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Tim’s Complex Care Story: Supporting Independence After an Acquired Brain Injury

Tim’s Complex Care Story – How Secure Healthcare Solutions helped Tim fulfill his life to the fullest.

Tim was 52 years old and had an acquired brain injury. Like everyone, he had his own interests, personality and things that brought him happiness. He was a passionate Wolverhampton Wanderers supporter and loved cooking!

For Tim, receiving the right support was about more than meeting his care needs. It was also about helping him maintain his independence, enjoy the things that mattered to him and continue taking steps forward in everyday life.

Through the support provided by Secure Healthcare Solutions, Tim experienced progress that was meaningful to him. He was able to take steps he had not been able to take before, highlighting the importance of personalised support that recognises the individual behind the care needs.

Understanding Acquired Brain Injury

An acquired brain injury (ABI) is damage to the brain that occurs after birth. It can happen for a variety of reasons and may affect people differently, depending on the nature and severity of the injury.

Some people experience changes in their movement, communication, memory, thinking or ability to manage everyday activities. The support they need depends on their individual circumstances, abilities and goals.

For Tim, the focus was on providing appropriate support while recognising his individuality and helping him develop greater independence.

Personalised Complex Care That Recognises the Individual

Complex care should be built around the person, taking account of their needs, preferences, routines and personal goals.

Secure Healthcare Solutions provides care and support for people with a range of health and social care needs, working in partnership with commissioners, local authorities, case managers and self-funded individuals.

Tim’s experience demonstrated the importance of having a supportive team around him. His feedback highlighted the professionalism and training of the staff supporting him, as well as the difference this support made to his ability to carry out tasks more independently.

Helping Tim Take Steps Towards Greater Independence

Progress can mean different things to different people. For someone living with an acquired brain injury, being able to do more independently can be an important part of everyday life.

Tim’s case study highlighted positive progress following support from Secure Healthcare Solutions. He was able to take steps that he had not been able to take before, and he described being able to complete tasks more independently.

These changes mattered because care is not simply about providing assistance. It is also about recognising a person’s abilities, supporting their individual goals and helping them maintain as much independence as possible.

Tim’s love of cooking and his enthusiasm for his football team were reminders that his interests and personality were just as important as his care needs.

Feedback From the man himself!

Tim shared positive feedback about the support he received from Secure Healthcare Solutions, particularly the quality and training of the staff.

“Professional agency, well trained brilliant staff, since Secure healthcare has supported me, I can do tasks more independently”.

His words reflect the importance of reliable, well-trained staff who understand the value of supporting people in a way that promotes independence.

Putting People at the Heart of Complex Care

Tim’s story highlights why complex care must be personalised. Every person has different needs, interests and goals, and the right support should reflect those differences.

For Tim, being supported to take steps forward and complete tasks more independently was an important part of his experience. His feedback also demonstrated how much confidence people can place in a team that provides professional, well-trained support.

At Secure Healthcare Solutions, we recognise that effective care is about the person, not just their condition. By focusing on individual needs and working to support independence, care teams can help people pursue meaningful progress in their everyday lives.

Looking for Complex Care Support?

If you or someone you care for needs specialist support at home, Secure Healthcare Solutions can discuss your requirements and help you explore the available options.

Contact our team to learn more about our complex care services and how personalised support may help meet individual needs.

Mary’s Complex Care Journey | Secure Healthcare Solutions

Getting to Know Mary

Mary was 29 years old and had a learning disability, epilepsy, a tracheostomy and a PEG (percutaneous endoscopic gastrostomy). She also required 24-hour ventilation.

Despite her complex health and care needs, Mary was shown smiling and enjoying time with her dolls. These moments offered a glimpse into her personality and the activities she enjoyed.

Understanding Mary’s Conditions

Mary had several conditions and medical needs that required specialist support. Understanding these needs helps explain the importance of appropriate care tailored to the individual.

  • Learning disability: A learning disability can affect how a person learns new skills, understands information and manages some everyday activities. The support needed varies from person to person.
  • Epilepsy: A neurological condition that can cause recurrent seizures. The type and impact of seizures vary between individuals.
  • Tracheostomy: An opening created at the front of the neck through which a tube is inserted into the windpipe to help with breathing or provide access for respiratory support.
  • PEG: A feeding tube inserted through the abdomen directly into the stomach, which can be used to provide nutrition, fluids or medication when required.
  • 24-hour ventilation: Mary required ventilatory support around the clock to assist her breathing.

Together, these needs meant that Mary required ongoing support tailored to her individual circumstances.

Mary’s Complex Care Package

Secure Healthcare Solutions provided care and support for Mary, whose needs required ongoing assistance and specialist care.

Her circumstances involved several complex health requirements, including a tracheostomy, PEG and 24-hour ventilation, alongside her learning disability and epilepsy.

SHS provide tailored care to clients with a variety of health and social care needs, working in partnership with CCGs, local authorities, case managers and more.

A Better Care Experience

Before moving to Secure Healthcare Solutions, Mary’s family had experienced difficulties with care provided by other agencies.

The decision to change providers resulted in a more positive experience, with Mary’s mum highlighting the improvement in the care and support received.

Her feedback reflected the importance of finding a care provider that families felt confident in and that delivered a positive experience for the person receiving care.

Feedback from Mary’s Mum

Mary’s mum shared her experience of changing care providers and the difference it made to the support Mary received.

Mary’s mum said:

“Previous care experiences with other agencies have not been great, changing to Secure Healthcare has resulted in great care & support”.

Putting the Individual at the Heart of Complex Care

Mary’s story highlighted the importance of appropriate support for people with complex health and social care needs.

Her family’s feedback demonstrated the value of a positive care experience and the importance of finding a provider that could deliver the care and support they needed.

At Secure Healthcare Solutions, Mary’s case formed part of the wider work supporting people with complex needs and their families.

Looking for Complex Care Support?

If you or someone you care for needs specialist support at home, Secure Healthcare Solutions is here to help. Contact our team to discuss your care requirements or explore opportunities to join our healthcare team.

Explore Complex Care Services

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Call our team: 0121 285 9449

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Ava’s Complex Care Story | Secure Healthcare Solutions

Every Child Has Their Own Story

Ava was four years old and had Type 1 Spinal Muscular Atrophy (SMA), a condition that caused muscle weakness and difficulties with movement.

Ava had her own favourite things to enjoy, including watching Peppa Pig and Ben & Holly on her iPad. Her care was supported by Secure Healthcare Solutions, with a focus on meeting her individual needs at home.

Understanding Spinal Muscular Atrophy (SMA)

Spinal Muscular Atrophy (SMA) is a rare genetic condition that affects the nerves responsible for controlling muscle movement. It causes muscle weakness and can affect movement, mobility and everyday activities.

Ava had Type 1 SMA, a severe form of the condition that typically begins in infancy. In Ava’s case, the condition caused muscle weakness and difficulties with movement, meaning her individual care needs required appropriate support.

Understanding how SMA affected Ava was important in recognising her needs and the role of personalised care in supporting her at home.

Ava’s Complex Care Package

Secure Healthcare Solutions provided care and support tailored to Ava’s individual needs, covering different aspects of her daily life.

  • Personal Care: Support with Ava’s personal care needs, helping maintain her comfort and wellbeing.
  • Daily Living Support: Assistance with Ava’s everyday needs as part of her care routine at home.
  • Communication Strategies: Using appropriate communication strategies to support interactions with Ava and help meet her individual needs.
  • Behavioural Support: Providing support tailored to Ava’s behavioural needs, with an approach suited to her individual circumstances.
  • Play, Engagement and Activities: Spending time playing and engaging with Ava, including interacting with her toys and supporting activities that interested her.

Care That Helped Her Family Feel Safe

As part of Ava’s care arrangements, Secure Healthcare Solutions provided care staff and supplied personal protective equipment (PPE) every week.

This was an important part of the support highlighted by Ava’s mother, who expressed her satisfaction with the staff and the care provided.

A Positive Experience for Ava’s Family

Ava’s mother rated the support and care provided by Secure Healthcare Solutions 10 out of 10. She also shared how safe she felt with the care staff and highlighted the weekly provision of PPE.

Ava’s mother said:

“I am happy with the staff provided, 10/10 support and care. We feel safe under Secure Healthcare’s carer and PPE is provided every week”

Putting Families at the Heart of Care

Ava’s story highlighted the importance of trusted care staff and the reassurance their support brought to her family.

Her mother’s positive feedback reflected her experience with Secure Healthcare Solutions and the confidence she felt in the care provided.

Looking for Complex Care Support?

If you or someone you care for needs specialist support at home, Secure Healthcare Solutions is here to help. Contact our team to discuss your care requirements or explore opportunities to join our healthcare team.

Explore Complex Care Services

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Call our team: 0121 285 9449

How Complex Care Improved Life for Yash and His Family

Every Person Is Different. Their Care Should Be Too.

Every person has different needs, challenges and goals. For individuals with complex needs, the right support can make a meaningful difference to everyday life, independence and family wellbeing. Yash was 15 years old and had autism and severe learning disabilities, with his needs having a significant impact on family life. His challenging behaviours, which could include lashing out, were causing distress and making everyday life at home difficult.

His family needed specialist support that understood Yash as an individual, responded to his needs and helped create a safer, more positive home environment. Secure Healthcare Solutions provided a personalised complex care package built around Yash, his individual needs and the things that mattered to him and his family.

Understanding Yash’s Complex Care Needs

Supporting someone with complex needs requires more than a standard care approach. It means understanding the individual, recognising their challenges and providing support that reflects their circumstances. For Yash, this meant understanding his behaviours, supporting his communication and helping him participate more positively in everyday life.

It was equally important to recognise the impact his care needs had on his family. His mum needed greater peace of mind, while the family needed support to feel safer at home and enjoy more positive time together. This understanding helped shape a personalised approach focused on Yash’s wellbeing, development and quality of life.

Inside Yash’s Personalised Complex Care Package

At Secure Healthcare Solutions, complex care packages are tailored to each person’s individual needs, preferences and goals. Support should reflect the individual rather than follow a one-size-fits-all approach. Yash received support from an experienced and passionate team of specialist complex care workers, with support available around the clock according to his needs.

His personalised care package included:

  • Personal Care: Support tailored to his individual care needs.
  • Daily Living Support: Help with everyday routines and activities.
  • Communication Strategies: Support to encourage expression, communication and interaction.
  • Behavioural Support: A person-centred approach to understanding and responding to challenging behaviours.
  • Community Outings: Opportunities to access the community and participate in activities beyond the home.

Yash also had a personalised care plan that was regularly reviewed to ensure his support continued to reflect his needs and progress. By combining specialist care, consistency and an understanding of Yash as an individual, the team worked towards meaningful goals for him and his family.

How Complex Care Helped Yash and His Family

The value of complex care is not measured only by the support delivered. It is also seen in the difference that support can make to everyday life.

With personalised support from Secure Healthcare Solutions, Yash and his family experienced positive changes.

  • Greater Safety and Peace of Mind: Yash’s family saw a reduction in challenging behaviours, helping create a safer home environment and easing some of the pressures they had been experiencing.
  • More Opportunities to Access the Community: Yash had more opportunities to get out into the community and participate in activities, helping him engage with experiences beyond the home.
  • Positive Progress with Communication: Yash became more vocal, creating new opportunities for communication and interaction.
  • More Time for Family Life: With greater peace of mind, Yash’s mum was able to focus on everyday activities and spend quality time with her daughter, who also felt safer at home.

These changes demonstrated the importance of looking beyond an individual’s care needs to understand what mattered to them and the people around them. Personalised complex care supported not only the individual receiving care, but also the wellbeing of the wider family.

A Message from Yash’s Mum

Reflecting on the difference the support made, Yash’s mum shared:

“Since Secure started working with my son, we have seen massive changes. My son has challenging behaviours, he lashes out and has targeted me for quite a few years causing some injuries to myself but since Secure Stepped in, these incidents have significantly reduced. My son has access to the community more often now and attends activities, he goes happily with the staff. My son is starting to understand his behaviours, and he is also being more vocal (he has been nonverbal for around four years prior to this). I’m now able to do things I need to do without worrying and spend quality time with my daughter who also feels a lot safer in our home.”

Personalised Complex Care That Puts People First

Yash’s story highlighted what mattered most when supporting people with complex needs: understanding the individual, providing the right support and working towards outcomes that improved everyday life. At Secure Healthcare Solutions, complex care solutions are designed around each person’s needs and circumstances. Through personalised care planning, specialist support and regular reviews, the aim is to help individuals develop their abilities, access their communities and achieve the best possible quality of life. Every care package is different because every person is different.

Looking for Complex Care Support?

Finding the right care for a loved one can feel overwhelming, particularly when their needs are complex. Secure Healthcare Solutions provides personalised complex care support designed around individual needs, with a focus on wellbeing, independence and quality of life.

Explore Complex Care Services

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Call our team: 0121 285 9449

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Understanding the Discharge to Assess (D2A) Model

Delayed discharges now account for over 11% of all NHS hospital bed days, costing the health service an estimated £2 billion a year and leaving thousands of patients stuck on wards longer than necessary. These are not just numbers — behind every delayed discharge is a person whose recovery is being held back.

If someone you care about has been told they are “medically fit for discharge” but still seems unwell, you are not alone in feeling anxious. It is natural to wonder whether leaving hospital is the right decision.

The Discharge to Assess model — commonly known as D2A — is designed to address exactly this concern. Rather than keeping patients in a hospital bed while lengthy assessments take place, D2A ensures they move to a more appropriate setting, ideally their own home, where their ongoing care needs can be properly evaluated.

In this guide, we explain how D2A works, what the four NHS discharge pathways involve, and how the right support can make all the difference.

What Is the Discharge to Assess (D2A) Model?

Discharge to Assess is an approach endorsed by NHS England as part of its national hospital discharge guidance, aimed at reducing unnecessary hospital stays and improving patient outcomes. The core principle is straightforward: once a patient no longer meets the criteria to reside in an acute hospital bed — sometimes referred to as being medically safe for discharge (MSFD) — they should not remain on a ward simply waiting for assessments to be completed.

Instead, their long-term health and social care needs are assessed after discharge, in a community setting or at home. This is often referred to as the “Home First” approach. The evidence is clear — people recover faster, regain independence more quickly, and experience better overall wellbeing when they are in familiar surroundings.

D2A is not a decision made by one person. It is a multi-agency process coordinated through local Transfer of Care Hubs and overseen by Integrated Care Boards (ICBs), bringing together NHS trusts, local authorities, multidisciplinary teams (MDTs), and care providers such as Secure Healthcare Solutions to ensure each patient receives the right level of support from the moment they leave hospital.

The Four D2A Discharge Pathways Explained

The NHS uses four numbered pathways — 0 through 3 — to match each patient with the appropriate level of support upon discharge.

Pathway 0 — Simple Discharge

This pathway applies to patients who are fully independent or already have adequate support in place at home. No new formal health or social care services are required. Pathway 0 accounts for the majority of all hospital discharges.

Pathway 1 — Support to Recover at Home

Pathway 1 is for patients who can return home but need short-term additional support to do so safely. This might include a domiciliary care package, reablement services — short-term, goal-oriented support designed to help people regain everyday skills and independence — physiotherapy, occupational therapy, or community nursing visits.

It is the most common D2A pathway and sits at the heart of the Home First philosophy. Secure Healthcare Solutions regularly supplies qualified healthcare assistants and registered nurses to support Pathway 1 care packages across England.

Pathway 2 — Rehabilitation or Short-Term Placement

Some patients require a higher level of rehabilitation that cannot be safely delivered in their own home. Under Pathway 2, they are discharged to a community rehabilitation unit, intermediate care bed, or temporary residential placement. The goal remains the same — to support recovery so the patient can eventually return home.

Pathway 3 — Long-Term 24-Hour Care

Pathway 3 is for patients with complex or ongoing needs who are likely to require permanent bed-based care. They are typically discharged to a care home or nursing home, where a formal assessment of their long-term requirements takes place. This pathway may also involve an NHS Continuing Healthcare (CHC) eligibility assessment.

How Does D2A Funding Work?

Funding is one of the most common concerns for patients and families, and rightly so. Under D2A, the NHS typically provides short-term funding free of charge during the initial assessment period following discharge.

This usually lasts between four and six weeks, during which time the patient should not be charged for care arranged as part of the D2A process.

Once the funded assessment period ends, a formal review determines ongoing needs:

  • If the patient qualifies for NHS Continuing Healthcare (CHC), their care continues to be fully funded by the NHS.
  • If they do not qualify, long-term social care is subject to a local authority financial assessment under the Care Act 2014, commonly known as means-testing.

It is important for families to seek advice early and understand their rights during this transition. Hospital discharge teams and local authority social workers can provide guidance, and organisations such as Secure Healthcare Solutions can help families navigate the process. If you feel the discharge is happening too soon, you have the right to raise concerns with the ward team and request a review of the decision.

Why D2A Matters — Benefits for Patients and the NHS

It is understandable to feel that being discharged from hospital seems premature. However, the evidence consistently shows that D2A leads to better outcomes for the vast majority of patients.

For patients and families:

  • Faster recovery in a comfortable, familiar environment
  • Reduced risk of hospital-acquired infections and deconditioning — the loss of mobility and muscle strength that often results from prolonged bed rest
  • More accurate assessments, because evaluating someone’s needs in their own home gives a far more realistic picture than assessing them on a hospital ward
  • Greater involvement of the patient and family in care planning decisions

For the NHS and wider health system:

  • Frees acute hospital beds for patients who need them most
  • Reduces delayed transfers of care and eases pressure on A&E departments
  • Supports better patient flow across the entire health and care system
  • Encourages integrated, multi-disciplinary working between health and social care teams

How Secure Healthcare Solutions Supports the D2A Process

As a CQC-registered, nurse-led healthcare agency, Secure Healthcare Solutions plays an active role in supporting safe and effective hospital discharge across England.

The agency provides:

  • Registered nurses and healthcare assistants to deliver post-discharge care packages at home, particularly under Pathway 1
  • Complex care specialists for patients with higher-acuity needs, including spinal injuries, acquired brain injuries, and ventilator-dependent conditions
  • Temporary and permanent staffing to NHS trusts, community services, and care homes managing discharge flow under Pathways 2 and 3

With 24/7 availability, rapid response times, and bespoke clinical training for all staff, the team ensures that every patient receives safe, person-centred care from the moment they leave hospital.

Getting the Right Support

The Discharge to Assess model exists to move patients out of hospital safely and promptly, so they can recover in the right setting with the right support around them.

Understanding the four pathways, knowing how funding works, and having access to reliable, high-quality care can make what feels like an overwhelming process far more manageable.

Whether you are a patient, a family member, a healthcare professional, or a commissioner looking for trusted staffing support, Secure Healthcare Solutions is here to help. Call the team on 0121 285 9449 or visit the website to find out how we can support your discharge and care needs.

References

  • https://www.gov.uk/government/publications/hospital-discharge-and-community-support-guidance
  • https://www.england.nhs.uk/urgent-emergency-care/improving-hospital-discharge/reducing-long-term-stays/
  • https://www.england.nhs.uk/statistics/statistical-work-areas/discharge-delays-acute-data/
  • https://www.gov.uk/government/publications/care-act-statutory-guidance/care-and-support-statutory-guidance
  • https://www.england.nhs.uk/long-read/nhs-continuing-healthcare-explainer-video-transcript/

Understanding Advanced MS: Symptoms & Progression

When a loved one’s multiple sclerosis stops behaving the way it used to, a fear strikes in. The relapses that once came and went, with recovery intervals, are replaced by something more relentless: a slow and steady loss of function that does not bounce back. This is Advanced MS and reality for the families living alongside it. Understanding what is happening and why is the first step towards feeling less alone.

This guide will walk you through what Advanced MS is and how a condition progresses to this stage, and the symptoms families should expect.

What Is Advanced MS?

Advanced MS is a condition of multiple sclerosis that has caused significant, cumulative disability or nerve damage in the brain and spinal cord, which builds up faster than the body can recover, and requires complex, often around-the-clock care. Its progression typically happens after years or decades of living with primary or secondary progressive MS.

Clinically, Advanced MS is often defined by EDSS (Expanded Disability Status Scale) with a score of 6.5 or higher. At this stage, the disease-modifying therapies that once slowed the relapse lose their effects, as the driving force behind the decline has shifted from inflammation to neurodegeneration.

How Does MS Progress to an Advanced Stage?

MS has different types that can later progress to advanced stages; the following are the types of multiple sclerosis and how it progresses further into Advanced MS:

  • CIS (Clinically Isolated Syndrome): A first encounter of nerve symptoms which can last for 24 hours and can later lead to an MS diagnosis.
  • RRMS (Relapsing-Remitting MS): RRMS is the most common type of MS (85% of MS patients start here), with clear flare-ups followed by recoveries.
  • SPMS (Secondary Progressive MS): Years after RRMS, the recovery gap between relapses shortens, and the symptoms start to get worse steadily, progressing into SPMS.
  • PPMS (Primary Progressive MS): 10% of people with MS are diagnosed with PPMS; the symptoms get worse from the start with no relapses or remissions.

For most people, MS starts with Relapsing-Remitting MS, then progresses to SPMS. Some people are rarely diagnosed with PPMS from the start. Both pathways eventually lead to advanced MS. A person’s timeline from MS or RRMS to advanced stages of MS varies person to person.

NHS data suggest that around 66% of people with RRMS eventually develop into progressive MS, although due to early access to disease-modifying therapies in the MS journey, this figure is dropping lower.

Common Symptoms of Advanced MS

For a family to witness a transition from managing MS symptoms to being consumed by it is one of the hardest situations. As the MS progresses, the symptoms become worse and more constant.

Common Symptoms of the advanced MS stage include:

  • Mobility issues: Needs support of a wheelchair for walking or standing; movement becomes dependent.
  • Profound Fatigue: Weakness in the body that cannot be relieved by rest alone.
  • Muscle stiffness: Spasms, muscle pain that disrupts sleep and comfort.
  • Bladder problems: Requiring catheters or continence support.
  • Swallowing difficulties: Difficulty swallowing food, which leads to the need for a feeding tube.
  • Cognitive changes: Problems with communication, concentration, memory and processing information.
  • Psychological strain: Anxiety, low mood or stress, grief for both the person with MS and the family.
  • Disorientation: Periods of confusion, caused by latent infections needing treatment.

MS is not a fatal condition, but the disease in itself can raise serious complications such as pneumonia. Each person experiences MS on a different scale; some retain clarity of mind while losing physical function, while others face the opposite.

Managing Advanced MS: A Whole-Person Approach

“Nothing more can be done” is rarely true while managing MS. What changes is the goal, as there is no single treatment for MS; the care shifts to comfort, dignity, and preserving whatever independence and quality of life remains possible.

A whole-person approach is about physical comfort, emotional well-being, cognitive support, and family needs to gather before a crisis instead of treating the symptoms in isolation. This approach includes:

  • Physiotherapy and occupational therapy: To better adapt to the home environment and maintain a comfortable lifestyle.
  • Speech and language therapy: To improve communication, speech and swallowing problems.
  • Symptom-focused medical care: To better manage the bowel, the bladder and pain, etc.
  • Advance care planning: Having a heart-to-heart conversation about the future needs and decisions, so later arrangements are by the person’s own choices.

A palliative care approach is suggested by clinical guidance for MS to improve the quality of life in advanced neurodegenerative conditions.

Living Well at Home with Advanced MS

For most people, staying at home in a familiar environment, routines, and rooms is something a care home or hospital can never replace or replicate. With the right support and management, it is possible to live at home with advanced MS. This can make a huge difference in the morale and dignity of a person.

Practical management includes:

  • Adjusting the home: Bathroom modifications, hand/grab rails, wheelchair for mobility reduce risks and boost confidence in a person.
  • A care team: A team of GPs, physiotherapists, nurses, and carers who understand the person’s medical history and preferences.
  • Respite plan: Taking rest for carers, family members, and nurses is a necessity to avoid burnout.
  • Stay in touch: Maintaining social contact through any means is essential, such as video calling or local support groups.
  • Watch for infection: Chest infection and urinary tract infection can cause weakness, rapid downturn in advanced MS.

The emotional toll of taking care of your loved one and seeing them change so drastically can be draining. Seeking support through counselling, carer groups, or practical tips can benefit the whole family in the end.

How Secure Healthcare Solutions Can Support People with Advanced MS

No Family or person should face advanced MS alone. Managing the condition while doing trial and error and being exhausted and overwhelmed. At Secure Healthcare Solutions, we understand that this condition needs more than clinical competence; it deserves patience, continuity, and genuine compassion from the carers.

From mobility to complex care such as feeding assistance and medication management, all delivered with the aim of helping people remain in the comfort of their home through our trained staff. We understand the toll this journey takes on the family carers, as we build flexible support into our care plans. To find out more about how compassionate, professional Multiple Sclerosis Care in the UK can support your family, get in touch with the Secure Healthcare Solutions team today.

Annual Health Checks for Learning Disabilities: Why They Are Vital

People with learning disabilities in the UK experience significantly worse mental and physical health outcomes than the general population. In many situations, people with learning disabilities die from potentialy tearable conditions. NHS England research says that only 37% of people with learning disabilities live longer than the age of 65, while the general population statistics are up to 85%.

So, it is important to have an annual health check to help you stay well. Talking about your condition or findings with your GP or nurse can help sort things out. In this blog, we will cover what annual health checks for learning disabilities are, why they are important, and what to expect during these checks.

What Are Annual Health Checks for Learning Disabilities?

Annual health checks are for people with learning disabilities aged 14 and over. This is an NHS enhanced service specially for people with learning disabilities who are on their GP’s learning disability register. In this annual health check, a GP or nurse generally review a person’s physical and mental health.

The check is more detailed and dedicated to the person than a standard check. Here is what it contains:

  1. A review of physical and mental health
  2. Checks for common conditions with learning disabilities: epilepsy, constipation, swallowing problems, vision and hearing issues.
  3. A check for conditions such as those linked to Down’s syndrome.
  4. A medication review under STOMP/STAMP programmes.
  5. A check to see if the vaccinations are up to date, such as flu, pneumonia, and hepatitis B.

These annual health checks are not compulsory, it can only be conducted with the consent of the person taking them.

Why Learning Disability Health Checks Are So Important

Research from LeDeR’s reports suggests that individuals with learning disabilities(LD) die 19.5 years earlier, and it goes up to 26.8 years for severe/profound LD. LeDeR’s reports further show that asian and asian british backgrounds often die younger than white backgrounds. People in the most deprived areas living with a learning disability are more likely to die younger than those in the least deprived areas.

These situations remind us of the impact of health inequalities and why the annual health checks for learning disabilities are so important.

This annual check is designed to catch commonly missed or misdiagnosed conditions. The most recent NHS data suggest that in the year 2025/26, around 267,000 learning disability health action plans were completed for about 78% of those aged 14+ on the learning disability register.

What to Expect During a Learning Disability Health Check

The check should be carried out by someone trained appropriately (a GP or learning disability nurse) who understands how to communicate accessibly and avoid diagnostic overshadowing.

As per NHS guidance, the learning disability health check follows:

  • A discussion about general well-being and whether the person needs help staying well
  • Checks for conditions more common in people with a learning disability (epilepsy, constipation, dysphagia, vision, hearing)
  • A urine sample or blood test may be requested
  • A medicines review, to make sure the right medication is being given at the right time (and to check no one is being over-medicated unnecessarily – see STOMP/STAMP)
  • Height, weight, and general physical checks
  • A discussion of any worries the person or their carer wants to raise
  • At the end, the doctor or nurse produces a health action plan — a written record of any follow-up actions, referrals, or health promotion advice, which is reviewed and updated at the next check

How Carers and Support Workers Can Prepare

  • Confirmation of Registration: A person should be on the GP’s learning disability register to be eligible for the health check. A family/carer can ask the GP practice to add them.
  • Pre-health questionnaire: GP practice offers a pre-questionnaire beforehand, or you can ask for it in advance. Some ICBs send these out in advance to gather information from carers before the appointment.
  • Health Passport/Hospital Passport: A document containing information about an individual’s needs, communication style, and health history that can be shared with any health professional.
  • Request reasonable adjustments in advance: Based on a person’s needs and disabilities, you may ask for reasonable adjustments such as a quiet waiting area, the first or last slot of the day, easy-read materials, etc.
  • Prepare the person beforehand: NHS England and organisations such as West of England Learning Disability Collaborative produce easy-to-read guides and videos accessible to all.
  • Follow up on the health action plan: After the appointment, carers play a key role in making sure agreed actions (referrals, follow-up tests, lifestyle changes) are actually completed before the next annual review.

Reasonable Adjustments – Know Your Rights

Under the Equality Act 2010, disability is one of the nine protected characteristics. All public sectors and NHS England and NHS-funded organisations are responsible for, and have a legal duty to, make reasonable adjustments for disabled people. This is an anticipatory duty in which organisations are expected to anticipate needs before problems arise.

Equality Act 2010 accepts a person with a physical or mental impairment with a substantial and long-term adverse effect on their ability to carry out normal day-to-day activities (learning disabilities, etc.) as a disabled person. This person is eligible for reasonable adjustments for annual health checks for learning disabilities under the Act.

A newer NHS-wide system confirms that it will let health care staff record, share and view a person’s reasonable adjustments for learning disabilities, so the staff can use this data for better and quicker preparations in the future. NHS and care providers in England must be able to use it by 30 September 2026. You can simply ask your GP for this information and about available adjustments.

How Secure Healthcare Solutions Can Help

Secure healthcare solutions as a provider that understands this enhanced service framework and can support GP practices, care homes, and services in identifying and registering eligible persons in the learning disability register.

Staff trained in learning disability and autism awareness can help with preparing for annual health checks and understanding reasonable adjustments, communication needs, and how to complete pre-check questionnaires. Furthermore, Secure Healthcare Solutions can ensure the health action plans are followed through between checks, since plans are only useful if actions are taken.

As one of the leading providers of Learning Disability Services in the UK, Secure Healthcare Solutions is committed to helping practices deliver consistent, person-centred care. Get in touch with our team today to find out how we can support your service in delivering high-quality annual health checks and ongoing care for people with learning disabilities.

References:

  • https://www.england.nhs.uk/statistics/wp-content/uploads/2021/06/C0962-i-annual-health-check-in-secondary-care-context-document.pdf
  • https://www.mencap.org.uk/press-release/mencap-responds-2023-leder-report
  • https://digital.nhs.uk/data-and-information/publications/statistical/learning-disabilities-health-check-scheme/england-march-2026
  • https://www.england.nhs.uk/learning-disabilities/improving-health/annual-health-checks/
  • https://digital.nhs.uk/services/reasonable-adjustment-flag
  • https://www.gov.uk/government/publications/reasonable-adjustments-a-legal-duty/reasonable-adjustments-a-legal-duty

Neurogenic Bowel: Symptoms, Causes & Long-Term Management

Some conditions reshape a person’s entire life through daily, minor, or ordinary routines. Neurogenic bowel is one of them. For those living with neurological conditions across the UK, it is a reality that millions navigate every single day – often in silence, and often without the support they truly deserve.

At Secure Healthcare Solutions, we believe that understanding a condition fully is a first step toward managing it with confidence. This guide is for their families, carers, and those who are living with neurogenic bowel.

What Is Neurogenic Bowel?

Neurogenic bowel is a condition or dysfunction in an individual with neurological disease or injuries, failing to evacuate the bowel or failing to contain the stool. This is not a condition but rather a consequence of damage or a disease affecting the nervous system.

The bowel is a sophisticated organ. It follows a series of nerve signals between the brain, the spinal cord, and the muscles of the gut, which keep the bowel functional and allow us to maintain control over when and where to empty the bowel. The profound impact of neurogenic bowel on the quality of life deserves an open conversation about how it changes your daily routines.

Neurogenic Bowel Symptoms

The bowel, without nerve control and normal functioning, can swing between extremes. Living with neurogenic bowel, maintaining a shifting landscape of symptoms can be challenging.

Neurogenic symptoms that affect your daily routine:

  • Constipation: It is the most common effect of neurogenic bowel. A UK postal survey of spinal cord-injured individuals found that up to 30 minutes was spent on each bowel care episode by 58% of respondents, with 22% spending between 31 and 60 minutes, and 14% spending over an hour.
  • Faecal Incontinence: This symptom causes the most psychological burden on a person, causing unexpected and unwanted passing of stool. Within the spinal cord injury population, 75% experience faecal incontinence.
  • Abdominal Symptoms: Neurogenic bowel dysfunction often causes a range of upper and lower abdominal symptoms such as cramping, pain, nausea, and a general feeling of discomfort in the abdomen.

Neurogenic Bowel Causes and Risk Factors

Neurogenic Bowel can cause different symptoms in each individual, which is why understanding its causes and risk factors is important. The cause is always a neurological disruption of the brain nerves that control the bowel.

This disruption can occur in many ways:

  • Spinal Cord Injury: The spinal cord acts as the main communication bridge between the nervous system and the bowel. The injury due to traumatic or non-traumatic causes can interrupt the communication. Spinal cord injury, both traumatic and non-traumatic, has an estimated prevalence of 15 per million in the UK.
  • Multiple Sclerosis(MS): MS is a progressive condition that affects the brain’s central nervous system and disrupts the brain signals. Within the MS population, it is usually estimated that a minimum of two-thirds suffer from bowel symptoms.
  • Parkinson’s: The loss of nerve cells in Parkinson’s disease weakens the autonomic nervous system, which governs bowel functions.
  • Stroke: The brain damage from strokes can result in constipation and faecal incontinence, sometimes resulting in permanent symptoms.
  • Neurological Conditions: Brain injuries and various forms of peripheral nerve damage can all lead to neurogenic bowel dysfunction.

Types of Neurogenic Bowel Dysfunction

Neurogenic bowel is typically classified into two types of dysfunction based on which part of the brain’s nervous system is damaged:

Upper Motor Neurone (UMN) / Reflexic Bowel

Reflexic Bowel occurs when the sacral region of the spinal cord (above S2-S4) is damaged. It affects the enteric nervous system, which connects the brain and the bowel’s own local network.

Due to this condition, the bowel retains automatic reflex activity, and voluntary control is lost. This results in constipation and hard stools. This is the type most commonly associated with cervical and thoracic level spinal cord injuries.

Lower Motor Neurone (LMN) / Areflexic Bowel

Areflexic bowel occurs when damage affects the sacral spinal cord or peripheral nerves, leading to the bowel. The bowel loses muscle tone, and the stool cannot move effectively, causing severe constipation. The anal sphincter may also become weak, which can lead to accidental stool leakage.

Understanding which type of dysfunction a person has guides everything from the techniques for bowel care to the medications prescribed and the management of outcomes.

How Neurogenic Bowel Is Diagnosed

Diagnosis of neurogenic bowel is a process rather than a single test, which may require a range of assessments and a thoughtful conversation between the patient and their clinical team.

  • Clinical History: Patient’s bowel history is taken carefully, exploring the nature, consistency, and frequency; symptoms such as bloating, pain; the impact on daily life. Assessment of prior bowel function is complete.
  • Neurogenic Bowel Dysfunction (NBD) Score: The NBD Score is a validated questionnaire that identifies the severity of the symptoms and is useful for initial assessment.
  • Imaging and Specialist Tests: In some cases, imaging such as plain abdominal X-rays may be used to assess faecal loading. Anorectal manometry, colonic transit studies, and neurophysiological tests may be arranged for more complex cases or where surgical intervention seems necessary.
  • Multidisciplinary Assessment: For many people, the most effective diagnostic and management pathway is delivered through a multidisciplinary team. In the UK, specialist centres such as spinal cord injury units typically have established pathways for this kind of comprehensive assessment.

Neurogenic Bowel Management

To manage neurogenic bowel, we need to find the right daily routine. A predictable, effective, and dignified routine that allows a person to get on with their life with as much independence and confidence as possible.

  • Conservative Management: The Foundation: The first-line approach includes:
    • Regular bowel routines timed after meals.
    • Suppositories and enemas to stimulate bowel emptying.
    • Digital rectal stimulation (DRS) for reflex bowel evacuation.
    • Digital removal of faeces (DRF) for severe impaction.
  • Transanal Irrigation (TAI)
    • TAI uses warm water introduced into the bowel through a rectal catheter or cone to achieve controlled evacuation. It improves symptoms and quality of life in many patients when conservative methods fail and is supported by NICE guidance in the UK.
  • Medications
    • Laxatives for constipation.
    • Anti-diarrhoeal agents (e.g., loperamide) for faecal incontinence.
    • Treatment should be tailored to the individual’s neurological condition.

Bowel Care Support at Home

Bowel care is a deeply personal territory that requires a level of trust, skill, and sensitivity. For people with neurogenic bowel, the majority of their care takes place at home, with the support of their family member or professional carer. Life with neurogenic bowel can be lived fully and actively if practical and professional help is given with the right management plan.

At Secure Healthcare Solutions, we provide specialist bowel care in Wolverhampton and across the West Midlands for people living with neurological conditions. Our compassionate, highly trained carers deliver personalised support that promotes comfort, dignity, and independence. If you or a loved one needs specialist care at home, we’re here to help.

Tracheostomy Suctioning: Purpose, Procedure & Care Guide

Every year, around 15,000 people in England and Wales require a tracheostomy – and for many of them, going home means taking this clinical need with them. Suctioning is at the heart of that daily care. Do it well, and life stays manageable. Miss the signs, or rush the technique, and things can deteriorate faster than most people expect.

Whether you’re a community nurse visiting a patient for the first time post-discharge, a family carer who’s just been handed a portable suction machine and a care plan, or an HCA freshening up your knowledge – this guide walks you through the tracheostomy suctioning procedure from start to finish: what it is, why it matters, and how to do it safely.

What Is Tracheostomy Suctioning – and Why Is Tracheostomy Airway Management So Critical?

Tracheostomy suctioning is the clinical procedure of passing a sterile catheter through a tracheostomy tube to remove secretions and maintain a patent airway. It is one of the most fundamental aspects of tracheostomy airway management.

When someone has a tracheostomy, their airway bypasses the nose and mouth entirely. The nose normally warms, filters, and moistens incoming air – without it, secretions thicken, pool in the trachea, and many patients simply cannot cough them clear. The tracheostomy stoma and tube itself can also increase mucus production, adding to the burden.

Left unmanaged, those secretions block the tube, drop oxygen levels, and quickly become a breeding ground for infection. In our experience at Secure Healthcare Solutions, carers who understand why they’re suctioning – not just how – respond far more calmly when a patient becomes distressed.

Signs That Tell You Suctioning Is Needed

The key signs that a tracheostomy needs suctioning include:

  • Audible bubbling or gurgling from the tracheostomy site
  • A drop in oxygen saturation (SpO₂) from the patient’s normal baseline
  • Visible secretions at the opening of the tube
  • Increased breathing effort — use of accessory muscles, restlessness
  • The patient pointing to their throat or appearing to struggle
  • Coughing that isn’t shifting anything

There is no fixed suctioning schedule. Frequency is based entirely on clinical assessment – some patients need it several times a day, others far less. Always encourage the patient to cough first; an effective cough is preferable to suction.

Open vs. Closed Tracheostomy Suctioning: Which Applies to Your Patient?

In community and home care settings, open suctioning is the standard method. If your patient is on a home ventilator, their care plan will specify closed suctioning – and you will have been trained on this before discharge.

Open suctioning disconnects the patient from any humidification or ventilator circuit. It works well but carries a slightly higher risk of deoxygenation and infection if technique is poor.

Closed (in-line) suctioning keeps the catheter within a sealed system – no disconnection, less contamination risk, less oxygen loss. Used primarily for ventilated patients.

Whichever method applies, maintaining adequate humidification via an HME (heat and moisture exchanger) is essential – it reduces secretion thickness and makes suctioning less frequent and less traumatic.

Choosing the Right Tracheostomy Suction Catheter Size

The correct tracheostomy suction catheter size should not exceed half the internal diameter of the tracheostomy tube – this is the standard rule across NHS trust guidelines. As a practical guide, most adult patients in the UK will use sizes 10, 12, or 14 FG, but the exact size must always be confirmed from the patient’s tracheostomy passport, where it is documented by the discharging hospital team.

The Tracheostomy Suctioning Procedure: How to Suction a Tracheostomy Safely

Before you begin, explain what you’re about to do. Even patients who can’t respond verbally are aware, and a calm explanation reduces distress for everyone in the room.

  1. Wash hands and put on gloves, apron, and eye protection
  2. Check equipment — suction pressure set to 80-120 mmHg for adults, correct catheter size
  3. Assess first — check SpO₂, listen, observe. Is suctioning actually needed right now?
  4. Pre-oxygenate if indicated — as per the care plan
  5. Attach catheter to suction tubing without activating suction
  6. Insert gently using a shallow technique — to the tip of the tube or 1-2 cm beyond. Deep suctioning risks carina trauma and is not recommended in community settings
  7. Apply suction on withdrawal only — rotating motion, no more than 10-15 seconds per pass
  8. Rest between passes — 20-30 seconds minimum, watch SpO₂ recover
  9. Repeat if needed — maximum 3 passes; beyond that, stop and reassess
  10. Flush and dispose — sterile water flush, single-use catheters discarded after the episode
  11. Document — colour, consistency, volume, patient tolerance, SpO₂ before and after

A note on saline instillation: routine use of saline before suctioning is no longer recommended by current UK guidance unless specifically directed by the patient’s care team.

Complications of Tracheostomy Suctioning – and How to Stay Ahead of Them

The main complications of tracheostomy suctioning – hypoxia, mucosal trauma, infection, cardiac arrhythmia, and patient distress – are mostly preventable with correct technique.

  • Hypoxia — limit suction duration, pre-oxygenate where indicated
  • Mucosal trauma or bleeding — correct catheter size, never force the catheter
  • Infection — strict Aseptic Non-Touch Technique (ANTT) every time; never reuse single-use catheters
  • Vagal response / cardiac changes — deterioration mid-procedure: stop immediately
  • Anxiety and distress — talk throughout; never work in silence

Escalate immediately if:

  • SpO₂ remains low after suctioning
  • Frank blood in secretions
  • Catheter cannot be passed
  • Tube appears blocked and won’t clear

→ Call 999. The emergency tracheostomy box lives at the bedside for a reason.

Tracheostomy Care at Home: What Families and Carers Need to Know

Family members and home carers can perform tracheostomy suctioning safely – and in the UK, they are trained by specialist nurses before discharge. You should not go home without that training and the right equipment in place.

A few things experienced home-care teams know well:

  • The Tracheostomy Passport — a formal NHS document developed in line with National Tracheostomy Safety Project (NTSP) guidance — records tube type, catheter size, humidification needs, and emergency instructions. It goes everywhere with the patient.
  • Secretions that change colour, thicken significantly, or develop an odour suggest possible infection — contact the GP or community team promptly.
  • Home suction machines need regular checks. Know who to call if equipment fails out of hours.
  • If secretions suddenly thicken, check the HME filter is in place and functioning.
  • In the longer term, some patients are assessed for decannulation — removal of the tracheostomy tube. This is a specialist multidisciplinary decision, not a community one.

Tracheostomy Care in Wolverhampton: How Secure Healthcare Solutions Can Help

Tracheostomy suctioning looks straightforward on paper – but the judgment around when to act, how to read the patient, and when to escalate takes experience. That’s something no checklist fully replaces.

At Secure Healthcare Solutions, we provide specialist tracheostomy care in Wolverhampton and across the surrounding community – from suctioning and airway management to tube changes and dedicated home care plans. Our trained team supports patients and families through every stage of tracheostomy care at home, so hospital discharge feels like a transition, not a cliff edge. Get in touch with our team today to discuss your needs.

References:

  • https://tracheostomy.org.uk/
  • https://www.nhs.uk/tests-and-treatments/tracheostomy/

How to Treat Skin Irritation Around a Stoma: Care Tips

Skin irritation around a stoma can start with something that seems small: a faint itch under the pouch, a slight sting during cleaning, or a red patch that appears after a leak. But peristomal skin can deteriorate quickly if faeces or urine sits against it. A systematic review found that peristomal skin complications affect between 36.3% and 73.4% of people following stoma surgery, which shows how common these problems can be.

The skin around a stoma is called peristomal skin. It should not feel sore, itchy, wet, burning or painful. If it does, it is usually a sign that something needs attention, such as a leak, poor pouch fit, trapped moisture, adhesive damage or irritation from a product.

For mild skin irritation, remove any leaking pouch, clean the skin gently with warm water, dry it completely and check that the pouch opening fits closely around the stoma. If irritation continues, worsens or the skin becomes broken, contact your stoma care nurse.

How to Treat Skin Irritation Around a Stoma

The most important part of treating skin irritation is finding the cause. If the same sore patch keeps returning, look carefully at where it appears. A ring of soreness close to the stoma often suggests output is touching the skin. Redness in the shape of the adhesive may suggest trauma from removal or sensitivity to a product.

When you first notice irritation:

  • Remove the pouch gently. Support the skin with one hand and slowly peel the adhesive away with the other.
  • Check the back of the pouch. Look for output under the flange or baseplate.
  • Clean with warm water only unless advised otherwise. Avoid scrubbing sore skin.
  • Dry the skin fully. Even slight dampness can stop the pouch from sealing properly.
  • Check the pouch opening. It should sit close to the stoma without rubbing it or leaving surrounding skin exposed.
  • Do not patch over a leak. Extra tape may hide the problem while output continues to damage the skin underneath.

In practice, one of the most useful checks is the back of the removed pouch. If the same area of adhesive is repeatedly damp or eroded, it often shows where the seal is failing. This can give a stoma care nurse clearer information than simply saying the pouch “keeps leaking”.

Barrier films, stoma powders and protective seals can be helpful in some situations, but they are not a cure-all. Too much powder or product can prevent the pouch from sticking. If you are unsure how to heal sore skin around a stoma, ask your stoma care nurse before changing products.

Common Causes of Skin Irritation Around a Stoma

Leakage is one of the most common reasons for sore skin around a stoma. Stoma output can be irritating, especially if it sits under the pouch adhesive. Once the skin becomes sore or moist, the pouch may stick less well, which can cause more leakage.

A poorly fitted pouch is another common issue. The stoma can change size after surgery, during weight changes or if the shape of the abdomen changes. Skin folds, scars, swelling, a flush or retracted stoma, and a parastomal hernia can all affect the seal.

A common pattern in home care is soreness returning in the same place, such as one side of the stoma or underneath a skin fold. This often suggests a fit or body-shape issue rather than a general skin problem.

Other causes include removing the pouch too quickly, trapped moisture or sweating, using too much powder or barrier product, sensitivity to adhesives, hair follicle irritation, existing skin conditions, or possible infection.

Itchy skin around a stoma can be an early warning sign. In home-care settings, carers often notice that people mention itching before they see an obvious leak. If itching keeps returning under the same part of the pouch, it is worth checking the seal and discussing it with a stoma care nurse.

How to Prevent Skin Irritation Around a Stoma

Good stoma skin care is built around routine and observation. The aim is to notice small changes before they become painful.

Check the skin at every pouch change. Look for soreness in the same place, damp skin, adhesive residue or signs that output has crept under the baseplate. Empty the pouch before it becomes too heavy, as the weight can pull on the seal.

Regularly remeasure the stoma, especially after surgery, weight changes or changes in abdominal shape. A template that fitted well a few months ago may no longer be right.

Helpful habits include:

  • Removing the pouch slowly
  • Drying the skin fully before applying a new pouch
  • Avoiding unnecessary product layers
  • Keeping supplies in a cool, dry place
  • Recording repeated leaks or irritation
  • Asking for a pouch review if leaks happen often

Small patterns matter. Repeated leaks overnight, after meals or during movement can give your stoma care nurse useful clues. Care teams also often notice that irritation is worse when pouch changes happen under pressure, such as before leaving the house or late at night.

When to Contact Your Stoma Care Nurse, GP or NHS 111

Contact your stoma care nurse or GP if irritation does not improve, keeps returning or prevents the pouch from sticking securely. You should also seek advice if the skin becomes painful, broken, wet, bleeding or weeping.

You should also request a review if you notice frequent pouch leaks, new ulcers, unusual skin growths or a sudden change in the stoma’s size, shape or position. If possible, take a clear photograph during a pouch change so your nurse can see what is happening.

Some symptoms may indicate a serious complication rather than routine skin irritation. Contact NHS 111, ask for an urgent GP appointment or seek urgent medical help if you experience severe abdominal pain, vomiting, signs of dehydration, lots of blood from the stoma or a high temperature.

You should also seek urgent help if your stoma stops producing output for much longer than normal, or if it suddenly becomes very dark, purple or black.

Practical Support With Stoma Care at Home

Skin irritation often becomes worse when small leaks are missed or when a pouch change feels rushed. Families may also feel unsure whether soreness is caused by the appliance, moisture, stoma output or the way the pouch is being removed.

A trained carer can support a calmer routine by helping the person change their pouch at the right time, checking for early signs of leakage and making sure the surrounding skin is fully dry before a new pouch is fitted. They can also record patterns, such as repeated leaks overnight, after meals or during movement, so these can be discussed with a stoma care nurse.

At Secure Healthcare Solutions, our care team often finds that people feel more confident when they have a consistent routine and know when to ask for clinical advice. Our personalised Stoma Care in Wolverhampton helps make daily stoma care feel less stressful while protecting dignity, comfort and independence.

Frequently Asked Questions

What cream is good for irritated skin around a stoma – and can I use Sudocrem?

Avoid ordinary creams including Sudocrem — they prevent the pouch from sticking and can make things worse. The right product depends on the cause. Ask your stoma care nurse before changing anything.

Is red skin around a stoma normal?

Temporary pinkness after removing the pouch may settle quickly. Persistent redness, discolouration, soreness, itching or broken skin is not considered healthy and should be assessed.

How do you treat raw or weeping skin around a stoma?

Raw or weeping skin should be assessed by a stoma care nurse. Avoid applying ordinary creams or dressings without professional advice.

Sources

  • https://pmc.ncbi.nlm.nih.gov/articles/PMC9819694/
  • https://www.nhs.uk/tests-and-treatments/colostomy/complications-of-a-colostomy/
  • https://www.colostomyuk.org/information/stoma-problems/sore-skinleakage/
  • https://ascnuk.org/