Deb Gascoyne was recognized after she visited the GP for a sore throat

Deb and her household in Beijing in 2012 (Picture: PA Actual Life)
A mother-of-two who feared she would not reside to see her youngsters develop up after a sore throat led to an incurable blood most cancers prognosis has expressed feeling “fortunate” to be alive 16 years later. Deb Gascoyne, 50, from Hagley, West Midlands, revealed {that a} precautionary blood take a look at detected her smouldering myeloma – an early stage of the blood most cancers – in July 2009, aged 34, when she visited her GP for a sore throat.
Deb, who resides together with her 50-year-old husband Nick and their two youngsters, Rebecca, now 21, and Sam, 19, stated the nurse’s last-minute resolution to take bloods that day resulted in an early prognosis and will have even saved her life. Regardless of experiencing two relapses over time, she has been capable of have fun many vital milestones and has devoted herself to fundraising, with the aim of reaching £250,000 to help analysis into remedies and a treatment.
So far, she has raised £248,100 for the charity Myeloma UK – though this determine is more likely to be increased because the system is just up to date month-to-month – and she or he is gearing up for her remaining fundraising problem in Might, a cycle journey from London to Paris, to succeed in her goal. Whereas Deb has grappled with survivor’s guilt and even felt like a “fraud” for outliving the standard prognosis, she stated she feels “fortunate that (she’s) had 16 years” and desires to supply “hope” to others.
“If I take into consideration the buddies I’ve misplaced alongside the best way, and what their households have missed out on, I’m remarkably fortunate to have a slower and fewer aggressive type of myeloma,” Deb informed PA Actual Life. “I’ve seen my youngsters hit their main birthdays, I’ve watched my son together with his girlfriend and my daughter changing into a paramedic, and also you simply assume, these had been issues I may solely have dreamt of once I first received that prognosis. I’m actually fortunate and actually blessed to have seen them by way of all of that.”
Earlier than receiving her prognosis in 2009, Deb was a busy mother-of-two working in Human Assets (HR) – and together with her youngsters aged two and 4 on the time, she was ready to “kickstart (her) household”. Nonetheless, every little thing shifted when she started affected by a relentless sore throat.
“It felt like a golf ball in my throat and I used to be worn out from it each month, so I went to the GP,” Deb recalled. “The nurse stated, ‘We’ll do a throat swab and if that comes again adverse and you are still having the sore throats, we’ll ship for bloods’.
“Then, simply earlier than I left, she stated, ‘Really, have you learnt what? We’ll simply ship your bloods off now anyway’.”
Deb revealed this snap resolution to take blood assessments that day resulted in an “early prognosis that (she) may not have had in any other case”. Following extra testing, together with scans and a bone marrow biopsy, it was confirmed in July 2009 that Deb had smouldering myeloma – an early stage of the blood most cancers – aged 34.
Left “completely shellshocked”, as docs initially informed her she was “too younger” to be recognized with the situation, she started conducting her personal analysis and found life expectancy statistics.

Deb and her youngsters throughout her chemotherapy therapy (Picture: PA Actual Life)
“On the time, there wasn’t a lot data from the UK, most of it was from the US, however it was saying two to 5 years’ life expectancy,” she stated. “So, then there was that complete concern and emotion of not seeing your youngsters develop up, not getting previous with Nick – all of the issues that we had plans for and had been a no brainer in our heads had been all of a sudden up within the air.”
Roughly a yr later, Deb’s myeloma superior to energetic most cancers and she or he was enrolled within the Myeloma XI trial in 2010, which concerned chemotherapy. Nonetheless, throughout that interval, Deb defined she immersed herself in fundraising as she “wanted to take management of one thing”, and first accomplished the Yorkshire Three Peaks together with her household and associates.
She admitted feeling “morbid” at instances, enjoying melancholy songs and even deciding on her funeral playlist, however when she linked with different sufferers by way of Myeloma UK’s help community, this helped shift her outlook. “There have been two ladies particularly who, sadly, aren’t with us anymore,” Deb recalled.
“However on the time, they had been actually instrumental in serving to me realise that I may nonetheless have a life and have myeloma, that I may nonetheless have quite a few years forward of me.”
Following her first stem cell transplant in July 2011, Deb was positioned on upkeep chemotherapy, which stored her in “partial remission” for eight years. Regardless of the “concern behind (her) head” about relapsing, she remained dedicated to fundraising, organising occasions together with a “glitz and glamour ball” that raised greater than £30,000.
Discussing her fundraising efforts, Deb defined: “I then did 40 challenges earlier than I used to be 40, together with studying 40 books, doing a pub crawl round 40 pubs in 40 hours and consuming 40 Brussels sprouts in 4 minutes. Then I did £50,000 earlier than I used to be 50, however within the center, I did different issues like a meals and wine tasting occasion, which raised about £11,000 and silent discos and auctions.”
Myeloma UK states that the situation sometimes follows a relapsing-remitting sample, whereby profitable therapy can obtain remission, although the illness is more likely to return. Deb skilled her first relapse in 2019, present process her second stem cell transplant in September 2020, earlier than struggling one other relapse in November 2024.

Deb after her first stem cell transplant (Picture: PA Actual Life)
She started a brand new upkeep therapy in December 2024, which she continues to obtain, and while she has skilled some “blips” and hospital admissions all through, she stays dedicated to fundraising. She is presently getting ready for her second London to Paris biking problem in Might, the place she can be accompanied by household, her marketing consultant, two of her medical analysis nurses, the spouse of a affected person who just lately handed away and different sufferers and associates. Throughout this era, she additionally hopes to step again from work to savour high quality time together with her household.
“My husband’s about to take a while out in order that we are able to make some reminiscences and never wait till it is too late,” she stated. “I feel we wish to see a little bit of Europe, and for Nick’s fiftieth birthday, we have got just a few presents of meals out or afternoon tea. It will likely be good to have time as nicely to help the children with out attempting to separate time between work and therapy, so we are able to make the priorities the proper ones.”
Deb stated she has had appreciable time to “replicate” since her prognosis, and she or he incessantly wonders what might need occurred if that blood take a look at had not been carried out. Nonetheless, as she approaches 17 years since her prognosis in July, she feels “grateful” as she didn’t imagine she would “have this a lot time”.

Deb and her son Sam (Picture: PA Actual Life)
She desires to proceed elevating consciousness of myeloma and to encourage others to “hearken to (their) physique and be their very own advocate”. “The entire journey with myeloma has been a rollercoaster for everybody, however what’s good is there’s a group on the market… they usually assist you to do not forget that you are not alone,” she expressed.
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“I would say to others, attempt to assume positively the place you’ll be able to, as a result of it doesn’t matter what you learn, I prefer to assume that tales like mine present that there’s all the time hope.”
To be taught extra or to contribute, go to Deb’s most up-to-date fundraising web page at journey.myeloma.org.uk/deb-gascoyne or try Myeloma UK’s web site at www.myeloma.org.uk.


















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