PACIFIC SOUTH COAST CHAPTER

The mission of the National MS Society is to mobilize people and resources to drive research for a cure and to address the challenges of everyone affected by MS. Locally, the Pacific South Coast Chapter provides programs and services designed to help the 18,000 people and families affected by

MS in San Diego, Orange and Imperial counties move their lives forward. All programs and services are offered at minimal or no cost to participants; fees are often waived for those with financial need. Most programs are offered on an ongoing basis throughout the chapter territory.

Visit www.MSpacific.org or call 1-800-344-4867 for details.

WHAT IS MS?

Multiple sclerosis (MS) is an unpredictable neurological disease that

interrupts the flow of information within the brain and between the

brain and body. The progress, severity and specific symptoms in any

one person cannot yet be predicted, and may range from numbness

and tingling to blindness and paralysis. Most people with MS are

diagnosed between the ages of 20 and 50, with more at least two

to three times more women than men being diagnosed with the

disease. MS affects more than 400,000 people in the U.S., and

2.1 million worldwide.

www.MSpacific.org

www.nationalMSsociety.org

1-800-344-4867 (1-800-FIGHT-MS)

JOIN THE MOVEMENT

TWO OFFICES TO SERVE YOU

3000 Airway AvenueSuite 125

Costa Mesa, CA 92626

5950 La Place CourtSuite 200

Carlsbad, CA 92008

PACIFIC SOUTH COAST CHAPTER

The mission of the National MS Society is to mobilize people and resources to drive research for a cure and to address the challenges of everyone affected by MS. Locally, the Pacific South Coast Chapter provides programs and services designed to help the 18,000 people and families affected by

MS in San Diego, Orange and Imperial counties move their lives forward. All programs and services are offered at minimal or no cost to participants; fees are often waived for those with financial need. Most programs are offered on an ongoing basis throughout the chapter territory.

Visit www.MSpacific.org or call 1-800-344-4867 for details.

WHAT IS MS?

Multiple sclerosis (MS) is an unpredictable neurological disease that

interrupts the flow of information within the brain and between the

brain and body. The progress, severity and specific symptoms in any

one person cannot yet be predicted, and may range from numbness

and tingling to blindness and paralysis. Most people with MS are

diagnosed between the ages of 20 and 50, with more at least two

to three times more women than men being diagnosed with the

disease. MS affects more than 400,000 people in the U.S., and

2.1 million worldwide.

www.MSpacific.org

www.nationalMSsociety.org

1-800-344-4867 (1-800-FIGHT-MS)

JOIN THE MOVEMENT

TWO OFFICES TO SERVE YOU

3000 Airway AvenueSuite 125

Costa Mesa, CA 92626

5950 La Place CourtSuite 200

Carlsbad, CA 92008

PACIFIC SOUTH COAST CHAPTER

The mission of the National MS Society is to mobilize people and resources to drive research for a cure and to address the challenges of everyone affected by MS. Locally, the Pacific South Coast Chapter provides programs and services designed to help the 18,000 people and families affected by

MS in San Diego, Orange and Imperial counties move their lives forward. All programs and services are offered at minimal or no cost to participants; fees are often waived for those with financial need. Most programs are offered on an ongoing basis throughout the chapter territory.

Visit www.MSpacific.org or call 1-800-344-4867 for details.

WHAT IS MS?

Multiple sclerosis (MS) is an unpredictable neurological disease that

interrupts the flow of information within the brain and between the

brain and body. The progress, severity and specific symptoms in any

one person cannot yet be predicted, and may range from numbness

and tingling to blindness and paralysis. Most people with MS are

diagnosed between the ages of 20 and 50, with more at least two

to three times more women than men being diagnosed with the

disease. MS affects more than 400,000 people in the U.S., and

2.1 million worldwide.

www.MSpacific.org

www.nationalMSsociety.org

1-800-344-4867 (1-800-FIGHT-MS)

JOIN THE MOVEMENT

TWO OFFICES TO SERVE YOU

3000 Airway AvenueSuite 125

Costa Mesa, CA 92626

5950 La Place CourtSuite 200

Carlsbad, CA 92008

EMOTIONAL SUPPORT

In addition to its physical symptoms, MS may have profound emotional implications. It may be difficult to adjust to a disease that is unpredictable and carries a risk of progressing over time. In addition to these emotional reactions to the disease, demyelination and damage

to nerve fibers in the brain can also result in emotional changes. The chapter offers support to help people with MS cope with the ever-changing symptoms and challenges that MS presents.

Newly diagnosed programs cover topics such as fatigue, treatments, disclosing diagnosis, medical management and the impact of MS on families. Knowledge is Power is an educational

series held via mail and email; specialist-led Moving Forward seminars are held throughout the year.

Professionally-led support groups offer an opportunity to learn about adapting to life with MS.

Counseling sessions help individuals learn to manage their reactions to the effects of living with or being affected by MS.

Self-help groups which are facilitated by people with MS, for people with MS, range from general discussion to special interest. Meetings are offered throughout the community as well as over the phone.

Angel Visitation volunteers provide companionship to individuals with MS who may be isolated.

WELLNESS

For a person living with MS, the road to wellness involves more than treatment of the disease. Equally important are health promotion and prevention strategies, satisfying personal relationships, a strong support

network, fulfilling work and leisure activities, a meaningful place in the community, and adequate attention to one's inner self.

Specialized exercise classes such as strength training, balance training and yoga may help improve strength, balance and flexibility as well as relieve symptoms such as spasticity or stiffness. Aqua classes, held in temperature-controlled swimming pools,

encourage mobility and flexibility in the enhanced freedom and comfort of water.

MS clinics at local affiliated centers offer specialized multidisciplinary care including diagnoses and second opinions. Each clinic is reviewed and approved by the chapter’s Clinical Advisory Committee and National Clinical Care Committee. Each Clinic’s staff, directed by MS Specialists, include a neurologist, nurse practitioner, physical therapist, care manager and chapter staff trained in managing the unique needs

of people living with MS.

EMOTIONAL SUPPORT

In addition to its physical symptoms, MS may have profound emotional implications. It may be difficult to adjust to a disease that is unpredictable and carries a risk of progressing over time. In addition to these emotional reactions to the disease, demyelination and damage

to nerve fibers in the brain can also result in emotional changes. The chapter offers support to help people with MS cope with the ever-changing symptoms and challenges that MS presents.

Newly diagnosed programs cover topics such as fatigue, treatments, disclosing diagnosis, medical management and the impact of MS on families. Knowledge is Power is an educational

series held via mail and email; specialist-led Moving Forward seminars are held throughout the year.

Professionally-led support groups offer an opportunity to learn about adapting to life with MS.

Counseling sessions help individuals learn to manage their reactions to the effects of living with or being affected by MS.

Self-help groups which are facilitated by people with MS, for people with MS, range from general discussion to special interest. Meetings are offered throughout the community as well as over the phone.

Angel Visitation volunteers provide companionship to individuals with MS who may be isolated.

WELLNESS

For a person living with MS, the road to wellness involves more than treatment of the disease. Equally important are health promotion and prevention strategies, satisfying personal relationships, a strong support

network, fulfilling work and leisure activities, a meaningful place in the community, and adequate attention to one's inner self.

Specialized exercise classes such as strength training, balance training and yoga may help improve strength, balance and flexibility as well as relieve symptoms such as spasticity or stiffness. Aqua classes, held in temperature-controlled swimming pools,

encourage mobility and flexibility in the enhanced freedom and comfort of water.

MS clinics at local affiliated centers offer specialized multidisciplinary care including diagnoses and second opinions. Each clinic is reviewed and approved by the chapter’s Clinical Advisory Committee and National Clinical Care Committee. Each Clinic’s staff, directed by MS Specialists, include a neurologist, nurse practitioner, physical therapist, care manager and chapter staff trained in managing the unique needs

of people living with MS.

EMOTIONAL SUPPORT

In addition to its physical symptoms, MS may have profound emotional implications. It may be difficult to adjust to a disease that is unpredictable and carries a risk of progressing over time. In addition to these emotional reactions to the disease, demyelination and damage

to nerve fibers in the brain can also result in emotional changes. The chapter offers support to help people with MS cope with the ever-changing symptoms and challenges that MS presents.

Newly diagnosed programs cover topics such as fatigue, treatments, disclosing diagnosis, medical management and the impact of MS on families. Knowledge is Power is an educational

series held via mail and email; specialist-led Moving Forward seminars are held throughout the year.

Professionally-led support groups offer an opportunity to learn about adapting to life with MS.

Counseling sessions help individuals learn to manage their reactions to the effects of living with or being affected by MS.

Self-help groups which are facilitated by people with MS, for people with MS, range from general discussion to special interest. Meetings are offered throughout the community as well as over the phone.

Angel Visitation volunteers provide companionship to individuals with MS who may be isolated.

WELLNESS

For a person living with MS, the road to wellness involves more than treatment of the disease. Equally important are health promotion and prevention strategies, satisfying personal relationships, a strong support

network, fulfilling work and leisure activities, a meaningful place in the community, and adequate attention to one's inner self.

Specialized exercise classes such as strength training, balance training and yoga may help improve strength, balance and flexibility as well as relieve symptoms such as spasticity or stiffness. Aqua classes, held in temperature-controlled swimming pools,

encourage mobility and flexibility in the enhanced freedom and comfort of water.

MS clinics at local affiliated centers offer specialized multidisciplinary care including diagnoses and second opinions. Each clinic is reviewed and approved by the chapter’s Clinical Advisory Committee and National Clinical Care Committee. Each Clinic’s staff, directed by MS Specialists, include a neurologist, nurse practitioner, physical therapist, care manager and chapter staff trained in managing the unique needs

of people living with MS.

EMOTIONAL SUPPORT

In addition to its physical symptoms, MS may have profound emotional implications. It may be difficult to adjust to a disease that is unpredictable and carries a risk of progressing over time. In addition to these emotional reactions to the disease, demyelination and damage

to nerve fibers in the brain can also result in emotional changes. The chapter offers support to help people with MS cope with the ever-changing symptoms and challenges that MS presents.

Newly diagnosed programs cover topics such as fatigue, treatments, disclosing diagnosis, medical management and the impact of MS on families. Knowledge is Power is an educational

series held via mail and email; specialist-led Moving Forward seminars are held throughout the year.

Professionally-led support groups offer an opportunity to learn about adapting to life with MS.

Counseling sessions help individuals learn to manage their reactions to the effects of living with or being affected by MS.

Self-help groups which are facilitated by people with MS, for people with MS, range from general discussion to special interest. Meetings are offered throughout the community as well as over the phone.

Angel Visitation volunteers provide companionship to individuals with MS who may be isolated.

WELLNESS

For a person living with MS, the road to wellness involves more than treatment of the disease. Equally important are health promotion and prevention strategies, satisfying personal relationships, a strong support

network, fulfilling work and leisure activities, a meaningful place in the community, and adequate attention to one's inner self.

Specialized exercise classes such as strength training, balance training and yoga may help improve strength, balance and flexibility as well as relieve symptoms such as spasticity or stiffness. Aqua classes, held in temperature-controlled swimming pools,

encourage mobility and flexibility in the enhanced freedom and comfort of water.

MS clinics at local affiliated centers offer specialized multidisciplinary care including diagnoses and second opinions. Each clinic is reviewed and approved by the chapter’s Clinical Advisory Committee and National Clinical Care Committee. Each Clinic’s staff, directed by MS Specialists, include a neurologist, nurse practitioner, physical therapist, care manager and chapter staff trained in managing the unique needs

of people living with MS.

DIRECT FINANCIAL ASSISTANCE

Assistance is provided to qualified individuals on a first-come, first-serve basis; eligibility requirements, application and needs assessment apply.

Durable medical equipment loans are available for up to one year. Loaned items such as canes, walkers, scooters, wheelchairs, hoyer lifts, hospital beds and many other items enhance the mobility, activity and independence of individuals living with MS.

Educational scholarships help individuals with MS and their children further their education. Annual recipients of the Bob

Webster and Helen Marocco Angel scholarships receive awards for tuition, books and other education-related expenses.

FAMILY & SOCIAL SUPPORTSupport for families can increase their understanding of the potential impact of MS on family life and help to strengthen the family unit. Fun and educational activities can help families maintain healthy and happy family and social relationships!

Caregiver education and support -- social events, educational seminars, and peer and professionally-led support groups address the special needs of the spouse, partner or family caregiver.

Respite care offers caregivers relief and may improve the health of the whole family. Caregivers are relieved by in-home assistance and a family consultant to help arrange respite hours with the home health agency. Subject to application, availability and waiting list, grants provide specific service allotments based on client needs.

Social events - families coming together find that they are not alone in coping with the challenges that MS might bring. Events such as Day at

the Bay include lunch, family fun and adaptive sailing. Our Thanksgiving Meal Delivery Program and Annual Family Holiday Brunch held in December offer families an enhanced sense of celebration. Multi-component Family Education Day events foster effective coping and communication skills.

Financial assistance is available to provide meaningful assistance to as many people living with MS as possible. The program assists people in maintaining their personal independence, safety, well-being and quality of life. Items considered include automobile or home modifications, long-term durable medical equipment needs, transportation assistance, health and wellness support, and critical short-term needs such as rent or utilities.

The MS van is an accessible van that can be rented for medical appointments, family outings or social events.

DIRECT FINANCIAL ASSISTANCE

Assistance is provided to qualified individuals on a first-come, first-serve basis; eligibility requirements, application and needs assessment apply.

Durable medical equipment loans are available for up to one year. Loaned items such as canes, walkers, scooters, wheelchairs, hoyer lifts, hospital beds and many other items enhance the mobility, activity and independence of individuals living with MS.

Educational scholarships help individuals with MS and their children further their education. Annual recipients of the Bob

Webster and Helen Marocco Angel scholarships receive awards for tuition, books and other education-related expenses.

FAMILY & SOCIAL SUPPORTSupport for families can increase their understanding of the potential impact of MS on family life and help to strengthen the family unit. Fun and educational activities can help families maintain healthy and happy family and social relationships!

Caregiver education and support -- social events, educational seminars, and peer and professionally-led support groups address the special needs of the spouse, partner or family caregiver.

Respite care offers caregivers relief and may improve the health of the whole family. Caregivers are relieved by in-home assistance and a family consultant to help arrange respite hours with the home health agency. Subject to application, availability and waiting list, grants provide specific service allotments based on client needs.

Social events - families coming together find that they are not alone in coping with the challenges that MS might bring. Events such as Day at

the Bay include lunch, family fun and adaptive sailing. Our Thanksgiving Meal Delivery Program and Annual Family Holiday Brunch held in December offer families an enhanced sense of celebration. Multi-component Family Education Day events foster effective coping and communication skills.

Financial assistance is available to provide meaningful assistance to as many people living with MS as possible. The program assists people in maintaining their personal independence, safety, well-being and quality of life. Items considered include automobile or home modifications, long-term durable medical equipment needs, transportation assistance, health and wellness support, and critical short-term needs such as rent or utilities.

The MS van is an accessible van that can be rented for medical appointments, family outings or social events.

Information is available through the National MS Society’s Information Resource Center at 1-800-344-4867, the chapter’s web site www.MSpacific.org and through chapter newsletters such as the MSConnection, e-communications and mailings.

Research updates help keep constituents informed. The quarterly Research Bulletin details current MS research from international

sources including the National MS Society, National Institute of Health and pharmaceutical clinical trials. The research list provides updated research information monthly via e-mail. Clinical Updates containing basic information about MS, current research results and clinical practices are provided to healthcare providers several times a year.

EDUCATION

Multicultural outreach and community education helps engage the general public as well as under-represented groups, while teaching about MS and the programs and services offered by the National MS

Society. The chapter is a resource for non-native English speakers by providing literature in Spanish, a bilingual newsletter, and self-help groups in Spanish.

Professional education is offered to a select segment of healthcare professionals. Programs include topics such as rehabilitation techniques, psychosocial needs of people with MS and pharmacologic management of MS.

ADVOCACY

Until a cure is found, we must pursue legislative progress and improved government programs to help people living with MS and their families overcome many challenges. We work for increased MS research

funding, disability rights, access to quality health care, long-term care resources, and accessible, affordable insurance.

MS California Action Network (MS-CAN)is an e-mail campaign that drives instant awareness of local and state political happenings that affect people with MS. The alerts focus on housing, transportation, access accommodations and disability rights. The network is also used to promote advocacy and mobilize

the MS community

MS Action Network is comprised of individuals living with MS and their friends and relatives who send letters to local, state and federal legislators. The nationwide commitment of this grassroots-lobbying network makes the National MS Society one of America’s most respected voices on healthcare issues.

Government relations priorities are determined by the chapter’s nonpartisan Government Relations Committee (GRC), which is comprised of volunteers including people with MS, their loved ones, legal professionals and other experts. The GRC monitors and advocates for favorable legislation through face-to-face meetings with municipal and state lawmakers.

Information is available through the National MS Society’s Information Resource Center at 1-800-344-4867, the chapter’s web site www.MSpacific.org and through chapter newsletters such as the MSConnection, e-communications and mailings.

Research updates help keep constituents informed. The quarterly Research Bulletin details current MS research from international

sources including the National MS Society, National Institute of Health and pharmaceutical clinical trials. The research list provides updated research information monthly via e-mail. Clinical Updates containing basic information about MS, current research results and clinical practices are provided to healthcare providers several times a year.

EDUCATION

Multicultural outreach and community education helps engage the general public as well as under-represented groups, while teaching about MS and the programs and services offered by the National MS

Society. The chapter is a resource for non-native English speakers by providing literature in Spanish, a bilingual newsletter, and self-help groups in Spanish.

Professional education is offered to a select segment of healthcare professionals. Programs include topics such as rehabilitation techniques, psychosocial needs of people with MS and pharmacologic management of MS.

ADVOCACY

Until a cure is found, we must pursue legislative progress and improved government programs to help people living with MS and their families overcome many challenges. We work for increased MS research

funding, disability rights, access to quality health care, long-term care resources, and accessible, affordable insurance.

MS California Action Network (MS-CAN)is an e-mail campaign that drives instant awareness of local and state political happenings that affect people with MS. The alerts focus on housing, transportation, access accommodations and disability rights. The network is also used to promote advocacy and mobilize

the MS community

MS Action Network is comprised of individuals living with MS and their friends and relatives who send letters to local, state and federal legislators. The nationwide commitment of this grassroots-lobbying network makes the National MS Society one of America’s most respected voices on healthcare issues.

Government relations priorities are determined by the chapter’s nonpartisan Government Relations Committee (GRC), which is comprised of volunteers including people with MS, their loved ones, legal professionals and other experts. The GRC monitors and advocates for favorable legislation through face-to-face meetings with municipal and state lawmakers.

Information is available through the National MS Society’s Information Resource Center at 1-800-344-4867, the chapter’s web site www.MSpacific.org and through chapter newsletters such as the MSConnection, e-communications and mailings.

Research updates help keep constituents informed. The quarterly Research Bulletin details current MS research from international

sources including the National MS Society, National Institute of Health and pharmaceutical clinical trials. The research list provides updated research information monthly via e-mail. Clinical Updates containing basic information about MS, current research results and clinical practices are provided to healthcare providers several times a year.

EDUCATION

Multicultural outreach and community education helps engage the general public as well as under-represented groups, while teaching about MS and the programs and services offered by the National MS

Society. The chapter is a resource for non-native English speakers by providing literature in Spanish, a bilingual newsletter, and self-help groups in Spanish.

Professional education is offered to a select segment of healthcare professionals. Programs include topics such as rehabilitation techniques, psychosocial needs of people with MS and pharmacologic management of MS.

ADVOCACY

Until a cure is found, we must pursue legislative progress and improved government programs to help people living with MS and their families overcome many challenges. We work for increased MS research

funding, disability rights, access to quality health care, long-term care resources, and accessible, affordable insurance.

MS California Action Network (MS-CAN)is an e-mail campaign that drives instant awareness of local and state political happenings that affect people with MS. The alerts focus on housing, transportation, access accommodations and disability rights. The network is also used to promote advocacy and mobilize

the MS community

MS Action Network is comprised of individuals living with MS and their friends and relatives who send letters to local, state and federal legislators. The nationwide commitment of this grassroots-lobbying network makes the National MS Society one of America’s most respected voices on healthcare issues.

Government relations priorities are determined by the chapter’s nonpartisan Government Relations Committee (GRC), which is comprised of volunteers including people with MS, their loved ones, legal professionals and other experts. The GRC monitors and advocates for favorable legislation through face-to-face meetings with municipal and state lawmakers.

Information is available through the National MS Society’s Information Resource Center at 1-800-344-4867, the chapter’s web site www.MSpacific.org and through chapter newsletters such as the MSConnection, e-communications and mailings.

Research updates help keep constituents informed. The quarterly Research Bulletin details current MS research from international

sources including the National MS Society, National Institute of Health and pharmaceutical clinical trials. The research list provides updated research information monthly via e-mail. Clinical Updates containing basic information about MS, current research results and clinical practices are provided to healthcare providers several times a year.

EDUCATION

Multicultural outreach and community education helps engage the general public as well as under-represented groups, while teaching about MS and the programs and services offered by the National MS

Society. The chapter is a resource for non-native English speakers by providing literature in Spanish, a bilingual newsletter, and self-help groups in Spanish.

Professional education is offered to a select segment of healthcare professionals. Programs include topics such as rehabilitation techniques, psychosocial needs of people with MS and pharmacologic management of MS.

ADVOCACY

Until a cure is found, we must pursue legislative progress and improved government programs to help people living with MS and their families overcome many challenges. We work for increased MS research

funding, disability rights, access to quality health care, long-term care resources, and accessible, affordable insurance.

MS California Action Network (MS-CAN)is an e-mail campaign that drives instant awareness of local and state political happenings that affect people with MS. The alerts focus on housing, transportation, access accommodations and disability rights. The network is also used to promote advocacy and mobilize

the MS community

MS Action Network is comprised of individuals living with MS and their friends and relatives who send letters to local, state and federal legislators. The nationwide commitment of this grassroots-lobbying network makes the National MS Society one of America’s most respected voices on healthcare issues.

Government relations priorities are determined by the chapter’s nonpartisan Government Relations Committee (GRC), which is comprised of volunteers including people with MS, their loved ones, legal professionals and other experts. The GRC monitors and advocates for favorable legislation through face-to-face meetings with municipal and state lawmakers.

INDEPENDENCE

Employment referrals, resources and consultations are offered as related to job retention, reasonable accommodations, Social Security, disability benefits, health insurance, Americans with Disabilities Act (ADA),

Family Medical Leave Act and disclosure in the workplace. Structured education sessions are provided annually.

Financial planning services provided through a pro bono effort of independent financial service organizations teach skills such as money-management, prioritization of debt repayments and management of cash flow.

Care management provides one-on-one professional assistance to help individuals with MS achieve independence and autonomy.

MEM

BER

REG

ISTR

ATI

ON

FO

RM To receive more information about chapter programs and services, complete this form with all relevant information, place in envelope and mail to the address listed on the reverse side. Or, call 1-800 FIGHT MS (344-4867). All information will be kept confidential.

Please choose one I have MS I have a family member with MSof the following: I have a friend with MS Other relationship

Name: (First) (Last) (MI)Street Address: City: State: Zip:Home Phone: ( ) Work Phone: ( ) Date of Birth: / / (M/D/Y) Date of Diagnosis: / / (M/D/Y)Marital Status: Sex M F # of Dependents:Email: Primary Language:Occupation: Employer: Neurologist:

JOIN THE MOVEMENT®

Volunteer your time and talents to help the chapter. We have opportunities from everyday office activities to special events, and from professional services to direct services for people living with MS.

The chapter is supported through private donations, special events and grants from foundations (non-governmental).

Donate either personally through planned giving and bequests or through your employer by participating in workplace giving, company sponsorship of events or both! Enjoy the benefits of tax-deductible giving and the delight of contributing to a world free of MS. To donate online, visit www.MSpacific.org.

Participate in the chapter’s special event fundraisers to face physical challenge, increase community awareness of MS and raise funds.

Sponsor a program, service or event through tax-deductible underwriting.

FUNDRAISING EVENTS

Walk MS: A fun, family event with a festival atmosphere.

MS Golf Classic: Hosting corporations, friends and families.

Challenge Walk MS: Walk with purpose in this three-day, 50-mile life-changing event (hotel accommodations included).

Bike MS Bay to Bay Tour: A one- or two-day ride ranging from 30 to 150 miles. Challenge individuals and teams alike.

MS Dinner Auction: Hundreds of items up for auction – early holiday shopping!

Race to Stop MS: Professional training to complete your dream triathlon or marathon.

4 COLOR CMYK - 9”x8”

4 COLOR CMYK - 9”x8”

INDEPENDENCE

Employment referrals, resources and consultations are offered as related to job retention, reasonable accommodations, Social Security, disability benefits, health insurance, Americans with Disabilities Act (ADA),

Family Medical Leave Act and disclosure in the workplace. Structured education sessions are provided annually.

Financial planning services provided through a pro bono effort of independent financial service organizations teach skills such as money-management, prioritization of debt repayments and management of cash flow.

Care management provides one-on-one professional assistance to help individuals with MS achieve independence and autonomy.

MEM

BER

REG

ISTR

ATI

ON

FO

RM To receive more information about chapter programs and services, complete this form with all relevant information, place in envelope and mail to the address listed on the reverse side. Or, call 1-800 FIGHT MS (344-4867). All information will be kept confidential.

Please choose one I have MS I have a family member with MSof the following: I have a friend with MS Other relationship

Name: (First) (Last) (MI)Street Address: City: State: Zip:Home Phone: ( ) Work Phone: ( ) Date of Birth: / / (M/D/Y) Date of Diagnosis: / / (M/D/Y)Marital Status: Sex M F # of Dependents:Email: Primary Language:Occupation: Employer: Neurologist:

JOIN THE MOVEMENT®

Volunteer your time and talents to help the chapter. We have opportunities from everyday office activities to special events, and from professional services to direct services for people living with MS.

The chapter is supported through private donations, special events and grants from foundations (non-governmental).

Donate either personally through planned giving and bequests or through your employer by participating in workplace giving, company sponsorship of events or both! Enjoy the benefits of tax-deductible giving and the delight of contributing to a world free of MS. To donate online, visit www.MSpacific.org.

Participate in the chapter’s special event fundraisers to face physical challenge, increase community awareness of MS and raise funds.

Sponsor a program, service or event through tax-deductible underwriting.

FUNDRAISING EVENTS

Walk MS: A fun, family event with a festival atmosphere.

MS Golf Classic: Hosting corporations, friends and families.

Challenge Walk MS: Walk with purpose in this three-day, 50-mile life-changing event (hotel accommodations included).

Bike MS Bay to Bay Tour: A one- or two-day ride ranging from 30 to 150 miles. Challenge individuals and teams alike.

MS Dinner Auction: Hundreds of items up for auction – early holiday shopping!

Race to Stop MS: Professional training to complete your dream triathlon or marathon.

4 COLOR CMYK - 9”x8”

4 COLOR CMYK - 9”x8”

INDEPENDENCE

Employment referrals, resources and consultations are offered as related to job retention, reasonable accommodations, Social Security, disability benefits, health insurance, Americans with Disabilities Act (ADA),

Family Medical Leave Act and disclosure in the workplace. Structured education sessions are provided annually.

Financial planning services provided through a pro bono effort of independent financial service organizations teach skills such as money-management, prioritization of debt repayments and management of cash flow.

Care management provides one-on-one professional assistance to help individuals with MS achieve independence and autonomy.

MEM

BER

REG

ISTR

ATI

ON

FO

RM To receive more information about chapter programs and services, complete this form with all relevant information, place in envelope and mail to the address listed on the reverse side. Or, call 1-800 FIGHT MS (344-4867). All information will be kept confidential.

Please choose one I have MS I have a family member with MSof the following: I have a friend with MS Other relationship

Name: (First) (Last) (MI)Street Address: City: State: Zip:Home Phone: ( ) Work Phone: ( ) Date of Birth: / / (M/D/Y) Date of Diagnosis: / / (M/D/Y)Marital Status: Sex M F # of Dependents:Email: Primary Language:Occupation: Employer: Neurologist:

JOIN THE MOVEMENT®

Volunteer your time and talents to help the chapter. We have opportunities from everyday office activities to special events, and from professional services to direct services for people living with MS.

The chapter is supported through private donations, special events and grants from foundations (non-governmental).

Donate either personally through planned giving and bequests or through your employer by participating in workplace giving, company sponsorship of events or both! Enjoy the benefits of tax-deductible giving and the delight of contributing to a world free of MS. To donate online, visit www.MSpacific.org.

Participate in the chapter’s special event fundraisers to face physical challenge, increase community awareness of MS and raise funds.

Sponsor a program, service or event through tax-deductible underwriting.

FUNDRAISING EVENTS

Walk MS: A fun, family event with a festival atmosphere.

MS Golf Classic: Hosting corporations, friends and families.

Challenge Walk MS: Walk with purpose in this three-day, 50-mile life-changing event (hotel accommodations included).

Bike MS Bay to Bay Tour: A one- or two-day ride ranging from 30 to 150 miles. Challenge individuals and teams alike.

MS Dinner Auction: Hundreds of items up for auction – early holiday shopping!

Race to Stop MS: Professional training to complete your dream triathlon or marathon.

4 COLOR CMYK - 9”x8”

4 COLOR CMYK - 9”x8”

INDEPENDENCE

Employment referrals, resources and consultations are offered as related to job retention, reasonable accommodations, Social Security, disability benefits, health insurance, Americans with Disabilities Act (ADA),

Family Medical Leave Act and disclosure in the workplace. Structured education sessions are provided annually.

Financial planning services provided through a pro bono effort of independent financial service organizations teach skills such as money-management, prioritization of debt repayments and management of cash flow.

Care management provides one-on-one professional assistance to help individuals with MS achieve independence and autonomy.

MEM

BER

REG

ISTR

ATI

ON

FO

RM To receive more information about chapter programs and services, complete this form with all relevant information, place in envelope and mail to the address listed on the reverse side. Or, call 1-800 FIGHT MS (344-4867). All information will be kept confidential.

Please choose one I have MS I have a family member with MSof the following: I have a friend with MS Other relationship

Name: (First) (Last) (MI)Street Address: City: State: Zip:Home Phone: ( ) Work Phone: ( ) Date of Birth: / / (M/D/Y) Date of Diagnosis: / / (M/D/Y)Marital Status: Sex M F # of Dependents:Email: Primary Language:Occupation: Employer: Neurologist:

JOIN THE MOVEMENT®

Volunteer your time and talents to help the chapter. We have opportunities from everyday office activities to special events, and from professional services to direct services for people living with MS.

The chapter is supported through private donations, special events and grants from foundations (non-governmental).

Donate either personally through planned giving and bequests or through your employer by participating in workplace giving, company sponsorship of events or both! Enjoy the benefits of tax-deductible giving and the delight of contributing to a world free of MS. To donate online, visit www.MSpacific.org.

Participate in the chapter’s special event fundraisers to face physical challenge, increase community awareness of MS and raise funds.

Sponsor a program, service or event through tax-deductible underwriting.

FUNDRAISING EVENTS

Walk MS: A fun, family event with a festival atmosphere.

MS Golf Classic: Hosting corporations, friends and families.

Challenge Walk MS: Walk with purpose in this three-day, 50-mile life-changing event (hotel accommodations included).

Bike MS Bay to Bay Tour: A one- or two-day ride ranging from 30 to 150 miles. Challenge individuals and teams alike.

MS Dinner Auction: Hundreds of items up for auction – early holiday shopping!

Race to Stop MS: Professional training to complete your dream triathlon or marathon.

4 COLOR CMYK - 9”x8”

4 COLOR CMYK - 9”x8”

PACIFIC SOUTH COAST CHAPTER

The mission of the National MS Society is to mobilize people and resources to drive research for a cure and to address the challenges of everyone affected by MS. Locally, the Pacific South Coast Chapter provides programs and services designed to help the 18,000 people and families affected by

MS in San Diego, Orange and Imperial counties move their lives forward. All programs and services are offered at minimal or no cost to participants; fees are often waived for those with financial need. Most programs are offered on an ongoing basis throughout the chapter territory.

Visit www.MSpacific.org or call 1-800-344-4867 for details.

WHAT IS MS?

Multiple sclerosis (MS) is an unpredictable neurological disease that

interrupts the flow of information within the brain and between the

brain and body. The progress, severity and specific symptoms in any

one person cannot yet be predicted, and may range from numbness

and tingling to blindness and paralysis. Most people with MS are

diagnosed between the ages of 20 and 50, with more at least two

to three times more women than men being diagnosed with the

disease. MS affects more than 400,000 people in the U.S., and

2.1 million worldwide.

www.MSpacific.org

www.nationalMSsociety.org

1-800-344-4867 (1-800-FIGHT-MS)

JOIN THE MOVEMENT

TWO OFFICES TO SERVE YOU

3000 Airway AvenueSuite 125

Costa Mesa, CA 92626

5950 La Place CourtSuite 200

Carlsbad, CA 92008