The MS Australia website is set up in a simple manner so that anyone can easily navigate it to get to the information they are looking for.  The Multiple Sclerosis Australia homepage includes only the basic links in order to minimize clutter.  This makes it easy for people to quickly find what they are looking for, whether they are a patient, a family member, a contributor, or a medical professional.  Their front page also includes a way to make the text larger or smaller, depending on a person’s needs, and it also offers the opportunity to change the language that the website is displayed it.  This makes it accessible to more people across the world.

Also featured on the home page of Multiple Sclerosis Australia is a handy search box, powered by Google.  You can use this to search the entire website for specific keywords in order to quickly find …

For those who suffer from multiple sclerosis and have children, MS Moms can be a great resource.  It is geared towards women who have the chronic neurological disease and also deal with raising children and having a family at home.  Created by Lorna J. Moorhead, the MS Moms site aims to provide these women with information about the disease, how they can alter their lifestyle to increase their quality of life while living with a chronic disease, and how to juggle their disease and their family and home life.  The site also stresses the importance of being able to laugh in the face of struggle and being able to enjoy life at all times, regardless of the situation.

For any person who is diagnosed with multiple sclerosis, learning more about the disease is the first step.  MS Moms offers information about the chronic disease for anyone, whether they are a …

Many hospitals have different departments for certain ailments or treatment options.  One of these is special areas is multiple sclerosis hospitals.  Multiple sclerosis is a chronic, neurological disease that affects the body’s nervous system.  This means it is usually treated by neurologists, doctors who specialize in diagnosing and treating diseases of the nervous system.  Most major hospitals will have an area for treating multiple sclerosis, but it is important to make sure before visiting the hospital or trying to make an appointment there.  A hospital will usually list the departments they have and the types of doctors they employ on their website, or you can call them and ask.

If there is more than one hospital in your local area that can treat multiple sclerosis, consider checking them all out in order to find the one that suits you best.  Find the hospital that has the most suitable environment …

The National Multiple Sclerosis Society has many different chapters all over the United States.  This includes the MS Society WA and the MS Society NYC.  These are both very large chapters that serve a lot of the population on opposite ends of the country that struggle with multiple sclerosis and its effects.  The Multiple Sclerosis Society WA serves people in the states of Washington, Alaska, and Montana.  The Multiple Sclerosis Society NYC serves people in the five different boroughs of New York City.  Combined, they serve over 22,000 people afflicted with or affected by multiple sclerosis, providing them with information, raising money for funding research and support programs, and educating the general public about multiple sclerosis.

Both of these chapters feature online websites with information about the multiple sclerosis society.  They feature specific information about their chapters, as well as overall information about the national society in general.  National …

One of the most important things that the MS Society Scotland does is collect money for research.  Currently, multiple sclerosis is still a mysterious disease in many ways to medical professionals, and there is no cure.  Since it is a very disabling disease that progressively gets worse over time, doctors and researchers are struggling to find a cure as quickly as possible.  They are also always looking for ways to help slow down the progression of the disease to ensure people diagnosed with multiple sclerosis can still live long, full lives without the full effect of symptoms getting in the way of daily living.

In order to raise money for research purposes, the MS Society Scotland holds many different kinds of events.  Some of these are physical activities for the community.  These can include walks, races, obstacle courses, or even bike tours that are held for the multiple sclerosis cause.  …

All across the world, there are many different MS organizations.  It is important to find legitimate multiple sclerosis organizations that offer valid information, support to patients and their caregivers, and a place for medical professionals to share research and connect with each other.  There are many different ways to look for these organizations in a particular area.  The easiest way is to use the Internet.  A search engine can give someone a guide to the closest multiple sclerosis organization near them, what services they offer, and what information they have on their website.  A website can tell a person a lot about the organization.

One sign of a good multiple sclerosis organization is a well-organized website.  The website should have an easy to navigate layout with important links highlighted.  Some of the links that should be right on the home page include a donation link, a contact us page, …

Like the name suggests, the Myelin Repair Foundation conducts research into myelin repair for patients with the degenerative disease multiple sclerosis.  Multiple sclerosis is one of the many different diseases that affects the nervous system.  The disease causes demyelination in the body, which means destruction of the myelin sheath that protects the nerves.  Currently, there is no known way to reconstruct myelin that has been destroyed.  There is only medication available to slow the demyelination process down.  One of the main goals of the Myelin Repair Foundation is to find a way to repair damaged myelin in order to restore the nervous system and reduce symptoms.

Demyelination is the main cause of symptomatic problems in the neurological disease multiple sclerosis.  It can cause many different problems, such as tingling and numbness in the limbs and face, problems with vision, mobility issues, and widespread pain.  By eliminating destruction of the myelin …

The Multiple Sclerosis Assocation of America is a non-profit organization that helps people in the United States who are affected by the chronic disease multiple sclerosis.  The mission of the MS Association of America is to “enrich the quality of life for everyone affected by multiple sclerosis (MS).”  In order to help people more effectively, they have a website set up that is available to people all over the world.  The homepage features links to all the major parts of their website, including their calendar of events, recent news, the donation page, about MS, the contact us page, and more.

The website is able to give a lot of different people a wide variety of reliable information about multiple sclerosis.  This can be helpful for people diagnosed with multiple sclerosis, medical professionals who treat the disease, and people who care for or live with those with MS.  The website also …

A good website should have all the best information available while still being easy to navigate.  The Rocky Mountain MS Center website is a great example of a good multiple sclerosis website.  It provides plenty of information about the Rocky Mountain Multiple Sclerosis Center, the disease in general, how people can donate their time or money to help the cause, and more.  The major links are featured right on the front page, including a donate button, social networking buttons, their newsletter, events held by the center, education and information about multiple sclerosis and more.  This is a great opening point for anyone who reaches the homepage of the website.

If you want more information, delve further into the website.  There is a great list of links on the left hand side to give people even more information to look at.  Some of these pages include frequently asked questions, clinical …

It is important for anyone affected by multiple sclerosis to get all the information they can about the disease.  The MS Society Australia website is a great way to find resources and information for free on the Internet.  While the society is based in Australia, the website is available worldwide, in several different languages.  This makes it accessible to people in all different countries.  The information they provide about multiple sclerosis, what can cause it, what the symptoms are, and how it can be treated can be beneficial to anyone who is affected by the disease.

Learning about multiple sclerosis can help someone who is newly diagnosed with the disease.  It can also help someone who is a loved one of someone with multiple sclerosis.  Having more information will help someone to have a better understanding of the disease, feeling more in control of their treatment and their life.  Since …

There is a lot of different information that can be found on the Multiple Sclerosis Society of Ireland website.  It is geared to help those people who are affected by multiple sclerosis learn about the disease and get the help they need.  The front page of the MS Society of Ireland website features an instant way for people to get help in an emergency by providing the telephone number for the MS helpline right at the top.  They also have a services and resources section for people to use if they are looking for information in case they are experience a new symptom, need advice on a doctor’s visit, or are looking for information about a treatment option.

The Multiple Sclerosis Society of Ireland is very community focused.  They work hard in order to help the nation’s population that is affected by the chronic neurological disorder.  Through collecting donations on …

For anyone who is newly diagnosed with multiple sclerosis, the first step is learning about it.  This can be easy by using the MS Society of America website.  The Multiple Sclerosis Society of America website has a lot of information about the chronic neurological disease available for free in an easy to understand manner.  Some of the information they cover includes the disease’s history, how it can be caused, what the symptoms are, how it is diagnosed, and what the treatments are.  This information can be helpful to people who have multiple sclerosis, their loved ones, and medical professionals.

Learning more about multiple sclerosis can give people with the disease more confidence in everyday life.  Knowing about the disease can also help patients know how to keep their bodies healthier while living with a chronic disease.  This can help them to avoid relapses and flare ups throughout the course of …

The MS Society Ireland website is very easy to navigate, and they have a lot of important information right on the front page.  One important piece of information to notice is the MS hotline at the top of the page.  For patients living with multiple sclerosis and their families, this is a great phone number to have in case of emergencies.  The front page also lists any current events that are going on to help raise funds for multiple sclerosis research, making it easy for people in the local area to learn how they can contribute to the society in some way.  They are listed on a helpful monthly calendar.

The Multiple Sclerosis Society Ireland website also has many links on the left hand side of the page to take users to different areas of the site.  These links can be helpful for patients with multiple sclerosis, their families, and …

The MS Resource Centre is United Kingdom based organization that helps people who are affected by multiple sclerosis.  The Multiple Sclerosis Resource Centre website features a lot of information that is useful to many different people who are involved with the disease, such as people who are diagnosed with it, their loved ones or caregivers, and medical professionals who diagnose and treat it.  The website is easy to navigate, so everyone should be able to find the information they need quickly and easily, no matter what Internet browser they are using.

The main links for the website are featured on the left hand side of the homepage.  Some of these links are useful resources, ways to donate, the guest book, research news, multiple sclerosis information, Multiple Sclerosis Resource Centre services, and the online shop.  Other featured links may be displayed at the center of the page and may change depending …

For people living with multiple sclerosis, it can be inspirational to hear other people’s success stories, including celebrities.  Tamia MS is a story that many people with multiple sclerosis can relate to.  The story of Tamia multiple sclerosis is one of hope and inspiration that many people can use to lift their spirits when they are feeling like they are in a never ending struggle with their disease.  Inspirational stories such as this one can help people to feel like they are not alone and encourage them to keep striving for their dreams in the face of adversity when struggling with a chronic disease.

Tamia is an R&B singer who was diagnosed with multiple sclerosis in 2003 at the young age of 28.  At the time, Tamia knew nothing about the disease and it was a heart-wrenching diagnosis.  It was difficult to deal with the symptoms and attacks while trying …

The American Autoimmune Related Disease Association is an association located in the United States that is dedicated to learning more about all diseases that affect the human body’s immune system.  Multiple sclerosis is one of the autoimmune disorders that the association looks into and tries to research.  They have an entire page dedicated to the disease that provides general information about what causes the disease, what some of the symptoms are, and how many people are affected by it.  From this information page, people request that a packet of information be sent to them for free about autoimmunity problems and diseases.

Other than giving people information about a variety of autoimmune diseases and disorders, the American Autoimmune Related Diseases Association also tries to promote advocacy about the diseases so that both patients afflicted with diseases will be informed, as well as their families.  They also want to educate the general …

There are many different multiple sclerosis organizations and societies all over the world that can provide information and support to patients and families.  The Multiple Sclerosis International Federation is an organization that links different organizations from different nations.  This helps them to connect with each other in order to exchange information and resources.  While the foundation is based in London, their website is available worldwide, and they focus on global research that will be available to everyone who is afflicted with multiple sclerosis.  The goal of the Multiple Sclerosis International Federation is to eventually find a cure for  MS.

The Multiple Sclerosis International Federation has links to the many different societies that are located around the world.  This can be very helpful to anyone who is looking for a local organization near them that is supported by the Multiple Sclerosis International Federation.  They can easily use a map and the …

Founded in October 2000, The Montel Williams MS Foundation was created in order to help certain multiple sclerosis organizations and institutions conduct research into cures for the chronic neurological disease.  Some of the different places that the foundation has given funding to include Brigham and Women’s Hospital, Yale, Accelerated Cure Project, the University of California, and the Karolinska Institute.  All of the public’s donation money currently goes to research to find a cure for multiple sclerosis.  Since the foundation started collecting money, it has been able to distribute over 1.5 million dollars to various research institutions and organizations across the world that study multiple sclerosis.

The main goal of the Montel Williams MS Foundation is to provide funding to research institutions in order to eventually find a cure for the degenerative disease.  Currently, there is no cure.  The only treatments available for multiple sclerosis can slow down the progression of …

The Consortium of Multiple Sclerosis Centers is a network of different multiple sclerosis organizations and societies across the world.  The Consortium of MS Centers website includes links to many different organizations that are members so that people can find their local society and their contact information.  Other societies and organizations can also use this information in order to connect with other multiple sclerosis organization to spread information, share research, and more.  It is a great way to keep everyone up to date and on the same page, no matter what country they are in.

In order for a society or organization to become a member of the Consortium of Multiple Sclerosis Centers, they must meet certain professional qualifications.  They will be reviewed to ensure they meet the qualifications and that they are legitimate.  There is an annual fee to be a member of the consortium.  It varies depending on what …

There are many different organizations that relate to the chronic neurological disease multiple sclerosis.  The Multiple Sclerosis Society of Canada is one of these organizations that offers many different resources for all kinds of people in Canada who are related to the disease either through personal reasons or professional reasons.  While they are located in Toronto, Ontario, Canada, their website is available worldwide in more than one language.  This makes them accessible to many different people – whether they are patients, families, or doctors who are looking for information and support related to multiple sclerosis.

The Multiple Sclerosis Society of Canada offers a wide variety of information on multiple sclerosis.  They keep up on the latest news about the disease, including information about research being done, treatment options, and events that collect money to help with funding multiple sclerosis research and treatment.  They also have a backlog of information for …

For those who have been recently diagnosed with multiple sclerosis, it can be difficult to understand the chronic neurological disease.  At the MS Society of Canada, patients can find the information they need to feel more in control of their disease and their treatment process.  This Canada MS society offers a free website that is available to residents of Canada as well as other countries.  This easy to navigate page includes recent news relating to the disease, information about multiple sclerosis and its progression, treatment options and alternative treatment information, and donation options.  They also list any special events coming up that people can participate in, such as MS dinner parties, the MS Walk, or the RONA MS Bike Tour.  These special events are held in order to raise funding for research in the multiple sclerosis field and to help local programs that help people who are affected by …

There are many valuable resources online that can be used to gather information.  The MS Trust UK offers a lot of information on the chronic neurological disease multiple sclerosis.  It is a multiple sclerosis trust that collects money in order to fund research and multiple sclerosis services.  It is a United Kingdom charity, but anyone can use their website and donate to their cause no matter where they live.  They feature online news articles about the chronic disease, a store with books, publications, and MS Trust merchandise, and online information about multiple sclerosis for patients.  They also have a section for health professionals and research.

A person with multiple sclerosis can benefit a lot from visiting the MS Trust website.  They offer a lot of information about the disease for the newly diagnosed.  Someone who is feeling overwhelmed about the new diagnosis can find a lot of information about what …

Multiple sclerosis is a chronic neurological disease that can be very hard to deal with individually.  That is why there are many MS centers worldwide to provide support to those who are afflicted with the disease.  The best multiple sclerosis centers offer free online resources for patients, their families and loved ones, and medical professionals.  They also have ways to collect donation money to help provide assistance to research foundations and local programs that provide help to people with multiple sclerosis.  They should also include listings for local support programs, helpful programs like meal assistance or self-help groups, and more.

The information provided through multiple sclerosis centers can be very useful, since it is typically very reliable.  These are organizations that are legitimate and want to provide only the best for their viewers.  Many multiple sclerosis centers will feature news that is accurate and up to date, including featured news …

To find the online home of the Multiple Sclerosis International Federation, visit www.msif.org, the official site of the organization.  The site is available in many different languages.  Choose the appropriate language on the right hand side of the site in order to start navigating!   After selecting a language, more links will pop up to help users choose where to go.  There are selections for patients with multiple sclerosis, medical professionals who treat the disease, and even some for family members and loved ones who are looking for more information.  The front page also features important news events that may be relevant to anyone who has interest in the multiple sclerosis field.

The msif.org website is easy to navigate no matter what type of information you are looking for.  The top bar includes links to different areas of the website that include information about multiple sclerosis, how to live with …

A neurologist is a doctor that specializes in diseases that effect the nervous system.  Multiple sclerosis is one of these diseases, so there are many multiple sclerosis neurologists out there to work with MS patients.  MS neurologists have a working understanding of how the disease works in the body and how it progresses.  Anyone who has been diagnosed with multiple sclerosis will need to have a neurologist who they see regularly to help them treat the disease.  A neurologist is going to be the medical professional most knowledgeable about the disease and the best treatment options.  They typically work through hospitals and larger medical organizations and can be referred through insurance companies or primary care doctors.

It is important for anyone afflicted with multiple sclerosis to find a multiple sclerosis neurologist that they feel comfortable with.  Since multiple sclerosis is a chronic and lifelong disease, they will be working with …

Multiple sclerosis is a disease that gets a lot of attention, since it affects so many people worldwide.  Multiple sclerosis foundations are a way to draw attention to the disease and help raise money for things like research and assistance programs.  There are various MS foundations available worldwide, so people all across the world can find a foundation close to them to get the benefits they have to offer or to participate in their fundraising events.  There are typically multiple sclerosis foundations for each country, and in the United States, one for each state.  This ensures that resources are available for many different people who have a need for multiple sclerosis information.

Multiple sclerosis foundations will vary, but most of them serve the same purpose – they want to help find a cure for the chronic disease and they want to ensure that people diagnosed with multiple sclerosis get the …

In order to make the MS Society UK website accessible to everyone, it is very easy to navigate.  It has been designed for everyone, with a simple template.  The links are right on the home page, easy to read and simple to understand.  Links are even broken up on the side by user, so people can view the website whether they are a person with multiple sclerosis, a caregiver, a person looking to fundraise, or a professional.  It also features links to help people who are looking to find local services, find out about multiple sclerosis, get involved with the society, and connect with other people.  The website can even be translated into other languages from the homepage so that people who do not speak English can still navigate and use the website.

The home page of the website also includes several important links including the contact link, the glossary, …

Finding multiple sclerosis specialists is a key part of any patient’s care.  MS specialists are going to be the most knowledgeable medical professionals in the field about the chronic neurological disease.  That is why it is so important for anyone who has received a diagnosis of multiple sclerosis to start looking for a multiple sclerosis professional, such as a neurologist.  There are specialists available all over, including MS specialists in the UK and the US.  Referrals to specialists are available through private insurance companies, multiple sclerosis foundations or organizations, hospitals, and primary care physicians.

For someone who has received a positive diagnosis of multiple sclerosis, they will have support from their current doctor in finding a neurologist for keeping up on their care.  Since multiple sclerosis is a lifelong disease, they will want to find a specialist they are comfortable with and who is readily available.  They should accept their …

For people diagnosed with multiple sclerosis, finding a neurologist is an important first step.  A multiple sclerosis neurologist is going to be the medical professional with the most experience in treating multiple sclerosis, a chronic disease that affects the nervous system.  A MS neurologist specializes in diseases that affect the nervous system, so they will be familiar with treatment options and how the body is going to react to the demyelination process going on in multiple sclerosis.

Finding a neurologist in your local area is not difficult, especially if you are already working with another medical professional.  Most specialists are found through a referral either from another doctor or a private insurance company.  Hospitals will also have special departments for neurologists and other specialists.  Anyone who requires a neurologist should be sure to find one they are comfortable with.  Don’t be afraid to have a consultation visit in order to …

When someone is diagnosed with multiple sclerosis, they will need to have a comprehensive treatment team that includes a variety of different medical specialists and doctors.  The best treatment team will include only the best multiple sclerosis doctors.  This can include a primary care physician, a neurologist, a nutritionist, a physical therapist, and more.  Since multiple sclerosis is a chronic and lifelong disease for which there is currently no cure, it is important to have a reliable team of multiple sclerosis doctors that are knowledgeable and professional.  They should be people that you feel comfortable with and that you can reach if you have a medical emergency or a change in your symptoms or the progression of your disease.

Finding multiple sclerosis doctors doesn’t have to be a time consuming hassle.  Other doctors you already see can give you a referral to the best multiple sclerosis doctors in your …

Many people all over the world are afflicted with multiple sclerosis, a chronic neurological disease for which there is no cure.  Because of this, the Race to Erase MS was founded in 1993 by Nancy Davis, who was diagnosed with the disease.  Today, the Race to Erase MS event is held annually, raising money to for the Nancy Davis Foundation For Multiple Sclerosis.  This event is typically a gala for celebrities, with very exclusive invitations.  Since its start, it has raised over thirty million dollars for research into the neurological disease.  All proceeds go to the foundation’s Center Without Walls program, which includes seven of the top multiple sclerosis research centers.  The ultimate goal of the Nancy Davis Foundation For Multiple Sclerosis is to one day find a cure for this debilitating disease.

Many entertainment and fashion organizations are backing the Race to Erase MS.  People such as Tommy Hilfiger, …

A multiple sclerosis clinic is a medical environment that will specialize in treatment for patients who have this particular chronic neurological disease.  It caters to the needs of the people who have been diagnosed with this disease, so it will have many different options for people in the varying stages of multiple sclerosis, whether it is relapsing-remitting type or primary-progressive type and beyond.  Some people will have various stages of disability, so a multiple sclerosis clinic should be handicapped accessible for those with limited mobility.  Most clinics will also include on hand nurses or other medical caregivers to help people with disabilities get in and around the multiple sclerosis clinic for their treatment.

A clinic should be a comfortable environment where patients can get testing and treatment done.  Many multiple sclerosis patients will need to get intravenous drip treatments done on a regular basis and have regular MRI testing done …

A multiple sclerosis therapy centre can provide different care options for those people who have been diagnosed with the disease.  For someone who is looking for a place that caters to people with multiple sclerosis, a MS therapy centre could be the answer.  MS therapy centers are typically clinics that only take patients who have already been diagnosed with the neurological disease.  They will provide the best care possible for people with multiple sclerosis, having the most up to date treatment options.  They may also offer clinical trials or experimental treatment options to qualified patients.  Since these places are centered around the disease multiple sclerosis, they may have research doctors in the centre who are willing to try newer, alternative treatments.

To find these centers in your area, try asking your primary care doctor or your neurologist.  You can also ask around your local hospital.  Support groups with other multiple …

The MS Society Minnesota offers assistance to people living in Minnesota and also to people living in some areas of Wisconsin.  This MS Society MN is one of the chapters of the National Multiple Sclerosis Society.  They run a free website to offer a lot of information to people suffering with multiple sclerosis as well as their caregivers and their medical professionals.  They have various links on their homepage to direct people to the appropriate pages, depending on the type of information they are looking for.  This makes it easy to navigate.

The multiple sclerosis site also offers a lot of different ways for people with the disease to connect to one another.  They can share how they are feeling about the disease, what the disease means to them, how it effects their lives, and more.  This is a great way for people to meet up with others who have …

The National Multiple Sclerosis Foundation began making a change in 1986. The goal of the National MS Foundation is simple; to enrich the lives of people with MS in any way, shape, or form. This non-profit organization offers programs with an educational background for individuals interested in learning more about MS. Whether you or a loved one has Multiple Sclerosis, the services and programs are available at any time.

Making life easier is possible through various funding, as well as both money and assistive equipment which have been donated. When able, the MS Foundation provides items to help increase the amount of independence for a person with MS. Walkers, wheelchairs, shower chairs, and various other forms of assistive technology can be obtained on loan through MSF.

A toll-free phone number is also available to put a person in touch with someone who knows answers to questions about MS or where …

The National Multiple Sclerosis Association is an American non-profit organization. Not only does the National MS Association wish to enrich the lives of people directly affected by MS, but it also wants to promote awareness of the disease. There are numerous obstacles a person with MS faces daily. The more people learn about MS, the easier it is to be mindful of just how difficult life for a person with MS can be. The MSAA supports the promotion of information on MS through the use of literature and videos; free of charge.

One great thing about MSAA is that there are multiple chapters across the nation, making it much easier for people to obtain assistive equipment, gather educational materials to pass on to others, and join support groups nearby. Founded in 1970, the MSAA has been assisting not only people with MS, but also their family members, caregivers, and friends. …

The National Multiple Sclerosis Association was established as a nonprofit organization and has remained so for the past several decades. Individuals who keep the organization running smoothly are passionate about what they do. Their goals are to increase awareness about MS, provide assistance where needed to people with MS and their caregivers, family members, and friends, and they also have an influence on government issues concerning MS. Everyone involved with the National MS Association is very active in any way possible.

If there are challenges a person with MS is facing, the National MS Association is there to help. Whether the individual needs encouragement, a support group, equipment to aid with the limited mobility being experienced, or simply to talk to someone about what to expect after being diagnosed with Multiple Sclerosis, someone can be reached through this valuable organization.

Social networking is alive and well with the National MS …

When you have questions about Multiple Sclerosis, for you personally or for someone else, turning to the MS Association of America is an excellent way to find answers. Their web address is www.msaa.com and they can help you find what you are looking for. This non-profit organization has programs and services geared towards helping people with MS get what they need. Support groups are available to lend an ear and give support when necessary. Finding answers through an MRI or evaluating the progression of MS are also possible through MSAA. They have a supportive staff that is willing to assist people with MS and their friends and family members in any way, shape, or form. Even caregivers of an individual with MS can turn to MSAA.

The News Center offers information on the latest happenings within the MS community. Such as the denial of FDA approval on a recently formulated …

The MS Foundation was established in 1986 and is an organization that relies solely on public funding. Any funds collected through this organization are put to good use for people with MS. The money provides a better quality of life by supplying much needed equipment or assisting with home improvements necessary to keep the environment around the house safe. People with MS often have limited mobility as the disease progresses and their independence can be maintained through the use of additional equipment. Specific furnishings might make life a bit easier, such as a walker, a chair for the shower, or anything else needed.

The extent of assistance will depend on the amount of funds collected throughout the year. Even though the main headquarters for the MSF are located in Fort Lauderdale, Florida, it provides services to the entire nation.

An MS Foundation for Women and Men

Although more …

A long list of Multiple Sclerosis organizations includes the names of groups around the world that try to bring about awareness of this debilitating disease. Just about every country has at least one MS organization already established, but many larger countries have multiple offices set up, due to the increased size of the population. Each of these smaller branches has similar goals to those of the more expansive national offices. They hope to assist people who need it, whether it’s through information about MS, gathering equipment to make life easier, supplying means for an initial diagnosis of MS or an MRI, connecting them with others in a similar situation, or raising awareness about Multiple Sclerosis.

Whether the person seeking aid is an MS patient, a family member, coworker, spouse, friend, or acquaintance, answers can be supplied or sought out. Besides the direct branches of MS organizations, there are additional groups …

The MS Association of America has programs and services designed to assist people connected to MS in any way. Within the National MS Association, a total of 5 categories exist and they are labeled as followed: Offering Lifelines, Branching Out, Finding Answers, Breaking Down Barriers, and Easing Daily Life. Each category is aimed at helping not only people with Multiple Sclerosis, but also those surrounding them, including their family, partners, and acquaintances.

Offering Lifelines is a service MSAA has to help people with MS to face challenges, become more certain about the future, battle depression, and deal with anything that Multiple Sclerosis puts in their way. MSAA is there to give the encouragement and understanding needed.

Branching Out allows people to share their experience with MS and talk with others with similar situations. This can be a healing process for many. Sometimes talking to others who understand what is …

The information supplied by the main National MS Society is valuable to not only people who have MS, but also to anyone who is a caregiver, family member, friend, or acquaintance of an individual with Multiple Sclerosis. The MS Society provides services and offers programs designed specifically around MS. This organization can assist people in obtaining equipment, furnishings, or other supplies needed to help function on a daily basis. MS generally causes limited mobility, which sometimes means a loss of independence. Any branch of the National Multiple Sclerosis Society is able to find out about items that can be used on loan that would greatly help a person maintain a sense of independence.

Fundraisers, such as an MS Society walk or bike ride are a key component in collecting funds for research. Finding a cure for MS involves a lot of research and it doesn’t come cheap. A constant flow …

Joining a National MS Society walk is a magnificent way to raise awareness and increase the amount of funds coming in to the MS Society for continuing research. There is always a need for research money, since searching for a cure for MS doesn’t come cheap. Walk MS is a movement designed to bring people together for a similar purpose; to fight MS.

To join in on a walk, you can visit the website and find out where the nearest location is to you. A map is provided on the National MS Society’s website. Clicking on one of the ten regions will take you to a new map which has zoomed in on the region you chose. On this new map, places were an MS Walk is taking place will have an orange square next to them. Once the orange square of choice is clicked on, an information bubble appears …

The mission of the National MS Society is to help people with Multiple Sclerosis to remain mobile, address challenges these individuals face each day, and to drive the research of MS forward. When it comes to mobility, people with MS often become very limited in what they are physically capable of doing. Due to muscle weakness, spasms, paralysis of limbs, and other affects experienced in the muscles, being able to carry out daily functions sometimes requires assistance.

Obtaining the necessary equipment to remain independent is how this nonprofit organization helps people remain in their own homes and continue to be self-reliant for as long as possible. People at any stage of MS can receive much needed support when dealing with the daily challenges of having MS. A National MS Society toll-free number is provided for anyone to use when they need encouragement, answers to questions, or just someone to talk …

The Natl MS Society is solely a nonprofit organization which consists of a large group of individuals who are set on making the world a better place by ridding it of Multiple Sclerosis. This is an impossible feat for one person to do. However, this organization is made up of thousands upon thousands of volunteers and dedicated staff members throughout the world. Most countries have an MS society of their very own and larger cities tend to have more than one outlet for people to go to.

These individual branches are each equipped with resources to help people understand more about MS and not to become frustrated or feel so alone in their stand against the disease. The loaning equipment is also possibility through the National MS Society or its chapters. MS can be a severely debilitating disease and limited mobility takes away the freedom of an individual. One way …

The ultimate goal of the National Multiple Sclerosis Society is to eradicate the world of MS. While this goal is a desirable one, it isn’t able to be achieved overnight. There are many steps involved with reaching this goal and it will take a collaborative effort from people of all walks of life. What the National MS Society is capable of doing is raising awareness of MS and help those who already have it.

Working on prevention of the disease and providing support for those recently diagnosed are on the list of things to do for the National MS Society. Staff members and volunteers concentrate on being a sounding board for those frustrated by the difficulty of daily living MS has created and getting even the smallest community involved. Caring individuals donate their precious time to host awareness events, fundraisers, and to assist in any way imaginable.

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