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Episodes of Leukaemia Chatters
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After giving birth to her second daughter, Heidi began to experience night sweats and was overwhelmed with fatigue. A few months later, Heidi was diagnosed with acute myeloid leukaemia (AML) and was unable to work, resulting in her and her husb
On this episode on Leukaemia Chatters, we spoke to Emma Sinclair a CML patient diagnosed in 2021. We talked to Emma about the events that led up to her diagnosis, the changes that have come with living with a chronic leukaemia and the support a
On this episode of Leukaemia Chatters we spoke to Zack Pemberton Whiteley, Leukaemia Care's CEO live from the ASH conference. We discussed some of the newest developments in the treatment of leukaemia and how they might change the landscape for
On this episode on Leukaemia Chatters, we spoke to Dan Chapman a CML patient diagnosed in 2015. We talked to Dan about the events that led up to his diagnosis, the impact of a chronic leukaemia on his life and the challenges he has taken on to
On this episode on Leukaemia Chatters, we spoke to Lisa Southall 10 years down the line from her diagnosis with Essential Thrombocythaemia. We talked to Lisa all about her period of diagnosis 10 years ago, the complications she faced through he
On this month's episode on Leukaemia Chatters, we spoke to Majella Murphy on the 4 year anniversary of her diagnosis with AML. As well as marking this personal anniversary for Majella, September is also Blood Cancer Awareness Month and as such
On this month's episode of Leukaemia Chatters as we lead up to the #SpotLeukaemia campaign we talked to Eilidh Ann Dewar, an APML patient diagnosed in 2018. We talked to Eilidh Ann about her rapidly accelerating symptoms, how she had to pursue
On this episode of Leukaemia Chatters, we spoke to AML patient Debbie Greenwood. We discuss the impact of her 2020 diagnosis on herself and her family, the support they have received since then and how Debbie is going on to provide help for pat
In this episode of Leukaemia Chatters we spoke to our new poet-in-residence Jamie Woods, an acute promyelocytic leukaemia (APL) patient. We spoke to Jamie about the power over poetry, how it's impacted his experience with leukaemia and what he
In this month's episode, we mark the ten-year anniversary of Peter's stem cell transplant he received from his donor David. We discussed Peter's initial diagnosis with MDS, the reality of the transplant process from both of their perspectives a
On this episode of Leukaemia Chatters, we chatted with chronic lymphocytic leukaemia (CLL) patient Helen Wood, who spent two years after diagnosis on Watch and Wait. As a part of this April's Left to #WatchWaitWorry campaign, Helen shares her e
In this month's Leukaemia Chatters podcast, we talk to Bailey about his childhood diagnosis of acute lymphoblastic leukaemia (ALL), his journey into acting, and the notable stops he's made along the way including Watford Square, and most recent
In this month's episode we talk about Kes' struggle to get a diagnosis, how she handled active monitoring/ Watch and Wait and the wider impact her stem cell transplant has had on her life.
This month we chatted to Naomi Roberts about being diagnosed 3 days before the first lockdown in March 2020, her experience with stem cell transplant and the impact on her time at university
In this month's edition of Leukaemia Chatters we spoke to Anthony Hyde about his chronic myeloid leukaemia (CML) diagnosis, which happened to be during the festive season, how he went on to write his own book following his CML experience and mo
In this month's edition of Leukaemia Chatters we spoke to Nick York, LC's very own Patient Advocacy Healthcare Liaison Officer and chronic lymphocytic leukaemia(CLL) patient. We talked to Nick about the methods he's used to protect himself as
On this month's episode of Leukaemia Chatters we spoke to Dharmesh Mehta, LC Trustee and CML patient. We chatted about how he came to be diagnosed, jumping out of a plane in the name of fundraising and the steps he took to get to grips with his
In this final podcast for blood cancer awareness month we spoke to acute lymphoblastic leukaemia (ALL)patient Bansri Dhokia. We chatted to Bansri about her experience getting diagnosed mid-pandemic, her treatment and stem cell transplant and he
STV News Reporter Laura Boyd was diagnosed with chronic myeloid leukaemia (CML) in September 2009. This #WorldCMLDay, Laura was kind enough to speak to our Patient Advocacy Manager Charlotte on our podcast Leukaemia Chatters! They talk about ho
We chatted to Wilfred Emmanuel-Jones MBE about his life, the turns of his career that have culminated in his "The Black Farmer" range, and his diagnosis and treatment of acute myeloid leukaemia (AML)
This month we chatted to acute promyelocytic leukaemia (APL) patient, Jamie Woods. We discussed how he came to be diagnosed, coming to terms with his survivor's guilt, and the impact his leukaemia experience has had on his life - in particular
Welcome to the June podcast of Leukaemia Chatters!This month we chatted with Carina Patterson, a hairy cell leukaemia (HCL) patient, about her symptoms, diagnosis and what she's got out of volunteering for Leukaemia Care's buddy scheme.
In our World AML Awareness Day podcast, Charlotte talks to Julie and Trudi, two acute myeloid leukaemia (AML) patients who both have a medical professional background. They discuss their shift in perspective from practitioner to patient, the e
This month's edition of Leukaemia Chatters we talk to patients, Sam and Nick about shielding being paused and their feelings on the situation. We discuss their concerns and hopes for the period moving forward, and how this change might affect t
In this episode, we talk to Tom Hunt and Sophie Wheldon about their experiences dealing with a leukaemia diagnosis as young adults. We talk about how they came to be diagnosed, how their experiences have influenced their studies of Medicine a
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