Connectionsnewsletter fall 2015

FALL 2015

National Multiple Sclerosis Society

MS CONNECTION NEWSLETTER

COLORADO-WYOMING CHAPTER

Colorado-Wyoming Chapter

NOVEMBER IS

National Caregivers Month INSIDE THIS ISSUE:

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MS WELLNESS CENTER

MS AND NUTRITION

PILATES CLASSES FOR MS

PROGRESSIVE MS RESEARCH

Letter From the President Dear Friends: The days are becoming shorter and cooler, which are signs that we are entering the final quarter of another year. This is a wonderful season of gratitude when we pause to take stock of achievements, reflect on how we’ve spent our time and resources, and plan for upcoming holiday celebrations. It is also a time to feed our souls and recharge our spirits by connecting with family and friends, and helping others.

Holiday gatherings are ideal times to discuss what - and who - people are grateful for and why. You may be surprised to learn what is important to those around the table and the work of charities impacting lives, families and communities.

This is a season of gratitude when we take stock … reflect … and connect … and help others...

As a sign of our love and gratitude, this is the season that we also present loved ones with gifts.

Consider a tribute gift to the Society as a meaningful alternative to giving "things." It is an amazing way to honor someone and impact others.

This is also a good time for companies to get involved and give back. Philanthropy and profits go hand in hand, and engaging employees and community members in charitable endeavors is good for business. This can take the form of allowing employees time to volunteer, hosting a special fundraising event or adopting a family or charity. It’s a win-win for all involved.

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Newsletter Distribution—If you have a change of address or would like to receive MS Connection electronically, please call 800-344-4867.

Left Hand Brewing is an outstanding example of a business that has created a culture of community giving. The company was honored as the 2015 Outstanding Small Business by National Philanthropy Day Colorado for it charitable work.

In addition to its Bike MS team raising more than $1.4 million for the Society, the brewery supports health and basic needs, natural disasters, animals, arts and entertainment, and strives to contribute the equivalent of 1 percent of its annual revenue to charitable organizations. We congratulate them on receiving this prestigious honor and for their support!

The Chapter has had another successful year and we are thankful for everyone who has supported our work and the MS community. Our board, staff and volunteers remain committed to enhancing the lives of people affected by MS and look forward to continuing our quest for a cure in 2016.

Best wishes for a safe and healthy holiday season that is filled with joy and hope for the coming year.

Sincerely,

Carrie H. Nolan carrie.nolan@nmss.org 900 S. Broadway Suite 250 Denver, CO 80209

If you or someone you know has MS—studies show that early and ongoing treatment with an FDAapproved therapy can reduce future disease activity and improve quality of life for many people with multiple sclerosis. Talk to your health care professional, or contact the National Multiple Sclerosis Society (NMSS) to learn about ways to help manage multiple sclerosis and about the current research that may one day reveal a cure.

The NMSS does not endorse products, services or manufacturers. Such names appear here solely because they are considered valuable information.

The NMSS assumes no liability for the use of contents of any product or service mentioned. Information provided by the NMSS is based on professional advice and expert opinion. Information provided in response to questions do not constitute therapeutic recommendations or prescriptions. The NMSS recommends that all questions and information be discussed with a personal physician. The NMSS is dedicated to a world free of MS.

©2015 National Multiple Sclerosis Society, Colorado-Wyoming Chapter Chapter President Carrie H. Nolan Board of Trustees Kyle Ocasek, Chair Travis White, Chair Elect Brandt Wilkins, Immediate Past Chair Deborah O'Neil, Secretary Jason Sibley, Treasurer Brooke Allen, MD Carl Berglind Whit Conant John Corboy, MD Chris Doerr Rob Hartnett Marley Hodgson III Darrin Johnson Carin Knickel Deborah O’Neil Michael Pierce Jo Wilson Emeritus Trustees George Garmany, MD Ralph Holden David Lord Janet Savage

MS CONNECTION: FALL 2015

IN THE NEWS EVENTS

2015 MS ON THE MOVE LUNCHEON A crowd of 350 supporters convened at the Westin Downtown Denver for the Chapter's annual MS On the Move Luncheon on September 17. KOA’s April Zesbaugh opened this year’s motivational program and introduced Virginia Valenze from Novartis, sponsor of the Chapter’s Spirit Award, which is presented annually in recognition of service to the MS community and contributions to society and the common good.

Valenze presented the award to this year’s recipient, Michael King. King has been an outstanding, active supporter of the Society and served on the Chapter’s board of trustees for seven years, which included a term as chairman. He also championed his firm’s Bike MS

team for 12 years. In addition to his support of the Society, King is active in the community where he serves as a commissioner for the Denver Public Library, is president of Stapleton United Neighbors and provides pro bono legal services.

In accepting, King reminded attendees that at one time the March of Dimes mission was to end polio. When a cure was found the organization had to redefine its mission. His goal is to put the MS Society out of business and he looks forward to the day that he will be able to ride for a different cause.

Speaker Rebekah Gregory, survivor of the 2013 Boston Marathon bombing, shared her story and uplifting remarks about overcoming challenges and obstacles that life presents. Whether a life challenge results from a terrorist bombing or a diagnosis of MS, Gregory emphasized that “struggles are meant to make us better versions of ourselves”

Michael W. King,

Rebekah Gregory,

MS Spirit Award

Keynote Speaker

and encouraged everyone to band together, lean on each other and greet every day with new hope.

The program concluded with Carlyn Shaw, who was diagnosed with MS at 19. She views the Society as extended family that she can rely on wherever she lives. Shaw hasn’t let MS deter her from reaching goals such as participating in the Boston Marathon and the upcoming New York Marathon. Like King and Gregory, she reiterated that it’s not the challenge but your response to the challenge that carries the day. n

Save the date! Westin Downtown Denver MS on the Move Luncheon: Join the Colorado-Wyoming Chapter of the National MS Society for an extraordinary fundraising event that funds critical research and programs and services for those affected by multiple sclerosis.

SEPT

15TH cureMSco-wy.org

VISION AWARD WINNER DIANA DEGETTE The Society honored U.S. Rep. Diana DeGette with its prestigious Vision Award for her tremendous leadership on the 21st Century Cures Act. This bill promotes a comprehensive look at what steps can be taken to accelerate the pace of cures in America. Innovations are occurring at light speed and laws must keep pace with innovation; this means closing gaps between advancements in scientific knowledge and how therapies are regulated. The Act includes three Society priority issues: establishing a

data collection system to identify risk factors for MS; increasing resources for the National Institutes of Health and the U.S Food and Drug Administration: and incorporating patient perspectives into drug development and review. The Act has passed in the House of Representatives and will be taken up by the Senate this fall.

The award was presented at the Society’s annual Ambassadors Ball, which was held on September 8 in Washington.

U.S. Rep. Fred Upton was also honored during the evening for his leadership with DeGette on the 21st Century Cures Act. Secretary of State John Kerry and

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

Russell Parker (left), U.S. Rep. Michael Burgess, U.S. Reps. Diana DeGette and Fred Upton at the Society’s Ambassadors Ball.

Sen. John McCain were also honored for their support of the U.N. disabilities treaty. n

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RESOURCES

LIVING WITH MS

(Not) the Sound of Music By: MICHAEL WENTINK Are you claustrophobic?” asks the radiologist.

I awkwardly respond, “No, I’m not ...”

As I walk down the hallway and into the room with the MRI machine, I ponder … does another scenario exist where that is the opening question from someone I’ve never met before?

Magnetic Resonance Imaging (better known as MRI) is an annual ritual endured by most individuals with multiple sclerosis. The machine, which weighs over 11 tons, takes pictures of the lesions on my brain, neck and spine, which my neurologist then uses to evaluate the progression of my MS. The truth is, I am claustrophobic. But really, is there anyone who enjoys having his or her entire body in a tube — just big enough to fit your frame — for two hours? For previous MRIs, I took a sedative, which made me drowsy enough to fall asleep, even amid the loud, torturous sounds of the scanning process.

But this time I was scheduled for an “open” (i.e., no skinny tube) MRI was scheduled; however, when I arrive the MRI tech tells me that the quality of an open MRI scan doesn’t meet the standards for MS patients. I nod my understanding while struggling to hide my disappointment.

After answering a few additional questions and changing into a hospital gown, the process begins.

I lay in the cylinder, my legs slightly elevated by a pillow and my head held in place by a cage-like helmet.

A mirror is strategically placed within

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the headpiece so I can see out of the tube.

I wear headphones that the radiologist uses to communicate updates or reminders to remain as still as possible. He briefs me on how to use the panic button, should it be necessary. As the MRI starts, I’m distracted by seeing my eyebrows in the mirror. One long, stray hair is protruding. Annoyed, I make a mental note to take care of it later.

The noises begin to swell from the machine. They change rather frequently. There’s what sounds like rapid machine gunfire, then there’s the construction zone phase, which is followed by various other loud, jarring noises.

As my senses adjust to the chaos, several random thoughts pop into my head, including: After “The Wizard of Oz” came out, did parents who lived in Kansas stop naming their daughters Dorothy?

Does a woman who is born on Valentine’s Day get jilted with “combo” presents the same way people who are born on Christmas do?

Medically speaking, do people tend to itch more when they know they can’t scratch it?

If the intention is to reduce stress, can’t they think of a better name than “panic button”?

I wonder, why am I thinking these things? I’ve never even watched “The Wizard of Oz”! Music from the radio also plays through the headphones.

Unfortunately, most of the songs are marred by the loud noises.

Suddenly, there is moment of silence and, as if on a cruel (and ironic) cue, Celine Dion belts out “All By Myself” — the timing is perfect. I almost start laughing.

I wonder, did the radiologist plan that? I then realize that he is back in the room and I am exiting the tube. As is standard, a dye is then injected into my arm and I go back in to the machine. It’s a cruel tease, even though I knew to expect it. The radiologist informs me I have a “solid half hour” left. I politely thank him while musing over his choice of the adjective “solid.”

I start to fantasize about breaking free and making a run for it and wonder how my wife, who is in the waiting room, would react to seeing a flash of me in a hospital gown sprinting out the door as I make my escape.

What seems like an eternity has passed and the radiologist informs me I have 12 minutes left. I challenge myself to count down these final moments. Twelve 60-second intervals, how difficult can that be?

I count well past what I think is 720 seconds and disappointment sets in as sounds of the apocalypse continue to blare in my face. I worry that I misheard the number “12” and then suddenly, it ends.

The room is now silent. My body slowly glides out of the tube and the helmet is removed. Overcome with jubilation, I resist the urge to give the radiologist a hug.

Thoughts of William Wallace in “Braveheart” screaming “Freeedomm!” dance in my mind as another annual MRI is now complete.n

MS CONNECTION: FALL 2015

RESOURCES

WHAT FATIGUE MEANS TO ME By: Kellen Prouse

Most folks have a pretty good idea of what the word “fatigue” means. But for me, using that word to describe the kind of exhaustion I experience doesn’t seem specific or accurate enough.

When that kind of tired sets in, I can’t just wait it out. It’s not like being worn out from a workout, where you can recover with a few hours of rest.

The tiredness never comes on during bedtime; oh no, that would be way too easy. Instead, it comes on when I’m driving or trying to enjoy my son’s soccer game. I often think I can power through it. But if I don’t make it to the couch, you will see me slumped forward and most likely drooling in my lap. This can happen just about any time, anywhere. I have even fallen asleep mid-conversation.

If we go for a walk, I will be wiped out for a day, maybe two. Even showering

is tiring. But the harder part to explain is how emotional stress can knock me down just as much. Being nervous, upset, or stoked about something can really take it out of me. So, between the physical act of doing something, and the emotional stress of just about anything, I am pretty much always tired. That isn’t even counting the days where just sitting, doing absolutely nothing, kicks my butt.

Even though sleeping doesn’t necessarily make the tiredness go away, it’s something I do a lot of. That is one benefit to being on disability; there aren’t many, but I will take this one.

The doc also advised me to get brain rest (much like meditation). Basically,

I need to find a quiet place away from the computer and phone, and just be.

I think that’s good advice for anyone though.

I don’t speak for all people with MS when it comes to fatigue (since we all have different triggers), but our fatigue is very real, very hard to explain and very frustrating. I only fell asleep four times while writing this ... not too bad.n Originally published at MSconnection.org an online social network where thousands of people support one another and explore the issues that shape your world.

HEALTH INSURANCE

Review Before You Renew!

Open Enrollment is underway and it is time to evaluate your 2016 options for health insurance.

Better smart than sorry. Before you enroll for your 2016 health insurance, be sure to review health plan details and do not assume that your plan will remain the same if you chose to automatically renew.

Be diligent when selecting your plan and review important factors including:

For more helpful healthcare resources and information:

cureMSco-wy.org

• What is your monthly premium?

• What are your additional out-ofpocket costs (deductible,

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

copayments, coinsurance and outof-pocket maximum?

• Is your doctor in-network?

• Is your MS medication covered in the plan’s formulary?

Helpful information and a valuable “Application Checklist for the Health Insurance Marketplace” is available on the Chapter’s website under “Resources and Support.”

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PROGRAMS

SAVE THE DATE UPCOMING PROGRAMS

Meet Our Southern Colorado Team - Pueblo Located at The Gathering

Saturday | November 21, 2015 9am - 11am

Western Slope Holiday Celebration & Potluck - Grand Junction Located at First Presbyterian Church Thursday | December 3, 2015 5:30pm - 7:30pm

Maximizing Your Doctor Visits - Loveland

Located at Chilson Rec Center (Senior Center Entrance) Saturday | December 5, 2015 10:30am - Noon

Holiday Party and Volunteer Recognition - Casper Located at Ramada Plaza Saturday | December 5, 2015 6:30pm - 8:30pm

Maximizing Your Doctor Visits - Cheyenne Loveland, Colorado at The Gathering Tuessday | December 15, 2015 6:30pm - 8pm

Visit cureMSco-wy.org for more information and to register for upcoming programs in your area.

Medicare Part D – Time to Sign Up

You must sign up for Medicare Part D each year if you are on Medicare. Open enrollment for 2016 coverage has begun and the deadline for enrolling is Monday, December 7.

For assistance, contact the State Health Insurance Program (SHIP). Counselors and volunteers are available to answer your questions free of charge.

Find a SHIP location near you: COLORADO: dora.Colorado.gov/insurance/ship or call 1-888-696-7213 WYOMING: wyomingseniors.com or call 1-800-856-4398

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MS CONNECTION: FALL 2015

RESOURCES

FULLY ADAPTIVE WELLNESS SETTING

The PEAK Center at Craig Hospital Craig Hospital is home to the PEAK (Performance, Exercise, Attitude, Knowledge) Center, an adaptive health and wellness center for people with neurologic disabilities that is infused with cutting-edge rehabilitative exercise technologies.

Initially launched as a wellness program under the direction of physical therapist Julie Hartman, the program proved to be so popular and successful that when the hospital underwent a major expansion, it included the new two-story adaptive gym, which opened in August 2014.

The PEAK Center has more rehabilitative exercise technologies than any other center in the state.

Physical therapists provide oversight of the program and every aspect of the PEAK is designed with its users in mind, from entry to the equipped gym to accessible changing and locker rooms with showers, grab bars and overhead lifts.

Open Monday – Saturday, 30 to 50 members can be found working out

daily and personal trainers provide 200 hours of one-on-one training a week. “Everyone using the PEAK has some form of disability and the PEAK Center provides a way to maintain their health and fitness goals in a comfortable environment that is appropriate for them,” said Hartman.

with exercise specialists, and under supervision, participants have access to advanced technologies that range from mechanical vibration stimulus to robotics.

David Sloan, who has lived with MS since 1998, began working out at the PEAK Center in July and found it to be an ideal setting for him. “The things I like most are regaining control of improving my health, getting stronger and smiling with complete satisfaction of my body waking up and responding to rigorous exercise. I use my positive attitude to help make this happen and have demonstrated results every time I workout,” Sloan said.

The PEAK Center is open to the community and features several levels of personalized services: General membership Following a general gym consultation, general members use adaptive fitness equipment specifically designed for people in wheelchairs, such as bike circuit training and standing frames; Volunteers and interns are also available to assist when needed to ensure a safe environment. Gym members also have access to group fitness classes including: adaptive yoga, upper extremity cycling class, and PEAK performance strength and conditioning class.

One-On-One memberships These are available for people who need more assistance. Following a physical therapy evaluation, customized program is developed

Functional Electrical Stimulation (FES) Cycling FES cycling uses electrical stimulation on weak or paralyzed muscles to prompt the legs of an individual to “cycle” on an adapted stationary recumbent bicycle. The repetitive activity offers cardiovascular exercise, spasticity reduction, improvements in range of motion, and other individually specific benefits.

“I was blessed to be the physical therapist who got the incredible job of developing and coordinating this program,” said Hartman. “I loved the idea of providing an adapted fitness center where people with mobility impairments feel comfortable coming to receive the mind, body and spirit support they need,” said Hartman. n

PEAK Center scholarship funding is available and people can learn more about this support during the initial physical therapy evaluation. For membership pricing and more information, visit www.craighospital.org/PEAKCenter or call 303-789-8325.

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

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RESOURCES PEDIATRIC MS NETWORK EXPANDS TO 12 SITES

Society Funds Pediatric MS Center in Colorado The Society recently funded a Pediatric MS Center in Colorado, one of three new Centers added to its network established in 2006 to provide comprehensive care to children with MS and other related central nervous system demyelinating disorders. The addition of the new Centers expands the network to 12 sites nationwide.

NUTRITION AND MS

Eat Food.

Seriously.

“Is there a special diet I should follow to help with my MS?” As a specialist in multiple sclerosis, this is one of the most common questions I’m asked by patients. Whether they are newly diagnosed or have had MS for decades, people understandably want to do everything they can to improve their disease outcomes.

Unfortunately, I have to give them the complicated answer, “No, but…”

It turns out that like most things in the treatment of MS, this question is much more complex than we thought.

Over the years, many neurologists, patients, and others with an interest

8Tracey, diagnosed in 2005

The Colorado Center is at the University of Colorado, in collaboration with Children’s Hospital, and is led by Dr. Teri Schreiner, assistant professor of neurology and pediatrics at the University of Colorado School of Medicine, Anschutz Medical Campus.

Expanding this research network will enhance the ability to understand childhood MS and its treatment, which may unlock the mysteries of MS in adults. Since 2013, the Society has committed $2.8 million to support the research network to provide essential infrastructure to facilitate research, including searching for the cause of MS by studying risk factors for the disease in children, close to the time of its onset.

in MS have investigated the question of diet and its effect on the disease.

There have been well designed research trials and anecdotal reports of something working wonders. The overall conclusion, however, has been that no particular dietary restrictions or inclusions have been shown to be beneficial in patients with MS. That said, there is good evidence that a healthy diet and lifestyle does improve overall quality of life, health, and well-being in people with MS – just as it does for the rest of us.

The most famous “MS Diet” was proposed by Dr. Roy Swank in 1948. This was an extremely low fat diet which did not appear to have significant benefit to multiple sclerosis when fully analyzed. The key to the diet, however, was to consume less

The network has a close alliance with global research efforts through the International Pediatric MS Study Group, convened by the Society in 2002, which now includes leadership from the MS International Federation, other MS societies, and medical and scientific leaders from more than 15 counties. n

than 15 grams of saturated fat per day, which is a good recommendation for anyone’s general health. As to whether this has a specific benefit in people with MS, there is no real evidence.

Essentially, the guidelines for eating healthy are the same whether you have MS or not. Watch out for saturated fats and cholesterol, keep the processed sugars to a minimum, limit salt and caffeine, and drink plenty of water (probably more than you think). Most importantly, eat a variety of foods.

Note the word food is key here. Not processed, pre-packaged, chemical infused food-like-products. Food.

So to help manage your multiple sclerosis, manage your overall health.

The main gateway to your body is your mouth, so be aware of what you put in it and make sure it is actual food. n

MS CONNECTION: FALL 2015

VOLUNTEERS participating in Walk MS. Three years ago she decided it was time to reduce stress and take care of herself.

She stopped working full time and directed some of her newfound free time to support the Chapter.

JERI SPOONEMORE

Chapter Volunteer of the Year Congratulations Jeri at Spoonemore, Brent and his daughter,to Danica Walk MS the Chapter’s 2015 Volunteer of the Pueblo 2014.

Year. This recognition is presented annually to an individual for outstanding volunteer efforts and exemplary leadership on behalf of the Society.

Diagnosed in 1996 in her late 30s, Jeri started fundraising for and WANT TO MAKE A DIFFERNECE?

Jeri serves on the Walk MS Cheyenne planning committee and redesigned the Kids' Korner area to provide more information about pediatric MS, in addition to adding a healthy snack and penny pond activity. She also co-leads the local support group and recently completed the Society’s Ambassador training. “I enjoy being able to share my story and encourage others to engage with the MS Society to make an impact.

It’s critical for people to have information and know where to turn for resources, which is why it’s very important to me to bring attention to this disease and spread the word, especially since MS is so prevalent in Wyoming and Colorado. We may live with MS, but we’re still viable citizens

in the community. Volunteering is an ideal way to make a difference,” she emphasized.

“Receiving this award is hard to put into words,” Jeri said. “I don’t volunteer for rewards or recognition.

I like being behind the scenes and out of the limelight, but this is a huge honor.”

“We congratulate Jeri on this honor and for all her outstanding contribution,” said Chapter President Carrie Nolan. “Volunteers are a vital part of our community and we are thankful for all the generous support they continually provide to help move us closer to a world free of MS.” Jeri was selected from among the Chapter’s 1,800 volunteers who donate more than 15,000 hours of service annually to support the Chapter’s successful events, promote community awareness and assist with other needs.

Volunteering with the Chapter is a meaningful way to give back. Interested in getting involved? Want to learn about volunteer opportunities available? Visit cureMSco-wy.org and click on volunteer or call Sarah Ness, volunteer manager, at 303-698-5443.

2015 Volunteer Recognition Successful fundraising events, advocacy, efforts, and community outreach involves the contributions of countless individuals and organizations. We are pleased to honor the following for their outstanding support this year.

Chapter Volunteer of the Year . . . . . . . . . . . . . . . . . . . . . . . . . Jeri Spoonemoore Volunteerof the Year . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Kevin Vogt Event Volunteer of the Year . . . . . . . . . . . . . . . . . . . . . . . . . . Ellie Wise Programs Volunteer of the Year . . . . . . . . . . . . . . . . . . . . . . . . Margaret and Wiff Withey Tireless Spirit Award . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Suzanne Pershall Longstanding Wyoming MS Community Partner . . . . . . . . . . . . . Bicycle Station Southern Colorado Community Partner of the Year . . . . . . . . . . . . . . . . . . . . . . . . High Country Beverage

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

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EVENTS PILATES CLASSES BENEFIT PEOPLE WITH MS AND THE SOCIETY Health enthusiast Clara Gelatt, co-owner of Cherry Creek Pilates, is a strong proponent of this exercise method that places emphasis on alignment, breathing and developing a strong core, which improve posture, flexibility, coordination and balance.

She became interested in how this form of exercise could also benefit

people with disabilities and neurologic disorders as her husband has lived with muscular dystrophy since childhood and several of her clients live with MS. “Pilates is a wonderful exercise option for people living with MS and others with physical challenges, as it provides a

CONGRATULATIONS!

LEFT HAND BREWING HONORED WITH NATIONAL PHILANTHROPY DAY AWARD

Chapter President Carrie Nolan and Vice President of Development Kristin Gibbs, cheer on Chris Lennert, captain of Team Left Hand’s Bike MS team at Bike MS Colorado in June.

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nice workout, but is gentle,” Gelatt emphasized.

“I have several clients who have MS and knowing how Pilates had helped them, I approached the Chapter about offering a donation-based class for people new to this form of exercise. The idea was welcomed and we offered our first class in the summer.

“We start with one-to-one private session and then individuals go into a small group class that meets one hour a week for seven weeks. The classes usually average six people, which allows for highly personalized instruction from me and two other instructors, Lisa Wolf and Katie Ross,” Gelatt continued.

To ensure that cost was not an obstacle for people interested in trying Pilates, Gelatt offered the MS class free of charge, but requested participants make a donation. “Cost for the classes can be a hardship for people already facing daily challenges, so our MS classes are donation based – people pay what they can and no amount is too small. All the donations collected from the classes are then gifted to the Society. Our first class raised more than $1,000 and was Left Hand Brewing was named the 2015 Outstanding Small Business by National Philanthropy Day Colorado.

This prestigious award is presented to a small business that has demonstrated outstanding long-term commitment to philanthropy through financial support and the creation of a corporate philanthropic culture that encourages employees and others to take leadership roles in philanthropy and community involvement.

This honor is well deserved. Left Hand Brewery is the fourth largest craft brewery in Colorado and has fostered a genuine culture of community giving since its founding. The company

so well received that we added a second class in the fall.

“Teaching Pilates is such a joy. It’s fascinating to see how certain exercises impact certain people. When people use some of the equipment, they are able to experience movement in ways they can’t in their regular daily lives.

By working on breathing techniques, correct alignment and smooth movement, Pilates participants can increase awareness of their bodies and can better control their movements, which is very gratifying, she added. n Galatt plans to continue offering MS donation-based classes on a semi-regular basis. For more information about 2016 offerings, please call 303-329-8700. strives to contribute the equivalent of one percent of its annual revenue to charitable organizations. As one of its core values, Left Hand encourages its workforce to contribute positively to the communities where they work, live and play. In 2014 alone, the company donated more than $490,000 to charitable causes and has raised $1.4 million for the Society through Bike MS! Left Hand has created a business environment where work and giving back truly coexist. Congratulations and thank you for all you do to enhance lives and communities! n

MS CONNECTION: FALL 2015

EVENTS

Annual DIY Walk Spotlights MS in Rural Wyoming Anyone affected by MS is well aware of the challenges this disease poses.

Add residing in a rural community of a sparsely populated state and its impact is compounded. Access to resources and opportunities for people with MS to get together can be limited which is why Jhon Estes started a local support group. One step further, he also heads an annual “do it yourself ’ (DIY) MS walk to keep awareness top of mind in his community, Lyman, Wyoming.

Estes, a 73-year-old veteran, was diagnosed with MS in 1995 after suddenly experiencing seizures at work. “When I was diagnosed you could have hit me with a sledgehammer,” Estes said. “At that time I didn’t have any connection to MS. Later, two of my sisters were also diagnosed, so keeping the community aware of MS is important to me.

informed of information the Society sends out. Since I’m an American Legion Commander, I was able to secure a free meeting room at the post to host a support group. Each month a few people meet, and it’s a good opportunity for people living with MS in our area to connect.

“The closest Walk MS event is more than 30 miles away from here, so several of us started our own walk in 2000, which takes place the Saturday before Father’s Day each year,” Estes said. “We usually have 2 – 7 people participate in the six-mile walk from the town hall in Lyman to the town hall in Mountain View, which takes us two days. I use a walker and another area resident, Myrtle, participates in a wheelchair. We carry signs and banners to let people know why we are walking

and on average raise between $1,200 and $1,800 each year, thanks to the support of family, friends and community members. Our group also takes part in Lyman’s Fourth of July Parade each year, which is good for community awareness. We have a fun time and it’s our way to do what we can to support finding a cure.” n

“I have computer skills so I do a newsletter and keep people in the area

Bike MS Wyoming featured mild temperatures , beautiful scenery along the northeastern Wyoming route and a lot of enthusiasm. Nearly 160 cyclists took to the road with a goal of raising $260,000. Congratulations to Leslie Osen, the ride’s top fundraiser this year!

Hike MS 2015 ATTENDANCE AND FUNDS CLIMB! Hike MS Keystone set attendance and fundraising records this year! More than 450 hikers turned out to take on the mountain July 25, raising more than $130,000. The hiking experience was enhanced thanks to a partnership with the Keystone Bike Park, which treated hikers to new mountain routes following single-track bike trails. Great food along with time to relax and bond, rounded out this annual event in Colorado’s beautiful high country.

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

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EVENTS

Parker . . . . . . . . . . . . . . . . .

ING April 16 WYOM . . . . . . . . . . . . . . . . April 30 Laramie O 0 D 3 A il Apr ne . . . . . . . . . . . . . May 7 COLOR Cheyen 0 ming . . . . .

3 . . . . . . . . . . . . . . . . il r r e Ap est Wyo Denv w h May 21 t u o . . . . . . . . ction 7 S n y u a J M d n t 10 Gra Casper . . . . . . . . . . . . . . . . . . Sep 4 1 May Pueblo . . . . . . . . . . . . . . . . . . . une 4 te . . . . . . . . . . . . . . . . . g . . . . . J lorado . . . . . . ay 14 Gillet in o C m o n r y e est W North . . . . . . M Northw Springs 1 d 2 o y o a w M Glen . . . . . . . . .

County ay 21 Boulder . . . . . . M s g in r o Sp Colorad

Keystone . . . . . . . . . . . . . .

brates ampions Cele rs Dinner of Ch rado Community Leade lo o C Northern 5 Dinner of es at the 201 raised more re o n o h e th ns to hich Congratulatio tember 11 in Loveland, w cal programs. p lo e S d s n a n h Champio fit MS researc e n e b to 0 0 ,0 ope Award than $80 ices - 2015 H nity. rv e S n o ti ta S commu urorehabili Center for Ne rm commitment to the M , e -t for their long is volunteerism h r fo n io p m Cha an - 2015 MS .

Joseph Flanig dedication to the Society d n leadership a

July 16

July 30

Colorado . . . . . . . . . . June 25-26 Wyoming . . . . . . . . August 13-14

CONGRAT ULAT IONS T O OUR 2015 T OP EVENT FUNDRAISERS Walk MS Individual Max Cohen $76,153

Top F&F Team Bunion Bunch $64,001

Top Corp Team The Clinic Colorado $94,349

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Bike MS CO Individual Tim Beaudin $203,791

Top Corp Team Left Hand Brewing $314,627

WY Individual Lesley Osen $50,650

Top F&F Team RawHinies $407,631

Hike MS

MuckFest MS

Individual Julie Brubaker $20,065

Individual Michael Pierce $13,490

Top Hike Team CUREageous Stampede $21,565

Top MuckFest Team Muckin’ for Michael’s Mom $36,836

MS CONNECTION: FALL 2015

RESEARCH

Finding Answers to Progressive MS

An Early Start

People who live with progressive multiple sclerosis have many questions, but one I hear often is, “When will there be treatment options for me?”

Based on what I saw and heard at the American Academy of Neurology’s Annual Meeting in April, I’m pleased to report that researchers from around the world are making important progress toward treatments and therapies for people living with progressive MS. Several groups presented updates on large, ongoing studies involving people living with primary-progressive MS, including: • A study of oral laquinimod, an experimental immunomodulator, in 375 people with primary-progressive MS (www.clinicaltrials.gov/ct2/ show/NCT02284568).

• A clinical trial of oral ibudilast, an anti-inflammatory enzyme, in 250 people with primary- or secondary-progressive MS (www. clinicaltrials.gov/ct2/show/ NCT01982942).

• A study of ocrelizumab, an antibody cousin of rituximab delivered by infusion, in 740 people with primary-progressive MS (www. clinicaltrials.gov/ct2/show/ NCT01194570).

No results are available yet, but some should be next year, and it’s encouraging to see that these trials are getting under way.

MS CONNECTION

While it may seem counterintuitive, scientists need to sometimes test treatments for progressive MS in people with very early signs of the disease, such as optic neuritis, an inflammation of the optic (eye) nerve that is often the first symptom of MS, before progression is even evident. They do this because the nerve damage — and if successful, the repair or protection from damage — is more easily observed in this single location.

Digging Deeper In another study, 154 people with primary- or secondary-progressive MS were given experimental MD1003 (concentrated biotin, a B vitamin), or an inactive placebo, for 48 weeks.

The results showed that 12.6 percent of those given MD1003 showed improvement in disability, versus none of those on placebo, and there were no serious safety issues reported. More research is needed to figure out who might benefit from this approach and why only 12.6 percent responded. The manufacturer, MedDay Pharma, says that another trial is underway in people with MS and results are expected later this year.

Finally, I was impressed with a study from Dr. Mika Komori and a team at the National Institute of Health that looked “behind the scenes” to try and better understand why immunemodulating treatments have not been successful in progressive forms of MS as they have been in relapsing MS. The team examined spinal fluid samples from 386 people with all types of MS, as well as people without MS, to determine the exact numbers and characteristics of various immune cells.

What they observed is that attacking immune cells in people with progressive MS were more likely to be holed up in the brain and spinal cord, whereas the cells in people with relapsing forms were mobile and circulating. What does this mean? It may be that, for treatments to succeed at modulating inflammation and/or nerve damage in progressive MS, the therapies will have to be able to track the bad cells within the central nervous system.

Everyone with MS lives with the uncertainty of whether it will progress and whether he or she will lose the ability to do the things that matter most. I’m encouraged by the research reported at the meeting and strongly believe this kind of research will drive us to find ways to stop progression and restore or repair lost function. n Dr. Douglas Landsman is Associate Vice President, Biomedical Research at the National MS Society.

Originally published at www.MSconnection.org/blog.

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13

RESEARCH

Unlocking the Mystery of Memory

compared to the other tissue samples from people of the same age. MS brains were also positive for proteins that indicate biological stress, but showed no signs of the type of complement implicated in some other diseases.

By Bruce Bebo, PhD Memory challenges occur in more than half of people with multiple sclerosis, but the details on how and why have been mysterious. Microscopic connectors, or synapses, are the point of communication between individual nerve cells, and they are critically important for all functions of the nervous system, including memory.

Some research has shown that synapses may be lost in some parts of the brain during the course of MS. Now, a study published in May in Annals of Neurology by Drs. Iliana Michailidou, Valeria Ramaglia and colleagues in The Netherlands and Germany has uncovered evidence that a group of immune system proteins, called

“complement,” may play a role in the loss of synapses in the hippocampus, a part of the brain linked to memory.

The researchers examined samples of the hippocampus from brain tissue donated by people who had primary-progressive MS or secondary-progressive MS in their lifetimes. Compared to brain tissue donated by people without neurological disease, the investigators observed a decrease in the density of synapses in the hippocampus. Two specific types of complement proteins were increased in MS tissue at the site of synapses,

The results of the study suggest a role for specific components of complement activity in synaptic loss in the hippocampus in people with MS. In light of the important role the hippocampus plays in memory, this study also suggests that complement activity may contribute to cognitive problems experienced by people with MS. If these results are confirmed and refined through additional research, it is possible that in the future, therapies that target the complement system may be useful for preventing or treating memory problems in people with MS. n Visit nationalMSsociety.org/cognition to learn more about MS-related memory issues or cognitive challenges.

STAY UP TO DATE AND LEARN MORE ABOUT MS RESEARCH. Get the news you need to live your best life. New and promising treatments, legislation affecting your life, and new programs and services to help you move your life forward.

For more information regarding research news and updates, or to learn how to contribute , Please visit nationalmssociety.org/Research or contact the MS information recource center 800-344-4867.

SUCCESSFUL NOW RESEARCH CAMPAIGN ENDS DECEMBER 31

In 2010, the Society began its unprecedented No Opportunity Wasted (NOW) campaign that set an aggressive goal of raising $250 million for research over five years, targeting three key areas stopping MS, restoring lost function and ending MS forever.

Remarkable Achievements!

As the campaign nears closure, your gifts to research have already made a significant impact: • MS treatment options are increasing

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– five new therapies were approved in the past five years; • The MS pipeline has expanded and there are now more potential treatments in clinical trials than ever before; • The promise of myelin repair is moving toward reality as three potential myelin repair treatments have entered trials; and

• Understanding causes of MS has advanced – more than 100 genetic variants have been identified and several risk factors confirmed.

Of the nearly $900 million invested in MS research by the Society since 1946, the NOW campaign has generated more than 25 percent of that total. The campaign concludes December 31, 2015 and we need your support NOW to ensure the campaign goal is met and efforts that are delivering results continue. Make a year-end research gift as part of your holiday plans and be part of the bonding force that is fueling a future free of MS! To donate, visit curemsco-wy.org. n

MS CONNECTION: FALL 2015

OF NOTE SHOWING MUSCLE BUILDS STRENGTH AND MS AWARENESS Lori Wilson was just 29 years old in 1995 when she was diagnosed with MS.

started intense weight training, cardio exercises and a diet program in April.

Six days a week for more than an hour daily she prepared for the National Physique Committee’s “Battle at the Border” competition held in Grand

Through the years she took advantage of MS treatments available and was able to maintain an active lifestyle, but an episode that left the right side of her body and face numb spurred her to think about what else she could do. “I knew I didn’t want to use a cane or be in a wheelchair,” she said.

When she and her husband Rodney moved to Grand Junction several years ago, they found themselves living close to a gym. The couple had never joined a fitness center before, but something clicked this spring and Wilson, now 48, decided it was time to take charge and get fit. “I wanted to do whatever I could to strengthen my body and maintain my health, so I participated in a 12-week gym challenge. I liked the transformation and experience so much that I set a new goal – to compete in a bodybuilding contest,” she said.

With her husband at her side, and working with a personal trainer, she

It's National Caregiver Month!

THANK YOU

This month, take the time to thank the caregivers you know for the physical, emotional, spiritual, financial and/or logistical support they provide to the sick, elderly, and disabled friends and relatives. According the Department of Health and Human Services, family caregivers provide estimated $450 billion worth of uncompensated care to love ones annually.

Chapter care managers are available to help! If you live with MS, or care for a

Colorado and Utah who filled Grand Junction High School’s auditorium.

“It was an amazing day and I wasn’t nervous at all. I had a good time when I was on stage doing the mandatory poses for the judges,” Wilson said. At the conclusion of the day, all her hard work paid off. She not only met her goal of competing, but also took first place in her division.

“I’m still in awe and I accomplished more than I ever thought I would be able to do. When the head of the competition handed me the trophy, he shared with the audience that I had MS and I received a standing ovation. It was amazing.”

Junction on September 5. As she prepared, she experienced the benefits of her fortitude - she had fewer episodes of numbness, less fatigue and better balance.

The day of the competition she was ready. Barefoot and wearing the specific bathing suit required, she competed in the Women’s Physique True Novice category in front of judges and an audience of hundreds from across

Perhaps more important to Wilson, her accomplishment is having a residual impact. “People in the community learned that I had MS from publicity surrounding the event. I work full time at a local credit union and the week following the competition, I had a call at work from a member whose future daughter-in-law might have been diagnosed with MS and she wanted to talk with me about it. Getting the word out is so important. I want to help and inspire others, and if that’s what I accomplished, it’s wonderful.” n

loved one or friend with MS, and find yourself overwhelmed by decisions, help is just a phone call away. Chapter Care Managers are available to provide guidance, support and solutions that can make your life easier!

Our Care Manages are: • Specially trained to help you apply for Medicaid, social security and disability benefits • Certified Application Counselors who can review options and answer questions related to the Affordable Care Act and other health insurance plans • Able to connect you to resources ranging from cooling vests to home modifications and mobility equipment

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

• Able to guide you on work-related issues and much more. n

To learn more or to set an appointment with a Chapter Care Manager, call LeeAnn Bellum, Care Management Director, at 303-698-5407.

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GIVING

MEMBERS

N AT I O N A L M S S O C I

A SPECIAL THANK YOU

to our Golden Circle Members who donated $1,389,383 in FY2015. Golden Circle members are individuals who give a one-time gift of $1,000 or more annually. For more information about becoming a member visit:

Ron and Lori Abramson Roger Ackerman Christina Alderfer The Alfano Family Scott Stallard and Marlu Allan Dr. Brooke Allen Michael Allgood Casey Amidon Ray Anderson and Nancy Speer Seth Anderson Liz Armstrong Sandra Arnold Thomas August Gary and Sandy Autrey Herb and Laura May Bacon, Bacon Family Foundation Erin and Erik Bailey E Dorris T Y Baker Mavis Bakken Mary Balliet Crista Barlow Dr. Daniel and Kimi Barry Dr. Frank Barry Jim and Sue Bartlett Raymond and Mary Lou Barton Patricia Batchelor Ruth Benton Alex Berger Carl and Meghan Berglind Jim Berguson Gary and Carol Berman The Bermant Family John Biggers Casey and Leslie Bishop Cheryl Bivona Tim Blach Merida and Robert Blackwell La Verne Blecha John and Carolyn Bliley Katie and Daniel Bloomenthal Dee Blue Timothy and Leanna Boers Catherine Boggs Jordan Bonicelli Dean and Karen Borgman Neal Botie John and Vicki Box

Colin Breetz Virginia Brey Barbara Brischke Cory Brown Sherry Brown Frederick and Sharon Brubaker Stephen Bryan Gordon Buchan James Burke Susan Burke Cheryl Cain Jim Caldwell Patrick and Nicole Callahan Jack and Meredith Callison April Carlton Dr. Jeffrey and Lynne Carlton Kevin Cartin Dave and Nicole Cecil Kurt Cellar John Cheney Adam and Emily Chereck Robert and Donna Chereck Brad Cherry Phil Childs The Chrisman Family Shawne Cihak Phillip and Marje Clark Virginia Classon Joanne Clayton Frank Cohen Richard and Marsha Cole Jacquelyn Anne Coles John William Collins Estate of Ruth Combs Marycatherine Comeau Mona Comeau Virginia Conwick Bart Cooper Elfriede and Gary Cooper Travis and Lindsey Cooper Darden Coors Henry Coors Corbin West Family Foundation Dr. John and Alix Corboy Brian Corcoran Jacqueline Cotshott Brian Cox

nationalMSsociety.org/goldencircle or contact sophia.conti@nmss.org 16

MS CONNECTION: FALL 2015

GIVING Dr. Carl Craig Peter Curnyn Claudia Curry Hill Charlene Curtis Glenn and Cecilia Curtis David and Virginia Cyganiak Janet Czachura Carolyn Daigre Carol and Rene Daigre Jr. Rivet Daigre Richard Dailey Cindy Dalton James and Jackie Davis Sarah Curry Davis David Denman Dr. Doug and Debbie Dennis Helen Dickens Katharine Dickson Kim and Christy Dittmar Christopher Dobbins Chris and Mary Doerr Deane Dolben Judee Donner Jean Dorans Elizabeth Douglass Andrew Doyle Andrew Dudiak Diane Duplissis Samantha Dwyer Susan Dyke Lyle Armen Eastham Bob and Margaret Eddy Stan and Carol Eilers Philip and Deborah Eisenhart Mike and Michelle Elings Dean Elliott Jack Emerson Bryson and Rylee Engel Brian England Alan and Linda Englander Doug Fairless Tom and Janet Falconer George and Carolyn Fancher Brian and Wendy Farley Andy and Chrissy Fedorowicz David Feese The Figge Family Kevin and Susan Fink Patrick Finney Marilyn Firstenberg Carl Fitch

Frances W. Burton Foundation Julie and Scott Forsyth Anne Foster and Kurt Duldner Mark and Nancy Foster Angela Fox Taryn Frenzel John Freyer Sr. Donald Fritschie Kristin Froehlich Fuller Family Fund Dustin Fulton Timothy Gablehouse Jason Gaedtke John and Barbara Galeotos Charles and Diane Gallagher Miss Teri Gallimore Roy Gamble Mary Gantz Gary Garcia John and Martha Gart Laura Gentry Sherry Gibson Tamara Gillespie Patrick Gilliland Darlene Gilson Mark Giordano Estate of Marianne Gjelsteen Jennifer and Jim Glennon Gary Goldberg Ellen Golden Peggy Goldman Joseph Goldstein Sheryl and Jon Goodman Richard Gorton Estate of Brian Grams Laura Granier Andrea Grant Jonathan Gray Gary Clark and Bettie Greenberg Caithlin Grimes and Deirdre Dwyer The Gustafson Family Bradley and Melissa Gustafson H. Fort Flowers Foundation Estate of Emmet W. Haas Nick and Anne Hackstock Arlene Ham Laurel Hammer Eric and Heather Hammond Chris Hansen Melody Hardy Anne Harrill

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

Denise and Hugh Harrington Rob and Melissa Hartnett Jeffrey Harvey Kevin Hatcher Todd and Marie Hauer The Hennessey Family Kathleen Henry Mike and Linda Hensal Teri Hernandez Joshua Herrenkohl James Hertwig Tad Herz Tom Herzog Chad Hester Sarah Higgins Donna Hill Kathleen and Heath Hill Daniel Hillen Sarah and Eric Hilty Mary and Owen Hobson Marley and Jennifer Hodgson Nancy Holden Ralph Holden Dirk Howell Dr. Eric Hoyer David and Jill Hughes Dave and Margie Hunter Mike and Kaye Hurtt Barbara and Roberto Iglesias The Irvin Family Doak and Connie Jacoway Brad and Carol James Michael and Twila Jenkins Richard Jenkins Darrin Johnson Michael Johnston Michele Johnston The Jones Family Keith Jones Donald Jump Craig and Cheryl Kane Joseph Kasputys Edward and Diane Keely Stephen and Kim Keen Robin and Richard Kelly Andrea and Michael Kennedy Robert Kessler Michael and Elizabeth King Marie Kinnard Neil Klein Kenneth Kline

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GIVING Dalton and Elaine Knauss Brad and Carin Knickel Buz and Sherri Koelbel Robert Kolbe Dr. Gloria and Mike Komppa Joseph Kopchik Margaret Kopchik Estate of Howard Kopet Robert Kornahrens The Kotlarczyk Family DeeAnna and Edwin Kraft Matt Kramer Robyn Krampitz James Kreitman The Krivel Family Craig Kruckeberg Thomas Kujawski LP Brown Foundation Jennifer Land Jack Landon Tommy and Pamela Lane John and Judith Lanning Elsie Larson Nancy Law Patricia Lechler Left Hand Foundation Tanya Leeper Donald Leforge Beth and Jason Leleck Chari Leleck Ryan Lepro Dr. Stuart and Arlene Lerman The Levengood Family Michael Linderman Nathan Lipke Cynthia Little The Locke Family David Lord Klaus Lorenz Carl Norgren Chester Luby The Lux Family Albert Wilson Lyle II The Lynch Family Carolyn Lyons Dr. Wendy B. Macklin Jerad Madeo Lisa Madigan Mark Maguire Dave Maheu The Markisohn Family

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Stephen and Courtney Marsters Marusi Family Foundation Leonard and Sylvia Marx Mark and Valerie Mashburn Thomas Massalone Brant Massman Chad McAllaster Yvonne and Bill McCallum Beth Ellyn McClendon Dr. Logan McDaneld Matthew McGee Daniel and Jean McKee Dr. Mark and Jennifer McKenna Teresa McKenzie Alex McLean Michael McRoberts Jackie Meadows Luke Meadows Ken Melies Janell Mellish Anne and Thomas Merrill Keith and Susan Metcalf Tammy Meunier David Middleton Carol Miller Douglas Miller Gary Keith and Ellen Miller Tom Miller Carl Minnig Chad Mitchiner Albert Mitterer Daniel Myers and Gretchen Mitterer Jim and Ellie Mohler Kristi Mollis Melissa Morelli Axson and Bryan Morgan Roger and Elaine Morin Bill and Margie Moskoff Christopher Moskoff Russell and Sandra Mowrer Dean Mueller Mark Muhich The Honorable Mary Mullarkey and Rev. Tom Korson The Mullen Family Gregory Mutz Jill and David Myers Marilyn Nadeau Charles Nail Jr. Marcia Naiman William and Rita Neff

Carl Nelson Andrew Newberry David and Katie Nichols Rodney Nielsen Paul Niemann Rylee Niesent Carrie Nolan John Norm Rhanda Nusbaum Kyle and Sarah Ocasek Tracy Olson Steffi and Patrick O'Malley Deborah and Shawn O'Neil Philip Orda Leah Orlinski David Ottewell Robert Overton Ruth Owens Phillip and Margaret Parrott Fred and Karen Pasternack Charles Paul Carrie Paulson Christopher Mark Pearson Lindsey Pederson Steve Penn Kerry and Bill Penney Sarah and Zach Pennington Gary and Sue Perkins LaNee Perkins Patricia Petersen Bob D. Peterson Bob Peterson The Peterson Family Jean and Peter Petrillo Catherine Pharis Phillip H. Corboy Foundation Marjorie Phye D L Pickering Lynne Pickett Ralph Pickett Michael and Paula Pierce Mary Porter Redneck Porter Jim and Karen Possehl Jennifer Quigley Jane Quinette Albert Rabil III Ralph C. and Joyce L. Vossler Fund Ron and Kim Ranes Dahna Raugh Beth Rauh MS CONNECTION: FALL 2015

GIVING Patricia Rawlings Dick and Jane Raymond Dr. Doug Rea Marion Reeder Molly Rehrig Mary and Ryan Rhinehart Tina Richardson Rusty Riggs Pam Ritchey Jenny Roberts Kevin Roberts PJ Robinson Phyllis Robsham Rachel Rodawig Arthur Rodecker Timothy Romani David Rosenblum Angela Ross Randi Ross Elizabeth and Rick Rossa Michael Rothschild Donna and Joseph Routzon Tara Ruberg Steven Saba Estate of Vernon Sachs Jennifer Sales and Greg Lyon Dale Sand Gary Sanders Ann Sandquist Paul Sandquist Matthew and Kimberly Sands Raymond Satter J. and Mary Sawyer Christiane Schild Susan Schmetzer Shauna and Dan Schmitz Andrea and Nicholas Schommer Mark Schouten Thom and Joani Schultz Bethany and Wayne Schultz Tim Schulz Annetta and Roy Schwalm Mark Schwarz Tory See Jeffrey Sepich Dr. William and Kristi Shaffer Robert and Mary Shanahan Robert Shaw Chris Sheehan Marie and Collin Sherick Carolyn Shogrin

Jason and Austin Sibley Benjamin Sieber Toma and Betsy Sinclair William Skewes II David and Andrea Sloan Christopher Smith Jeffrey Smith Sid and Billie Busby Smith Larry and Brenda Smith Minyoung Sohn Michelle and Mark Solari Carol and George Solich Bernadette Spille Katy and Marc Spritzer Jonah and Kathy Staller Dr. Douglas States Robert Steel Elena Stefanopoulos Leonard and Angela Stegman Jan and Bob Steiert Kathy Stein William Stein Louise Steinhauer Lynette and Bradley Steininger Coy and Catherine Stewart Gary and Teresa Stewart Margaret Stockover Katherine Straus Robert and Celia Stretmater Clarence and Emily Stump The Sullivan Family John Svoboda Sara Swalnick The Swanson Family Foundation Glenna Swanson Lloyd and Nancy Sweet Linn Syz TWC Foundation Inc. Douglas Tashiro The Carter Chapman Shreve Family Foundation The Chrysalis Fund The Darlene M. and Reuben T. Swanson Foundation The John and Kathleen Schrieber Foundation The Ozmen Family Foundation The Phyllis M. Coors Foundation The Rifkin Foundation The Rosemary & David Olsen Foundation

cureMSco-wy.org 1-800-FIGHT-MS (344-4867)

The Ryan Foundation The Toney Family Foundation David and Susan Thomas Peter Tilley Thomas Toomey Tim Travis Timothy Travis Bill and Sarah Trimarco Tim Trumble Bill Turner Amy and Joel Vaccher Grant van Rooyen Rich VanDewater Dr. Thomas and Cindy Voelker Joseph and Linda Vumbaco Kay Wagner Adam Wahl Bill and Midge Wallace William Walsh Molly Walters Adam Warner James Warren Thomas and Susan Washing Robert and Kay Watson Barbara and David Weaver Dave and Susie Wehrfritz Suellen and Travis White Kevin Yoder and Bekkey Wiebe Brandt Wilkins and David Alexander Tad Willenbrock William C. Kuzell Foundation M.A. and Carrie Williams Jo Wilson Hubchik Pat Wischmann Polly and John Wojnaroski Karen Woods Frederick Woodward John Woollam Keith Worfolk Dr. Janet and Arthur Worrall Chuck Wright Sybil and Shelby Yastrow Eric Yen Kevin Yoder and Bekkey Wiebe Barbara Zaneri Donald Zimmerman Michael Zimmerman

THANK YOU to our many anonymous Golden Circle donors!

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24 HOURS

TO GIVE WHERE YOU LIVE. Colorado Gives Day is Tuesday, December 8 this year!

Join your neighbors on this special day of giving.

Mark your calendar to support the National MS Society Colorado-Wyoming Chapter

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