winter 2011 ms connection

Championing the CauseWinter 2011

MS Snowmobile TourPowers the Movement

Special Message from the Chapter President

If you or someone you know has MS: Studies show that early and ongoing treatment with an FDA-approved 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 MS Society at nationalmssociety.org or 1-800-344-4867 to learn about ways to help manage multiple sclerosis and about current research that may one day reveal a cure. The National MS Society does not endorse products, services or manufacturers. Such names appear here solely because they are considered valuable information. The National MS Society assumes no liability for the use of contents of any product or service mentioned. Information provided by the Society is based upon professional advice, published, experience and expert opinion. Information provided in response to questions does not constitute therapeutic recommendations or prescriptions. The National MS Society recommends that all questions and information be discussed with a personal physician. The National MS Society is committed to seeing a world free of MS.

©2012 National Multiple Sclerosis Society-Wisconsin Chapter

2 JOIN THE MOVEMENT: wisMS.org MS CONNECTION: Winter 2011

Kenneth Minor, ChairSonic Foundry, Inc.

Michael Lutze, Vice ChairErnst & Young David Rodgers, Vice ChairBriggs & Stratton Corporation

Alyson Zierdt, Past ChairAttorney, Retired

James Rose, TreasurerBaker Tilly Virchow Krause LLP

Robert Sowinski, SecretaryDiversified Insurance Services, Inc.

Colleen Kalt, President & CEONational MS Society - Wisconsin Chapter

Robert Buhler Open Pantry Food Marts of Wisconsin, Inc

Dennis ChristiansenCommunity Advocate Robert EngelRetired, M&I Bank

Tom GoldenM3 Insurance Solutions for Business

Martin McLaughlinReinhart Boerner Van Deuren, S.C. Bruce OlsonThe Marcus Corporation Shelley Peterman SchwarzMeeting Life’s Challenges

David RaysichPlunkett Raysich Architects

Patricia RaysichCommunity Advocate

Jeffrey SterenSteren Management/McDonald’s

Robyn TurtenwaldCommunity Advocate

Molly WalshWaisman Center

Wisconsin Board of TrusteesNational Multiple Sclerosis Society

Wisconsin Chapter

Tuesday, December 6

AnnuAl Meeting

the Wisconsin Chapter’s Annual Meeting is scheduled for tuesday, December 6 from 6-8 p.m. at the Chapter offices, 1120 James Drive in Hartland. the Annual Meeting is held for the purpose of electing a Board of trustees, reviewing the treasurer’s report and considering other appropriate business and reports that may be presented. individuals can submit names to the Chapter’s governance Committee for consideration for Board of trustees membership by contacting Melissa Palfery at 262-369-4419 or [email protected].

the event is open to the public. Reservations are required. For more details or to R.S.V.P. by December 1, please call (800) 242-3358.

Separate recognition events for fundraisers and volunteers are currently being planned. Watch for more information as it becomes available.

3tOll FRee nuMBeR 1 800 242 3358

How Will You Champion the Movement? Each of us contributes to this Movement to end MS in our own way. In doing so, we each share a connection. We each become a champion for the cause. We each embrace our ability to lead the way. Father Charlie Brooks, featured on the cover of this magazine and profiled beginning on page 12, has been leading the way for more than 20 years. He’s a familiar face on the annual MS Snowmobile Tour. He has donated to the Scholarship program. He has named the Society in his will. He has made a decades-long commitment in honor and memory of a sister who lived with MS for most of her adult life. He does it all – riding the trails to raise awareness, writing letters to raise funds, remembering the National Multiple Sclerosis Society in his estate planning – in ways that are personally meaningful to him. He does it in his own way … just like you. Regardless of what you can give to the Movement at this moment – whether it’s time, talent or treasure – it makes a difference. Whether it’s riding a bike, writing a check or volunteering with a do-it-yourself fundraiser, your efforts propel this movement forward. Where will they take us? Where will we be a year from now? What will have been discovered and what will have been improved? None of us can say, but that doesn’t stop us from trying. If we’ve come this far together, imagine how much farther we can go. If you start recruiting for your Walk MS team now, begin training for Bike MS: Best Dam Bike Ride one month earlier, or add a few dollars more when you make your annual personal contribution, how much faster will we get to our ultimate goal – a world free of MS?

Father Brooks has brought a lot to the Movement and been a leader in what we’ve accomplished so far. So have others you’ll read about in this magazine – people like Dr. Douglas Woo, Nina Slowik and the 217 Challenge Walk MS participants who made the 4th anniversary event a record-setting success.

Who will be the next leaders moving forward? As we approach the end of the year, we hope you will be inspired to take action in your own way to help fund further research for a cure, address the needs of those diagnosed, and attract more promising bright minds dedicated to serving those affected by MS.

Thank you for moving us forward.

Sincerely,

Colleen G. KaltPresident & CEO

We all share this connection. We are all champions for the cause. We all have the capacity to lead the way. - Colleen Kalt

Chapter President & CEO Colleen Kalt with Father Charlie Brooks, a champion of the Movement.

4 JOIN THE MOVEMENT: wisMS.org

College is a fresh start, a chance to grow ones skills, develop new talents and fulfill lifelong dreams. For those living with multiple sclerosis, it’s an opportunity that’s too often sacrificed as families are forced to accommodate the disease that has intruded on their lives. The compounding costs of lost wages, expensive drugs and medical care can leave little to cover additional expenses like college tuition.

The National Multiple Sclerosis Society’s scholarship program was created to help offset those expenses and fill a void in scholarship assistance for those diagnosed with multiple sclerosis and their families. Launched in 2004, the program has since provided $1 million in scholarships to 639 students nationwide. In Wisconsin, 190 students have been funded through awards totaling $265,000. In addition to scholarships at the Chapter level, recipients are eligible to be named Top Scholars by the National Multiple Sclerosis Society. Wisconsin’s Rebecca LeBeau was one of 17 students selected from across the U.S. in 2011, joining an elite group of five other Top Scholars from Wisconsin in the past eight years. With the Top Scholar designation comes additional funding that LeBeau will use along with the T. Ferguson Locke MS Scholarship from the Wisconsin Chapter to help fund her studies.

Your gift can help the class of 2012 The scholarship program is only possible because of individuals and foundations that recognize the value of a college education, particularly for those touched by MS. With the cost of tuition at a public four-year

college averaging more than $8,000 per year, and without the assistance of programs like the Wisconsin Chapter MS Scholarship Program, even more young adults affected by MS would need to defer or entirely forego their dream of a college education. Given the increased financial pressures families today are facing, the Wisconsin Chapter again expects to receive more applications in 2012 than it will be able to fulfill.

Donations to the program will help offset the costs these deserving students face, and could help ensure that even more young adults affected by

MS can afford to further their education. To contribute to the future of the promising young minds who have been touched by MS in some way, contact Denise Jendusa at 262-369-7166 or [email protected].

Bright MindsScholarship Program is an Investment in Growth

ForJennaWolfsohn,theNationalMultipleSclerosisSociety’sScholarshipProgramcreatedsomethingpositiveforherfamilyfollowinghermother’s2009diagnosis. AsophomoreatHartland’sArrowheadHighSchoolwhenhermomwasdiagnosed,Wolfsohnfounditdifficulttoconcentrateonherschoolwork,wantinginsteadtohelphermomandenjoyhercompanywhileshewasstill“themobileandwonderfulwomanI’llalwaysholdinmyheart.”Redoublinghereffortsandfocusingonherschoolwork,Wolfsohnwentontoperforminnumeroustheatreproductions,runCrossCountryandgraduateinthetopfivepercentofherclasswithhighhonorsinsixadvanced-levelcourses.Shealsofoundtimetovolunteerwithanumberoforganizations

One Scholar’s Story

After college, I hope to be working at a job that I enjoy and can put my math and science skills to work. - Katherine Hager, 2011 scholarship recipient


The MS Scholarship Program is designed to open doors for young adults affected by MS who have demonstrated strong leadership potential, academic excellence and financial need by ensuring the financial impact of MS doesn’t stand in their way of achieving a college education.

Applications are being accepted through January 13, 2012.

To qualify, applicants must: • Beahighschoolseniororhighschool(orGED) graduate. • Haveaparentwhohasmultiplesclerosisorhave MS themselves. • Beattendinganaccreditedpostsecondaryschool for the first time. • BearesidentofWisconsin.

Applications are processed by the ACT national nonprofit organization before being sent to the Wisconsin Chapter for further review by the MS Scholarship committee. Comprised of leadership

volunteers, the committee provides guidance on the program, selects scholars, determines award amounts,

engages and mentors past scholars, and provides financial support through donor cultivation. Applications are currently available through the Wisconsin Chapter website, wisMS.org. They must be completed and submitted electronically no later than January 13, 2012. To learn more, contact Dawn Thaves at 262-369-4403 or [email protected].

AcademicperformanceandpotentialLeadershipandparticipationinschoolor communityactivitiesWorkexperienceStatementofeducationalandcareeraspirationsCompellingpersonalorfamilycircumstancesFinancialneedAnessayontheimpactofMSontheapplicant’slifeAnoutsideappraisal

Scholars are selected on the basis of:

includingtheNationalMSSociety,goingsofarastoorganizeaHoopsforHopebasketballtournamentthatraisedmorethan$7,000. NowafreshmanattheUniversityofSouthernCalifornia,WolfsohnisdoublemajoringinBiologyandEnglishintheBaccalaureateMedicalProgramthanksinparttothescholarshipshereceived. “Thisprogramtooksuchanegativeaspectofourlivesandturneditintoanopportunitytomoreeasilyfundmyundergraduateeducationandmydreamofbecomingadoctor,”sheexplained.“WeallhavehadtheunfortunatesituationofhavingMSafflictsomeoneinourfamily,buttheprogram’ssupportremindsusthatpeoplearewatchingoutforusandthatwecanpursueoureducationalgoals.”

Jenna Wolfsohn

Bright FutureApplications Being Accepted for 2012 Scholarship Awards


MS Clinic at Froedtert & the Medical College of WisconsinDr. Douglas Woo Leads MS Clinic with a Focus on the Future

Dr. Douglas Woo, who at age 37 is the youngest member of the Wisconsin Chapter Clinic Advisory Committee(CAC),isanassistantprofessorofneurologyand the director of the residency program in the Department of Neurology at Froedtert & the Medical College of Wisconsin. OriginallyfromHawaii(alsothebirthplaceoffellowCACmemberDr.JohnFleming),Dr.Woocame to Wisconsin to do his undergraduate program at

Marquette University before going to medical school at the Medical College of Wisconsin. After he completed a clinical fellowship in multiple sclerosis, he returned to Froedtert & the Medical College of Wisconsin, where he has worked since the summer of 2006. Patients with MS make up about 75 percent of his practice. “I like working with the people I have as patients,” he said. “The field in multiple sclerosis is very innovative, with a lot of new things coming on.” The Multiple Sclerosis Clinic at Froedtert & the Medical College of Wisconsin is one of six National MS Society Affiliated Centers for Comprehensive Care in Wisconsin. It offers multiple programs to help those with MS, including a spasticity clinic, neurology clinic and other areas of specialty. “We do a range of treatments,” Dr. Woo said. The clinic offers physical, occupational and speech therapists. Psychiatric care is also available. “Even with MS, you can still live well through thinking well,” Dr. Woo explained.

“I think the most important thing for each patient is making sure their individual needs are met,” he said. “Each patient is different. They are not a cookie cutter. You have to get to know each individual’s needs. “I think our relationship with the National MS Society gives us the ability to tap into resources we wouldn’t have otherwise,” he added. “There’s literature, networking abilities and the fellowships which are important for increasing the number of MS physicians.”

The National MS Society fellowship program brings young investigators and doctors into the field of MS. In fact, Dr. Woo took part in the MS Clinical Fellowship Program at the University of Texas Southwestern

Medical Center in 2005 and 2006. He returned to the Medical College of Wisconsin after his fellowship to be the program director of the residency program, training up-and-coming neurologists. He has a comprehensive approach to education with a program that includes exposure to a range of conditions, including multiple sclerosis.

He said, “It’s important that neurologists learn as much about MS before they go into their general practice.” According to Dr. Woo, physicians at the Froedtert & Medical College of Wisconsin Multiple Sclerosis Clinic are involved in a wide range of research in addition to patient

care. That includes Dr. Woo, who is collaborating on a project with Marquette University looking at fatigue in MS. Alexander Ng, whose previous research has been supported by the National MS Society, is also a principal investigator on that study.

The most important thing for each patient is making sure their individual needs are met. - Dr. Woo

Dr. Douglas Woo (left) is a member of the Clinic Advisory Committee along with (from left to right) Drs. Loren Rolak, Bhupendra Khatri, John Fleming and Stanya Smith. Not pictured: Drs. Eric Maas and Merle Teetzen.


Disability BenefitsWhat to Do If You’re Asked to Take a Consultative Exam By Attorney Thomas E. Bush

A claimant for disability benefits from the Social SecurityAdministration(SSA)maybeaskedtoattendaconsultative examination by a doctor who has a contract with SSA to perform such examinations. If you get a notice to attend a consultative examination, you should go to the appointment and participate fully in the examination. Do your best on any tests administered. Answer the doctor’s questions truthfully, neither exaggerating nor minimizing your physical or mental problems. Usually a consultative examination is scheduled simply because the disability examiner does not have enough information to decide the case. Perhaps a claimant with MS mentioned depression or some other

mental impairment as part of the reason the claimant cannot work but has never been treated by a mental health professional. Thus, a psychological consultative examination may be scheduled. In Wisconsin, consultative examinations are usually scheduled because the disability examiner wants to do a thorough job. They are not scheduled because the disability examiner is looking for reasons to deny the claim. If your MS is treated by a reputable neurologist, SSA likely will rely on examination findings in your neurologist’s records. It is so unlikely that SSA would schedule a physical consultative examination when it has your neurologist’s records, if you get a notice that one is scheduled it might be worthwhile to telephone the disability examiner to inquire if there has been a mix-up. The answer could be that they have been unable to get your neurologist’s records, that the records are unreadable, or that your doctor has not done

a thorough examination recently. You can ask to be allowed to resolve these problems instead of attending a consultative examination. You can get the records. You can ask your doctor’s staff to transcribe the records. You can ask your doctor if he or she is willing to perform a consultativeexaminationforthe(relativelylow)feepaidby SSA for such examinations. Under an SSA regulation that is seldom applied, if your doctor is “qualified, equipped and willing” to perform the examination, your doctor is the “preferred choice” for doing an SSA consultative examination. At your request, the disability examiner will reschedule the consultative examination with your own doctor. Your doctor likely brings to the examination a lot more information about your impairment than a consultative examiner can glean from records.

Tom Bush is the preeminent expert on SSDI in Southeast Wisconsin. A Wisconsin Chapter volunteer for 20 years, he was inducted into the National MS Society’s Volunteer Hall of Fame in 2008. Tom’s website is www.tebush.com.

Wisconsin’s Tom Bush shares SSDI expertise gleaned over 20 years.

In Wisconsin, consultative examinations are usually scheduled because the disability examiner wants to do a thorough job. They are not scheduled because the disability examiner is looking for reasons to deny the claim.

Under an SSA regulation that is seldom applied, if your doctor is “qualified, equipped and willing” to perform the examination, your doctor is the “preferred choice” for doing an SSA consultative examination.


Matching Gift ProgramsYour Employer Could Double or Triple Your Donation

The impact of Matching Gifts in 2011

Nina Slowik has been raising money for the Movement for the past 10 years, riding in Bike MS: Best Dam Bike Ride in support of a co-worker’s wife who was diagnosed with multiple sclerosis. A dispatcher at Rexnord, the leading worldwide power transmission and water management product manufacturer headquartered in Milwaukee, Slowik has utilized the company’s matching gift program each year to grow the size of her donations. “I saw it as a good opportunity to increase

my fundraising,” she said of tapping into the company-sponsored resource. “It helped me raise more money for the people that are affected by this dreaded disease and made more money available for research.” The process, she adds, wasn’t difficult. “With minimal effort you’re able to increase your donations.”

While guidelines vary by company, the results of employer-sponsored matching gift programs are the same: more money that moves Wisconsin toward a world free of MS and supports the services that help those who have been diagnosed. While not all organizations offer such a benefit, those that do often match dollar-for-dollar what their employees donate; some double or triple it. Check with your human resources department or visit the Chapter’s Donations page at wisMS.org and usetheMatchingGiftSearchTool(locatedundertheMatchingGiftsheadline)tofindoutifyourcompany

has a program. If it does, be sure to find out how the matching gift request needs to be submitted. Contact the Wisconsin Chapter at [email protected] or 1-800-242-3358 for more information.

131companiesmatchedgifts

totheNationalMultipleSclerosisSociety-WisconsinChapter

*All numbers reflect totals for fiscal year 2011.

394MatchingGiftswerereceived

130,000inMatchingGiftdollarsweredonated

Morethan

I saw it as a good opportunity to increase my fundraising. It helped me raise more money for the people that are affected by this dreaded disease and made more money available for research. - Nina Slowik

Nina Slowik uses her employer’s matching gift program every year.


Income Tax Donation ProgramWhat’s Raised in Wisconsin Stays in Wisconsin

In 2005, committed volunteers helped the Wisconsin Chapter successfully lobby Madison to include a check-off option on the state’s annual income tax forms allowing residents to make a donation to MS. The benefit to Wisconsinites affected by MS was dramatic with nearly $85,000 raised that first year alone. By donating specifically through the Make a Mark for MS program:

• 100%ofthemoneystaysinWisconsin. • Thegiftremainsanonymous. • You’llhelpdirectlysupporttheneedsofthose with MS in our state.

Funds that come from Make a Mark for MS are used to help those who have the disease cover the cost of

programs, services or equipment that aids in mobility and maintained independence. These could include the installation

of a wheelchair lift that would allow the mother of five to continue driving the family mini-van to work and school, or allowing a grandmother to watch her grandson play soccer for the first time thanks to a scooter purchase. With the average annual cost of MS estimated to be nearly $70,000 per person in medical-related expenses and lost wages, it’s easy to see why the funds provided through Make a Mark are so important. Last year 90 people were helped.

Although more than $425,000 has been raised through Make a Mark since it first appeared on Wisconsin income tax forms, the annual amounts have

been decreasing year-to-year due in part to economic conditions. You can help reverse that by making your own tax check-off donation and letting family, friends, neighbors and your tax professional know what earmarking an income tax donation for MS can do.

Make Tax

Donation

for MS

14 Donations (decreases refund or increases amount owed)

a Endangered resources f Firefighters memorial

b Packers football stadium g Prostate cancer research

c Breast cancer research h Military family relief

d Veterans trust fund i Feeding America

e Multiple sclerosis j Red Cross WI Disaster Relief

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A donation area similar to this will be on 2011 state tax forms. All dollars designated for MS stay in Wisconsin.

Make a Mark for MS

How you can help: • Whenit’stimetocompleteyourstateincome taxes,findthedonationslineandenterthe amountyouwouldliketodonatetomultiple sclerosis. • Tellyourfamily,friends,neighbors,co-workers, Facebookfriendsandanyoneelseyoucanthink ofabouttheMakeaMarkforMSincometax donationprogram.Lettingthemknowyouhave aconnectiontoMSmayencouragecontributions. • Askyouraccountantortaxpreparerifyoucan provideinformationaboutMSforthemtoshare withtheirclients. • Askyouremployertodisplayinformationto promotetheMakeaMarkforMSprogram. (Aposterandflyerareavailableonthe WisconsinChapterwebsite,wisMS.org.) • PlaceanoticeabouttheMakeaMarkforMS programinthebulletin,newsletterorwebsiteof yourplaceofworship.


Break Out Your Dancing ShoesNew Event Would Blend Movement, Music and Fun

Tax Deductions Beyond Medicine

Hines Ward. Buzz Aldrin. Wendy Williams. Mike “The Situation” Sorrentino. If these and other famous “Dancing With the Stars” contestants have demonstrated anything, it’s that no one can deny the growing popularity of—and diverse participation in—ballroom dancing. But not only is it a fun social event, it’s good exercise. “There are a lot of potential benefits for people with multiple sclerosis,” said Alexander Ng, an associate professor at Marquette University in Exercise Sciences who studies fatigue in MS and has previously been funded by the National Multiple Sclerosis Society. After hearing about studies on ballroom dancing for people with Parkinson’s disease, Ng thought it might have potential for people with MS. That’s the idea behind “Ballroom Dance for MS,” an informal event designed to be fun, get people moving and help gauge the potential for future dance-specific training or intervention study. Led by Ng and his colleague, Pamela Landin, a fellow exercise physiologist at Marquette University and

professional dance instructor, the event is tentatively being planned for early 2012. More details will be made available as they are finalized. In the meantime, anyone interested in volunteering to help with or take part in the event should contact Meghan Schnabl at 262-369-4420 or [email protected].

ManyoftheexpensesassociatedwithmanagingMSmightbetaxdeductible,beyondmedicines.(Keepinmindthatonlyunreimbursedmedicalexpensesthatexceed7.5%ofyouradjustedgrossincomearedeductible.)Hereareadditional possibilities:

• Equipment and extras,suchasservicedogs(anddogfood!)andtransportationtodoctorappointmentsviacar service or taxi if you can no longer drive. • Home modifications that don’t increase a home’s value. “Get a doctor’s prescription for ramps, wider doorways, grab bars, even a swimming pool, as well as a letter from a real estate agent stating that these changes don’t make your home more valuable,” suggests Anne Davis, program director of Legal Services for the Society’s New York City and Southern New York Chapter.

For people receiving SSI or disability benefits, impairment-related work expenses may be deducted from their earnings, if their income might otherwise jeopardize their government benefits. TwoIRSPublications–907,TaxHighlightsforPersonswithDisabilities(www.irs.gov/pub/irs-pdf/p907.pdf ) and502,MedicalandDentalExpenses(www.irs.gov/pub/irs-pdf/p502.pdf )–maybehelpful.Consultanaccountantto make sure your particular situation is in line with current IRS regulations.

Dr. Alexander Ng is interested in learning if people with MS would benefit from ballroom dancing.


Living With MSInformation on Preparing For Pregnancy

The good news about planning a pregnancy when you have MS is that there’s no evidence that MS has any effect on fertility; pregnancy usually reduces exacerbations(althoughflaresdotendtoincreasepostpartum);andgoodoutcomesarethenorm. Nevertheless, making the decision to get pregnant can be complicated, primarily because of the physical challenges of MS, says Barbara Green, MD, director of the West County MS Center, St. Louis. “I also suggest women think about and discuss with their partners the emotional and financial challenges of raising a child, which could affect work and managing the disease.”

Meds, pregnancy and MS Noneofthedisease-modifyingdrugs(DMDs)areapproved for use during pregnancy, and most should not be taken for a few months beforehand. “The risk time is when you’re attempting to conceive,” noted Dr. Green. Plan a discussion with your neurologist about when to stop DMDs—and when, after delivery, to begin them again. “Until recently, most studies were neutral about whether breastfeeding was protective in preventing relapses,” says Dr. Green. “But a new study quotes a beneficial effect on relapse. People with non-aggressive disease may be able to wait to resume DMDs, which can’t be taken while nursing.” Include any symptom-management medications in the discussion with your doctor. From bladder problems to fatigue, pregnancy can make MS symptoms worse, yet many meds are not safe for pregnant women. “We advise people on non-pharmaceutical approaches: getting enough sleep, adjusting work schedules and exercising,” says Dr. Green. “Symptoms during pregnancy are probably not MS—tiredness doesn’t mean your symptoms are coming back,” says Eileen Davis, APN, who has worked with people with MS for 12 years in New Jersey and New York. Keep exercising, she recommends, “so you aren’t carrying unnecessary weight post-pregnancy, which can affect symptoms such as falling.”

Connect the team Connect your obstetrician and neurologist to coordinateyourcare.Visitwww.nationalMSsociety.org/pregnancy for “Pregnancy, Delivery and the Post-Partum Period” to share with health-care professionals. If anesthesia is part of your birth plan, arrange a meeting with the anesthesia team. All forms of anesthesia are considered safe for women with MS. Don’t wait to plan for what happens after delivery. Tap family and friends about helping with housework, foodand,ofcourse,watchingthebaby!

CheckouttheSociety’scollectionofvideos,books,bookletsandWebpagesthatyoucandownload,orcallforfreeprintcopies.

www.nationalMSsociety.org/pregnancy

“MS and Starting a Family”Momentum,Winter2010-2011nationalMSsociety.org/Momentum(click“BackIssues”)

Kara’s Story – Part I and II TheNationalMSSocietyfollowsKarafromherfirsttrimesterallthewaythroughthebirthofherbabyboy

youtube.com/watch?v=f1-heWHC7jI

youtube.com/watch?v=npgN99NeD1k&feature=channel

The MS Daily Minute nationalMSsociety.org/dailyminuteSixty-secondvideospackedwithinformationon •BeginningMSTherapyafterPregnancy •RelapsesDuringPregnancy •BreastfeedingwithMS •SupportDuringandAfterthePregnancy

Resources on MS and Pregnancy


The Legacy of a Brother’s LoveAcross Multiple Decades and Countless Miles,

Love for his sister has driven Father Charles Brooks to raise significant funds for multiple sclerosis over the past 27 years. Brooks, 74, is a long-time rider and top fundraiser of the MS Snowmobile Tour. He became familiar with the National Multiple Sclerosis Society’s mission after his older sister, Theresa, was diagnosed with multiple sclerosis in the late 1970s. The MS Snowmobile Tour meant the chance to do something to help his sister while participating in one of his favorite activities. The Tour, celebrating 29 years in 2012, has raised more than $6 million to power MS research andsupportthoseaffectedbyMS.(Formoreinformation on the MS Snowmobile Tour, see page14.) An avid snowmobiler since he was 29, Brooks took every opportunity to ride the trails near his home. It had become a hobby of his, a way to escape into the beautiful woods of Wisconsin and pass time during cold winters. Brooks grew up in a little community called Askeaton, 18 miles east of Appleton. From a large family,

he was the 13th of 16 children. Theresa was about five years older than him and struggled with symptoms the family thought were due to a back injury. It was 20 years before she was diagnosed with MS. “She went from the back injury to being disabled in a matter of about three years,” he explained. “It went very fast. I think she first had paralysis in her late 20s.” Once his sister was diagnosed, Brooks threw himself into fundraising, asking for support from his congregation, friends and family.

“I’m terrible at asking a person face-to-face to contribute,” explained Brooks, who entered seminary in the early ’50s and was ordained in May of 1965. “But as a priest I knew a lot of people in the parish – so I wrote to all of them. Other parishes gave me permission to write to them as well.” His efforts paid off, garnering

donations that have moved the mission forward. “I am motivated to raise funds by a need to help all those who have MS, as many as I can, and see if we can come up with a cure soon,” he said. “We are certainly

getting much closer I think and people are at least improving with the new medications.” Every year that Brooks rides is his way of helping his sister and others affected by MS. “It all began for her and others like

her,” he said. “I wanted to do something to help them out. And now I know lots of people with MS.”

Inducted Into the Volunteer Hall of Fame In 1999, two years after Theresa passed away after a battle with breast cancer, Brooks was inducted into the National MS Society’s Volunteer Hall of Fame for fundraising. “That was certainly one of my highlights, there is not doubt,” he said of his induction in the Volunteer

I’m terrible at asking a person face-to-face to contribute. But as a priest I knew a lot of people in the parish – so I wrote to all of them. - Father Brooks

Father Charlie Brooks has been a dedicated fundraiser for MS research, programs and services for nearly 30 years.

Hall of Fame. “That was remarkable. I sure met a lot more of the same kind of people: charitable, generous, good people committed to MS.” He shared that he appreciates the dedication of people who work on behalf of those with MS, including MS researchers. “I’m grateful for the many scientists who work on MS,” he said. “I have had great chances to meet a number of them over the years. They are truly top notch scientists.”

Supporting the Scholarship Program Over the years, Brooks has designated a portion of the funds he raises to the MS Scholarship program. (FormoredetailsontheMSScholarshipprogram,seePages4-5.)

“Helping these young adults, who have parents that are struggling with the disease, it frees them up a little bit from worrying about the total cost,” he explained. In 2008 for the 25th anniversary of the MS Snowmobile Tour, the Father Charles Brooks Scholarship was established in recognition of Brooks’ contribution to

the program, an experience he called “very humbling.” “It was very humbling without a doubt,” Brooks said of the named scholarship.

In addition to his many contributions to the Society throughout the years, Brooks is a Lawry Circle member. The Lawry Circle is a distinguished group of people who have remembered the National MS Society in their estate plans by designating the Society as the beneficiary of a bequest, annuity, life insurance policy or other deferred gift.

Committed to the Cause Brooks served as a hospital chaplain for 16 years and was able to spend a lot of time with his sister who lived nearby. “I used to stop and visit with her almost every day, to spend time with her and her husband and four kids.” His service continued in a parish in De Pere for another 12 before settling in at St. Edward Parish of Mackville in Appleton. He retired almost five years ago and now spends his winters in Mesa, Arizona. This year, he will come back to Wisconsin for Christmas and stay the month of January to attend the 29th MS Snowmobile Tour. “I am most impressed with the ‘Snow’ group’s community spirit, their love for others, their concern for others,” Brooks said. “I think that is one of things that has really kept me going back. It should be an enjoyable year with the group at the MS Snowmobile Tour.”

Bethany Sievert contributed to this article.


A familiar face on the MS Snowmobile Tour, Father Brooks (left) also supports the Scholarship Program and is a member of the Lawry Circle.

Father Charlie Brooks’ Dedication Endures

I am most impressed with the Snow group’s community spirit, their love for others, their concern for others. I think that is one of things that has really kept me going back. - Father Brooks


MS Snowmobile TourSmiles and Meaning in Every Mile

Billed as a fun ride for a great cause, the annual MS Snowmobile Tour brings together nearly 200 enthusiasts for a weekend traversing the trails in northeast Wisconsin, with the hope that the money they raise will power the research that will end MS forever.

Led by event co-chairs Mark Schmidt and Marty Iverson, the family-friendly event is a fun, all-inclusive, fully-supported experience that features:

• Guidedtrails • Eveningcelebrations • ThreenightslodgingatthePotawatomiCarter Casino Hotel • Sixmeals(twobreakfast,twolunch,twodinner) • Mechanicalsupportthroughouttheweekend • Silentauction,raffleandprizes,andmore!

Participants are asked to raise a minimum of $650 each, although many have been so successful that the MS Snowmobile Tour has raised more than $6 million throughout its 28-year history for MS research and related services.

There’s still time to register!Visit MSsnowmobiletour.org or call 1-800-242-3358. First-timeriderscanregisterforfree!EntercodeMSSTrookie2012,orcall262-369-4400(800-242-3358)and ask for your MS Snowmobile Tour Ticket to Ride. (Refundscannotbegiventofirst-yearriderswhoarealreadyregistered.)

Don’t have your own sled? Don’t let that stop you! You can rent one or ride with someone else! For details contact the Wisconsin Chapter at 1-800-242-3358 or [email protected]

The MS Snowmobile Tour is a great time for riders of all skill levels, and first-time participants can register for free.

January 26-29, 2012, Carter, Wisconsin

John DownsMonika IversonRandy MurdockKeith Paul

Donnie RoweBob SchmidtCraig SchmidtScott Smith

Additional thanks to committee co-chairs Mark Schmidt and Marty Iverson.

Special Thanks to the 2012 MS Snowmobile Tour Volunteer Committee!


Olympic Medalist Named MS Ambassador Ski Event Again Names the Society as Charity of Choice

Participants in the 2012 American Birkebeiner Skiers for Cures weekend in February will have the chance to win a trip to Norway and spend time with one of the biggest names in cross-country skiing, Vegard Ulvang, fresh off his trek to the South Pole. It will be the fourth year that American Birkebeiner has named the National Multiple Sclerosis Society as its Skiers for Cures beneficiary. To date, Birkie skiers and their supporters have pledged more than $220,000 to power MS research.

American Birkebeiner is the largest Nordic ski event in North America. Held in Wisconsin near Hayward, the weekend includes ski races, sprints and family events along with equipment demos, music, food and entertainment. It’s billed as an event for both the “super fit and like-minded fitness buffs” as well as “those wanting pure and simple recreation.” Participants are invited to fundraise for the National MS Society as the event’s charity of choice. Ulvang, a six-time Olympic medalist and three-time Holmenkollen 50K winner recognized as one of Norway’s Top Ten Nordic skiers of all time, will participate as a “Research Ambassador” for the Wisconsin Chapter. Currently the executive director of FIS Nordic and the creator and director of the hugely successful Tour de Ski, Ulvang will be coming off an 800-mile planned

trek across Antarctica commemorating the 100th anniversary of the discovery of the South Pole by fellow Norwegian Roald Amundsen. Those contributing $2,000 or more to Skiers for Cures will have the opportunity to ski with Ulvang and enjoy a private lunch with him afterwards. More details about Skiers for Cures are available at wisMS.org, by calling 262-369-4407 or by e-mailing [email protected].

Win a Trip to Norway’s 2013 Birkebeinerrennet Donors will receive one entry in a drawing to win a trip for two to Norway’s 2013 Birkebeinerrennet for every $250 contributed to Skiers for Cures. The trip includes two race entries, three night’s lodging and a $1,500 voucher for air travel.

Skiers for Cures Pins The popular Ski for the Cure pin will once again be available for $20 at the American Birkebeiner Expo (or online at wisMS.org). Those wearing the pin on their Birkebeiner or Kortelopet race bib when they cross the Finish Line will be randomly selected to win prizes.

Other Skiers for Cures Opportunities

Leading Skiers for Cures donors will have the chance to ski with Olympic-medalist Vegard Ulvang.


Community Events Reflect Do-It-Yourself MentalityNew Tools for Raising Money Everywhere, In Every Way

The Movement for a world free of MS has benefitted immeasurably from those who go beyond the Society’s signature events to raise money that drives research and funds services. Through their own ingenuity and passion, these do-it-yourselfers put together their own community event fundraisers that last year contributed more than $200,000 locally to the mission. From denim days and luncheons to poker tournaments and Zumbathons, they get involved in ways that are fun and have a direct impact in helping those affected by the disease. The Carney Roundup Rodeo 2nd Annual Chilly Willy Open Horse Show was

one such event held recently. Encouraging participants to “take the reins for MS,” it featured 106 horses and a T-shirt sale that together raised $1,500. For its second annual fundraiser, the Milwaukee area Generation OptiMiStic hosted a Miller Brewery Tour. Free food and beverages were provided by MillerCoors, and donations of $15 in advance and $20 at the door were requested.Togetherwitharaffleandsilentauction, more than $4,000 was raised. Those types of third-party fundraisers,

previously referred to as community events, have now been renamed “Do It Yourself Fundraising.” Emphasizing the critical role these events, and their dedicated organizers, play in raising money for the mission, the new name comes with a set of new online resources to help make their efforts even easier. Available through the Wisconsin Chapter website, the DIY Fundraising pages include tips, tools and answers to commonly asked questions about creating your own events. Find them online at wisMS.org.

Generation OptiMiStic enjoyed free beer and raised more than $4,000 with their Miller Brewery Tour event.

In taking the reins for MS, the Carney Roundup Rodeo 2nd Annual Chilly Willy Open Horse Show recently raised $1,500. It’s an example of the type of community events the new Do It Yourself Fundraising tools were developed to help with.


Challenge Walk MSBelieving in the Possibilities Leads to Record-Setting Success

They came for the CHALLENGE.

They came for the CELEBRATION.

They came because they BELIEVE.

A record 217 people participated in Challenge Walk MS 2011: 133 walkers, 17 Super Crew members and 67 crew members. Dedicated in their belief that anything is possible to overcome the challenges of multiple sclerosis, they came from 15 states, brought 72 first-timeparticipantsandraised$385,000,a29%increasefrom2010! The weekend began on a picture-perfect day for walking, with participants meandering through beautiful Peninsula State Park at the start of their 20-mile route and enjoying a variety of themed rest stops from Egan’s Irish Pub to Multiple Screwballs’ Chocolate Shoppe. Day Two brought rain and weather challenges, but determined walkers and supportive volunteers worked together and ultimately were rewarded with a beautiful sunset at day’s end. Day Three took participants to a special finish line event. Special congratulations to top team fundraiser Heller’s Multiple Screwballs and top individual fundraiser Connie Plier. Plans are in the works for next year’s fifth anniversary event, September 21-23 at the Alpine Resort in Door County. More than 100 people have alreadycommittedtobeingpartofit.Jointhem!VisitChallengeWalkMSwi.org to register. When asked what they liked about the walk, this year’s participants spoke of the camaraderie, the sense of

mission, the “family reunion” type atmosphere, and the enthusiastic and welcoming environment. Here’s what a few others had to say:

“Those who participate in the weekend are forever linked together in their heart-felt belief that the world will be free of MS someday! So much love for one another - so many positive people pulling together - so much HOPE!”

“It is a way for all involved to feel that they are, in some small way, contributing to better the lives of their loved ones and all who suffer from MS.”

“We really felt like we made a difference.” “The energy and spirit of the event was inspiring.” “I loved the small close knit feel.” “I have a whole new extended family people I love to be around and can’t wait to see next year.”

“It was such an emotional experience to go from using a cane when first diagnosed almost two years ago to being able to complete the 50 mile walk (and

even run a bit of it). It was so emotional to cross the finish line….It was also such a blessing to meet a few other people that weekend who have overcome similar (or even greater) obstacles.”

Challenge Walk MS is a fully supported, three-day, 50-mile walk. And “fully supported” means just that: the logistics of accommodations, meals, entertainment and route assistance are taken care of so you can focus on fundraising and enjoying the walk with family and friends in one of the most beautiful areas of Wisconsin.

Daniel DeNoble (left) and son Matthew from the team Multiple Screwballs were among the 217 Challenge Walk participants who together raised $385,000 – a 29% increase from 2010.


Challenge Walk MS 2011


AfterreturningtoworkattheMilwaukeeCountySheriff’sOfficefollowingChallengeWalkMS,FranMcLaughlinthoughttheremightbeamentionduringtheweeklystaffmeetingabouthertakingpartintheevent.Imaginehersurprisewhensheinsteadlearnedthat,inherabsence,thestaffattheagencyhadraisedmoneytohelpherreachhergoal.Bailiffsraised$400sellinghotdogs.Jailstaffgeneratedanother$400withabakesale.Acorrectionalofficersentheracheckfor$420withanotesayingheappreciatedherdedicationtoagoodcause.Thecommandstaffmadecashdonationsforatotalofmorethan$2,000.“Iwasoverwhelmedandspeechless,”saidthefour-yearChallengeWalkMSparticipantofherco-workers’generosity,whichhelpedherexceedher$5,000,$100-for-every-milegoal.“Aren’tpeoplewonderful?”

McLaughlin already registered for the 5th Annual Challenge Walk MS event. Join her by signing up at ChallengeWalkMSwi.org.

Co-Workers Take Up the Challenge


walkMSwisconsin.orgor1-800-242-3358

Thank You 2011 Challenge Walk MS Sponsors

WALK MS: 2012DOLLARByDOLLAR,WALKMSISCHANGINGLIvES.

REGISTERANDSTARTFUNDRAISINGTODAy!

walkMSwisconsin.orgor1-800-242-3358

saturday APRil 28

Fond du lacla CrosseMenomonee FallsWausau

sunday APRil 22

Brown County

sunday APRil 29

eau Claire-Chippewa ValleyFox CitiesKenosha-RacineWaukesha

saturday MAY 5

graftonManitowoc-two RiversPlatteville

sunday MAY 6

Janesville-Rock RiverMadisonMilwaukeeSheboygan

Wisconsin ChapterWalk 2012


Participate from HomeLearn More About MS with New Midwest Teleconference Series

The National Multiple Sclerosis Society-Wisconsin Chapter is proud to introduce the Midwest Teleconference Series, an educational program that you can participate in from the comfort of home. The Wisconsin Chapter hosts the Midwest Regional Teleconference on the second Monday of each month at 7 p.m. CST. Each hour-long call features expert information on different aspects of living with multiple sclerosis. There is no charge for these calls, but registration is required. Register online at wisMS.org or by calling 800-344-4867 by the Thursday before each teleconference.

You are Not AloneDecember 12

2012Making Connections Thru Social NetworkingJanuary 9

What About Progressive MSFebruary 13

Research: Where are we now, where are we going?March 12

Maximizing Your Physical Therapy for Optimum BenefitApril 9

Me, Myself and I: The Art of Being Your Own Care PartnerMay 14

Give Yourself a Hand: Tools for Everyday LifeJune 11

The Cycle of MS Symptoms and their Effect on Bowel and BladderJuly 9

Spasticity, What’s Under Your ControlAugust 13

MS What a PainSeptember 10

If you miss a teleconference, you can listen to the recorded calls by going to wisMS.org. The October teleconference, “Eating for Healthy Living with MS,” is already available. In this call, you’ll learn how to get the best out of the foods you eat, what foods to focus on and what to watch out for. In addition, you’ll learn about food allergies.

The November 14 teleconference, “Hot Flash or MS Moment?,” will be available online in the next few weeks.

BecausenooneshouldfaceMSalone,theMSNavigatorinformationhotlineisavailabletotakeyourcalls.StaffedbyMSexperts,MSNavigatorprovidespersonalizedservice,up-to-dateinformationandpracticalresourcesandreferrals.

CallMSNavigator1-800-344-48677a.m.to6:30p.m.CST,MondaythroughFriday

Questions About MS?Call an MS Navigator


Registration is Open! The 2012 Walk MS dates have beenannouncedandregistrationisnowopen! • Register by January 1 for your free Walk MS 2012 bandana. • Register before January 24 and make a self pledge of $24 or more(incelebrationofthe event’s 24thanniversary)foryourpairof commemorative Walk MS 2012 shoelaces.Both make great accessories for MS Awareness Week in March!

Want More Walk MS Wear? Raise $100 or more and gettheofficialWalkMS2012T-shirt,too.(Children9andundercanearnonebyraising$25ormore.)

Last year more than 12,000 walkers raised more than $1.5 million for MS research, programs and services. Go to walkMSwisconsin.org to register.

Translating the Cognitive Challenges of MS. The second edition of Jeffrey Gingold’s award-winning

book “Facing the Cognitive Challenges of MS” is being translated into Polish and will be released in Poland in 2012. Gingold discussed his book in a recent interview with the Polish magazine, “Pozytywny Impuls,” translated as “Possitive Impulse.” Jeffrey continues to donate all of his author royalties from the sales of his books directly to MS research and education.

Order directly from the publisher and receive a special discount. Visit demoshealth.com and utilize this code: SSGINGOLD30 when you make your purchases.

Informative MS Videos Available Online. More than 50 videos are now available at the Society’s MS

Learn Online website, and new productions are added monthly. There are Spanish Learn Online videos, too. Visit nationalMSsociety.org to view the MS Learn Online videos – and sign up for e-mail alerts so you’ll know when a new feature is available for screening.

Wisconsin Chapter Calendar of Clinic Visits Representatives of the Wisconsin Chapter regularly visit several of the organization’s official clinics. During these visits, Chapter staff is available to meet confidentially and answer questions plus share informative literature. The current schedule of clinic visits is as follows: • Aurora Baycare MS Clinic, Green Bay: 4th Friday of every month • Marshfield Clinic MS Center, Marshfield: 3rd Tuesday of every month • ProHealth Care Oconomowoc Physician Center, Oconomowoc: 3rd Friday of every month • Regional Multiple Sclerosis Center, St. Luke’s Medical Center, Milwaukee: 1st Monday, 2nd Thursday, 3rd Wednesday, 4th Tuesday of each month • ProHealth Care Neuroscience Center, Waukesha Memorial Hospital, Waukesha: 4th Tuesday of each month • UW Hospital and Clinics Neurology/MS Clinic, Madison: 4th Wednesday of each month

Support Groups. There are nearly 50 MS support groups in Wisconsin and new groups sprout up regularly. For a complete listing including meeting dates, please visit wisMS.org or call 800-242-3358.

Sign Up for Action Alerts and Read the Blog. Sign up today to receive Action Alert e-mails. These informative updates will keep you connected to the issues that matter most to individuals with MS. E-mail [email protected] for details or call 800-242-3358. You can also read the MS Activist blog to keep up with news on federal-level issues at MSactivist.blogspot.com.

Wisconsin Chapter News and NotesThis is How We Move It

Wisconsin ChapterWalk 2012

MS Connection is a publication of the National Multiple Sclerosis Society-Wisconsin Chapter. For information or to share story ideas, please call 262-369-4421. Editor: Maureen Waslicki, Assistant Editor: Amanda Gasper, Art Director: Amy Malo.

SECOND EDITION

FACING THE

COGNITIVE CHALLENGES

OF MULTIPLE SCLEROSIS

FACING THE COGNITIVE CHALLENGES OF MULTIPLE SCLEROSIS

GINGOLD

SECO

ND

EDITIO

N

DISTRIBUTED IN NORTH AMERICA BY PUBLISHERS GROUP WESTCOVER DESIGN BY CARLOS MALDONADO

11 W. 42nd Street, 15th FloorNew York, NY 10036

www.demoshealth.com

$19.95

Jeffrey N. Gingold is the internationally acclaimed author of the Award-winning book, Facing the Cognitive Challenges of Multiple Sclerosis and an outspoken volunteer advocate on MS and

cognitive disability. He has been a guest on The Montel Williams Show, NPR affi liates, numerous webcasts and national talk radio shows. In his second book, Mental Sharpening Stones: Manage the Cognitive Challenges of Multiple Sclerosis, Jeffrey provides strategies from people who have MS and medical providers, sharing their tactical advice on how to manage the “invisible MS.”

He was recently inducted to the 2010 National Multiple Sclerosis Society Hall of Fame for his Advocacy. Jeffrey is a published freelance writer and has authored numerous articles for U.S and international publications. He enjoys spending family time with his wife, Terri, two adorable daughters, Lauren and Meredith, and one cat named Mickey - named after the baseball player, not the mouse.

ABOUT THE AUTHOR:

“ As recently as the 1980’s, people diagnosed with multiple sclerosis were assured that their thinking skills would be spared when looking at the possible range of symptoms. It was not true then or now. Cognitive issues are bad players because they can signifi cantly affect the lives of those who have them and their families, while remaining largely invisible to most of us. Jeffrey acknowledged his struggles and then moved forward by looking for solutions for himself and then by sharing them with others. We can all learn from his journey.”

— PATRICIA KENNEDY RN, CNP, MSCN NURSE EDUCATOR, Can Do Multiple Sclerosis and author of the forthcoming Can Do Multiple Sclerosis Guide to Lifestyle Empowerment

“ Jeffrey Gingold, in this the second edition of his book, has not only provided an intimate look into the personal experiences with which he has had to contend with his MS, he has created a work that is informative, highly personal, incredibly supportive and realistic in its advice. It is a truly outstanding work that I can recommend without reservation to those both with MS as well as anyone who wants to know more about this aspect of MS.”

—PATRICIA A. FARRELL, PHD, author of It’s Not All in Your Head and How to Be Your Own Therapist

“ In his latest and most moving book, Jeff Gingold takes us on a journey into the ‘hidden’ precincts of multiple sclerosis – cognitive changes. Not only people with MS, but those with any connection to MS, personal or professional, should read this book.”

— NICHOLAS G. LAROCCA, PHD, Vice President of Health Care Delivery and Policy Research, National Multiple Sclerosis Society, author of Multiple Sclerosis: Understanding the Cognitive Challenges

“Multiple sclerosis can be a scary, lonely disease. Jeffrey Gingold has given us some weapons to fi ght where we can. He also demonstrates the wisdom to accept

situations that are not what we had envisioned for ourselves, while showing that a ‘new’ reality doesn’t mean defeat. Buy this book.

You will be stronger for reading it.”

—JULIE STACHOWIAK, PHD, About.com guide to Multiple Sclerosis, author of The

Multiple Sclerosis Manifesto and The Diabetes

Manifesto

SECOND EDITION

FACING THE COGNITIVE CHALLENGESOF MULTIPLE SCLEROSIS

“...a poetic testament to one man’s courage” —CONSORTIUM OF MS CENTERS


Generation Optimistic GreatDanePub-HilldaleMadisonDecember8

Midwest Teleconference“youareNotAlone”December12

Generation Optimistic Mo’sIrishPubWauwatosaDecember15

2012Midwest Teleconference“MakingConnectionsThruSocialNetworking”January9

MS Snowmobile TourCarterJanuary26-29,2012

Midwest Teleconference“WhatAboutProgressiveMS”February13

Generation Optimistic CaribouCoffeePewaukeeFebruary16

Birkie Skiers for Cures February23-25

Midwest Teleconference“Research:Wherearewenow,wherearewegoing?”March12

MS Awareness Week March12-16

Midwest Teleconference“MaximizingyourPhysicalTherapyforOptimumBenefit”April9

Generation OptimisticvinoCappuccinoBrookfield,WIApril19

Walk MSBrown County Sunday,April22

Fond du Lac Saturday,April28

La Crosse Saturday,April28

Menomonee Falls Saturday,April28

WausauSaturday,April28

Eau Claire-Chippewa Valley Sunday,April29

Fox Cities Sunday,April29

Kenosha-Racine Sunday,April29

WaukeshaSunday,April29

Grafton Saturday,May5

Manitowoc-Two Rivers Saturday,May5

PlattevilleSaturday,May5

Janesville-Rock River Sunday,May6

Madison Sunday,May6

MilwaukeeSunday,May6

Sheboygan Sunday,May6

Midwest Teleconference“Me,MyselfandI:TheArtofBeingyourOwnCarePartner”May14

MS Summit WisconsinDellsMay18-19

MS World Day May30

Midwest Teleconference“GiveyourselfaHand:ToolsforEverdayLife”June11

Generation Optimistic MilwaukeePublicMarketMilwaukeeJune21

On the Move Luncheon MilwaukeeJune27

On the Move Luncheon MadisonJune28

Midwest Teleconference“TheCycleofMSSymptomsandTheirEffectonBowelandBladder”July9

Bike MS: Best Dam Bike Ride August4-5

Midwest Teleconference“Spasticity,What’sUnderyourControl”August13

Generation Optimistic AlterraattheLakeMilwaukeeAugust16

Midwest Teleconference“MSWhataPain”September10

Challenge Walk MS September21-23

Please visit the wisMS.org Calendar of Events for the latest listing of Chapter activities and Community Events.

Wisconsin Chapter Calendar of Events

®

wisMS.org • Toll Free 1 800 242 3358 • 262 369 4400

NoN-Profit orgaNizatioN

U.S. PoStage

MilwaUkee, wi 53202PerMit No. 2868

PAID1120 James Drive Suite A Hartland, WI 53029

Mailing Label ChangesPleasechecktheappropriateboxbelow,correctthelabelandreturntotheWisconsinChapter. Namechangeormisspelled Addresschange Removefrommailinglist Receivedmorethanonecopy PleasesendmemyMSConnection viae-mail.Mye-mailaddressis:__________________________________________

ON YOUR TAx RETURN … Make a Mark to Help Create a World Free of MS

While doing your 2011 Wisconsin income taxes, please check the box under the “Donations” heading to make a charitable contribution to the National Multiple Sclerosis Society. Importantly, 100 percent of your contribution will support the more than 10,000 Wisconsin residents diagnosed with MS. Your small mark

will make a big difference in the movement to create a world free of MS.

Contact the National MS Society-Wisconsin Chapter or your tax preparer for information.

262.369.4400 | 800.242.3358 | 1120 James Dr. Suite A, Hartland, Wi 53029 | [email protected] | wisms.org

early and ongoing treatment with an FDA-approved therapy can make a difference for people with multiple sclerosis. learn about your options by talking to your health care professional and contacting the national MS Society at nationalMSsoci ety.org or 1-800-FigHt-MS (344-4867).

winter 2011 ms connection

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