{"id":212593,"date":"2025-06-25T07:46:12","date_gmt":"2025-06-25T07:46:12","guid":{"rendered":"https:\/\/www.europesays.com\/uk\/212593\/"},"modified":"2025-06-25T07:46:12","modified_gmt":"2025-06-25T07:46:12","slug":"i-have-adhd-and-pay-200-a-month-for-treatment-after-the-nhs-refused-to-help","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/uk\/212593\/","title":{"rendered":"‘I have ADHD \u2013 and pay \u00a3200 a month for treatment after the NHS refused to help’"},"content":{"rendered":"

A Lanarkshire mum living with ADHD says she has to pay \u00a3200 every month for medication despite her private diagnosis being accepted by an NHS psychiatrist.<\/strong><\/p>\n

Gemma Wardlaw turned to private healthcare in January after years of struggling with undiagnosed ADHD \u2013 a neurodevelopmental condition marked by symptoms such as difficulty concentrating, hyperactivity, and impulsive behaviour.<\/p>\n

Her diagnosis followed a thorough assessment process that involved several evaluations and input from her husband and mother.<\/p>\n

Gemma says she was initially told by her GP that shared care arrangements could be made after her diagnosis.<\/p>\n

However, in May she received a letter saying the GP practice would not proceed with shared care and that no adult ADHD clinics were operating within the local health board area.<\/p>\n

That meant she had to fund her prescription privately.<\/p>\n

Gemma, who works as a baker, told STV News: \u201cI was so crushed and emotional. I hadn\u2019t felt like that in a long time. Honestly, at that moment, I felt I was back at square one with no route to care.<\/p>\n

\u201cIt\u2019s very disheartening. I feel ADHD doesn\u2019t get treated like other conditions. If I had depression or high blood pressure, I\u2019d get access to treatment straight away. But with ADHD, the door\u2019s shut. There\u2019s such a stigma around it.\u201d<\/p>\n

Gemma is taking on extra working hours to afford the unexpected cost of her medication.<\/p>\n

She added: \u201cWith that money, I could have taken my family on another holiday this year. That\u2019s upsetting \u2013 I could be making more memories with my children, going to new places. I feel guilty, but in a way, the medication is essential. I can\u2019t be the best mum I can be without it.\u201d<\/p>\n

NHS guidance allows GPs to consider shared care agreements following a private diagnosis on a case-by-case basis and advises against blanket refusals.<\/p>\n

\"GemmaSTV NewsGemma has founded The Fair Care Circle, a support group for neurodivergent people and their families STV News<\/p>\n

Gemma told her story as a Holyrood committee launches an inquiry into treatment pathways and support for ADHD and Autism Spectrum Disorder (ASD).<\/p>\n

ADHD affects around 5% of school-aged children and between 2.5% and 4% of adults. ASD is a lifelong developmental condition that affects communication, interaction, and information processing, with an estimated prevalence of about 3% in the population.<\/p>\n

Gemma says she has experienced ADHD symptoms since the age of nine.<\/p>\n

\u201cI struggled with sleep for years, and found it hard to complete even basic tasks, like work around the house. I\u2019d get overwhelmed very easily. I missed appointments, let customers down by missing orders, and lost things constantly.<\/p>\n

\u201cSince starting medication, my eating has improved significantly. You have to eat daily \u2013 even that was exhausting for me.\u201d<\/p>\n

Gemma is also a mother to two neurodiverse children, who had to wait six years for their own diagnoses.<\/p>\n

\u201cMy eldest was diagnosed earlier this year through the NHS, and my youngest is currently at the top of the list and undergoing assessment,\u201d she said.<\/p>\n

Her family\u2019s experiences have led her to launch The Fair Care Circle, an online support group for the neurodivergent community.<\/p>\n

Gemma lodged formal complaints with the GP surgery and NHS Lanarkshire, and submitted a Subject Access Request for her medical records and related correspondence, some of which she says remains outstanding.<\/p>\n

She also claims that her chosen GP had never seen her diagnosis or medication titration plan.<\/p>\n

Gemma has taken her case to the Scottish Public Services Ombudsman, which is now reviewing it.<\/p>\n

Reflecting on the past few months, she said: \u201cI hit a wall and went right back to how I was before. I was struggling with work \u2013 people noticed the impact it was having on me.\u201d<\/p>\n

Gemma says she has heard from many others across Scotland facing similar difficulties accessing NHS ADHD care after a private diagnosis.<\/p>\n

\u201cIt\u2019s a widespread problem,\u201d she said. \u201cThere\u2019s no consistency with policies across GP practices. It\u2019s like a postcode lottery. They\u2019re supposed to follow NHS board guidelines and avoid blanket refusals, but that\u2019s not happening.\u201d<\/p>\n

She is building a network of resources for individuals and families affected by ADHD and is campaigning for a national, consistent policy on ADHD care.<\/p>\n

\u201cI want a framework that ensures all patients, regardless of postcode or route to diagnosis, are treated with dignity, equality, and transparency,\u201d said Gemma. \u201cEveryone deserves a fair chance.\u201d<\/p>\n

\u2018People are being left in limbo\u2019\"ScottishSTV NewsScottish Autism\u2019s director of practice and innovation, Joe Long STV News<\/p>\n

Joe Long, director of practice and innovation for Scottish Autism, describes the situation for people seeking referrals for ADHD and autism diagnoses and treatment as a \u201ccrisis\u201d.<\/p>\n

\u201cIt\u2019s really inconsistent across Scotland,\u201d he said. \u201cMany people face difficulties just getting referred in the first place. One key issue is poor information and communication \u2013 understanding when they might be seen, what\u2019s involved, who they will see.<\/p>\n

\u201cWe\u2019re also finding that once people have assessment and diagnosis, there isn\u2019t really adequate post-diagnostic support to make sense of that, to find out how to advocate for their needs effectively, and to get adjustments for their education setting or their workplace.\u201d<\/p>\n

Joe highlighted the financial burden many are facing by going down the private route.<\/p>\n

\u201cPeople are going through real hardship, borrowing money from families, going into debt, or selling possessions just to afford a diagnosis that should be available to them from the state,\u201d he said.<\/p>\n

\u201cPeople are feeling upset and stressed, left in limbo for long periods, with great uncertainty about their future.<\/p>\n

\u201cThey feel let down by the system and are genuinely concerned on quite a lot of fronts.\u201d<\/p>\n

A Scottish Government spokesperson said: \u201cTogether with NHS boards, local authorities and community partners we are working to improve access to the best possible neurodevelopmental care and support services for children and adults.<\/p>\n

\u201cFor many people, such support is likely to be community-based and should be quickly and easily accessible, and is not dependent on a formal diagnosis.<\/p>\n

\u201cWhere patients have obtained a private diagnoses for conditions like ADHD, it remains the clinical discretion of each individual GP to decide the best course of action for their patients including ongoing care and medication.\u201d<\/p>\n

NHS Lanarkshire have been contacted for comment.<\/p>\n

STV News is now on WhatsApp<\/p>\n

Get all the latest news from around the country<\/p>\n

Follow STV News <\/a>Follow STV News on WhatsApp<\/p>\n

Scan the QR code on your mobile device for all the latest news from around the country<\/p>\n

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