Hi everyone

New fundraising treatment plan incoming

(May 2026 Update)

I’m so sorry I’ve been so quiet - I’ve had some big decisions to make over the last few weeks and it’s taken its toll on me. Plus the fact that the pain from the cancer tumors has ramped up a hell of a lot of- I’ve been really struggling both with the pain and also with my mind. Living in a state of panic and fear is a difficult place to be.

So we have now moved out of our rented house which had 5 bedrooms and enough space for 2 adults , 6 children, two are 19 so only stay sometimes as usually they are away at university, a dog and 2 cats into my mums semi detached falling down house (I mean this literally- the bathroom has fallen into the kitchen) so we can put the rental money we save towards my treatment. Every penny counts here

We’ve now got 2 bedrooms between us all and we are all swapping on and off the sofa the dog Agnes has gone to my step dads , one cat has gone to my friends and we’ve managed to sneak one cat in, so it’s less that ideal but hopefully it’s temporary and will all be worth it if it gives me more of a chance to fight this cancer and ultimately have more time with my girls.

You will have noticed I have changed the treatment that I have been fundraising for as I had my consultation with America for the Histotripsy procedure I was hoping for and the surgeon told me that out of the 5 largest tumors he could only guarantee to get to 1 of them. This is not the news I was hoping for and has really spun me out and I’ve been a bit of a mess as you can imagine.

Again though I’ve kind of got my head together somehow (lorazepam thank you ) and I’ve been researching and I’ve found a brand new treatment called NK cell therapy- it’s Natural Killer Stem Cell therapy which essentially harvests donor NK stem cells and then the doctor injects them into you daily for 4-6 weeks and these cells go after the abnormal cancer cells and try to revert them back to normal cells.

Its similar to dendritic cell therapy but hopefully more intense. Again though its not available in the UK outside of a trial - which I’m not eligible for as I’ve not had chemotherapy (even though I have been told that chemotherapy wouldn’t be appropriate for me) The UK system is fatally flawed sadly.

So, pushing on, I have paid £10,000 from my fundraising funds (thank you all so much for getting me to this point) for the deposit and preparation of the cells and I’m flying out to Kuala Lumpar on June 1st for my first infusion of cells on the Wednesday at a cost of £25,000 which I’m hoping and praying I manage to fundraise. Big ask I know but I HAVE to try.

If all goes to plan and my liver doesn’t explode mid flight (it’s enlarged to 19cm and is stretching its capsule causing it to press on nearby nerves causing a me tonne of pain) then I’ll be there for 6 weeks - all on my own - I’m just hoping and praying that my body accepts the donor cells and they do their job on these tumors.

It’s so bloody difficult and awkward asking the same people over and over for help but honestly every single £ donated is helping me reduce the cancer cells in my body and giving me a chance at a longer life. Even if you just share share share my fundraiser please do so - and as always anything you can donate is appreciated so so much.

If you know anyone with a large social media following pls pls pls ask them to share for me

Any questions at all pls pls don’t hesitate to ask me on 07539255717- i want to share my knowledge and help anyone going through cancer in any way that I can.

I appreciate you all so much

Emma xxxx

Old News (Feb 2026 update)

Hi my name is Emma. I’ve had stage 4 cervical cancer since November 2023 and I’ve been managing it well with my concoction of off label drugs, intravenous vitamin C, hyperbaric oxygen therapy, Bioresinence, Ayurvedic interventions, alkaline water, infrared light therapy plus a whole host of other weird and wonderful things.

I’ve tried medicinal cannabis- THC- cold plunging - saunas- sound baths- anything that might help- I’m there.

I’m not new to this fundraising stuff- I raised money for my treatment when I was initially diagnosed and I honestly wholeheartedly believe that the treatment I have been able to fund has kept me alive.

Over the past 12 months I’ve definitely not been as diligent with treatment and unfortunately on the last scan I had in January 2026 it has shown some new tumors on my liver. The largest one and the one causing the most problems is around 3.2cm.

I’m not a candidate for surgery on the NHS as with stage 4 disease it’s considered not resectable. Also The Christie hospital has said that as the cancer is slow growing it’s not a fit for chemotherapy so I’m left with very little options here other than to seek treatment abroad.

I’m so upset about my scan and that there is essentially nothing that Christie’s can offer me treatment wise. I’ve always had chemotherapy to fall back on and now it’s not an option I feel more scared.

I do have some treatment options available to me but they are in America and expensive and I’m going to have to fundraise and I feel so awful asking everyone for help after you’ve all been so generous in 2024.

The treatment is $50,000 which I understand is an insane amount of money- but if it gives me more time then it’s worth it!

I’m going to have to come up with some sort of a fundraising plan to achieve this goal and time is really of the essence.

Please donate what you can and share, share, share!

Thank you so so much for your love and support. It means the world to me

Emma xx