Hey everyone

ive never done anything like this before it feels uncomfortable to be fundraising for myself I’ve always been so independent but cancer took that all away from me.

In August 2024 I was diagnosed with stage 4 metatastic melanoma cancer after lots tests scans seeing surgeon I was booked in for a operation in October I had a huge melanoma removed breast tissue and lymph nodes.

After having a petscan in November I was clear and began on aduvent treatment of immunotherapy

I was scanned every other month and I remained clear for 7 months however I started to reacting to treatment black and blue bruises aching legs upset stomachs so my oncology team requested a pet scan if was still clear they would stop the treatment.

unfortunately.

in may 2025 melanoma deposits were found in my left breast one in my stomach 2 small ones in my lungs and one on my arm

I was put on 4 rounds of ipilumab alongside my nivolumab

only managing 3 out the 4 rounds as it made me incredibly ill and my liver function bloods to spike so high all treatment was stopped.

the tumour in my stomach had also seemed to be bigger protruding from my skin I was taken in hospital and this was removed in surgery. I was put on intravenous steroids very high dose causing me to bloat out get puffy and caused two cataracts which I’ve also had to address.

in November after being weaned off steroids and after not being on NHS treatment since August we tried treatment again just with my original nivolumab treatment unfortunately my liver failed again and I was back on the high dose steroids.

.

my pet scan in December showed I’d cleared all the tumours through my holistic approach apart from 2 small ones in my lungs despite having no NHS treatment.

however 4 new ones have appeared recently however this proves that my holistic approach has definitely had a positive impact on my cancer health journey.

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on Friday 16th January I was told I can never have immunotherapy again

initially my oncologist said this was last option otherwise we’d go no further and nhs may not be able to have any other options recently ive been told as I’m B RAF mutation gene I am eligible for short course of tablets with a 60% chance of success

however these targeted therapy tablets stop working after 8-12 months then will be relying on if a trial comes out with at this moment in time no other options available

.

I’m now trying to raise funds to continue my holistic therapy to keep me fit and healthy and help fight the cancer as I’ve done in past but also to raise funds to travel abroad for treatment to get into remission this is life saving treatment not available on the NHS but I need help getting the funds to be able to do this once the tablet is no longer working

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My go fund me is to support me maintain my private alternative holistic treatments giving me better chances of survival I’m under a private dr holisticly working to get rid of the cancer on 1-2-1 basis and heal my cells and dna and build up my immune system with alternative therapy

My go fund me is enabling me to do this

and also to raise funds for treatment abroad not available here in uk on NHS

thankuou for reading my story I’m very grateful of your unwavering support abc love ❤️

thank you so much for reading my story and I hope you can support me & help me get this treatment and beat this cancer and keep it away

lots of love

Becky ❤️