![\"Beth](\"https:\/\/www.europesays.com\/uk\/wp-content\/uploads\/2025\/07\/0_CapturePNG.png\")
Beth was a capable and independent teenager before she could no longer recognise her loved ones(Image: Mirror)<\/p>\n“It is like someone has flipped a switch and you don\u2019t recognise that person in front of you.”Beth was a capable and independent teenager before she could no longer recognise her loved ones(Image: Mirror)<\/p>\n
A teenager was left unrecognisable to her friends and family after she suffered a sudden personality <\/a>change.<\/p>\n Beth Shepherd was diagnosed with a mysterious condition known as PANS <\/a>in 2022 when her whole personality instantly transformed. The 16-year-old’s behaviour suddenly became violent and she would fly into fits of rage, often subjecting her mum, Toni, to beatings.<\/p>\n She struggled to recognise her family members and feared she would be kidnapped<\/a>. Other times the teen hid under tables believing she was going to be murdered.<\/p>\n Mum Toni had to give up work for five weeks after Beth’s first symptom.<\/p>\n Speaking of her daughter’s condition, she told the Mirror<\/a>: \u201cAbsolutely terrifying. You cannot imagine. You have a baby, they hand you the baby on your chest and say, \u2018Here is your healthy <\/a>baby girl. And that will never leave me, because the comparison to now\u2026 I don\u2019t recognise her. On a good day I do.<\/p>\n “But when we are rolling around for two hours and I put myself between her and a wall so she can\u2019t injure <\/a>herself… It is like someone has flipped a switch and you don\u2019t recognise that person in front of you.\u201d<\/p>\n Toni, who had been a childminder before it became too dangerous to have other kids in the house with Beth, hopes to raise awareness of her daughter’s condition and get her child the help <\/a>she desperately needs.<\/p>\n Toni, from Matlock, Derbyshire<\/a>, said her daughter’s first symptom was an unusual one.<\/p>\n She said: \u201cShe started making strange noises. But I didn\u2019t really address it. I left it because I know with Tourettes <\/a>that sometimes the more you talk about it the worse it gets.\u201d<\/p>\n Asked to describe the sound, she said: \u201cKapow! Kapow! She would be sitting on the sofa <\/a>watching telly and she would randomly go \u2018kapow\u2019. It was just odd. We didn\u2019t try to make a thing of it.\u201d<\/p>\n However, things escalated quickly, and Beth rang her mother from school one day with the ominous statement: \u201cMum, something is happening to me.\u201d She thought she might be having a seizure and Toni said she was \u201cjerking all over the place\u201d when she arrived. The family rang an ambulance. At the hospital<\/a>, they were told it could be motor tics.<\/p>\n They went home <\/a>and were told to return in a year, where they might then get a diagnosis of Tourettes. Verbal tics came four days later but soon her personality and behaviour transformed.<\/p>\n Describing the change, Toni said: \u201cReally really rapidly, she became really anxious, she was paranoid<\/a>, she was having hallucinations, she didn\u2019t recognise her family, she thought we were going to kidnap her.<\/p>\n \u201cShe was screaming for me, I\u2019m right in front of her, but she is screaming for me because she didn\u2019t recognise <\/a>me. And she thought I was a stranger. She thought the whole world was falling to pieces. Then the rages started, she would literally erupt, and excuse my language, but she would physically attack me. It was scary, it was really really scary.\u201d<\/p>\n More symptoms arrived in the form of seizures, up to 80 a day, and despite lasting just a few seconds, they resulted in Beth falling to the floor. She then started having paralysis for up to four days at a time because her body simply forgot how to work. After countless visits to A&E, Toni, completely desperate for answers, staged a sit-in, and begged someone from CAMHS <\/a>(Child and Adolescent Mental Health Services) to see them.<\/p>\n Beth also started having restrictive eating where she would refuse certain foods because <\/a>they \u201ccame from a farm and farms were dirty\u201d. Along with irrational thoughts, she regularly smashed her head against the wall. They proved to be particularly devastating moments for the family that includes Beth\u2019s younger sister, 11, who has been hugely impacted by her sibling’s decline.<\/p>\n However, eventually a diagnosis <\/a>was found, and Toni remembered: \u201cIt was my mum. We had spent hours trawling the internet trying to find what the hell is happening. It was actually my mum who found PANS (Paediatric Acute-Onset Neuropsychiatric Syndrome) and she rang one day and said I\u2019ve got it.\u2019 I was a bit sceptical because so many symptoms overlap with different things but it was just spot on.\u201d<\/p>\n She said there were 20 symptoms on a PANS <\/a>criteria and at the time Beth had 19, before eventually developing the one she did not have. It is a neuropsychiatric condition caused by a misdirected immune response to an unknown trigger causing inflammation in the brain and leads to both physical and psychiatric symptoms. These include rages, anxiety, tics, hallucinations, chronic fatigue and pain, sleep difficulties and being unable to walk.<\/p>\n It is a syndrome<\/a> that develops incredibly suddenly and impacts the physical and mental health of children and young adults. It can develop after common infection, and in Beth\u2019s case, it may have appeared after she had Covid-19 in July 2021. Despite being recognised by the World Health Organisation, there are no treatment guidelines for it in England, making Beth\u2019s situation particularly turbulent.<\/p>\n Toni spent up to \u00a38,000 finally getting Beth diagnosed privately and was prescribed <\/a>antibiotics and steroids. The latter caused her to become manic, resulting in her climbing walls and thinking her skin was covered in spiders. As of today, Beth now has invaluable chiropractic care every week that regulates her nervous system. If she does not attend, her mum notices symptoms immediately, and her daughter will become more agitated, fiery and in pain.<\/p>\n She also has counselling <\/a>once a week, and all of these things are funded privately, with Toni stressing she has not been able to get any support. Toni has spent countless hours contacting every local statutory body in the hopes someone will take responsibility to provide what Beth needs to function \u2013 but said it has been a year of hitting brick walls.<\/p>\n However, after starting a GoFundMe in recent weeks to fund private care, more than \u00a33,000 has been raised, meaning her daughter has started hyperbaric oxygen therapy<\/a>. And writing on the fundraiser, Beth, who is falling behind in her education because of the lack of support, said: \u201cI haven\u2019t given up on life; I\u2019m still here and I am still fighting this debilitating illness. With your help, I hope to be able to strengthen my body and mind and become more like the person I was.\u201d<\/p>\n Get the latest news sent straight to your messages by joining our WhatsApp community today.<\/p>\n You’ll receive daily updates on breaking news as well as the top headlines across Scotland.<\/p>\n No one will be able to see who is signed up and no one can send messages except the Daily Record team.<\/p>\n All you have to do is click here if you’re on mobile<\/strong><\/a>, select ‘Join Community’ and you’re in!<\/p>\n If you’re on a desktop, simply scan the QR code above with your phone and click ‘Join Community’.<\/p>\n We also treat our community members to special offers, promotions, and adverts from us and our partners. If you don\u2019t like our community, you can check out any time you like.<\/p>\n To leave our community click on the name at the top of your screen and choose ‘exit group’.<\/p>\n If you\u2019re curious, you can read our Privacy Notice.<\/a><\/p>\n The therapy, which involves breathing pure oxygen in a pressurized chamber<\/a>, will hopefully reduce Beth\u2019s inflammation and infection. That may lead to an increase in energy and sleep (currently she only gets three hours per night).<\/p>\n Giving an insight into her daughter\u2019s life now, Toni said: \u201cShe spends probably two to four days a week in a wheelchair<\/a>. Another couple on her specialised crutches. She usually gets one day a week where she is mobile, but she has to have rested all the way up to that and needs to rest three days after.<\/p>\n \u201cShe lives for one day a week and that is the only light she has left.\u201d<\/p>\n Toni hopes the alternative therapy will help with that and any proceeds from the fundraiser will go towards a possible purchase of a hyperbaric oxygen machine<\/a>, adaptations to the house so Beth can live downstairs in her own space and eventually a therapy dog for support.<\/p>\n![\"Beth](\"https:\/\/www.europesays.com\/uk\/wp-content\/uploads\/2025\/07\/1751359463_559_0_CapturePNG.png\")
Beth was thriving in life before antibodies latched on to the part of the brain that controls emotions and mobility(Image: Mirror)Symptoms<\/p>\n![\"The](\"https:\/\/www.europesays.com\/uk\/wp-content\/uploads\/2025\/07\/1751359464_618_0_CapturePNG.png\")
The mum and daughter have endured difficult times together in recent years (Image: Mirror)<\/p>\n![\"Beth\"](\"https:\/\/www.europesays.com\/uk\/wp-content\/uploads\/2025\/07\/1751359465_455_0_CapturePNG.png\")
Beth(Image: Mirror)Diagnosis<\/p>\n![\"It](\"https:\/\/www.europesays.com\/uk\/wp-content\/uploads\/2025\/07\/1751359465_86_0_CapturePNG.png\")
It has been a challenging three years for the teenager \u2013 but she is refusing to give in(Image: Mirror)Treatment \/ Fundraiser<\/p>\n![\"\"](\"https:\/\/www.europesays.com\/uk\/wp-content\/uploads\/2025\/05\/1747398730_254_0_WACOMMUNITYQR3.jpg\")
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