Educational Teleconference Programs 2011-2012
Parenting Skills - Developing a Tool Kit
This teleconference will help you to identify your parenting strengths, and trouble spots in managing MS and parenting responsibilities. It will focus on the importance of communication, planning, prioritizing and developing a support network.
Speaker: Nancy Lowenstein, OT
Mount Auburn Hospital Comprehensive MS Care Center, Cambridge, Massachusetts; Assistant Clinical Professor at the Occupational Therapy Program, Boston University.
Speaker: Ronnie Hochberg, MS, CRC, LMHC
Mt. Sinai Medical Center, Department of Psychiatry New York, NY
Date: Thursday, November 10, 2011
Time: 6:30 – 7:30 p.m.
REGISTRATION DEADLINE: Thursday, November 3, 2011
Where is My Memory? Cognitive Changes in MS
This teleconference will explain cognitive issues in MS and delve into the impact of cognitive dysfunction on everyday life. Additionally, we will explore tools to help people with MS manage and adapt to their effects.
Speaker: John DeLuca, PhD
Speaker: Jeffrey Gingold, author of the Award-winning book, “Facing the Cognitive Challenges of Multiple Sclerosis” and person living with MS.
Date: Tuesday, January 24, 2012
Time: 6:30 – 7:30 p.m.
REGISTRATION DEADLINE: Tuesday, January 17, 2012
Emerging Therapies
The emergence of new MS therapies is both exciting and challenging for people living with MS and the clinicians who treat them. Our speaker, an MS specialist neurologist, will discuss the most recent information concerning newly emerging MS therapies to promote a better understanding and educate participants on treatment options.
Speaker: Stephen Krieger, MD
Corinne Goldsmith Dickinson Center for MS at Mt Sinai Medical Center, New York, NY
Date: Thursday, March 15, 2012
Time: 6:30 – 7:30 p.m.
REGISTRATION DEADLINE: Thursday, March 8, 2012
Using Assistive Technology for People Living with MS
Mark Surabian, Assistive Technology Practitioner, will discuss a variety of assistive technologies that can enable people living with MS to function better at home, at work and at leisure. He will also address resources that may be available in the community for funding of equipment.
Speaker: Mark Surabian, Assistive Technology Practitioner
Pace University, New York, NY www.Cognitechcafe.com
Date: Thursday, May 3, 2012
Time: 6:30 – 7:30 p.m.
REGISTRATION DEADLINE: Thursday, April 26, 2012
Management and Rehabilitation of Advanced MS
Dr Kraft will present a brief overview of advanced MS, current status of research and practical application of symptom management.
Speaker: George H. Kraft, M.D., M.S.
Director of the Western Multiple Sclerosis Clinical Center and Alvord Professor of MS Research; Professor, Rehabilitation Medicine and Neurology at the University of Washington in Seattle
Date: Wednesday, July 18, 2012
Time: 6:30 – 7:30 p.m.
REGISTRATION DEADLINE: Wednesday, July 11, 2012
Staying Healthy With Vitamins and Oral Supplements
Learn about the benefits of oral supplements and discuss some of the most commonly used vitamins, minerals and herbs.
Speaker: Patricia Melville, NP-C
Stony Brook MS Comprehensive Care Center, Stony Brook, NY
Date: Thursday, September 13, 2012
Time: 6:30 – 7:30 p.m.
REGISTRATION DEADLINE: Thursday, September 6, 2012
Register today! Registration is FREE.
For more information or to register, please call 1-800-344-4867, option 1 or visit the Teleconference Series page.
National Multiple Sclerosis Society, Greater New England Chapter
101A First Avenue, Suite 6 | Waltham, Mass. 02451-1115
tel: 1 800-344-4867 | fax: 1 781-890-2089 | MSnewengland.org
Monday, October 17, 2011
Wednesday, October 12, 2011
The Promise of NOW: Annual Meeting of Members Research Update & Conference
*** Less than 2 weeks left to register! ***
The Promise of NOW: Annual Meeting of Members Conference & EXPO with Stanley F. Waterman Research Update
This year’s Annual Meeting of Members will include educational workshops, a research update and a product EXPO at each of our four locations. Conference attendees will have the opportunity to visit the EXPO to learn about health, recreation, and independence products and services, and to network with others living with MS. This FREE program includes lunch. Limit 2 adult guests per registrant.
PRE-REGISTRATION IS REQUIRED.
Date: Saturday, October 29, 2011
Location – choose the site you wish to attend:
Best Western Royal Plaza Trade Center, Marlborough MA
Stanley F. Waterman Research Update- Opening Doors in the MS Research Pipeline: 20 years of Progress in MS Diagnosis and Treatment presented by Mayo Clinic Neurologist and Researcher Dr. Brian Weinshenker Winner of the 2011 John Dystel Prize for MS Research
Clarion, Portland ME
Stanley F. Waterman Research Update- How are Cognition and Fatigue Affected by MS presented by John DeLuca, Ph.D., ABPP, Professor, Dept of Physical Medicine and Rehabilitation, Dept of Neurosciences Univ. of Medicine & Dentistry of New Jersey - New Jersey Medical School
Church Landing, Meredith NH
Stanley F. Waterman Research Update- Coming Soon - a New Treatment Option for Secondary Progressive MS presented by Carolina Ionete, MD, Ph.D, University of Massachusetts Medical Center Multiple Sclerosis Clinic Neurologist & Researcher
Hilton Burlington Hotel, Burlington VT
Stanley F. Waterman Research Update- Hope Through MS Research: Recent Advances and Emerging Therapies presented by Angela Applebee, MD, Assistant Professor, University of Vermont College of Medicine, Director of the MS Center of Northern New England, Burlington, VT
Registration deadline: October 22, 2011
Agenda:
8:30 am Continental Breakfast & Registration
9:00 am Welcome & EXPO
9:30 am Workshops
12:00 noon Lunch
12:30 pm Annual Meeting
1:30 pm Stanley F. Waterman Research Presentation
Learn something new about current MS research directions, MS treatments, symptom management, resources, services & products available to you. Feel more confident in managing MS & its effects on your life. Learn something new about the National MS Society & the Greater New England Chapter and join the movement!
To register: Follow the links for the location you want to attend
Call 1-800-344-4867.
If you are not able to attend and wish to assign your proxy vote, please use this link:
Eligibility: Person with MS and adult guests.
This program not suitable for children. This program is handicapped-accessible.
The Promise of NOW: Annual Meeting of Members Conference & EXPO with Stanley F. Waterman Research Update
This year’s Annual Meeting of Members will include educational workshops, a research update and a product EXPO at each of our four locations. Conference attendees will have the opportunity to visit the EXPO to learn about health, recreation, and independence products and services, and to network with others living with MS. This FREE program includes lunch. Limit 2 adult guests per registrant.
PRE-REGISTRATION IS REQUIRED.
Date: Saturday, October 29, 2011
Location – choose the site you wish to attend:
Best Western Royal Plaza Trade Center, Marlborough MA
Stanley F. Waterman Research Update- Opening Doors in the MS Research Pipeline: 20 years of Progress in MS Diagnosis and Treatment presented by Mayo Clinic Neurologist and Researcher Dr. Brian Weinshenker Winner of the 2011 John Dystel Prize for MS Research
Clarion, Portland ME
Stanley F. Waterman Research Update- How are Cognition and Fatigue Affected by MS presented by John DeLuca, Ph.D., ABPP, Professor, Dept of Physical Medicine and Rehabilitation, Dept of Neurosciences Univ. of Medicine & Dentistry of New Jersey - New Jersey Medical School
Church Landing, Meredith NH
Stanley F. Waterman Research Update- Coming Soon - a New Treatment Option for Secondary Progressive MS presented by Carolina Ionete, MD, Ph.D, University of Massachusetts Medical Center Multiple Sclerosis Clinic Neurologist & Researcher
Hilton Burlington Hotel, Burlington VT
Stanley F. Waterman Research Update- Hope Through MS Research: Recent Advances and Emerging Therapies presented by Angela Applebee, MD, Assistant Professor, University of Vermont College of Medicine, Director of the MS Center of Northern New England, Burlington, VT
Registration deadline: October 22, 2011
Agenda:
8:30 am Continental Breakfast & Registration
9:00 am Welcome & EXPO
9:30 am Workshops
12:00 noon Lunch
12:30 pm Annual Meeting
1:30 pm Stanley F. Waterman Research Presentation
Learn something new about current MS research directions, MS treatments, symptom management, resources, services & products available to you. Feel more confident in managing MS & its effects on your life. Learn something new about the National MS Society & the Greater New England Chapter and join the movement!
To register: Follow the links for the location you want to attend
Call 1-800-344-4867.
If you are not able to attend and wish to assign your proxy vote, please use this link:
Eligibility: Person with MS and adult guests.
This program not suitable for children. This program is handicapped-accessible.
Saturday, October 8, 2011
Ask the Employment Specialist: Telephone Q&A Sessions
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JOIN THE MOVEMENT
ASK THE EMPLOYMENT SPECIALIST: TELEPHONE Q&A SESSIONS
Do you have an employment question you would like answered?
Are you curious about workplace disclosure, social security benefits, need a reasonable accommodation or are you thinking about returning to work?
On October 19, November 16 and December 14, employment specialist Barbara McKeon, CRC, LMHC, Director of Employment for the NYC - Southern NY Chapter of the National MS Society, will be available to address your questions regarding employment concerns for people living with MS.
Participants may register for any one session of their choice:
October 19 12 p.m. – 1 p.m.
November 16 6 p.m. – 7 p.m.
December 14 12 p.m. – 1 p.m.
Dial-in information will be provided with registration confirmation. Participants will be asked to present their question in advance during registration.
Register online or for more information, call 1-800-344-4867 and have your question ready!
Print all
Ask the Employment Specialist: Telephone Q&A Sessions
Inbox
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National MS Society, Greater New England Chapter amber.stalker@nmss.org to me
show details 4:53 PM (15 hours ago)
Images are not displayed.
Display images below - Always display images from amber.stalker@nmss.org
JOIN THE MOVEMENT
ASK THE EMPLOYMENT SPECIALIST: TELEPHONE Q&A SESSIONS
Do you have an employment question you would like answered?
Are you curious about workplace disclosure, social security benefits, need a reasonable accommodation or are you thinking about returning to work?
On October 19, November 16 and December 14, employment specialist Barbara McKeon, CRC, LMHC, Director of Employment for the NYC - Southern NY Chapter of the National MS Society, will be available to address your questions regarding employment concerns for people living with MS.
Participants may register for any one session of their choice:
October 19 12 p.m. – 1 p.m.
November 16 6 p.m. – 7 p.m.
December 14 12 p.m. – 1 p.m.
Dial-in information will be provided with registration confirmation. Participants will be asked to present their question in advance during registration.
Register online or for more information, call 1-800-344-4867 and have your question ready!
Friday, October 7, 2011
Federal Focus - October 2011
Weigh-in with Your Member to Protect MS Research
As many of you have probably heard, Congress has appointed a "Supercommittee," a bipartisan body consisting of six Senators and six Representatives, to find ways to reduce spending and tackle the federal deficit. This committee is tasked with drafting and voting on a proposal to find at least $1.5 trillion dollars in savings over ten years, by November 23.
Although an important task, we must ensure that federal cuts don’t harm research and critical programs for people with chronic diseases and disabilities, like MS. While the Society is advocating for many investments like Medicaid and Social Security to be protected, our community has prioritized maintaining MS research as a top priority.
Senate and House committees have until October 14 to provide recommendations to the Supercommittee. Click here to contact your members today and urge them to remind the Supercommittee of the importance in investing in MS research.
Federal Appropriations Update
This week, Congress cleared and the President signed a “Continuing Resolution” (CR) that will fund the federal government and its programs through November 18. Congress was to have completed work on its 12 annual appropriations bills by the beginning of the fiscal year--October 1. Because this did not happen, the CR grants Congressional appropriators and leadership time to determine final funding levels for Fiscal Year (FY) 2012.
The Society has been and will continue to urge robust appropriations for MS research and many programs that support people affected by MS. Last month, the Senate Appropriations Committee moved forward the Department of Defense appropriations bill, which funds the Congressionally Directed Medical Research Programs (CDMRP). This vote comes months after the House approved its bill in June. As in years past, the Senate did not include a specific line item for the MS Research Program in the CDMRP. The MS program received $3.8 million in the House Appropriations bill. The Society will continue to urge Congress to adopt the House’s appropriation as the process moves forward.
The House Appropriations Majority recently released a draft of its Labor-Health and Human Services appropriations bill that funds critical research and health programs. The draft provides $31.7 billion in program funding for the National Institutes of Health (NIH), which is $1 billion over last year’s level, while the Senate Appropriations Committee bill would provide $30.5 billion for NIH. The House draft bill also includes $2.495 million for the Lifespan Respite Care Program, which is the same funding level that the Senate Committee provides.
As November 18 approaches, stay tuned for opportunities to urge your federal lawmakers to provide meaningful support for people with MS in the FY 12 budget.
Lifespan Respite Grants
At the end of July, the U.S. Administration on Aging (AoA) announced more than $1.1 million total in grants to the following six states to implement statewide respite system to serve family caregivers: Colorado, Hawaii, Montana, New Jersey, Ohio, and Virginia. The Lifespan Respite Care Program was enacted in 2006 to increase access to and quality of respite services for some of our nation’s 65 million family caregivers, including those that support people living with MS. Just last Friday, AoA announced another $1.1 million in grants to the following six states that have received previous grants to expand their programs: Delaware, Nevada, North Carolina, Rhode Island, South Carolina, Tennessee, and Texas, and the District of Columbia. These grants stem from the program’s funding FY 2011 funding that MS activists advocated for at the Society’s 2010 Public Policy Conference.
As many of you have probably heard, Congress has appointed a "Supercommittee," a bipartisan body consisting of six Senators and six Representatives, to find ways to reduce spending and tackle the federal deficit. This committee is tasked with drafting and voting on a proposal to find at least $1.5 trillion dollars in savings over ten years, by November 23.
Although an important task, we must ensure that federal cuts don’t harm research and critical programs for people with chronic diseases and disabilities, like MS. While the Society is advocating for many investments like Medicaid and Social Security to be protected, our community has prioritized maintaining MS research as a top priority.
Senate and House committees have until October 14 to provide recommendations to the Supercommittee. Click here to contact your members today and urge them to remind the Supercommittee of the importance in investing in MS research.
Federal Appropriations Update
This week, Congress cleared and the President signed a “Continuing Resolution” (CR) that will fund the federal government and its programs through November 18. Congress was to have completed work on its 12 annual appropriations bills by the beginning of the fiscal year--October 1. Because this did not happen, the CR grants Congressional appropriators and leadership time to determine final funding levels for Fiscal Year (FY) 2012.
The Society has been and will continue to urge robust appropriations for MS research and many programs that support people affected by MS. Last month, the Senate Appropriations Committee moved forward the Department of Defense appropriations bill, which funds the Congressionally Directed Medical Research Programs (CDMRP). This vote comes months after the House approved its bill in June. As in years past, the Senate did not include a specific line item for the MS Research Program in the CDMRP. The MS program received $3.8 million in the House Appropriations bill. The Society will continue to urge Congress to adopt the House’s appropriation as the process moves forward.
The House Appropriations Majority recently released a draft of its Labor-Health and Human Services appropriations bill that funds critical research and health programs. The draft provides $31.7 billion in program funding for the National Institutes of Health (NIH), which is $1 billion over last year’s level, while the Senate Appropriations Committee bill would provide $30.5 billion for NIH. The House draft bill also includes $2.495 million for the Lifespan Respite Care Program, which is the same funding level that the Senate Committee provides.
As November 18 approaches, stay tuned for opportunities to urge your federal lawmakers to provide meaningful support for people with MS in the FY 12 budget.
Lifespan Respite Grants
At the end of July, the U.S. Administration on Aging (AoA) announced more than $1.1 million total in grants to the following six states to implement statewide respite system to serve family caregivers: Colorado, Hawaii, Montana, New Jersey, Ohio, and Virginia. The Lifespan Respite Care Program was enacted in 2006 to increase access to and quality of respite services for some of our nation’s 65 million family caregivers, including those that support people living with MS. Just last Friday, AoA announced another $1.1 million in grants to the following six states that have received previous grants to expand their programs: Delaware, Nevada, North Carolina, Rhode Island, South Carolina, Tennessee, and Texas, and the District of Columbia. These grants stem from the program’s funding FY 2011 funding that MS activists advocated for at the Society’s 2010 Public Policy Conference.
Tuesday, October 4, 2011
MSConnection Fall 2011
Table of Contents — Fall 2011 Issue
Passes For MS Logo
Passes for MS Campaign Gains Yardage for People with multiple sclerosis
Top Stories
From the President
Passes for MS Campaign Gains Yardage for People with multiple sclerosis
Annual Meeting of Members
News
Medicare “Improvement Standard” Challenged
Potential Anti-Spasticity Treatment Boosted by the Society’s Fast Forward Program
Welcome to Digital Momentum!
New Free App!
You’ll be seeing a lot more of this thing!
Judy Hallam Receives New Hampshire Governor’s Accessibility Award
Newly Diagnosed
The Benefits of Denial
Programs
Medical Student Fellowship
Regional Programs Offer Many Opportunities!
Program Highlights
Building a Life of Inclusion in Fall River
Research
Understanding CCSVI and MS
Resources to find Clinical Trials
MS NOW
Research News
Advocacy
MS Activist Blog
Action Alert
Government Relations Committee
Health Care Reform Implementation
Federal Update
Maine
Massachusetts
New Hampshire
Vermont
Volunteers
Passionate People = Productivity
Fundraising
Thank you to our sponsors!
The Golden Circle
Students conduct penny drive for MS
Ride to be Cool
Zumba
Cape Cod Getaway
NH Seacoast Escape
Bike MS Season Starts Strong!
Journey of Hope 2011
30th Annual MS Harborfest!
Fashion Plates Luncheon & Fashion Show
Boston Volvo 5K Road Race
Calendar of Events - see current calendar
Classified Ads - see current listings
Community Programs Catalog Fall 2011
Facebook Become a fan of the Greater New England Chapter on Facebook
You are receiving this email because you chose to subscribe electronically to the MS Connection. To update your email preferences, including unsubscribing from MS Connection, please click the Unsubscribe link below.
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 http://main.nationalmssociety.org/ or 1-800-FIGHT-MS (344-4867).
Our postal address is:
National Multiple Sclerosis Society
733 Third Avenue
New York, New York 10017
Passes For MS Logo
Passes for MS Campaign Gains Yardage for People with multiple sclerosis
Top Stories
From the President
Passes for MS Campaign Gains Yardage for People with multiple sclerosis
Annual Meeting of Members
News
Medicare “Improvement Standard” Challenged
Potential Anti-Spasticity Treatment Boosted by the Society’s Fast Forward Program
Welcome to Digital Momentum!
New Free App!
You’ll be seeing a lot more of this thing!
Judy Hallam Receives New Hampshire Governor’s Accessibility Award
Newly Diagnosed
The Benefits of Denial
Programs
Medical Student Fellowship
Regional Programs Offer Many Opportunities!
Program Highlights
Building a Life of Inclusion in Fall River
Research
Understanding CCSVI and MS
Resources to find Clinical Trials
MS NOW
Research News
Advocacy
MS Activist Blog
Action Alert
Government Relations Committee
Health Care Reform Implementation
Federal Update
Maine
Massachusetts
New Hampshire
Vermont
Volunteers
Passionate People = Productivity
Fundraising
Thank you to our sponsors!
The Golden Circle
Students conduct penny drive for MS
Ride to be Cool
Zumba
Cape Cod Getaway
NH Seacoast Escape
Bike MS Season Starts Strong!
Journey of Hope 2011
30th Annual MS Harborfest!
Fashion Plates Luncheon & Fashion Show
Boston Volvo 5K Road Race
Calendar of Events - see current calendar
Classified Ads - see current listings
Community Programs Catalog Fall 2011
Facebook Become a fan of the Greater New England Chapter on Facebook
You are receiving this email because you chose to subscribe electronically to the MS Connection. To update your email preferences, including unsubscribing from MS Connection, please click the Unsubscribe link below.
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 http://main.nationalmssociety.org/ or 1-800-FIGHT-MS (344-4867).
Our postal address is:
National Multiple Sclerosis Society
733 Third Avenue
New York, New York 10017
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About Me
- Steve
- North Grafton, Massachusetts, United States
- Well-educated, disabled at this point with Multiple Sclerosis. I am very glad that I was able to do the things that I have been able to do over the years. had to change the picture, this one's more realistic.