In a brand new Sky Sports activities Information documentary, Jo Wilson opens up on her most cancers journey in ‘Soccer, Most cancers and Me’.
The presenter was identified with stage three cervical most cancers in 2022, shortly after the beginning of her daughter, Mabel. She has now been cancer-free for the final two-and-a-half years.
Jo is joined by 4 soccer figures who’ve additionally been affected by the sickness. They focus on their very own experiences with most cancers when the documentary airs on Sky Sports activities Information on Wednesday at 4pm.
She chats with David Brooks and Henri Lansbury, who have been each identified whereas taking part in, Tony Mowbray whereas supervisor at Birmingham and Sky Sports activities reporter Emma Saunders. Jo additionally meets St Johnstone proprietor, Adam Webb.
In her personal phrases, Jo takes us by her journey with most cancers, the way it affected her life and household, and why there may be hope for anybody going by the identical expertise…
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It was on the thirty first of July 2022 once I was informed I had most cancers.
It hit me like a truck. I did surprise if I’ll die. I would ready myself for the worst – I believe you must.
I truly did not inform anybody. It was onerous as a result of I did not need to put it on anybody. I nearly assume if I might’ve executed it with out telling anybody, that will’ve been higher as a result of I simply did not need anybody to fret about me.
If one individual can see this and make a telephone name with a physician due to one thing they really feel is not proper, then it is price speaking about.
So many individuals are affected by most cancers whether or not instantly or not directly and if having these conversations, placing it on the market so folks do not feel alone, and that there’s life after most cancers.
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I knew one thing wasn’t proper so I went to get checked out. I completely thought I would be informed ‘oh it is a bit of a hangover from giving beginning’, however I used to be informed that day that it regarded like I might have most cancers.
It is not one thing you ever count on to listen to and your life modifications immediately.
However the weirdest factor was how nothing modifications for just a few weeks as a result of you’ve got that time frame the place you are going for additional checks and scans. They should know what sort of most cancers it’s and give you a remedy plan.
There have been a few weeks the place I used to be residing my life as regular. I went to a wine pageant in Cheltenham that weekend and I used to be wanting round at everybody having a very good time considering ‘I’ve received most cancers’.
It is mad how life simply carries on, however on the identical time, your entire life has modified and is about to vary.
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My remedy plan was 5 weeks of radiotherapy every single day, Monday to Friday. 5 weeks of chemotherapy as soon as every week, each Wednesday, then three days of brachytherapy, which is kind of an intrusive type of inner radiotherapy.
I did not inform anybody about my analysis till I had that remedy plan as a result of I needed to have the ability to telephone my mum and inform her ‘that is occurring, however that is the plan and that is how we’ll get by this’.
It was onerous as a result of I did not need to put that on anybody. I nearly felt like ‘I can deal with this’, however I did not need anybody else to fret and stress about me.
I knew my mum and pa can be actually upset and they’d really feel fairly helpless as a result of there’s actually nothing they may do to assist me in that second.
As a mum myself, you’d do something to your youngsters and you do not need them to have any struggling. I knew how onerous they’d discover it.
Chemotherapy days have been the toughest. I keep in mind the nurse speaking me by it and I stated ‘how is that this going to make me really feel?’ and he or she stated ‘everybody reacts otherwise so there is no method of figuring out’.
Not figuring out I discovered fairly troublesome to cope with since you’re it going ‘OK, this liquid goes into me, I do not know the way it’ll make me really feel, I do not know the way my physique goes to react’, however on the identical time, it is the factor that is hopefully going to make me higher.
There have been moments the place I used to be on the ground crying, being like ‘I can’t do that, I can’t go to my remedy’.
The final a part of my remedy was brutal. It was three days in hospital, I received put to sleep and had 14 metallic rods inserted inside me, then for these three days, I needed to lie flat on a hospital mattress. I could not eat, I could not transfer.
I additionally wasn’t allowed to see Mabel as a result of she’d need to cuddle and climb on me and I did not need her to see me like that anyway.
Nevertheless it was the primary time I would been other than her since I would given beginning. That was in all probability the darkest time, mendacity in that hospital mattress.
I say she received me by my remedy and it was solely three days, but it surely was the primary three days I would spent other than her.
After I was first identified, Mabel was 18 months previous. She grew to become my focus and why I received up every single day regardless of the illness and exhaustion.
With the ability to slip again into mum mode saved me going as a result of even on my darkest days, she was my motive for every thing. With out figuring out it, Mabel was my rock.
I did say my first query was ‘am I going to die’ and that wasn’t about me. I got here to phrases with demise and that it may very well be the truth for me, however what I wasn’t OK with was the prospect of leaving her with out a mum.
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When the remedy stops, it is onerous since you’re all of a sudden simply left there to cope with what’s occurred.
You’re feeling just like the assist has been taken away a bit bit since you’re not entering into for remedy and that restoration is difficult since you nonetheless really feel ailing. I used to be nonetheless very drained and making an attempt to cope with the psychological results as nicely.
Issues like scans in a short time develop into a giant a part of your life, as does the nervousness of the illness probably coming again.
I discover some folks assume ‘you’ve got had most cancers, you’ve got had the remedy, now you are higher’, but it surely would not work like that. I in all probability give it some thought each single day in some kind.
I awakened with a extremely sore again some time in the past and with the kind of most cancers I had, one of many largest signs for a recurrence is a sore again, and I assumed ‘it is again’.
It is fairly a tough factor to get your head round that you simply now want to attend and hope that it is labored.
I nonetheless did not need to see folks as a result of I would misplaced a number of weight and I felt like I did not look wholesome. I additionally did not know if it had labored or not and I wasn’t able to have these conversations with folks.
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Being informed I used to be cancer-free felt unimaginable. You possibly can’t even describe the sensation while you hear these phrases, that the remedy has labored, as a result of it is all you’ve got hoped and wished for.
It’s the hardest factor that I’ve ever needed to cope with, however I’ve received by it and I am cancer-free, I am alive and life is sweet.
It is so horrendous that you simply assume you need to be celebrating getting the all-clear, but it surely’s maybe not as a result of it is a horrible factor to have gone by.
I am now two and a half years cancer-free, however I do not know in the event you ever actually are as a result of it is nonetheless one thing I take into consideration every single day. As the times go on, you concentrate on it much less and fewer, but it surely’s nonetheless one thing I take into consideration.
I’m residing with negative effects as nicely. I am 40 years previous, but it surely’s aged me. I used to be plunged into early menopause, I am infertile so I used to be informed my remedy would imply I could not have any extra youngsters.
Even psychologically, it is troublesome. I do not assume it is one thing that ever leaves you.
I felt so joyful for Mabel. You nearly begin to image your little lady’s life and I keep in mind having ideas about not seeing her begin college.
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I’ve at all times been sporty in order that aggressive spirit comes out in something I do. That helped me so much once I was going by my remedy by way of with the ability to cope with it and that resilience as nicely, it performs an element in taking part in sport my entire life.
Then the broader soccer household, being concerned in sports activities media, the assist that I received from there meant completely every thing to me.
The outpouring of assist I received from the footballing and sporting world, folks I’ve by no means met or spoken to… once I got here again to work, I posted on social media and the quantity of messages from individuals who have been genuinely so joyful and happy to see me come out of the opposite aspect.
Life is sweet, life is joyful. Life is about having fun with the little moments, spending time with folks you like and doing issues that make you cheerful.
It modifications you completely. You possibly can’t undergo one thing like this and never be modified. It places every thing into perspective. None of us know the way for much longer we have got on this earth so it is about having fun with every single day.
You may get by it. Individuals will assist you to get by it and there may be life after most cancers.
When you or somebody has been affected by most cancers, you are not alone. For assist and data, please go to: cancerresearchuk.org or macmillan.org.uk. You can even communicate to your GP or name the Macmillan Help Line on 0808 808 00 00.
Watch ‘Soccer, Most cancers and Me’ with Jo Wilson on Sky Sports activities Information at 4pm on Wednesday. The documentary can even be out there On Demand.

