logo
Hundreds attend Turner Syndrome Football Festival in Glasgow

Hundreds attend Turner Syndrome Football Festival in Glasgow

Glasgow Times6 days ago
More than 200 girls from across the West of Scotland arrived at Petershill Park in Springburn on Sunday, July 27, for the annual Turner Syndrome Awareness Football Festival.
For the first time, teams had the chance to play across the entire complex in North Glasgow, which allowed even more girls to take part.
(Image: TSSS)
The event was organised by the Turner Syndrome Support Society (TSSS) in an effort to raise awareness of the rare genetic condition, which is said to affect one in every 2000 girls.
Arlene Smyth, executive officer of the TSSS, highlighted the importance of early diagnosis.
She said: "Events like these are absolutely essential in raising awareness of Turner Syndrome.
"If a girl is not achieving expected growth or development, it's important not to ignore the signs -early diagnosis makes a real difference.
'We're grateful to everyone who helped make today possible."
(Image: TSSS)
READ NEXT: Glasgow youth project in desperate bid for new building
According to NHS Scotland, Turner Syndrome (TS) is a rare genetic condition that only affects females and is usually diagnosed at birth.
There is currently no cure, but treatment and support are available to help manage symptoms.
It is understood that everyone with the condition is affected differently; however, it can impact growth, height, and general development.
This year's football festival saw an increase of more than 50 per cent in attendance and was described as both a 'significant milestone' for girls' football and raising awareness of TS.
Teams from Phoenix Girls travelled from Hamilton, Renfrew, West Park United, Kilmarnock and Glasgow City to take part.
Gus MacLean, chair of Phoenix Girls FC, said: "This event wouldn't have been possible without the commitment of our partners, the Partick Thistle Charitable Trust, and the tireless work of coaches, parents, and volunteers.
'Together, we're making a real difference."
Iain Stuart, Scottish Women's Premier League competitions officer, presented the medals on the day.
(Image: TSSS)
He praised the event as a 'testament' to the power of partnership and community.
READ NEXT: Man hits out at 'unbelievable' state of Glasgow cemetery
Speaking at the festival, Mr Stuart commented: "Festivals like this simply didn't exist a decade ago.
"It's fantastic to see hundreds of girls out playing football together, raising awareness, and showing just how far the women's game has come.
'Today is a testament to the power of partnership and community."
The event was delivered through a partnership between the TSSS, a Clydebank-based charity, and Phoenix Girls FC, who built on the previous year's success with the support of the [[Partick Thistle]] Charitable Trust.
(Image: TSSS) (Image: TSSS)
It was dedicated to the memory of Emma Woods, who lived with TS and sadly died aged 20.
The Emma Woods Memorial Fund, created by her friends and family, continues to raise vital funds to support awareness campaigns and initiatives such as the festival.
Fraser Cromar, CEO of the Partick Thistle Charitable Trust, said: "Petershill Park is synonymous with women's football in Scotland, being home to both Glasgow City and Partick Thistle Women.
'When we heard about the vision behind the Turner Syndrome Awareness Football Festival, we were fully committed to supporting it.
'Bringing communities together through football to raise awareness for such an important cause is exactly the kind of initiative we want to champion."
For further information on TS visit the TSSS's website HERE.
Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

I had multiple cancer symptoms - doctors thought it was probably anxiety
I had multiple cancer symptoms - doctors thought it was probably anxiety

Daily Mirror

time3 hours ago

  • Daily Mirror

I had multiple cancer symptoms - doctors thought it was probably anxiety

Gail Whiteford was experiencing various cancer symptoms, but was prescribed antidepressants A woman has spoken out about her ordeal, claiming she felt as though she was "going insane" after doctors misdiagnosed her cancer symptoms as anxiety and prescribed her antidepressants. Gail Whiteford, 39, battled for four years to get her GP to take her numerous health symptoms seriously. ‌ She experienced back pain, jaw pain, earaches, skin rashes, and blood in her urine, but was given antidepressants. After initially seeking help for a persistent backache via her GP's appointment app in August 2019, she was reassured there was nothing to worry about. ‌ In November, the Scottish mum reported an ear infection and jaw pain that lasted two weeks, only to be dismissed once again. In 2020, following a chest infection and a period of personal stress, Gail was prescribed antidepressants and signed off work, reports Glasgow Live. ‌ It wasn't until 2023, when she was urgently hospitalised after losing function in her kidney, that doctors diagnosed multiple myeloma, a serious form of blood cancer. "The test results in 2019 said there was nothing of concern - so I thought, okay, fine," Gail recalled. "My next contact with them was 12 November, and it was for a sore ear, aches and pains. I had a sore ear for about two weeks and the pain was getting worse and going down into my jaw. It sounds like nothing, but these are all recurring infections, which is a sign of myeloma." ‌ Gail, an insurance broker, was told that her symptoms were likely due to anxiety from her high-pressure job and the sudden loss of her father. She trusted her GP's advice and accepted a prescription for a low dose of antidepressants. However, her physical discomfort persisted, now exacerbated by the side effects of starting SSRI medications. "I remember being really busy at work, and they put all of my symptoms down to stress," Gail recalled. "My dad passed away in December 2020, and it was sudden - he was diagnosed with cancer and was gone within three weeks. I felt like they jumped on that, and it automatically became related to mental health. In all my years of being a broker, I'd never gotten to the point where I had to go off work. ‌ "I think they signed me off for two or three weeks and started me on antidepressants. You take the advice that's given, and I put my trust in these people. I was going backwards and forwards to the doctors for pains and aches, and being signed off. Nobody could give me any straight answers - sometimes I couldn't even get to see the doctor." Her condition deteriorated further that summer, as Gail began to experience severe skin itching and burning. Doctors at her local GP practice assumed her childhood eczema had returned, prescribing her creams to treat the rashes, while her aches and pains continued unabated. ‌ Gail started working from home as her skin symptoms persisted and her exhaustion grew worse. "When I was a child, I suffered badly with eczema, but this was different," she said. "This wasn't eczema. The only way I can describe it, that my skin was raw, and it was possibly an indication that my kidneys were struggling, because itchy skin is a byproduct of kidney issues. None of that was ever considered - it was just put down to potentially eczema. "I spoke to doctors in July, August, November, December - I was literally begging for them to help me. In March 2022, it was pain in my neck, shoulder, head and jaw - that was one of the first things I ever said to them back in 2019. Three years later, I was still suffering. September 2022 was when it was getting bad - probably a year before I was admitted into hospital. ‌ "I was still working, but I really struggled. I was working a lot from home because I couldn't get up in the morning." In July 2023, Gail found herself unable to keep food down whilst her heart raced uncontrollably. Alarmed, she rang her GP, who arranged blood tests - but her nurse suggested her symptoms stemmed from anxiety, and recommended she boost the dose of her antidepressant. "I contacted them and said I was continuously vomiting and my anxiety - because I'd been led to believe my heart racing was to do with anxiety - was out of control," Gail said. ‌ "I'll never forget a conversation I had with the nurse, where she took my blood and said she could see I was on 50mg of antidepressants. She said, 'do you know that's not a lot? I recommend you up it to 100mg'. At that point, I thought, maybe she's right - maybe this is all in my head. I genuinely thought I was going insane. Maybe I don't have these pains in my back and my shoulder and my ribs. It sounds ridiculous, but at the time, I was so desperate. I took her advice. "I remember coming home, and I was constantly being sick. I couldn't keep any food down, couldn't get out of bed, had no energy, and my body was screaming in pain." Eventually, after returning home from having her blood test on August 1, 2023, Gail received a call from her doctor, telling her to get to hospital immediately. She rushed to the hospital, where medics revealed her kidneys were functioning at just 12%. Days afterwards, she received her devastating diagnosis of multiple myeloma - and was informed she needed to be put on kidney dialysis and undergo six months of chemotherapy. ‌ "At 3pm that day, the doctor called and told me to get myself straight to hospital, because my kidneys weren't doing what they needed to," she said. "After I'd been in hospital for a week, I'd had a kidney biopsy and CT scans, spoken to pharmacists and senior consultants. "I'll never forget when the consultant came to me and said to prepare myself - and used the words multiple myeloma. The doctors were telling me it was treatable and they would help, but it takes time to accept it and understand it. In some weird way, I felt absolutely relieved - I was being validated. "A nurse looked at my blood and asked me when the last time I felt well? It hit me like a ton of bricks - because I couldn't answer that, I didn't know. I started getting dialysis three times a week, then going upstairs to the cancer unit and getting my chemo. The consultants and the nurses were just so compassionate, so helpful, and they got me through it." ‌ Following her initial round of chemotherapy, Gail has received stem cell treatments, and is now free from dialysis whilst preparing for a kidney transplant. "I got my stem cell treatment in March last year," Gail said. "My kidneys are just now sitting about 22% which sounds ridiculous, but for somebody who has kidney failure, it's amazing to be at the point where you don't need to be on dialysis." Throughout her treatment, Gail started attending the Ayrshire Myeloma Support Group - and discovered that her battle to be taken seriously was anything but unusual. She is now campaigning to raise awareness of myeloma symptoms and the vital importance of standing up for your own health. On Sunday, July 27, Gail and her support group organised a charity walk around Dean Park in Kilmarnock to raise funds for Myeloma UK, with the aim of funding research into a cure. "It's difficult to look back at previous online GP requests, because I can hear the way I'm begging the doctor for help," she expressed. "The saddest part of all is when I speak to so many different people, it's exactly the same thing. They're told doctors can only look at one thing or speak about one thing in the appointment. I'm angry, I'm frustrated, and I just feel there's got to be a better way." A link to the fundraiser can be found here.

'My mum went with my dad to AA and then realised she was an alcoholic'
'My mum went with my dad to AA and then realised she was an alcoholic'

The Herald Scotland

time5 hours ago

  • The Herald Scotland

'My mum went with my dad to AA and then realised she was an alcoholic'

Maree Todd was given the post by First Minister John Swinney in June, and has never spoken of her personal link to addiction. Scotland's drugs minister has told how her mother was persuaded to go to Alcoholics Anonymous (AA) with her father, before realising she too had a drinking problem. But with her father celebrating four decades of sobriety this year, the minister said she hopes his story will show people 'that change can happen'. In her childhood, Ms Todd's parents John and Christina drank heavily, but when she was 12, the pair decided to get sober. It was not until a friend from their west Highland village – who was in recovery himself – approached her father to ask him to seek help that the process truly began. READ MORE: Accepting the invitation to AA, her mother was eventually persuaded to go along, but only after being erroneously told it was normal for spouses to attend with their partners. 'They persuaded my mum by telling her, and it's a funny thing, they said it was normal for wives and spouses to go along to the meeting as well, because she was not at all convinced that this was an issue for her,' Ms Todd told the PA news agency. 'My mum went along to this meeting and literally had this road to Damascus moment as she sat there listening to the testimonies around the table and thought 'actually this is where I am'… she realised that there and then.' Ms Todd's father did not engage much with AA again, but this year he celebrated his 40th year sober. Undated handout photo of Maree Todd (right) with her mother Christina, father John, and sister Fiona. (Image: Maree Todd/PA Wire) The minister's mother died in 2022, with 38 years of sobriety behind her – excluding a 'handful' of relapses. While there was no ill will between her father and AA, Ms Todd described him as a 'typical west Highlander'. 'He's a lovely, lovely man, but talking isn't really his thing,' she said. 'He actually feels guilty about that sometimes, he says he thinks he sets a bad example to other people who are trying to stop because it's so important to access help and it's not common to be able to stop on your own.' Ms Todd – who was elected to the Scottish Parliament in 2016 after 20 years as a pharmacist – said her childhood was generally a good one other than her parents drinking, and she speaks emotionally of the impact recovery programmes like AA had on the lives of her parents and her own. 'My mum's relationship with AA continued and it was a profound part of her life, a profound part of our lives as we grew up,' she said. Fighting back tears, she added: 'When my mum died, it was a really profound experience for myself and my sister to be able to say thank-you to the fellowship for what they had done to help our parents to get sober and to recognise the impact, particularly my mum, had on so many other people's lives.' Undated handout photo of Maree Todd (left) with her mother Christina. (Image: Maree Todd/PA Wire) During the period her parents were drinking, Ms Todd said the local community where she grew up ensured her and her sister Fiona were taken care of. 'When I was minister for children and young people I used to say it takes a village to raise a child, and I came from a good village,' she said. 'So when my parents were drinking, I had adults all around me who were looking out for me and who made sure I was fed and safe. 'That is a really important thing from the community that I grew up in, people knew what was happening and they looked out for us.' Going through university to a job in the health service, then to Parliament and eventually ministerial office is not the usual path trodden by someone whose parents struggled with addiction, but Ms Todd said her family never normalised the situation. 'We knew that what was happening in our house wasn't normal, we knew that other houses weren't like that,' she said. 'That's another thing about growing up in a close-knit, small community.' That is not to say that the girls did not feel 'shame', she said, adding: 'We did, but we did not have that burden of trying to cover up what was happening at home, it wasn't possible, it was very visible and, actually, I look back and I think that's a real blessing.' Despite there being anger and shame in growing up with parents struggling with addiction, Ms Todd said she never lost the love for her family. 'I was 10, 11, 12 years old and there were moments of real shame, moments of real anger,' she said. 'Throughout this I loved my parents, they were really loving. 'I don't want anyone to get the wrong impressions. 'One of the reasons that I'm so sorted is because the only thing my parents got wrong was the drinking.' Despite being in the public eye for almost a decade, Ms Todd has not spoken about her parents' struggles. She said her father is happy with her discussing it now, because they both hope his four decades of sobriety will inspire others. 'One of the reasons I'm so keen to talk about it is because I want people who read your work or come across your work to understand that change can happen,' she said.

Sandie Peggie NHS Fife tribunal: 'Mass discrimination' legal action warning if nurse wins case over Beth Upton
Sandie Peggie NHS Fife tribunal: 'Mass discrimination' legal action warning if nurse wins case over Beth Upton

Scotsman

time9 hours ago

  • Scotsman

Sandie Peggie NHS Fife tribunal: 'Mass discrimination' legal action warning if nurse wins case over Beth Upton

Sign up to our Politics newsletter Sign up Thank you for signing up! Did you know with a Digital Subscription to The Scotsman, you can get unlimited access to the website including our premium content, as well as benefiting from fewer ads, loyalty rewards and much more. Learn More Sorry, there seem to be some issues. Please try again later. Submitting... It has been one of the most contentious and high-profile employment tribunals in modern British legal history and its outcome could wield significant influence at a time when policies and guidance around gender are in a state of flux. All eyes are on the Dundee employment tribunal that has heard every blow and counter in the case brought by Sandie Peggie against NHS Fife. In legal proceedings that have made headlines around the UK, the nurse is pursuing a claim for sexual harassment, belief discrimination and victimisation against both the health board and Dr Beth Upton, a trans woman colleague at Kirkcaldy's Victoria Hospital with whom she clashed over a women's changing room. Advertisement Hide Ad Advertisement Hide Ad With the final evidence sessions concluding last week, the legal teams of those involved have until August 25 to provide any supplementary statements effectively summarising their case. The tribunal will then briefly reconvene at the start of September for two days for oral submissions alongside any legal questions. Supporters of nurse Sandie Peggie protest outside the employment tribunal hearings in Dundee. Picture: Lisa Ferguson | Lisa Ferguson Only then will the panel, helmed by employment judge Sandy Kemp, be in a position to issue a written ruling. But while many tribunal judgements are given relatively quickly after the final submissions have been made, the intricacies of this particular case mean it could be weeks, if not months, before a legally binding decision is announced. One source indicated 'the end of 2025' as a 'likely timeframe', given the panel has to consider not just the evidence from more than 15 witnesses, but thousands of pages of documentation. When the moment eventually arrives, the implications could well be far reaching. Around the UK there are a number of ongoing employment tribunals and other legal cases which span the kind of gender-critical and trans issues that have been discussed at length throughout the Peggie tribunal. Advertisement Hide Ad Advertisement Hide Ad And according to gender-critical campaign and advocacy groups involved in various legal activities, there is likely to be similar employment tribunal cases in Scotland - and potentially, even a large, class-action style legal action. 'There are more employment tribunals' Susan Smith, co-founder of For Women Scotland, the gender critical group that successfully fought the Scottish Government all the way to the Supreme Court over sex-based protections, said there were other women planning legal action around such issues. She indicated there may also be cases similar to the judicial review brought to the Court of Session in April by parents in the Scottish Borders, which ultimately led to a judge ordering that Scottish state schools must provide single sex toilets for pupils. Ms Smith said: 'I know there are more employment tribunals. It's always hard to say how many, because people are at different stages of the process, but I understand there are a couple of court dates that have been set. Susan Smith, left, celebrated with colleagues and supporters of For Women Scotland after the Supreme Court ruling that the word 'woman' in the 2010 Equality Act refers to a biological woman. Picture: Lucy North/PA | PA 'There is also consideration underway about whether judicial reviews will be brought against anyone at any point for not adhering to the law. It can be a difficult process, but ultimately, we're not going anywhere. And if things aren't being done, we're keeping an eye on what we need to think about doing.' Advertisement Hide Ad Advertisement Hide Ad Maya Forstater, chief executive of the Sex Matters group, stressed the law on single sex spaces was 'already clear' in the wake of April's landmark Supreme Court ruling. The court decision set out the terms 'woman' and 'sex' refer only to a biological woman and biological sex in the Equality Act. But should the Dundee tribunal find in Ms Peggie's favour, Ms Forstater said it would 'help bring home to foot-dragging employers all over the country that complying is not optional'. 'Any employer that continues to flout health and safety regulations concerning toilets, changing rooms and washing facilities is putting itself at risk not only of a high-profile legal case involving a single brave claimant like Sandie, but a mass discrimination and harassment case taken jointly by large numbers of female employees,' she said. Appeal could lead to legal precedent being set As is to be expected, the extent of the repercussions of the Peggie case depends on the ruling the Dundee tribunal issues, which could be fully or partly in favour of one side or the other, and the similarity of circumstances in future cases. Advertisement Hide Ad Advertisement Hide Ad Either way, the outcome will be consequential, not least because there is little in the way of existing case law around the question of workplace changing rooms. And although judgements in Scottish tribunals are not binding in England, Wales or Northern Ireland due to the separate legal jurisdictions, they can be used as persuasive arguments by the parties involved. One legal source familiar with the Peggie case said in the event the judgement goes to appeal - a process that could end up in the Supreme Court - the outcome could set a legal precedent similar to that seen in the case of Ms Forstater's High Court appeal win against an employment tribunal in 2021, which found her gender-critical beliefs fell under the Equality Act. Above all, the source said, the Peggie case would be a 'cautionary example' to public bodies 'not to play fast and loose with the law and its interpretations'. Nurse Sandie Peggie, centre, alongside Maya Forstater, left, and employment lawyer, Margaret Gribbon, outside the Scottish Parliament after a meeting with MSPs in June. Picture: PA | PA Such developments could prove important in a case such as that brought to a Newcastle tribunal by a group of nurses, who are challenging the decision by the NHS foundation trust in County Durham and Darlington to allow one of their trans colleagues to use female changing rooms. The group has filed claims at an employment tribunal on the grounds of sexual harassment, discrimination, victimisation and breaches of the right to a private life, under article eight of the European Convention on Human Rights. The case is not scheduled to be heard until October. But it has been reported the Royal College of Nursing has urged the trust to comply with statutory provisions laid down in the Workplace (Health, Safety and Welfare) Regulations 1992, which require all changing rooms to be male or female-only except when they are 'single lockable rooms'. Advertisement Hide Ad Advertisement Hide Ad Ms Smith said if Ms Peggie wins her case, it will become all the more important for health boards, and Scottish ministers, to ensure they are complying with existing legislation. 'The immediate implications for the NHS in Scotland will be to ensure that they have lawful policies,' she said. 'It might focus minds at health boards that they are going to have to take some responsibility for sorting things out. They can't leave these kinds of policies to graduates with no background in law or human resources, and they're going to have to review all their policies for staff and patients. 'They are responsible whether they like it or not' 'Ever since the Supreme Court ruling, we have been pushing the government on policies which we don't regard as lawful, especially around schools and prisons. Their argument a lot of the time is that these organisations, like the NHS, are arms-length and that it's not up to the government to provide guidance, even though they've done just that in the past. They are responsible whether they like it or not.' Ms Smith added: 'A lot of organisations are putting off any changes because of the false narrative that's been created, which says the ruling is not law until the statutory guidance is approved by Parliament. But that's utter rubbish - the law is what the Supreme Court says it is. Unfortunately, a lot of people choose not to believe that.' Advertisement Hide Ad Advertisement Hide Ad Sandie Peggie | Lisa Ferguson Ms Smith also suggested the intense scrutiny of NHS Fife's processes and practices may prevent other public bodies from contesting similar cases raised at employment tribunals in the future, describing it as a 'real embarrassment' for the health board. 'Even if they were to win at this stage, which I don't think is likely, I am sure it would go to appeal, and ultimately, they would lose,' she said. They have spent a vast amount of taxpayers' money on this, and it's been humiliating to hear some of the evidence, and the gossiping and bitchiness in the workplace. 'I think there'll be more cases and I think there will be more settlements. Wiser lawyers will be telling their clients that it is better for them to swallow whatever disadvantage comes from settling, because they're not going to win in the long term.' Political pressure and cost concerns The Peggie judgement will also have repercussions for NHS Fife. Already, senior figures in Scotland and elsewhere have reflected at length on the case, with many calling for changes even before a judgement is issued. Advertisement Hide Ad Advertisement Hide Ad As part of cross-party condemnation of the health board, Scottish Conservative leader Russell Findlay is among those who have said senior managers should step down over its handling of the case, while SNP MSP Michelle Thomson has called on the members of NHS Fife's board to consider their positions. Elsewhere, Scottish Labour's Carol Mochan has said Holyrood's health committee should investigate the way in which the health board has handled the case. NHS Fife has come under extensive criticism. Picture: Fife Free Press | Fife Free Press That criticism is likely to continue, especially as the costs of defending the tribunal case mount up. NHS Fife has confirmed that as of the end of June, it had spent more than £258,000 on legal costs relating to the tribunal - a sum that includes counsel fees and services provided by NHS Scotland. But given the hearings that have taken place since then, one source suggested the total bill could reach in the region of £500,000 to £700,000 if not more. That sum would exclude any remedy made in Ms Peggie's favour should the health board lose its case. 'The costs of defending such a case, and eventually paying compensation, is likely to be enormous,' Ms Forstater said. Advertisement Hide Ad Advertisement Hide Ad

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store