Bladder problems are one of the most common symptoms for people with Multiple Sclerosis and can have a big impact on quality of life. Bladder issues can be divided into two main types.
Bladder problems in MS are caused by nerve damage to areas of your brain and spinal cord which are related to your bladder. The type and severity of problem will depend on where the damage is.
There are many ways that you can be supported with your bladder. It is important you speak to your MS team if you are having problems with your bladder.
Storage problems can show themselves as needing the toilet right away (urgency) and needing the toilet more often (frequency). You may also have bladder accidents such as incontinence or leakage of urine. These can be brought on by things such as sneezing and coughing (stress incontinence) or can be unexpected.
Issues with emptying your bladder can show themselves in different ways.
There are several things you can do to help your bladder problems, as well as contacting a medical professional. These include:
Different bladder problems are treated differently. Certain investigations will be completed by a healthcare professional to decide the right treatment for you. These may include:
Treatment for bladder urgency, frequency, and incontinence could include:
Treatment for bladder hesitancy and retention could include:
It is common to feel anxious about going out if you have bladder issues. If finding a toilet is something you are worried about, there are several tips which can help.
Bladder incontinence | MS Trust
Supporting Your Bladder & Bowel Health | Bladder & Bowel Community (bladderandbowel.org)
Benefits are available to help with living costs, support those on low income and provide support for those who may not be able to work due to their MS. Below are some of the benefits you may be entitled to.
If your MS affects how much you can work, then you may be able to claim ESA.
https://www.gov.uk/employment-support-allowance
PIP may be available for people with MS if it affects your daily living or mobility.
If you are unemployed and applying for jobs, then you may be able claim this allowance.
https://www.gov.uk/jobseekers-allowance
This is a payment to help with your living costs. You may be able to get it if you're on a low income, out of work or you cannot work.
https://www.gov.uk/universal-credit
This helps with extra costs if you have a disability severe enough that you need someone to help look after you.
https://www.gov.uk/attendance-allowance
You may be able to apply for a blue badge if your walking is reduced or you have certain other disabilities. This will allow you to park in disabled parking spaces. The website below gives clear information on who may be successful in getting a blue badge.
Apply for or renew a Blue Badge - GOV.UK (www.gov.uk)
If you require adaptions (changes) in your house because of your MS, you may be able to get a grant to help pay for these.
https://www.gov.uk/disabled-facilities-grants
Your carer, spouse or relative may be able to claim this if they care for you for more than 35 hours a week.
https://www.gov.uk/carers-allowance
You could apply to your local council. You may get a discount on your bill if you're eligible.
https://www.gov.uk/apply-council-tax-reduction
WaterSure is a scheme which helps some people with their water bills. To apply for the scheme, you must be on benefits and need to use a lot of water for medical reasons.
WaterSure scheme – help with paying water bills - Citizens Advice
Pension credit is for people of pension age on a low income.
https://www.gov.uk/pension-credit
For people with children under 16 years old or under 20 years old if they are in education.
https://www.gov.uk/child-benefit
The MS Society has further information about benefits which you can access from this link.
Brief Guide to MS Benefits - Financial Support | MS Society
You can also get in touch with one of their MS benefits advisers by calling the MS Society Helpline on 0808 800 8000 or emailing on This email address is being protected from spambots. You need JavaScript enabled to view it.
Your local Citizens Advice Bureau can also provide support with benefits.
Benefits calculators - GOV.UK (www.gov.uk)
https://dorsetaccesswellbeing.co.uk/about_us/
Some information sourced from Hereford MS Wellbeing Hub (herefordmshub.co.uk)
The MS Service has a pharmacist who supports with the MS disease modifying drug (DMD) pathways.
They support with getting the prescriptions for the DMDs written and delivered to where they need to go to ensure you get the medication. This includes overseeing the team in the hospital that links with the pharmacy homecare delivery companies, for the DMDs which use these services.
On behalf of the MS Neurologist, the Pharmacist will also conduct the full annual DMD review (which will take the place of your neurologist drug appointment). They ensure that everything is in place for our team to be able to prescribe the MS DMDs (from a Hospital Trust perspective) and ensure that we are complying with NHS England requirements as a prescribing centre for MS DMDs.
In addition to supporting the service with MS DMDs, the MS Pharmacist also provides advice to the service practitioners when there are complex queries relating to medications used to help manage MS symptoms.
For more information on MS DMDs see DMD section.
Please see Appointments and clinics section for more details.
Living a healthy lifestyle helps you feel better, stay well, and cope more easily with any health problems that may come your way.
For people with MS this is even more important, as evidence clearly shows that maintaining good health and wellbeing will have a positive effect on MS disease course and management of symptoms.
It can be hard to find the time or the energy to make lifestyle changes, however your efforts will pay off in many ways, both in terms of your MS and your general health. Often small changes can lead to bigger ones so even small changes are worth making.
Most of steps you can take will be as recommended for the general population, they benefit everyone's health and wellbeing. Evidence shows that these are particularly important for people with MS. There are also other things that are specific for people with MS which are likely to be of benefit.
Maintaining a healthy diet and body weight is important for everyone's overall health and wellbeing and will help to manage some symptoms of MS. Research has shown people who are obese are likely to have higher numbers of MS lesions (areas of MS damage) than people who maintain a healthy weight. Obesity is also associated with a higher risk of disability in people with MS.
See Diet for more information.
Water is really important to your health and makes up over half of your body weight. It plays an essential role in many of your body's functions, including bringing nutrients to cells, getting rid of waste, protecting joints and organs, and in maintaining body temperature. It also plays a crucial role in your bladder and bowel function.
Fluid intake is particularly important in MS as research has shown that even mild dehydration can make energy levels and fatigue worse and lead to poorer thinking processes.
See Cognition for more information.
Drinking plenty of water is especially important if you have bladder and bowel symptoms. If you don't drink enough, your urine will be more concentrated which can irritate your bladder and lead to urinary tract infections and drinking enough fluid can help prevent and relieve constipation.
See Bladder and Bowels for more information.
Water is the best thing to drink. Other fluids will hydrate you to different levels, and some may have effects which aren't so good on your body (for example the caffeine found in tea and coffee can make us produce more urine, and acidic fruit juices or carbonated drinks can irritate your bladder). More information can be found here: Hydration Information - British Nutrition Foundation
There is a lot of evidence demonstrating that exercise and activity is beneficial to you and specifically for people with MS. It can help manage symptoms of MS and improve your general health and wellbeing. It also helps to prevent other health conditions, which in themselves may have a negative impact on MS.
See Exercise and Activity for more information.
The health risks associated with smoking are well known, but there is growing evidence of the specific negative effects of smoking for people with MS.
Studies have shown if you smoke:
(Reproduced from the MS Trust – see link to webpage below)
Smoking is also known to influence MS symptoms such as pain and cognitive problems.
It is never too late to stop smoking and there are lots of resources available to support you with this. If you are considering stopping smoking, it is not recommended that you use 'vaping' as some research has suggested that vaping could be as bad for the blood brain barrier for someone with MS as smoking. For support and advice for stopping smoking please see Stop Smoking With LiveWell Dorset | Help To Quit Smoking In Dorset · LiveWell Dorset.
See Smoking and MS | MS Trust and Lifestyle factors and living well with MS | MS Society for more information
There's no clear guidance on how alcohol affects MS, but we do know that drinking too much can harm your general health and increase the risk of problems like liver disease, heart issues, and mental health concerns.
Although we don't know exactly how alcohol affects MS itself, it can affect people with MS differently. Even small amounts of alcohol might make symptoms like balance, coordination, or thinking problems (cognition) worse for a while.
Anything that affects your body or your health can be a trigger for worsening of MS symptoms, or the return of symptoms which you may have had previously. This is described in more detail in What is a relapse? in the sections 'What isn't a relapse?' and 'Triggers for symptoms worsening or coming back'.
It's really important to look after your overall health. This means trying to prevent other health problems, or getting them treated early, and managing any conditions you already have so they don't make your MS worse.
These are some of the things that you can do to help this aspect of managing your general health:
There is evidence that suggests that people who live with other health conditions, as well as MS, (such as high blood pressure, heart disease, diabetes, asthma, anxiety, depression) have worse outcomes throughout the disease course in MS, than people who don't have comorbidities. It is therefore vital that any other health condition that you have is well managed. How these are managed will be determined by what the health condition is and what has been advised by your doctor or health care team.
As described above, managing other health conditions is really important for your MS. Mental health is no exception. Mental health isn't just about people who have been diagnosed with anxiety, depression or other mental health conditions, it includes things like managing stress and maintaining healthy relationships and social connections.
Stress - Every Mind Matters - NHS (www.nhs.uk)
Maintaining healthy relationships and mental wellbeing - NHS (www.nhs.uk)
Our Mood page also has useful information and links, and you may find our pages on Relaxation and Mindfulness useful.
Your MS Service will advise you if you are eligible for and if it is recommended that you take medication for MS itself (disease modifying drug (DMD) treatment). If it is recommended that you take a DMD, it is because it is evidenced that there are better outcomes for people who have a presentation of MS where DMDs can be effective. See Disease Modifying Drugs (DMD) for more information.
It is also important to take other medications that you have been prescribed and to take them as advised by the person prescribing the medication. These medications could be to help with symptoms of MS or other health conditions. Both are important in helping you to live well with MS.
There isn't a lot of research in the field of MS and menopause, but many symptoms of menopause are similar to MS symptoms, and symptoms of menopause can be a trigger for worsening of existing or previous MS symptoms.
If you are experiencing symptoms which you think are related to menopause, it may be useful to speak to your GP to have this confirmed, and to look at whether treatment such as Hormone Replacement Therapy (HRT) may be appropriate for you.
The MS Trust and MS Society have information which may be useful on menopause and MS:
Problems with sleep are very common in people living with MS. It is important that you address them, as quality sleep is good for your overall health and lack of sleep (or poor-quality sleep) can make your MS symptoms worse. See Sleep for more information about sleep and MS and for tips for sleeping well.
It is important for all of us to try and have a good work-life balance, but even more important for someone with MS as there are different MS symptoms which will make finding this balance more challenging. If you don't have a good work-life balance it can make your MS symptoms being worse and can lead to you using all your energy on work. Not being able to enjoy anything outside of work can lead to poor mood and mental health.
Creating boundaries, learning how to say 'no' politely, listening to your body, and taking regular breaks at work can all be useful in helping to achieve a work-life balance.
See Work and MS for more information specific to work.
Many people with MS notice that their symptoms feel worse when the weather is hot or humid, or for some people when it's cold.
For people who are sensitive to heat, activities such as exercising, and having hot baths or showers can worsen MS symptoms temporarily. These usually improve again after you cool down.
Strategies for staying cool:
Although not as common, cold can also affect some people with MS. Some symptoms, particularly spasms, stiffness and spasticity, can get worse with the cold.
Optimising brain health in MS is really important. Many of the healthy behaviours discussed above are shown to benefit brain health. To find out more about brain health and the MS Brain Health consensus group please see Brain Health.
Having a positive mindset and trying to make your diagnosis of MS part of who you are, rather than being all-encompassing can not only be useful in managing your mental health and wellbeing, but it can also help you to manage other symptoms of MS and your MS journey overall.
You may feel pulled in different directions and experience stress from different aspects of your life, leaving little time for yourself. Learning to balance your life with some time for yourself and making small changes towards a healthier lifestyle will pay off with big benefits – a healthy outlook and better health.
If this is something you are struggling with, there are services which can support you. Please see Mood and The Dorset Supported Self-Management Service · Help & Care (helpandcare.org.uk) for more information.
Although support from professionals in the MS Service is important, there is a lot that you can do for yourself to keep yourself well and manage your symptoms. Use the information here and on our other webpages to help you to best manage your MS.
LiveWell Dorset has excellent resources to help you with your general health and wellbeing: LiveWell Dorset | Health & Wellness Coaching | Free Advice & Support · LiveWell Dorset
They have a workbook which you may find useful in taking your first steps in making changes to your lifestyle or creating new habits which can be found here:
In relation to patients, the MS Administrators are responsible for:
The MS Administrators also have several work-streams which are not related to patients.