Support with AAC devices

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Support with AAC devices

Here is some information about what to do for some common issues with AAC devices.  

Please only contact AAC WEST about devices that we are responsible for. 

Our contact details are at the bottom of this page.  

Mounting problem

Issue with a current mount? 

  • Contact AAC WEST Tech Team (see details at the bottom of the page).

Need a new mount? 

AAC device mounted to wheelchair

Hardware problem 

Issues with:

  • Screens
  • Camera
  • Charger
  • Turning device on

Contact AAC WEST Tech Team (see details at the bottom of the page).

AAC icons of plug, cracked tablet screen, switch, tablet charging port, and charger

Software problem

Issues with:

  • Device not speaking. 
  • Device freezing/crashing.
  • Device not working as normal. 

First try:

  • Power off and turn it on.
  • For iPads, try a hard shut down.
  • Complete all hardware and software updates. 

If not resolved first contact:

  • The local team, for example teacher, support worker, and local speech and language therapist.
  • The supplier see (details at the bottom of the page).

If not resolved:

Contact AAC WEST Tech Team (see details at the bottom of the page). 

AAC software logos

Editing

Need to make changes to the vocabulary such as:

  • Adding words.
  • Changing symbols.
  • Adding pages. 

First explore:

If not resolved first contact:

  • The local team, for example teacher, support worker, and local speech and language therapist.
  • The supplier (see details at the bottom of the page). 

If not resolved:

  • Contact AAC WEST Tech Team (see details at the bottom of the page). 
Icons for editing AAC software

Supporting AAC users

Support with: 

  • Help to learn how to use their AAC.
  • Modelling AAC.
  • Communication partner skills.

First explore:

If not resolved first contact:

  • The local team, for example teacher, support worker, and local speech and language therapist.
  • The supplier (see details at the bottom of the page).

If not resolved:

  • Contact AAC WEST Tech Team (see details at the bottom of the page). 
Person supporting another person using an AAC device

Supplier contact details 

Check your device for the company name. Suppliers can support with a range of issues. If you give them consent they can have remote access to your device to provide support. 

AAC WEST contact details 

Please contact us if the above do not resolve your device issue. 

Admin

Tech Team

  • For hardware issues like faulty batteries, broken screens, missing equipment, and frozen iPads.
  • aacwesttech@nbt.nhs.uk                                     
  • 0117 414 5850

Support

  • Support for software issues like missing grid sets/cells, Dropbox/account issues, and connectivity.
  • aacwestsupport@nbt.nhs.uk
  • 0117 414 5850

© North Bristol NHS Trust. This edition published October 2025. Review due October 2028. NBT003817.

Cellular Immunology / Immunophenotyping Laboratory

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Leukaemia and Non-Hodgkin Lymphoma Diagnosis and Monitoring

The laboratory provides a comprehensive service in the investigation of Leukaemia and Non-Hodgkin Lymphoma. Immunophenotyping provides additional information to morphology and cytogenetics in the diagnosis, classification and monitoring of these disorders.

HIV Monitoring
Immunophenotyping is used serially to monitor CD4 levels.

Investigation of Cellular Immunodeficiency Disease
Wrong choice of tests, especially in the paediatric setting, can mean rare cases of immunodeficiency are missed. Vital information includes type and site of infections, family history, other pathology results, X-rays and clinical features. Please refer to the Clinical Immunologists: ward or clinic referral is the ideal.

  • Immunophenotyping identifies numerical defects in lymphocyte subsets, inherited or acquired, and are indicated in cases with recurrent viral, fungal or mycobacterial infection.
  • PNH Testing performed on peripheral blood samples looking for the absence of GPI-linked proteins on neutrophils, monocytes and red blood cells.
  • Functional Leucocyte Assays

These assays are technically complex and require prior discussion with the laboratory. Abnormalities are rare, most commonly due to poor sample quality, testing during drug therapy or intercurrent infection.  Abnormal findings should always be confirmed on a second sample.  True abnormalities may need further, more specialised tests to specify the disorder.

  • Lymphocyte function studies are indicated in cases of recurrent viral, fungal and mycobacterial infections in whom no numerical lymphocyte defect has been defined. The investigation provides a measure of lymphocyte activation. Lymphocytes are cultured for 5 days with mitogens which mimic antigen activation.
  • Neutrophil function studies screen for defects in the metabolic burst and adhesion molecules and are indicated in cases with recurrent fungal or bacterial infection with a normal neutrophil count (>1x109/1).A normal result excludes major defects in neutrophil function.

 

Quantiferon Assay

The QuantiFERON-TB test is an interferon gamma release assay (IGRA) used for the diagnosis of latent Tuberculosis (TB). The assay requires special blood tubes and has specific sample handling requirements. The laboratory can issue guidance and sample tubes to requestors. Interpretation of the result needs to be in the context of clinical history and other laboratory and clinical investigations.  The antigens used in the test are absent from all BCG vaccine strains of TB and from most known non-tuberculoid mycobacteria, it is possible to have a reactions to M. kansasii, M. szulgai and M. marinarum.  If such infections are suspected, alternative testing should be sought.

The QuantiFERON-TB test (and other TB IGRAs) may give false negative results in immunosuppressed patients. The laboratory provides a positive control tube for all tests to ensure the validity of results. Where the positive control fails (indeterminate result) the laboratory may suggest alternative testing. Please see guide below for interpreting indeterminate results.

Guide to interpretation

•    Negative: A negative result indicates that latent infection with M. tuberculosis is NOT likely. This result does NOT exclude active TB infection. The investigation of suspected active TB requires clinical, radiological and microbiological assessment.
•    Positive: A positive result is consistent with latent or active TB. This result may be due to exposure to M.tuberculosis complex (except M. bovis BCG), M. kansasii, M. szulgai or M. marinarum.  IGRA should not be used for the investigation of suspected active TB. The investigation of suspected active TB requires clinical, radiological, and microbiological assessment.
•    Indeterminate: The likelihood of the patient having M. tuberculosis infection cannot be determined from the blood sample provided. Please see the guide to interpreting indeterminate results below.

 

Quick guide to interpreting INDETERMINATE and EQUIVOCAL QuantifFERON-TB results

INDETERMINATE RESULTS

An indeterminate result from the QuantiFERON-TB assay means that the likelihood of the patient having M. tuberculosis infection cannot be determined from the blood sample provided.

The majority of indeterminate results are caused by a low T lymphocyte response to mitogen stimulation (reported as mitogen tube failure).  
This can be caused by:

•    An insufficient number of T lymphocytes in the blood sample. Is the patient immunosuppressed?
•    A functional inability of the patient’s lymphocytes to generate Interferon-gamma (IFN-γ) in response to mitogenic stimulation, for example if they are taking drugs that supress their immune system.
•    Reduced lymphocyte function due to improper sample handling.

Ideally repeat the QuantiFERON-TB test once with a fresh blood sample. If a mitogen tube failure is reported a second time, there is no value in repeating the QuantiFERON-TB test again until the underlying cause has been identified and resolved. 

Rarely a high background in the negative control (Nil) tube generates an indeterminate result. 
This can be caused by:

•    Excessive levels of circulating IFN-γ or the presence of heterophile antibodies in the sample. Stimulating the cells further as part of the QuantiFERON-TB test does not produce a further IFN-γ response.

Ideally repeat the QuantiFERON-TB test once with a fresh blood sample. If a high background is reported a second time, there is no value in repeating the QuantiFERON-TB test again until the underlying cause has been identified and resolved.

Other causes of indeterminate results can include:

•    Incorrect filling/mixing of the Lithium Heparin or QuantiFERON-TB tubes.
•    If the time between venepuncture and sample incubation in the laboratory is greater than 16 hours.

These indeterminate samples should be repeated using the correct sampling and handling procedures.

For further information please see:

https://www.qiagen.com/gb/tb-testing/what-is-quantiferon/how-does-qft-work/quantiferon-tb-test-result-interpretation

EQUIVOCAL RESULTS

An equivocal reference range of 0.2 – 0.7 IU/mL is now applied to the Q-TB results generated when subtracting the negative control tube value (NIL) from the TB1 and TB2 tube results: TB1-NIL and TB2-NIL.

Where both TB1-NIL and TB2-NIL results are within the equivocal range (0.2 – 0.7), or where one result is equivocal (0.2 – 0.7) and one is true negative (<0.2) the Q-TB results will be reported as EQUIVOCAL with the following interpretation applied:

The significance of this result is uncertain. The risk of progression to active TB disease is likely to be different when compared to patients with clear positive (>0.7) or clear negative (<0.2) results. Suggest repeat testing if clinically indicated; approximately one third of patients with equivocal results will revert to either a clear positive or clear negative result when a fresh blood sample is analysed within six months. We would recommend repeat testing again in 4-8 weeks where practical. Where this is not practical, we would recommend a repeat test in weeks rather than days.

Why have we implemented an equivocal reference range?

Reversion and conversion of low positive (TB-NIL: 0.35 – 0.7) and high negative (TB-NIL: 0.2 – 0.34) Q-TB results on repeat testing is a well-recognised phenomenon. To address this issue, multiple European centres have proposed an equivocal range of 0.2 – 0.7 IU/mL [1-7]; conversion to true positive results have been shown to occur most frequently when the first Q-TB result is between 0.2 – 0.35 IU/mL, and reversions to a true negative result have been shown to occur more frequently when the initial result is between 0.35 – 0.7 IU/mL [5].

The Royal Free hospital in London has implemented this equivocal range in line with other low-incidence TB European settings [6].  Data from the Royal Free lends support to the use of the equivocal range for the reporting of Q-TB results; ~1/5th of their results that fell just below the 0.35 cut-off were positive when repeated on a fresh blood sample, and half of those just above the 0.35 threshold were negative when repeated on a fresh blood sample. This data strongly implies that relying on results within the equivocal range could result in either over-treatment or under-treatment of patients.

  1. Torres Costa J, Silva R, Sa R, et al. Serial testing with the interferon-gamma release assay in Portuguese healthcare workers. Int Arch Occup Environ Health 2011; 84: 461–469.
  2. Schablon A, Harling M, Diel R, et al. Serial testing with an interferon-gamma release assay in German healthcare workers. GMS Krankenhhyg Interdiszip 2010; 5: Doc05.
  3. Schablon A, Diel R, Diner G, et al. Specificity of a whole blood IGRA in German nursing students. BMC Infect Dis 2011; 11: 245.
  4. Ringshausen FC, Schablon A, Nienhaus A. Interferon-gamma release assays for the tuberculosis serial testing of health care workers: a systematic review. J Occup Med Toxicol 2012; 7: 6
  5. Nienhaus A, Ringshausen FC, Costa JT, et al. IFN-gamma release assay versus tuberculin skin test for monitoring TB infection in healthcare workers. Expert Rev Anti Infect Ther 2013; 11: 37–48.
  6. Brown J, Kumar K, Reading J, et al. Frequency and significance of indeterminate and borderline Quantiferon Gold TB IGRA results. Eur Respir J 2017; 50: 1701267
  7. Hermansen TS, Lillebaek T, Langholz Kristensen K, et al. Prognostic value of interferon-gamma release assays, a population-based study from a TB low-incidence country. Thorax 2016; 71: 652–658.

Test Information

Sample vials for testing

Includes details of sample types, volumes, special precautions, turnaround times & reference ranges.

Cellular Immunology/Immunophenotyping Laboratory

Moving forward after breast cancer

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Introducing supported self-management

North Bristol NHS Trust (NBT) has introduced supported self-management and remote monitoring. This is done using a website called My Medical Record (MMR). This can be used to manage your follow-up care securely.

Regular follow-up appointments can involve organising travel and time off work, which can be costly and inconvenient. Although some people find these appointments useful and reassuring, some find them unnecessary unless they have something specific to discuss.

If individuals report symptoms and concerns as they occur, rather than waiting for a routine appointment, this can help address concerns more quickly.

Following breast cancer treatment, you will be followed up for a period of time (usually 5 years) when you can contact your Breast Care Team directly if you have any queries or concerns.

What does supported self-management and remote monitoring mean?

  • Supported self-management: This enables you to take a leading role in your follow-up with support as needed.
  • Remote monitored: The Breast Care team can monitor your health and plan of care even when you are not in a face-to-face appointment.

The main aim is to enable you to develop the skills and knowledge to:

  • Make positive choices about your health.
  • Manage the physical and emotional impact of breast cancer and its treatment.
  • Make healthy lifestyle changes.

Follow-up after breast cancer treatment

Depending on the type of treatment you have had, you may have a plan of regular mammograms or other imaging.

At NBT we use MMR to provide you with your monitoring plan, test results, and useful resources.

You can use it to message your cancer support team securely with non-urgent queries.

After finishing treatment, a Breast Clinical Nurse Specialist will discuss your monitoring plan and how self-supported management works.

Once introduced to MMR, you will be offered access to the website. You can access the website from your smart phone, tablet, or computer at any time.

Here is a short film about MMR: 

After watching this video, if you would like to use MMR, you will be provided with login details. You can also choose not to use MMR, your monitoring will continue with routine telephone appointments.

What tests will I have?

  • Yearly mammogram or MRI depending on your follow-up plan. We call this surveillance. Usually this is for 5 years.
  • Depending on your treatment pathway, you may be prescribed anti-hormone tablets. We call this endocrine therapy.
  • At the end of your monitoring period, you may continue to have imaging tests under the National Breast Screening Programme, depending on your age.

Imaging appointments will be arranged by the Radiology Administrative Team.

You will receive an appointment to attend the hospital typically 1 year from when you had your surgery, and yearly afterwards for the monitoring period.

Your mammograms will be carried out by the Radiology department at the Breast Care Centre during your period of follow-up.

MMR will show when future tests are due.

  • If your test results are normal, a digital letter confirming this will be available on MMR, as well as the date of your next test.
  • If your test results are abnormal, the Breast Cancer Team will contact you. You will likely be asked to come to an appointment at the Breast Care Centre.

Picture of the MMR homepage

My Medical Record homepage

Useful resources available on MMR

Information resources including websites, leaflets and videos are available on MMR. These cover topics such as:

  • Managing the side effects of treatment.
  • Self-examination.
  • Healthy lifestyle.
  • Support groups.

Contact information

Breast Care Admin Team

  • Queries relating to appointments.
  • 0117 414 7000

Breast Care Support Workers

  • Support and information relating to breast cancer.
  • 0117 414 7047

Radiology Administrative Team

  • Queries relating to mammograms and screening.
  • 0117 414 9132

Macmillan Wellbeing Centre

  • General support and information.
  • 0117 414 7051

If there is no answer, please leave a message and we will get back to you as soon as possible. We will aim to get back to you within 48 hours.

© North Bristol NHS Trust. This edition published February 2026. Review due February 2029. NBT003691

What to expect

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If you have been offered an appointment with us, it is because your local speech and language therapist has referred you. 

What to expect  

Appointments 

Your appointment may take place at your home, your school/college, your day centre/hospice/care setting or at one of our outpatient service buildings. 

Your appointments will usually last around 2 hours but may take longer. We will offer you regular breaks and can split the assessment over two appointments if needed.  

Who will be there? 

  • Your local speech and language therapist. 
  • An AAC WEST speech and language therapist. 
  • An AAC WEST occupational therapist.  
  • An AAC WEST assistant practitioner. 
  • Your school, college or day centre staff. 
  • Your family, carers or support staff. 

There may be lots of people at your appointment, please let us know if there is any way we can make it more comfortable for you.  

Appointment pathway 

  1. Referral – your referral is made by your local speech and language therapist.  
  2. Initial assessment – we will assess your communication access needs (how you select what you want to say). 
  3. Equipment provision – an AAC device is loaned to you and we will set your goals together.  
  4. Review/final review – your AAC and goals will be reviewed. At the final review we hand your care back over to the local team.  

What will happen in my initial assessment?

In this appointment we may: 

  • Explain the criteria set by the NHS for specialised AAC services in England. 
  • Talk to you and your communication partners to find out more about your communication strengths and needs.  
  • Look at how you can use AAC. We will look at your physical movements, and try out different methods for you to access AAC. 
  • Try out different types of AAC (these could be powered and/or paper based). 
  • Try out different types of communication software. 
  • Look at where to place the equipment. 
  • Decide on an AAC option to loan to you over a period of weeks (normally loaned to you in the equipment provision appointment). 
  • Ask you and your communication partners to think of words and phrases you may want to add to the AAC. 

What will happen in my equipment provision appointment?

In this appointment we may: 

  • Further assess some of the areas from the initial assessment. 
  • Show you and your communication partners how to use the AAC we are loaning. 
  • Set some goals with you and your team so that you can get the best out of your AAC trial. 
  • Demonstrate the technical and safety aspects – this may include charging, mounting, software updates etc. 
  • Check if there are any further words and phrases that you want adding to the AAC. 
  • Ask you and/or your team to write down some examples of the AAC use over the coming weeks. 

Sometimes we can combine the initial assessment and the equipment provision appointment.  

What will happen in my review?

In this appointment we may: 

  • Find out from you and your communication partners how the AAC trial has been going. 
  • Talk about any issues or queries and try to problem-solve these. 
  • Look at the progress you have made with your goals and offer more support if needed. 
  • Suggest a longer trial period if needed. 
  • Decide whether we are able to loan and fund the AAC long term. 
  • Look at alternative AAC if this is needed. 

Some people will just need one review – this will be their ‘final review’. See below. 

What will happen in my final review?

We will discuss similar points as above under ‘Review’. 

If we are able to loan AAC long term, we will: 

  • Agree to fund and maintain your AAC. 
  • Set some AAC goals for the future. 
  • Decide who will update words and phrases on your AAC (if you need help with this). 
  • Make sure you and your communication partners know who to contact if you have any problems with your AAC. 
  • Hand your care back to your local speech and language therapist, and communication partners. 
  • Discharge you from AAC WEST and tell you how to access re-referral in the future if needed. 

If we are not able to loan AAC long term: 

  • This may be because the timing is not right. We will discharge you, but you can be referred in the future if things change. 
  • We may suggest you work on building skills for AAC. 
  • Your local speech and language therapist can explore other options/services that may be able to support you. 

What is an Emergency Appointment?

Emergency appointments are for people whose condition is getting worse quickly, like Motor Neurone Disease (MND). They need to be seen urgently. 

AAC WEST schedules on average two emergency assessments a month, and they are scheduled for people who meet the following criteria: 

  • Are getting worse quickly rapidly. 
  • Can no longer able to rely on their speech. 
  • They can no longer easily use touch devices like tablets or Lightwriters because their hand function has declined. 

Referrals for emergency appointments are made by the local speech and language therapist. After this a series of 3 appointments will be made: 

  • An initial appointment where AAC WEST will assess the person and loan equipment for trial. We aim to do this within 4-6 weeks from referral acceptance. 
  • A review appointment that will take place 3-4 weeks later. 
  • A second review appointment that will be scheduled 3-4 weeks after the first review appointment. This appointment may not always be needed if everything is working well at the first review. 

Emergency appointments are usually done by an AAC WEST occupational therapist and assistant practitioner.  

What is a mounting appointment?

In this appointment we may: 

  • Talk about where you use your communication aid (such as at home, school or shopping). 
  • Talk about where you use your communication aid the most (such as your wheelchair, class chair, bed or table). 
  • Measure, build and attach the stand for your communication aid.  
  • Show your family/carers/staff how to put on and take off the device from the mounting solution.  

© North Bristol NHS Trust. This edition published December 2026. Review due December 2029. NBT003829.

Exclusive Enteral Nutrition (EEN)

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Introduction

This page will tell you about Exclusive Enteral Nutrition (EEN). It will answer some questions you may have about it.

What is Crohn’s disease?

Crohn’s disease can affect any part of your gut. It causes inflammation, ulcers, swelling and soreness on the lining of your gut.

When symptoms are under control, it is known as remission. When symptoms are more active, it’s called a flare-up.

Crohn's disease is a lifelong illness. It currently has no known cure. However, medications, surgery, or a mix of the two can help you stay well.

Symptoms of Crohn’s disease can include:

  • Feeling tired. 
  • Diarrhoea.  
  • Blood in your poo.  
  • Constipation.  
  • Bloating and wind. 
  • Tummy pain.  
  • Joint problems and/or weaker bones.  

What is EEN?

It is a liquid only diet. The aim is to put your Crohn’s into remission or to reduce your symptoms. The diet is followed for a short time of 6-8 weeks.

It replaces all food and most drinks with prescribed drinks. These drinks will provide all you need to stay healthy. These drinks come in a range of flavours. Your dietitian will tell you how many drinks you need.

We don’t fully know how it works. One idea is that it helps the gut ‘rest’. Some studies have shown it works for 45-75% of patients.

Sometimes you will need to follow it if you have a narrowing in your gut called a stricture. Your doctor will tell you if you have this.

How long will I need to follow EEN?

  • It should usually be followed strictly for 6-8 weeks. This depends on your response. 
  • Once you start to eat food again, you may need to continue some of the drinks. Your dietitian will advise on this.  

My target for EEN

Name of Nutrition drink(s)Number of drinks per day
E.g. Fortisip6
  
  
  
  • Extra fluid you need: 
  • Provides:
    • kcal:
    • g of protein:
    • ml fluid:

Following this diet can be hard! Here are some tips to make it easier:

  • Freeze your drinks into ice lollies.
  • Try lots of flavours. Your dietitian can discuss this with you.
  • Spread your drinks throughout the day.
  • Sip on the drinks slowly to make them last longer.

Contact your dietitian if you can’t finish all your drinks.

How do I know if EEN is working?

The treatment goal includes:

  • Remission.
  • Normal bloods.
  • Healing of your gut.
  • Better quality of life.

We can use The Harvey-Bradshaw Index to see if the diet is working. 

This table is at the back of the sheet for you to fill out. Please fill it out before, during, and after your diet. 

If you have an appointment with a dietitian, please take this completed with you.  

What happens after your EEN diet?

After following EEN for a minimum of 6 weeks, you can slowly reintroduce food over 5 days. This is an example based on a total based on total 2400kcal.

  • Day 1 - breakfast, 7 nutritional drinks.
  • Day 2 - breakfast, lunch, 5 nutritional drinks.
  • Day 3 - breakfast, lunch, dinner, 3 nutritional drinks.
  • Day 4 - breakfast, mid-morning snack, lunch, afternoon snack, dinner, 1 nutritional drink.
  • Day 5 after EEN - follow your normal diet. You may need to continue the nutritional drinks for weight gain or support. You can discuss this with your dietitian.

Going forward

There is no specific diet you need to follow when your Crohn’s is in remission. No diet has been proven to help keep you in remission. Also, no foods can cause flare-ups. Some foods may trigger symptoms, but they can’t cause a flare-up. If that happens, use the food and symptom diary at the back of this booklet. It may help you spot trigger foods when you are in remission.

Key points for diet in remission

  • Aim for a healthy, balanced diet that gives you all the nutrients you need to stay healthy.
  • Avoid cutting out foods or food groups, as you would miss out on important nutrients.
  • Try to eat a variety of fruits, vegetables, nuts, seeds, proteins, and whole grains.
  • Limit high-fat, high-sugar, and high-salt foods, especially animal fats and processed meats.
  • You don't need to cut back on fibre unless you have a narrowing in your gut (called a stricture).

Always talk to your GP, IBD team, or dietitian before making major changes to your diet.

Harvey-Bradshaw Index for Crohn’s

Please fill out this form on day 1 of starting the EEN diet. It is useful to bring this completed if you are due to see a Dietitian. If you are unsure what each section means, please speak to your clinician. 

Week12345678
Your general wellbeing (for previous day)
0 = very well
1 = slightly below par
2 = poor
3 = very poor
4 = terrible
        
Abdominal pain (for previous day)
0 = none
1 = mild
2 = moderate
3 = severe
        
Number of liquid stools per day (for previous day)
Score 1 per movement
        
Abdominal mass
0 = none
1 = dubious
2 = definite
3 = definite and tender
        

Complications (score 1 per item)

  • Joint pain.
  • Inflammation of the middle layer of the eye (uveitis).
  • Red nodules on shins.
  • Mouth ulcers.
  • Necrotic tissue.
  • Tear in the the anus (anal fissure)
  • A new fistula.
  • Abscess.
        
Total:
Remission: less than 5
Mild disease: 5-7
Moderate disease: 8-16
Severe disease: more than 16
        

Food and symptom diary

Use this template for any day of the week. 

Day:FoodSymptomsTime of day and how long symptoms lasted
Breakfast   
Mid-morning snack   
Lunch   
Mid-afternoon snack   
Dinner   
Notes   

© North Bristol NHS Trust. This edition published February 2026. Review due February 2029. NBT003821

Privately funded devices

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AAC WEST process for working with people who have a privately funded AAC device 

If an individual has an AAC device funded through private, medicolegal, or charity routes, they may still be referred to AAC WEST by a health, education or social care SLT if they meet NHS specialist services criteria. (See How AAC WEST work with independent professionals, suppliers and charities)

Please note the following important points: 

  • AAC WEST will carry out an impartial assessment of the individual’s AAC needs before making decisions about next steps.  As part of this assessment we will review all privately purchased elements and make a decision about whether this best meets the person’s needs. This would include reviewing the device, software, access method, accessories, and mounting solutions.  
  • Decisions are made at the conclusion of the assessment process. This may be a single assessment appointment, but will usually (though not always) include a trial/review period. 
  • AAC WEST’s assessment may include consideration of other assistive technology needs, but the primary focus will be on the individual’s communication needs. 
  • Our recommendations may differ from previous advice. 
  • We do not reimburse any costs associated with purchasing or hiring devices privately. 

Potential outcomes following AAC WEST assessment 

Where the AAC user/family accept the above points, we would proceed with an AAC WEST assessment. The following outlines the typical potential outcomes of an AAC WEST assessment for people who have a privately funded AAC device. 

A. Current AAC setup is appropriate and NHS criteria is met. 

If the AAC WEST assessment indicates that the current AAC setup (device, access method, vocabulary, mounting) is appropriate and NHS Specialised Services criteria has been met, AAC WEST will: 

  • Offer to take on responsibility for the device. 
    See section below: What does it mean for AAC WEST to take on responsibility for a device?
  • Recommend and provide mounting solutions. 
  • See section below: What if the AAC user/family does not wish for AAC WEST to take on responsibility? 

B. Current AAC device is appropriate, but setup needs adjusting.

If the AAC WEST assessment indicates the device is suitable, but changes are needed to optimise the set up, AAC WEST may recommend a trial period to explore some of the following: different access method, vocabulary package, or software settings.

If the trial is successful and NHS criteria is met: 

  • AAC WEST will offer to take on responsibility for the device. 
  • Provide mounting solutions. 
  • See section below: What if the AAC user/family does not wish for AAC WEST to take on responsibility? 

C. A different AAC solution is recommended and NHS criteria is met.

If the AAC WEST assessment indicates a different AAC solution is needed, AAC WEST may recommend a trial of an alternative AAC solution. This trial will follow our standard pathway.

See section below: What if the AAC user/family does not wish to follow AAC WEST's recommendation.  

D. NHS criteria is not met 

AAC WEST assessment indicates the individual does not meet NHS Specialised Services criteria, and therefore their AAC needs should be met locally. 

  • AAC WEST will provide recommendations in a written report.
  • Responsibility for the AAC device and support remains with the family and/or local team. 
  • Mounting solutions will not be provided. 

Important notes 

  • AAC WEST will only be responsible for one AAC device per person. If a device has previously been provided by AAC WEST, it must be returned before we take on a new privately funded device. 

What does it mean for AAC WEST to take on responsibility for a device?

If AAC WEST agrees to take on responsibility for a privately funded device, this includes: 

  • Maintenance, repairs, and replacement when required. 
  • Labelling the device and charger with a inventory code (STC number) for linking to our patient records. 
  • Annual safety checks of the device and charger.  

Benefits include: 

  • Coverage of repair costs. 
  • Device replacement where appropriate. 
  • Regular assurance that the device is safe and fit for purpose. 
  • The device being accepted in all settings. Some local authorities have policies to not permit privately funded devices in their settings.  

These benefits will continue as long as the patient remains on the NHS pathway. 

 

What if the AAC user/family does not wish for AAC WEST to take on responsibility of the device?

If AAC WEST does not take on responsibility: 

  • Recommendations will be provided in a written report. 
  • Responsibility for the device remains with the family and/or local team.

What if the AAC user/family does not wish to follow AAC WEST’s recommendations?

If AAC WEST’s recommendations are not accepted: 

  • Recommendations will be provided in a written report. 
  • Responsibility for the device and support remains with the local or independent SLT. 
  • Mounting solutions will not be provided. 
  • If circumstances change and the AAC user/family wish to take on AAC WEST’s recommendations in the future, they can be referred for another assessment.  Please include information about the current situation and an update about what has changed. 

How AAC WEST work with independent professionals, suppliers and charities

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Independent Professionals  

Definitions: 

  • A statutory professional is employed or commissioned by health, education or social care.  
  • An independent professional (also referred to as ‘private’) is not directly employed or commissioned by these services. They may be funded by individuals, families, charities or by medicolegal settlement.  We will use ‘independent professional’ to include Speech Therapists, Occupational Therapists, Physiotherapists, AAC Consultants, AAC Teachers, and home school tutors. 

At AAC WEST, we value collaborative working to achieve the best possible outcomes for our AAC users.  We encourage input from independent professionals, however only statutory Speech Therapists can refer to AAC WEST due to the way that NHS AAC Specialised Services are funded.  

Working with independent professionals can work well when: 

  • The statutory SLT and the independent professionals work together. They can both contribute to the AAC assessment and the AAC WEST referral form. 
  • Everyone knows their role from the start and respects each other’s work. You can use tools such as ‘Choosing Roles in AAC Decision Making’ to help (can be found on the I-ASC Resources website). 
  • The team shares the same goals, with the AAC user at the centre. 
  • There is clear and open communication. Everyone is kept up to date. 
  • Everyone supporting the AAC user follows the plan made by AAC WEST. 
  • The AAC user, family, and professionals understand: 
    • The AAC WEST assessment process 
    • The criteria for NHS AAC specialised services 
    • How funding works 
    • That AAC WEST will: 
      • Carry out impartial assessments. 
      • Aim to find the best AAC option for the user, whether it’s low tech (paper based) or high tech (powered). 
      • Make recommendations that may differ from previous advice, even if devices were already tried or bought. (See also Privately funded devices).

If the AAC user or team want to try something different to AAC WEST’s recommendations, they can choose a private AAC pathway instead of the NHS one. 

AAC Suppliers and Assistive Technology Charities  

(visits, trials, loans for people not seen by AAC WEST)  

Some families or clinicians arrange visits from AAC suppliers. This can help the team to explore potential AAC options, but it may also make things more confusing, as the AAC user and their family will receive advice from multiple people. 

We recommend: 

  • The clinician (statutory and/or independent) maintains responsibility on these visits, and makes the clinical decisions. 
  • Everyone knows their role: 
    • AAC suppliers bring technical knowledge of their company’s devices. 
    • Clinicians bring knowledge about the AAC user.  
  • The clinician considers arranging visits from multiple suppliers to explore different options. 

If the AAC user is referred to AAC WEST, we will: 

  • Carry out an impartial assessment 
  • Aim to find the best AAC option for the user, whether it’s low-tech (paper-based) or high-tech (powered). 
  • Make recommendations that may differ from previous advice, even if devices were already tried or bought. We do not refund money spent on privately bought or hired devices. (See also Privately funded devices).

Information about your referral, assessment, and what we offer

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This page has information for people who have been referred by your GP or specialist to the Bristol M.E. Service for an assessment.

What happens now?

Your first appointment normally takes about an hour. We can offer face to face, video, and telephone assessments. We hope to offer a time that works for you. If you need to take a break part way through your assessment, please let us know.

The assessment appointment will give us more information about your health problem and the effect this has on your everyday life. It does not involve any kind of physical tests.

We will also send you a link to some questionnaires which include the questions we ask in the assessment so you have time to think about your answers. This is so that we can build up a clearer picture of your difficulties, and answer any questions you may have. We can then work out with you the best way to take things forward.

We offer a variety of approaches depending on your needs. Our main focus is to help you develop a range of coping strategies to improve your quality of life. You may be offered one or more of the following:

  • Individual contact based on your needs. 
  • Group self-management programme using video conferencing/calls. 
  • Us giving advice to existing services or organisations involved in your care. Face to face, video, or telephone appointments.
  • Face to face, video, or telephone appointments.

Who is involved in running the service?

This service includes:

  • Occupational therapists
  • Physiotherapists
  • Psychologists
  • Specialist dietitians

All these professionals are specialists in helping people to manage ME/CFS and post viral fatigue syndromes such as long COVID. We are all committed to understanding your individual difficulties. Fatigue and other symptoms can affect your life in many ways and this varies between people. Because of this we tailor our approach to meet your needs.

Where can you find out more about ME/CFS, post viral fatigue syndrome and long COVID?

You might find these web pages from our website to be helpful:

Please note that not everyone that we assess will have (or be given) a diagnosis of ME/CFS, post viral fatigue syndrome, or long COVID. So, please be aware that this information might not be appropriate to everyone referred to the Service.

© North Bristol NHS Trust. This edition published February 2026. Review due February 2029. NBT003856

Editing vocabulary - dos and don'ts

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Don’t

Screenshot o editing page on AAC device

Do not move around existing vocabulary cells – there is a lot of research behind where cells are placed. Moving cells also impacts on the motor patterns the AAC user has learnt.

Do not give out the guided access code (if the device has one) to a young AAC user or others who may not understand these guidelines around editing.

Do not delete words or phrases – your AAC user or someone who models on the device may still need access to these.

Do not duplicate words or phrases to another part of the vocabulary without a good reason – check this with your local SLT.

Do not have lots of different people editing the device – this can quickly make the vocabulary disorganised and confusing.

Do

AAC icon of open book with AAC icon examples

Get your AAC user involved in suggestions of what words and phrases they would like on their device.

Ask for vocabulary suggestions from other places your AAC user spends time – family members, friends, day centres, clubs etc.

Have a system in place for reviewing your AAC user’s vocabulary and do this regularly – at least every term.

Ask for support from AAC WEST (if the AAC user is still being seen by them) or your local SLT.

Agree on a main device editor – others can still be involved in contributing, via email, a shared notebook, whatever works for you.

Understand the colour coding system for different word types on your vocabulary. Ask AAC WEST or your local SLT for more information. It’s important to stick with this system for new words you are adding to help your AAC user learn them.

Attend AAC WEST Software Training to help you learn/refresh your editing skills.

Attend AAC WEST Keeping Vocabulary Updated training for further resources and information about how to ensure your AAC user has access to words they need.

Hypersensitivity pneumonitis

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What is hypersensitivity pneumonitis? 

Hypersensitivity pneumonitis is a condition in which your lungs develop an immune response (hypersensitivity) to something you breathe in and results in inflammation of the lung tissue (pneumonitis).

What are the causes of hypersensitivity pneumonitis?

One example is farmer’s lung. This is caused by breathing in mould that grows on hay, straw and grain. Another is bird fancier’s lung, caused by breathing in particles from feathers or bird droppings. The disease can also develop from inhaling fungus in humidifiers, heating systems, and air-conditioners found in homes and offices, especially if they are not well maintained. 

Sometimes patients develop hypersensitivity pneumonitis and no obvious cause can be found.

What are the symptoms of hypersensitivity pneumonitis?

Symptoms of cough, shortness of breath and sometimes fever or flu-like symptoms can occur suddenly after you’ve been exposed. This is the acute form of the condition and can go away without causing permanent damage to the lungs, if the substance that caused the attack can be permanently avoided. 

In other cases, symptoms of cough and breathlessness can come on more gradually, perhaps over months or years; following repeated exposure to a particular substance, and can result in permanent scarring or fibrosis of the lungs. This is called fibrotic hypersensitivity pneumonitis and often a specific cause cannot be found.

What tests will I have?

Your specialists will take a detailed medical history and perform a thorough physical examination. You may be asked to have the following investigations:

  • Lung function tests – breathing tests which see how well your lungs are working. These can be used to monitor your lung disease and also to see whether it is responding to treatment. You may be asked to have a walk test to measure how far you can walk and to make sure you are getting enough oxygen into your blood when you are walking. As part of this test you will be asked to rate how breathless you are on a scale. 
  • A CT scan of your chest which shows a detailed picture of your lungs. There are characteristic patterns on these pictures that can help your specialist to identify either scarring or inflammation of lung tissue.
  • Blood tests are performed to detect the presence of antibodies against the specific agents (allergens), for example bird proteins in bird fancier’s lung or moulds in farmer’s lung. Antibodies are developed by your immune system to try to protect you when an unknown or unwanted substance enters your body. It is possible to have antibodies and not become ill. 
  • Some people may also have a bronchoscopy, where a small flexible tube is passed down into your lungs, allowing collection of cells which may help with diagnosis. 
  • Finally, if the diagnosis remains unclear, the specialist might wish to remove a small piece of lung through a surgical procedure (surgical lung biopsy) to confirm the diagnosis.

What happens to patients with hypersensitivity pneumonitis?

If the cause can be identified and removed, individuals with early hypersensitivity pneumonitis should make a full recovery. However, they will remain sensitised and should they be exposed to the allergen in the future, their symptoms will often return.

For individuals with more chronic (long-term) disease, removal of the allergen hopefully stops the disease getting worse, although unfortunately this is not always the case. Your specialist may advise some treatments to try to slow or stop the disease getting worse (see below).

How is hypersensitivity pneumonitis treated?

If we can identify a specific cause, the most important aspect of treatment is to try to avoid it. This may require rehoming household pets, a change in employment or the use of a specialist mask when exposed to the allergen. Not being able to stop exposure increases the chance that hypersensitivity pneumonitis will progress to irreversible lung damage. 

Your specialist may advise a trial of specific medications as detailed below.

Medications 

Steroids are produced naturally in the body by the adrenal gland. Additional steroid in the form of prednisolone can be given to attempt to reduce inflammation in some patients. They are usually given in tablet form but may be given by injection into a vein. If you are prescribed steroid tablets on a long-term basis, you should not stop them abruptly. You will be given a ‘steroid emergency card’ which you should always carry with you. The specialist may also assess the need for bone protection medication and anti-reflux treatment to protect against some side effects whilst on steroids.

Immunosuppressive medication is commonly used to dampen down the hypersensitive immune response in the lungs. Some examples of these medications are cyclophosphamide, mycophenolate mofetil and azathioprine. One of these medications will usually be prescribed alongside a steroid such as prednisolone. It can allow the dose of the steroid to be reduced and in some cases, may allow the steroids to be stopped altogether. As a result, they are sometimes also called ‘steroid sparing agents’. Whilst you are taking immunosuppressant medication you will require regular blood tests to monitor your response to treatment.

If your condition worsens despite taking a steroid and/or immunosuppressive medication, your specialist may suggest an antifibrotic medication that aims to slow further progression. Other medications and therapies are used to relieve symptoms, such as cough and breathlessness. Your specialist will discuss options with you on an individual basis.

Other treatments

Pulmonary rehabilitation is an exercise and education programme that can help you to learn to manage your breathlessness and remain active. The programmes are multidisciplinary, meaning that the team includes respiratory physiotherapists, nurses, dieticians, doctors and others, and can help improve energy, strength, and your quality of life.

Supplemental oxygen: As lung scarring can reduce the amount of oxygen getting from your lungs into the bloodstream, some individuals may require oxygen therapy. Where the levels of oxygen are low, oxygen therapy may help with breathlessness and enable individuals to be more active. Correct levels of oxygen in the blood are necessary for normal body functions and reducing additional health problems.

Clinical trials: You should also discuss with your team if there are any clinical trials in which you can participate. Clinical trials are voluntary research studies, which are designed to answer specific questions about your care or the safety and/or effectiveness of medications.

Lung transplantation: A small minority of patients may require assessment for and be suitable for lung transplantation.

How can I help myself?

Have your annual respiratory vaccinations (COVID-19 and Flu) and the pneumonia vaccination (you only have this once).

You may be eligible for a variety of benefits such as Attendance Allowance or Personal Independence Payment if you need help with personal care or getting about.

Our specialist nurses run a regular Pulmonary Fibrosis Support Group which is a space for discussion with other patients with similar lung problems. Here we also aim to provide several presentations from a variety of guest speakers and charities. 

Keep active and do what you enjoy!

© North Bristol NHS Trust. This edition published June 2023. Review due June 2026. NBT002702