rules went into effect July 1, 2014.
While some applaud the increased availability of parking spaces, others think it puts an unfair burden on people with disabilities. There are good points on both sides, but the reality is this is now the law – and we ignore it at our own peril (of getting a ticket)!
So in a salute to reality, we had decided to provide a quick update on the law. Coincidentally, just as we were putting the finishing touches on it, the Portland Bureau of Transportation (PBOT) told us they were releasing some new information about how it is all working out. We’ll get to that in a minute. But first, here is a quick review of the changes:
by Jennifer Meacham
“How many of you are personally associated with someone with MS?”
Such was the question posed by David Osmond, National MS Society ambassador and keynote speaker for A Night in the Park: Gala 2014. Roughly half of the 220 seated in downtown Portland’s Director Park on September 11 raised their hands.
David’s father, eldest of the world-famous Osmond Brothers, was diagnosed with primary-progressive MS in 1987. Twenty years later, David received his own diagnosis, for relapsing MS.
“My daughter Saffron prays at night and says ‘And please bless my daddy, that his MS will go away,’” David said to the crowd. “She’s 5. And when I hear those words, how can I not do everything in my power to fight back and make sure that I beat MS?”