17/05/2026
Hi everyone,
We just want to say a huge thank you to everyone who continues to share Maisie’s story, and to all the incredible people who have donated. We are beyond grateful, and we will never forget your kindness and support.
Maisie is now scheduled to have surgery in June. We are hopeful that this will help reverse her most debilitating daily symptoms, including severe cognitive impairment, constant nausea, and dizziness. Most importantly, we hope it will allow her to be a mum again and start living life outside of these limitations.
There is, unfortunately , a possibility that Maisie may need another surgery in the near future which will mean fundraising again and costing more money🥲. Right now, this first operation is absolutely essential and life saving.
after surgery, Maisie could experience issues in her lower neck, as she currently has two herniated discs. If this happens, it may require additional surgery to remove the discs and extend the fusion. We truly hope this won’t be necessary but it’s a possibility— Maisie is young and just wants to move forward and live her life as fully as possible.
If further treatment is needed, we may have to fundraise again to ensure it can be done quickly, before symptoms become severe again. Maisie wants to just get back to work and living so she can save for future issues but she may not get the chance to save before she needs a second surgery fingers crossed this doesn’t happen. We shouldn’t have to rely on the public to help us fund such life saving important surgeries it’s just disgraceful! And sad that there’s no options because this condition without treatment leads to paralysis and permanent neurological damage. There have been so many cases in the uk and still no change!
As many of you know, the NHS currently does not provide surgery for Maisie’s condition, and private hospitals in the UK are also unable to offer this procedure. This means fundraising remains our only option.
We do hope things will change in the future. There have already been discussions in Parliament, as more people across the UK are being left without treatment for this condition. Without proper care, it can lead to permanent neurological damage and, in the most serious cases, paralysis.
If you would like to continue following Maisie’s journey, we will keep sharing updates on Facebook.