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After his heart failure diagnosis, Barry Newman from East Ardsley near Wakefield was told he had to start planning his funeral, until one call changed everything. Barry came across an interview featuring a groundbreaking stem cell procedure funded by the Heart Cells Foundation which supports pioneering research and clinical trials where a patient’s own stem cells regenerate their damaged heart. After being deemed a suitable candidate, Barry embarked on a transformative journey - here's his story.

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00:00My name's Barry Newman, formerly known as Barry Newman, now I'm stem cell baz.
00:05That'll come later. In 2014, through no fault of my own, I got a virus, got a heart condition,
00:13dilated cardiopathy. After an MRI scan my heart was working at 13% and it was slightly larger than
00:20it's supposed to be. For a guy that doesn't drink, doesn't smoke, likes to keep fit, always strong
00:24as an ox, daft as a brush, it's not looking good at all. For a few years on, the medication
00:29just
00:29weren't working, I couldn't tolerate a lot of tablets, my blood pressure kept falling through the floor.
00:34Initially I'd been told I was looking at a heart transplant and it's like, this can't be true.
00:39Me and my partner sat watching TV, watching The One Show and there's this article about
00:43Heart Cells Foundation that work with Barts Hospital in London and they have this unbelievable treatment
00:51where they take your stem cells, they'll nick them out your bone marrow in your hip, jiggle them,
00:56the jiggling bits the clever bit clearly, going through your wrist, put the stem cells into your heart.
01:01It's an amazing procedure which I am now absolutely committed to help them get it onto the NHS,
01:07which it needs to be there for everyone that needs it. So Heart Cells Foundation have been going now for
01:1220 years, trying to get this fantastic modern day miracle onto the NHS. They're now at the stage where they're
01:20at
01:20phase three, which is they have to go through phase three to prove to the NHS that this is a
01:27viable thing
01:27in every way, shape and form. So there we are now, obviously pushing for awareness, that's what I'm
01:34doing every day is I speak to patients every day that need it. I speak to people about the fundraising,
01:40I speak to people about awareness, but the phase three bit is the critical bit now where
01:44this is the final push to get it exactly where it needs to be for everyone that needs it. It's
01:50available.
01:51In this time from getting diagnosed before the stem cells, my choice of clothing were my pyjamas and
01:58my best friend in my bed. And it's like, wow, how can this go from being that bad to being
02:04this good
02:05with such a simple procedure? My son Robert, obviously being part of the entire journey from day one with
02:11me being ill. Rob's actually taking on the challenge of the London Marathon to raise funds for Heart
02:19Cells Foundation, which is fabulous and fantastic. And a lad called Josh, my lad's called Robert Newman,
02:25Josh's dad, he saw me on TV with another patient that had it done. He had it done last summer
02:30and he's on the mend.
02:31So it's a life-saving, life-changing thing. And it isn't just the patient, it's the families. The families
02:39get their family member back and they stop worrying about the family member that's going to die or they've
02:45got this horrendous thing that's going on that they don't know what's happening. That's gone. No one
02:49worries about Bazdemore because he's nutted a fruitcake and doing all sorts of strange things that he
02:54shouldn't be doing. This is my 60th year in life and it's like, you're not stopping me.
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