MSAA Terms & Conditions
Web Terms and Conditions
The Multiple Sclerosis Association of America (MSAA) is a nonprofit organization whose mission is to enrich the quality of life for everyone affected by multiple sclerosis. The goal of this website is to provide a source of information to our clients, their care partners, and the general public on MS. The information that is found on this website is based on professional advice, published research, and expert opinion, but does not represent therapeutic recommendation or prescription. MSAA Strives to provide useful, up-to-date information on matters of concern to MS patients and their families. This material is intended for general informational purposes only, and it does not constitute medical advice. You should not use the information presented as a means of diagnosis or for determining treatment. For diagnosis and treatment options, you are urged to consult your physician. Those affiliated with this website and MSAA cannot be held responsible for any unintentional errors in the writing of this website or changes in information that may occur, possibly affecting certain details of an explanation, assumption, or treatment. MSAA does not endorse nor recommend, products, services or items that appear on this website.
The entire contents and design of msassociation.org are protected under U.S. and international copyrights. Msassociation.org is for your own personal noncommercial use. You may download materials for personal use only. You may not modify, distribute, transmit, display, or publish any materials contained on msassociation.org without the prior written permission of msassociation.org or the appropriate copyright owner. Please refer to the copyright notice for more information. Certain names and logos are trademarks and service marks of msassociation.org and third parties and may not be used without permission.Msassociation.org is funded through various grants and donations.MSAA does not have or accept any paid links or advertising on its website msassociation.org
Thank you for visiting the MSAA website. We hope that you find it informative and a valuable research tool in understanding and coping with MS.
Contact Information
MSAA National Headquarters is located at:
706 Haddonfield Road
Cherry Hill, NJ 08002
Email: msaa@msassociation.org
Phone: (800) 532-7667
Cookies
We use cookies (small files that are sent to your web browser and stored on your computer’s hard drive) to improve your website experience. The cookie is used to speed up your access to the website and the information you wish to see, but it does not contain any personal information. When you log on to our website our web server automatically records domain name and standard information about the operating system and web browser. To track your progress through the site and help us evaluate usage of the site, the server places a “cookie,” a small text file with an identification number, on your machine. This automatically collected information is used for statistical purposes to help us manage our site.
Opting –Out
The majority of web browsers accept cookies but the “help” menu on your browser should give you options for preventing and accepting or receiving notice of new cookies. However, please be aware that if you block cookies, some website functionality may be lost. After gathering any user information, MSAA offers users the opportunity to remove their information from our active database so as not to receive further communication and/or to no longer interact with the website.
Data Use
We collect information on you only if you volunteer it. There are several ways you may volunteer information on the site. These include completing a survey, sending an email inquiry to us, contributing online, or registering for or contributing to a participant in an event online. The information provided is collected and used to provide you with information about our programs and services available to you through MSAA. We generally respond to your request via postal service mail, email, or telephone depending on your request with our resources.Sometimes we will use the information that you volunteer on several instances:
| • | Mailings with information about multiple sclerosis and MSAA ’s programs and events |
| • | Mailings to invite you to join MSAA or to help MSAA fulfill its mission |
| • | Telephone contact to invite you to help MSAA achieve its mission |
| • | Email contact to respond to your questions, comments, or suggestions |
| • | Email contact to alert you to multiple sclerosis news updates and programs, as well as invitations to join MSAA or to help MSAA fulfill its mission. |
Acceptance of These Terms
By using our website, you consent to the collection and use of this information by MSAA. If we decide to change our privacy policy, we will post those changes on this page so that you are always aware of what information we collect, how we use it, and under what circumstances we disclose it.
Link Policy
Multiple Sclerosis Association of America, Inc (MSAA) website may contain links to other sites. MSAA is not responsible for the content or accuracy of the information, or the privacy practices of these sites. You should review the privacy policy of these sites to learn more about what and how they collect and use any personal identification information. All websites who wish to link to msassociation.org must be reviewed by a website editorial board and in some way represent MSAA's mission to enrich the quality of life for everyone affected by multiple sclerosis. If you are interested in linking to MSAA's website please contact MSAA's webmaster . MSAA reserves the right to determine which links to provide on the website as well as the right to terminate links at anytime. MSAA does not have or accept any paid links or advertising on its website msassociation.org
Donor Rights
MSAA has created and follows the Fundraising Standards established by the Board of Directors. These standards include:
Truthfulness in communication
Communications and donor expectations and intent
Reporting to donors
Controls over solicitors
Acknowledgements of grants,donations, and gifts in-kind
Donor requests
Registration of fundraising consultants
Acceptance of gifts
MSAA adheres to the Donor Bill of Rights, created by the American Association of Fund Raising Counsel (AAFRC), the Association for Healthcare Philanthropy (AHP), the Association of Fundraising Professionals (AFP), and the Council for Advancement and Support of Education (CASE). The full text of the Donor Bill of Rights can be found at www.afpnet.org/ethics/ethics_and_donors .
Donor Bill of Rights
As Published by the Association of Fundraising Professionals at www.afpnet.org
Philanthropy is based on voluntary actions for the common good. It is a tradition of giving and sharing that is primary to the quality of life. To ensure that philanthropy merits the respect and trust of the general public, and that donors and prospective donors can have full confidence in the nonprofit organizations and causes they are asked to support, we declare that all donors have these rights:
- To be informed of the organization's mission, of the way the organization intends to use donated resources, and its capacity to use donations effectively for their intended purposes .
- To be informed of the identity of those serving on the organization's governing board, and to expect the board to exercise prudent judgment in its stewardship responsibilities.
- To have access to the organization's most recent financial statements.
- To be assured their gifts will be used for the purposes for which they were given.
- To receive appropriate acknowledgement and recognition.
- To be assured that information about their donation is handled with respect and with confidentiality to the extent provided by law.
- To expect that all relationships with individuals representing organizations of interest to the donor will be professional in nature.
- To be informed whether those seeking donations are volunteers, employees of the organization, or hired solicitors.
- To have the opportunity for their names to be deleted from mailing lists that an organization may intend to share.
- To feel free to ask questions when making a donation and to receive prompt, truthful and forthright answers.
If you have any questions please contact MSAA's Development office by phone (800) 532-7667, ext. 159 or through email at bwilliams@msassociation.org.
Security of Donation
If you are making a donation to MSAA online you will be directed to a secure website where you can make a donation to MSAA via credit card. MSAA will not be sharing this information you provide with any outside parties. All donations that are made online will only be handled by those who are either contracted by MSAA or are members of the internal staff. We have put in place appropriate physical, electronic, and managerial procedures to safeguard and help prevent unauthorized access, maintain data security, and correctly use the information we collect online.
Although we take appropriate measures to safeguard against unauthorized disclosures of information, we cannot assure you that personally identifiable information that we collect will never be disclosed in a manner that is inconsistent with this privacy notice. Inadvertent disclosures may result, for example, when third parties misrepresent their identities in asking the site for access to personally identifiable information about themselves for purpose of correcting possible factual errors in the data.
What We Do
The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization dedicated to enriching the quality of life for everyone affected by multiple sclerosis. MSAA provides ongoing support and direct services to individuals with MS and their families. MSAA also serves to promote greater understanding of the needs and challenges of those who face physical obstacles.
Programs and services provided by MSAA include:
| • | National toll-free information and support Helpline (800-532-7667) |
| • | Compassionate and responsive consultation with MS clients and their families |
| • | Support groups for individuals with MS, their care partners, their children, men’s groups, and teens with MS |
| • | Equipment Distribution Program (wheelchairs, walkers, scooters, etc.) for those who are physically challenged |
| • | Cooling Assistance Program to provide relief for heat-sensitive individuals |
| • | Barrier-free housing for physically disabled adults who wish to remain independent |
| • | Funding of diagnostic MRIs for those who have been denied insurance coverage |
| • | Insurance advocacy and financial assistance to individuals in need of follow-up MRI exams through the MSAA MRI Institute |
| • | Educational literature on topics ranging from medical research and treatments to managing symptoms and coping with MS |
| • | Free lending library of books and materials on topics related to multiple sclerosis |
| • | Awareness events including conferences with educational workshops, guest speakers, and information on helpful products and services |
Multiple sclerosis – a disease with no known cause, cure, or prevention – is the most common neurological disorder of young adults. Many of the estimated 350,000 individuals with MS are diagnosed between the ages of 15 and 50. Women are twice as likely as men to develop MS.
Since 1970, MSAA’s philosophy and efforts have focused on improving the quality of day-to-day life for people with MS and their families. MSAA relies heavily on volunteer efforts and the ongoing support of the general public.
MSAA invites everyone in the community to join our cause – working together to break down barriers (physical, emotional, and social) and build up hope for those who are physically challenged.


