SUPERBAD BIKE MS CHALLENGE FOR MAY: 2 EASY WAYS TO WIN GOOD BIKE STUFF
1. For every $100 YOU raise between May 11-May 22, you’ll be entered to win a Bike MS-branded windbreaker from our apparel sponsor, Primal. Woot!
2. For every $1000 your TEAM raises between May 11-22 (or every $2.5k for teams larger than ten) you’ll be entered to win a cooler full of ice-cold, carbonated and super fizzy Izzy sodas to keep you and your team refreshed (between beers) during Bike MS weekend.
How sweet is that? Read more…
Hosted by Western Bikeworks
Saturday, May 16 @ 10 am
Starts/Ends at Western Bikeworks
1015 NW 17th Ave
Portland, OR 97209
Join us for a super awesome ride hosted by our friends at Western Bikeworks. Great for all rider levels. Includes lunch and a drink. Bring along a friend and your Bike MS teammates. A great way to get moving this spring!
By Nan Devlin
Merilee McDowell was just 22 years old when she began to experience numbness on her right side. Her balance was off, and she often felt sleepy and exhausted. For a normally energetic and active young woman, this was cause for concern, so she saw a doctor. The last thing she expected to hear was a tentative diagnosis of MS. Tentative, because in 1977, MS was harder to diagnose, and there was really no medication given other than prednisone, an immunosuppressant steroid.
“A lot of progress has been made since then,” said Merilee, who later was officially diagnosed and treated at Oregon Health and Science University in Portland by Dr. Roy Swank, a pioneer in MS research. “And it’s the main reason I am a supporter of Walk MS.”
2015 Public Policy Conference Recap, pt I
by Helen Russon
We know a lot about the symptoms of MS, but what exactly do we know about who gets it?
Well, women are about three times as likely to get it as men. While it’s not contagious, it does tend to run in families. There is also evidence that it could be related to a Vitamin D deficiency. And the further north of the border you grew up, the more likely you are to get it.
Confounding, right? If there was ever a disease that cried out for more scientific research and exploration, this is it. And although scientists are putting in mega-hours trying to find these answers, they are hampered by a huge and unanticipated problem: There is currently no nationwide system for collecting data about who gets MS, where they live, their gender, their age, their diet and many other factors that could be crucial in discovering the cause – and ultimately the cure –for this disease. Read more…
by Helen Russon & auGi
Want to join a big party to stomp MS?
…a family-friendly, 4-hour party packed with playful music, interactive exhibits, free food, tasty refreshments, a kid’s play zone, “selfie stations,” colorful costumes and so much more? And as if that wasn’t enough, every penny you invest goes to a meaningful cause.
If this sounds too good to be true, you need to meet Andrea Kofoed, the fun-loving Manager of Walk MS Oregon.
According to Andrea, thousands of Oregonians and SW Washingtonians will join Walk MS in 9 locations this April and May. All to show their love of the 8,100 who live with MS in our Chapter.
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.