Health
Better pregnancy or baby loss bereavement care for people in Wales
SANDS the UK’s leading pregnancy and baby loss charity, is supporting the National Strategic Clinical Network for Maternity and Neonatal Services to create tailored bereavement care pathways for those who have experienced pregnancy or baby loss in Wales.
The pathways aim to reduce inequalities and improve the quality of bereavement care provided to parents and families, and has been made possible by funding from the Welsh Government. The pathway materials will include guidance for healthcare professionals based on evidenced best-practice, and a set of standards relating to important aspects of bereavement care.
Good quality bereavement care is vital for parents who have experienced the loss of a pregnancy, or whose baby has died. It includes sensitive communication with parents, providing a bereavement room away from maternity or labour wards, and parents being given informed choices about decisions relating to their care and the care of their babies.
Clea Harmer, Sands’ Chief Executive, said: “Everyone affected by pregnancy loss or the death of a baby deserves high quality bereavement care and support.
“We know that no level of care can remove the grief that many parents will feel after pregnancy loss or the death of a baby, but good care can make this devastating experience feel more manageable. We also know that poor quality or insensitively delivered care can compound and exacerbate pain.
“This launch follows a huge amount of hard work and determination from our partner organisations, the generous support of many bereaved parents and families, and medical professionals who have shared their experiences.
“We hope that through supporting the National Strategic Clinical Network for Maternity and Neonatal Services, we can work together to make sure everyone affected by pregnancy or baby loss gets the care that they need.”
In developing the pathways for Wales, Sands carried out a series of listening events for parents and health professionals during 2024, to understand how bereavement care in Wales can be improved.
These insights will be incorporated into work with the National Strategic Clinical Network for Maternity and Neonatal Services to introduce pathways to address specific needs after miscarriage, Termination of Pregnancy for Foetal Anomaly (TOPFA), stillbirth, neonatal death or Sudden Unexpected Death in Infancy (SUDI).
Chief Midwifery Officer for Wales, Karen Jewell said: “We are delighted that we have been able to support this important initiative to develop and implement a National Bereavement Care Pathway for Pregnancy and Baby Loss.
“Pregnancy loss or the death of a baby is devastating, and this initiative will help to ensure that every family who suffer from this are appropriately and compassionately supported.
“Our significant investment into bereavement services will improve care and ensure consistency across Wales, the Bereavement Support Grant will continue to support organisations like Sands to extend and deepen bereavement support and fill the gaps that currently exist.”
Healthcare professionals are an important part of the Sands community, and the charity wants to support them to deliver good bereavement care. The pathways will introduce dedicated support for medical staff who care for bereaved families in Wales.
Cara Moore, Lead Midwife from the National Strategic Clinical Network for Maternity and Neonatal Services said: “We are thrilled to be leading the development and implementation of the development and implementation of bereavement care pathways in Wales in collaboration with Sands. The development of pathways will ensure consistent high quality and sensitive bereavement care is offered to all bereaved parents in Wales. This will be supported through training, interdisciplinary collaboration and continuous monitoring and promises a sustained improvement in the experiences of bereaved parents.
“We are also pleased that the implementation of the pathways align with and supports long term plans for the delivery of high quality maternity and neonatal care in Wales.”
Marc Harder, Head of Bereavement Care & Hospital Liaison at Sands, said: “Earlier this year, bereaved parents and families in Wales generously shared their stories of pregnancy and baby loss with us during a series of listening events. Key themes that arose included gaps in compassionate care, inappropriate and insensitive medical terminology, care outside of the hospital and inconsistency in bereavement care provision.
“We are delighted to be working in partnership with the National Strategic Clinical Network for Maternity and Neonatal Services to develop bereavement care pathways that will begin to address these concerns and lead to higher quality care at such a difficult time for parents and families. We will continue to work with parents, professionals and other stakeholders to ensure an evidence-based and community-led approach to the development of Wales-specific pathways.”

More information about the bereavement care pathways in Wales
The project in Wales is led by Sands in collaboration with a number of other charities and professional organisations, and funded by the Welsh Government. The project provides dedicated, evidence-based care pathways designed for all healthcare professionals and staff involved in the care of women, birthing people, partners and families at all stages of pregnancy and baby loss.
Five experiences of pregnancy or baby loss are included in the pathway project including miscarriage, TOPFA, stillbirth, neonatal death and SUDI.
Sands is here to support all bereaved families in Wales and across the UK. The charity provides support through its Freephone helpline, online community and resources, and through a network of regional support groups run by trained befrienders, all offering in-person peer support.
Find out more about all the ways the charity offers bereavement support.
Health
Patients in Wales waiting years for autoimmune diagnosis
Study led by Swansea University says long delays, limited specialist access and referral barriers are leaving some patients worse off than those elsewhere in the UK
PEOPLE in Wales with autoimmune and rheumatological conditions are facing long waits for diagnosis, poor access to specialist care and repeated obstacles when trying to secure treatment outside their local area, according to new research.
The study, led by Swansea University, examined the experiences of patients with illnesses including lupus and other autoimmune disorders. It drew on interviews, survey findings and Freedom of Information responses from health boards across Wales.
Researchers found that specialist provision remains limited in some parts of the country. Some patients reported having no access to a lupus specialist in their area, while FOI responses indicated there is only one NHS neuro-ophthalmologist in Wales for patients with neurological or visual problems linked to autoimmune disease.
The report also highlighted a lack of diagnostic services. None of the Welsh health boards that responded said they currently provide nailfold capillaroscopy, a test used to help identify conditions such as scleroderma.
Diagnosis in rheumatology can also be difficult because many of the conditions involved are complex and may develop gradually over time. Illnesses such as ankylosing spondylitis can be mistaken in the early stages for more common causes of pain, while autoimmune disorders often present with symptoms that overlap with other conditions.
Patients may require a combination of investigations before a diagnosis can be confirmed, including HLA-B27 testing, routine blood work, MRI scans, X-rays and detailed clinical assessment. Doctors also rely heavily on patient interviews to build up a picture of pain, stiffness, mobility and the wider pattern of symptoms.
There have also been local pressures on services in west Wales. At Withybush Hospital, delays were caused after the departure of a specialist consultant, and it took some time for that post to be filled. That consultant has now been replaced. However, it is understood the workload remained heavy, with the specialist working through a backlog of cases.
In some cases, patients may also feel rheumatology is treated as a lower-profile service. At Withybush Hospital, for example, the department has been based in a portacabin in the hospital car park, which it shares with the lymphoedema service — a setting that can give the impression that two important but often overlooked specialties are being accommodated on the margins of the wider hospital system.
Rheumatology also places a significant burden on the NHS because of the cost of long-term treatment and follow-up care, although that is not the main focus of the study. Biological drugs used to treat conditions such as rheumatoid arthritis and ankylosing spondylitis can cost around £500 for a pack of four injections, according to local hospital sources. Patients on those medications often also require regular blood monitoring, consultant reviews, specialist nurse support and physiotherapy. The Herald understands that more than 1,000 patients in Pembrokeshire are currently being managed through this treatment pathway.
Researchers said patients were also being held back by the referral system. Under current NHS Wales rules, doctors must apply to their local health board for permission to send patients for treatment outside the area or across the border into England. The study said decision-making around those requests was often inconsistent and unfair.
One patient with systemic lupus erythematosus told researchers he waited two years for approval to be referred to England, despite believing the process should only have taken weeks.
The study found that patients in Wales often face longer journeys to diagnosis than elsewhere in the UK. In the sample reviewed by researchers, the average time from first symptoms to diagnosis was around 11 years, compared with around seven years across the UK.
Patients described the effect those delays had on their health. One woman in her 30s said requests to see a specialist in a neighbouring health board had been turned down, and that her lupus had worsened as a result. Another patient said access to care became more difficult after moving from England to Wales.
The research was led by Rupert Harwood of Swansea University Medical School, who himself lives with several autoimmune conditions.
His own experience reflects the wider concerns raised in the report. After developing visual symptoms in 2016, he was advised to see a neuro-ophthalmologist, but no such service was then available in Wales. A referral to England was not successfully made until 2025, and he is still waiting for an appointment.
Mr Harwood said the present system can leave patients at a disadvantage if they cannot afford to seek private treatment outside Wales.
The study concludes that while NHS Wales rheumatology teams provide high-quality care, patients in Wales face additional barriers compared with those in England.
Researchers are calling for a review of the out-of-area referral system, better access to specialist services and greater investment in diagnostic testing to reduce delays and improve outcomes.
Health
Lib Dems vow to keep Palantir out of Welsh public services
Party says it would use its influence in the next Senedd to block any move to bring the firm into the NHS or government systems in Wales
THE Welsh Liberal Democrats have pledged to use their influence in the next Senedd to keep controversial technology firm Palantir out of Wales’ NHS and wider public services.
The party said it would oppose any attempt to introduce the company into Welsh Government systems, citing concerns over data security, transparency and Palantir’s wider links to military and intelligence work.
The move comes amid increasing scrutiny of Palantir’s £300m contract with NHS England and reports that UK ministers are considering whether to activate a break clause.
The Welsh Liberal Democrats said Wales must not follow what they described as a risky approach to the handling of sensitive public data.
A debate on the issue is due to be led in Westminster today by Liberal Democrat MP Martin Wrigley.
The party said it supported better data integration to improve patient care and help reduce waiting times, but argued that this should not come at the expense of public trust or national security.
Instead, the Lib Dems are calling for investment in what they describe as trusted and transparent alternatives, including British-based providers, to modernise digital infrastructure without raising concerns over foreign influence or the handling of personal data.
The party also said that, in a finely balanced Senedd, it would use its votes to block any effort to bring Palantir into Welsh public services.
It warned that once contracts involving critical digital systems are signed, they can be difficult to reverse, and said ministers in Wales should take a precautionary approach now rather than try to solve problems later.

Commenting, Welsh Liberal Democrat Westminster spokesperson David Chadwick MP said: “People across Wales will rightly be asking why a controversial foreign tech company with links to military and intelligence operations is being trusted with something as sensitive as our health data.
“The Welsh Liberal Democrats are clear: Palantir should be nowhere near our NHS or our public services. Trust in how data is handled is absolutely fundamental, and once that trust is lost, it is incredibly difficult to rebuild.
“In the next Senedd, we will use our votes to make sure this company is kept out of Wales. There can be no compromise when it comes to protecting people’s personal information and safeguarding our national security.
“We all want to see better joined-up care, shorter waiting lists and a modern NHS fit for the future. But that must be delivered in a way that puts patients first, not by handing over the keys to organisations that many people simply do not trust.
“Wales should be leading the way in building secure, transparent digital systems that the public can have confidence in, not going down a path that risks undermining that trust.”
Health
Tracy’s firewalk raises £528 for Withybush rheumatology unit
Long-serving staff member and patient took on 800°C embers to give back to service that has supported her family for years
A MEMBER of staff at Withybush Hospital has raised £528 for Rheumatology Services after taking part in Hywel Dda Health Charities’ firewalk challenge.
Tracy Beynon, who has worked at Withybush for 23 years and has also been a rheumatology patient for 20 years, took part in the barefoot walk across 800°C embers in October to support the department.
She said she had always wanted to try a firewalk and jumped at the chance to do one for her local health board.
Tracy said: “Over the years, I have done some wild things to raise money for various charities, including shaving my head after a Six Nations rugby match 11 years ago.
“Rheumatology have looked after many generations of my family throughout the years, and I wanted to try and give something back to help the team and the patients they serve.
“I was stunned by how much money I raised. After I put a video on TikTok, I had a number of donations from people I have never even met. I will forever be thankful to my friends and family for supporting all of my mad fundraising ideas.”
Katie Hancock, Fundraising Officer for Hywel Dda Health Charities, said: “A huge thank you to Tracy for showing her support to the service that has taken such good care of her for so long.
“The generous charitable donations we receive do not replace NHS funding. Instead, they support additional items and activities outside core NHS expenditure. These small extras make a big difference, and we are so grateful for every donation we receive.”
Hywel Dda Health Charities said donations help provide added items and activities for local NHS patients and staff beyond core NHS spending.
For more information about the charity and how to support local NHS services, visit the Hywel Dda Health Charities website.
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