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Help Save Jade - Hodgkins Lymphoma

£51,320 of £120,000 goal

Raised by 985 people in 12 months
Who am I?
I'm someone that wants to live - a wife, a daughter, a sister, an aunt, a niece, a cousin, a friend, a colleague and sometimes a pain in the butt.

In February 2017, at the age of 34, I was diagnosed with Stage 4 Hodgkin's Lymphoma
It sounded bad but to be honest I felt slight relief at a diagnosis after 2 years of horrible symptoms and mental anguish.

Treatment on the NHS started quickly in March 2017, with a 6 month course of chemotherapy every 2 weeks.
It wasn't easy. It was definitely scary. It was the start of a new life for me and everyone around me.

After 2 months a PET scan showed remission (although I was still in and out of hospital with various infections) and thought ‘’could this be a sign of my immune system fighting back’’?

However, a PET scan at 6 months showed it was back and aggressive - on my spine, ribs, lungs, hip and lymph nodes (everywhere!).

I needed a second type of treatment.

I received this new treatment in November and December 2017.
It was harsh (to say the least) and most mornings I was still being sick as I arrived at the hospital.

A PET scan in January gave more bad news - the drugs had no effect on the cancer.

I needed a third type of treatment.

I was referred to UCLH Macmillan in London.
If you ever end up in a life or death situation like mine, this place and the people are amazing.
They helped me secure a place on a trial comparing a new drug to one that was currently being used by the NHS.
The new drug was showing particularly good results for my type of cancer but, to my despair, I was randomly placed to receive the drug that is already available.

Another 2 months passed and another PET scan showed mixed response to the currently available treatment
The cancer had cleared in some areas, but progressed in others – meaning that the current drug was no longer effective.

Was I running out of options?

I needed a fourth type of treatment.

The next session of chemotherapy was horrific - I was in hospital for 9 days and it resulted in me collapsing and having problems with my kidneys.
After 2 days at home I had to return to hospital as I had contracted sepsis.
2 weeks later, I had to receive another 5 days of this chemotherapy.

Another PET scan showed these treatments had made no impact.
The cancer is now in my liver, abdomen and in more areas on my lungs.

Update; Now having undergone further treatments of Pembro and mini-LEAM and spending weeks in hospital with sepsis, pneumonia and flu there are no more options funded by the NHS apart from palliative care.

A treatment was proposed to me by the specialists at UCLH Macmillan.
This drug is legal and available, but it is not available on the NHS for Hodgkin's Lymphoma.
This drug called Panobinostat.
The treatment costs an estimated £120,000

With this drug my consultant believes my cancer could be put into remission.
Which would mean I could finally have a Stem Cell transplant - which presents its own challenges (and is a hurdle for another time!).

I need to find a way to fund this hopefully lifesaving treatment.
To do that I need to call upon the generosity of you.

Please help. Every penny counts.

If you are unable to donate money, please consider signing up to the stem cell registry (link below).
They desperately need more people registered and the test is a simple swab of the mouth that you send away in an envelope.

Thank you for taking time to read and share this,
Jade xxx

Stem Cell Registration
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Time has gone quickly this year, and honestly at the beginning of the year I didn’t know if I’d be around today.

After spending Christmas and most of January in the London hospital, I had the news that I was considered palliative in February.

Luckily, my doctors don’t like to give up and they tried me on Panobinostat which we funded through this Go Fund Me page - thank you everyone.

Unfortunately, whilst it cleared some of the cancer up, it progressed too much and I was taken off of it after a few rounds.

Fast forward to today and I’m 2 weeks after an infusion of Bendamustine with another to come in June. We tried one go of this in the summer 2018, and my doctors thought it was worth trying again.

So here I am, waiting on drugs and a PET scan.

If this doesn’t work I believe the next step is for me to go onto palliative care drugs to try and slow the growth of the cancer; in the hope that a trial becomes available.

I’m getting as much time in with family and friends with small holidays in the UK and trips out. Because after all, it’s the people supporting me that make me smile, feel happy and keep my spirits up.
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A LOT has changed since my previous update and it would be far to long to write hear; so this is where we currently stand.

I’ve had a bunch of chemos some that looked like they were working but not enough to get me transplant as the cancer grew back too quickly.

I have an option of going on oral tablets to try and contain the cancer, or another drug called Panobinostat.

The hospital cannot get me this drug on compassionate grounds for me.

I need to fund privately for 6 sessions at £20k a go, £120k in total.

Please please help me and my family and friends to try and reach this new target. Anything at all is greatly appreciated.

I wish love was enough to keep me here x
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Had an amazing little wedding on Thursday, it was relaxed, fun and full of love and laughter! Perfect! ❤️
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PET scan done now the wait begins. All the specialists will discuss it at their meeting Thursday - the day I get married! Then I should have the results within a couple of weeks. Please keep everything crossed that the drug is helping x
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£51,320 of £120,000 goal

Raised by 985 people in 12 months
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