The Glow Edit by Maria

The Glow Edit by Maria

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14/09/2026

Life, Unedited

This week made me stop and think.

Last week, round 5 of chemo really knocked me for six.

I spent pretty much the whole week in bed, resting and taking it easy, which I found incredibly frustrating. I don’t like feeling unwell or feeling like I’m doing nothing. I’m much happier when I’m busy, so being forced to stop gave me far too much time to think.

Because I’ve spent the whole of chemo saying I’ve got through it relatively unscathed. But when I actually stopped, I realised I haven’t really thought about everything I’ve been through.

Each round meant around six hours in the chemo chair, then going home with a pump delivering more chemotherapy for another 48 hours. For two days I was literally tethered to it until it was disconnected.

There were medications, injections to help my bone marrow produce more white blood cells, and a couple of heart scares.

My hair has been shedding heavily every day. I’ve been incredibly lucky to keep it, but watching it get thinner and seeing all that hair coming away has been emotional. I started with a lot of hair and still have plenty, but it’s still hard to watch.

The neuropathy has been brutal. For about a week after each infusion, cold can cause intense nerve pain. Gloves to get things from the fridge. Wooden cutlery because metal hurts. No cold drinks because it feels like swallowing glass.

We even had to put covers permanently over the door handles because touching them can set it off.

There’s also been first bite syndrome, that horrible pain with the first bite of food, and mouth ulcers.

When I actually say it out loud, it sounds like quite a lot.

And yet, I’ve just carried on. I’ve adapted, found ways around things and got through the difficult days.

Maybe that’s why they call us warriors.

You don’t necessarily feel like one while you’re doing it. You’re just getting through the day in front of you.

Five rounds of intensive chemotherapy done.

And now I can finally stop and think, bloody hell… I actually did that.

First part of my cancer treatment complete.
Deep breath, sleeves up… onto the next.

10/09/2026

šŸ”” I rang the bell today. ā¤ļø

Five rounds of IV chemotherapy — DONE. 🄹

One big chapter finished, but the treatment isn’t over yet.

Next stop: chemo + radiotherapy.

One step at a time. ā¤ļø

Photos from The Glow Edit by Maria 's post 07/09/2026

Some weeks change everything ā¤ļø

Last week we had my oncology appointment to discuss the results of my latest scan. We were hoping for good news, but not daring to expect too much. Then my consultant said the words I’d been desperate to hear:

ā€œYour tumour has shrunk by 45%.ā€

45%. šŸ™ŒšŸ™Œ

After everything my body has been through, it was so good to know that it was actually working.

And because I’ve responded so well, I’ve been told I only need five rounds of chemotherapy rather than six. Tomorrow is my final round, then I move on to chemoradiotherapy.

But what I’ll never forget is Rich turning to me and saying, ā€œThis is the first time I’ve felt like I’m not going to lose you.ā€ 😢

One of the first things I did was call my sons. For once, I was able to give them some good news and, just for a little while, take some of the worry off their shoulders.

And as if that wasn’t enough for one week, I found out that my Maltese citizenship had been approved and I’m now officially a Maltese citizen. šŸ‡²šŸ‡¹

I’ve always been incredibly proud of my Maltese heritage, but being officially Maltese makes that connection even more special.

I was looking forward to reconnecting with my Maltese family and visiting my grandad’s old home, where I spent time as a child. I have so many lovely memories of Malta and family from when I was younger. Sadly, we had to cancel that trip, which makes this news feel even more special.

And to top it all off, we celebrated Rich’s birthday with a lovely Turkish meal. šŸŽ‚ It’s been such a long time since I’ve been able to enjoy something as simple as going out for a meal. Before chemotherapy, my symptoms had made even that difficult. Sitting there together, enjoying good food and celebrating his birthday felt really special.

For the first time in months, it felt like we could start planning our future again.

My journey isn’t over yet. There’s still chemoradiotherapy and surgery ahead. But this week has given me something I’d been missing, that feeling that there is a future to plan for.

Some news heals your body. Some news heals your heart. This week, I was lucky enough to receive both. ā¤ļø

31/08/2026

Life, Unedited: The Bit I Haven’t Shared

There’s something I haven’t really talked about in my cancer journey yet, and that’s my staging.

Before that appointment, I was convinced they were going to tell me I was going to die.

That sounds dramatic now, but honestly, that’s what I thought.

My thoughts went straight to Rich and my sons, and what I was going to tell the boys.

Greece. Our plans to retire.

My Maltese citizenship. Months of tracing hundreds of years of family history. I was so excited to finally be becoming a Maltese citizen.

In my head, all of it was gone.

And then there was my business. The hours, risks and hard work. I’d only just started getting busy.

And suddenly I was thinking:

What happens to all of this if I’m not here?

I’ve always been someone who puts her armour on when things get difficult. I put on the brave face and keep going.

But underneath it, I was terrified.

Then came the staging appointment.

There was one thing I needed to hear.

The ā€˜M’ Whether the cancer had spread to other organs.

I needed it to be zero.

M0.

And it was.

T3b N2 M0 V+.

Honestly, I barely heard anything else.

Rich and I almost high-fived each other walking out.

The doctor had to remind us it was serious. We hadn’t appreciated just how advanced the cancer was.

A few days later, the rest sank in.

Stage 3B. Locally advanced, with lymph nodes involved and venous invasion.

And then the treatment began.

I’m now three-quarters through the first part, chemotherapy. It’s been tough, but I’m getting through it and grateful for the days I feel well and feel like me.

My first progression scans are done, and this week I find out how the treatment is responding.

I didn’t realise how much this appointment had been sitting in my mind until the emotions caught up this weekend.

I remember how frightened I was waiting for those first scans.

This time I’m nervous, but I’m also feeling really positive about where I am.

I don’t know what I’ll hear, but I’m hopeful.šŸ¤ž

There’s still treatment ahead, but there’s also a future I’m still planning for.

And right now, that feels pretty bloody good. ā¤ļø

24/08/2026

Life, Unedited: Apparently I’m going to uni… and opening a bakery šŸ˜‚

After last week’s post about everything cancer has taken, this week feels like the complete opposite.

Somewhere amongst chemo, hospital appointments and everything that’s changed, normal life is still carrying on too.

And apparently normal life now involves me making a slightly ridiculous amount of bread.

So far I’ve made white bread, sundried tomato & olive bread and cinnamon & raisin loaves, and I’m getting far too pleased with myself every time one turns out properly.

My son has suggested that while The Glow Edit is on pause, I should launch The Loaf Edit instead. šŸž

Rich and I have also signed up for a part-time university course in Greek starting at the end of September. šŸ‡¬šŸ‡·

I did the same beginners course about 20 years ago and I’ve always loved languages, especially Greek, so for me it’ll be a refresher. Anyone who knows me well will also know I’ve attempted plenty of very confident, probably questionable Greek after a few drinks over the years. šŸ˜‚

For Rich, it’ll be the first time he’s learnt another language.

We’ll be going right back to the beginning — alphabet, greetings, numbers, food and drink, directions, conversation and the grammar bits I’ve probably forgotten.

Rich has already decided that with my head start and competitive streak, I’m going to be an absolute swat, desperate to get everything right and probably completely unbearable with it. He knows me far too well.

I’ve also told him there’ll be no slacking and he will be doing his homework.

His response? ā€œOK miss.ā€ 🤣

The last few months have been full of treatment dates, scans and bloods, so it feels nice having something normal to look forward to that has nothing to do with cancer.

Cancer may be taking up a huge part of my life at the moment, but it doesn’t get to take up all of it.

I want to remember the bread, the laughter, learning Greek with Rich, making plans and finding little things to enjoy too.

Although at this rate, by October I’ll be running The Loaf Edit from the kitchen while Rich is in the corner doing his Greek homework. 😜

17/08/2026

Life, Unedited | Cancer is a thief.

I read something last week that described cancer as a thief, and it stayed with me.

Because it doesn’t just steal your health.

One minute you’re living your ordinary life—making plans, booking holidays, working, worrying about things that now seem insignificant.

Then someone tells you that you have cancer.

Suddenly there’s a definite before and after.

Cancer steals the certainty you never realised you had. You assumed you’d be here next year, and the year after. There would be another summer, another holiday, another birthday.

Then you’re talking about tumours, lymph nodes, chemotherapy, radiotherapy, operations and stoma bags—things you never imagined you’d have to face.

It steals your relationship with your body too. Before cancer, an ache was an ache. Feeling tired meant you’d done too much. Now everything gets noticed.

Is that normal?
Is that the chemo?
Is that the cancer?
Should I be worried?

Your body stops feeling private. It’s scanned, prodded, needled and discussed by more strangers than you’d care to remember.

Your diary gets stolen too. Instead of clients, dinners and holidays, it’s blood tests, chemo days, scans and hospital visits.

And perhaps the strangest thing it steals is the ability to have a bad day without feeling you should be handling all this brilliantly.

People tell me how positive I am. And I am. I believe I’m going to get through this.

But being positive doesn’t mean I’m not frightened.

I still lie awake wondering whether the treatment is working. I still desperately want my old life back. And I don’t always feel brave.

Most of the time, I’m simply doing the next thing because there’s no other option.

But cancer hasn’t taken everything.

I laugh. I make plans and look at holidays I want to take. I think about my business. I still have ordinary days where I almost forget I’m ill.

And maybe that’s the bit I’m learning.

Cancer barged into my life without an invitation and took far more than I was willing to give it.

But it doesn’t get to have all of me.

And I’m certainly not handing over my future without a fight.

10/08/2026

Life, Unedited — The people carrying me through it…

Something I’ve realised over the last week is just how much all of this affects the people around me too.

Obviously I’m the one with cancer. I’m the one having the chemo, going through the side effects and wondering what the next few months are going to look like.

But I’m definitely not the only one living it.

I see it most with Rich.

His day-to-day life has changed so much too. He still gets up and goes to work every day, but he also cooks every day, cleans, does the shopping, walks Barney, comes to appointments and generally keeps our life ticking over when I can’t.

And apparently he now has to deal with my random food cravings too. šŸ˜‚

Last week I suddenly really fancied homemade bread-and-butter pudding.

Now, Rich has never baked anything in his life, but that didn’t seem to bother him. He decided he was making me one.

The district nurse happened to be here flushing my PICC line when he popped his head in and said:

ā€œTotally unrelated… what’s caster sugar?ā€

She explained what it was and told him that if we didn’t have any, he could try blending normal sugar.

Next thing I know, my district nurse has gone from flushing my PICC line to standing over Rich in the kitchen watching him trying to make caster sugar in the blender. šŸ˜‚

It really made me laugh, but actually that probably sums Rich up better than anything.

Whatever I need, he just gets on with it.

And I know it can’t be easy for him either. I can talk about how I’m feeling because everyone asks me. He’s the one watching the person he loves go through it, while still trying to hold everything else together.

It’s not just Rich either.

I’ve seen the effect this has had on all of my family.

One of my sons has decided to volunteer as a Macmillan Buddy so he can support someone else going through cancer. I can’t really put into words how proud that makes me. Something horrible has come into our lives and he’s decided to take something from it and use it to help somebody else.

My sons and daughter-in-law are always checking in, asking how I am and making sure I know they’re there.

And then there’s my teenage grandson.

Before cancer, getting a hug or kiss out of him could result in a full Perry and Kevin performance. šŸ˜‚

Now I get proper hugs and kisses, and even little text messages checking how I’m doing.

I’m making the most of that one because I fully expect normal teenage service to resume at some point. šŸ˜‚

I think one of the biggest things all of this has made me realise is just how lucky I am.

I’ve said to Rich a few times that I honestly don’t know how people go through this on their own.

There are days when I’m tired, scared, fed up or just don’t feel like myself, and there is always somebody there.

And I don’t take that for granted.

I’ve always believed you find out who your people are when life gets difficult.

The last few weeks have proved that to me over and over again.

I might be the one having the treatment, but there are a whole load of people going through this with me.

And I hope they all know just how much I love and appreciate them. šŸ¤

03/08/2026

Life, Unedited — Just when I thought I understood it…

One thing nobody really prepares you for is that cancer treatment isn’t always a fixed plan.

I still haven’t fully got my head around everything ahead of me, but I know I’m in for a long treatment plan. Three months of intensive chemotherapy, followed by 25 sessions of chemoradiotherapy and then surgery.

That’s the plan I’m trying to prepare myself for.

Then, after my very first round of chemo, it felt like that plan might already be changing.

When my pump was removed, I mentioned I’d been getting a burning pain in my chest. I honestly thought it was probably something simple… maybe heartburn, even though I’ve never actually had heartburn. I think I just wanted it to be something simple.

Things moved quickly from there. A doctor was called and I was sent to the assessment unit for four ECGs and blood tests. Thankfully, everything came back clear, so I went home hoping it had just been one of those strange things that would never happen again.

A few days later, I was back at clinic expecting to talk about my next round of chemo.

That conversation took a very different turn.

My oncologist told me they were thinking about changing my chemotherapy because one of the drugs can sometimes affect the heart, and after the chest pain they didn’t want to ignore that risk.

I’ll be honest… I don’t think I heard much after that.

My brain had already gone somewhere else.

ā€œHang on… you’re taking one of my chemo drugs away?ā€

ā€œDoes that mean I’ve got less chance of beating this?ā€

That was the only thing going through my head.

I’d started on an intensive three-drug treatment because the aim is to hit the cancer as hard as possible and give me the best chance of beating it. But my team also has to balance that with what my body can safely cope with. If one of those drugs is affecting my heart, carrying on regardless simply isn’t the right thing to do.

We talked everything through and agreed I could try the same treatment one more time, but with a very clear backup plan if the chest pain returned.

So I went into round two hoping the first time had just been bad luck.

Unfortunately, it wasn’t.

On pump removal day, the same burning pain came back.

Another call to the helpline.

Another trip back to hospital.

More ECGs. More blood tests.

One of the doctors told me they were satisfied I hadn’t had a heart attack. I have to admit, hearing those words stopped me in my tracks because I hadn’t realised that was one of the things they’d been checking for.

So now, although nothing will be confirmed until I see my oncologist on Friday, I’m preparing myself for the fact that the backup plan will probably become the plan.

Weirdly, I don’t think it’s the new drugs I’m struggling with now, It’s the fact I’d only just started understanding the first ones. I was beginning to learn the pattern… which days were hardest, which side effects belonged to which drugs and what helped me get through them.

Now it feels like I’m back at the beginning again.

This week has reminded me that treating cancer isn’t just about giving me the strongest treatment possible. It’s about finding the strongest treatment my body can safely cope with.

Some weeks it’s easier to stay positive than others, and this has definitely been one of the harder ones.

But I’m trying to remind myself that a change of plan doesn’t mean a change of goal. I’m still moving towards the same outcome, even if the plan to get there now looks a little different.

So for now, I’m waiting for Friday, trying not to get too far ahead of myself and taking it one step at a time. šŸ¤

27/07/2026

Life, Unedited — Things to look forward to

Over the past week, I’ve been trying to focus more on the things waiting for me on the other side of all this.

I’ve also started matching my PICC line covers to my outfits, because apparently one was never going to be enough. šŸ˜‚

Looking through our holiday photos made both me and Rich far more emotional than we expected. We’ve been so lucky to have had some amazing holidays and experiences, and it really brought home how much life has changed in such a short space of time.

We’ve also had to cancel both of the holidays we had planned for this summer, which has been hard. But looking back through those photos reminded us how much we still have to look forward to.

Not being able to plan anything properly is difficult because I’m usually happiest when I’ve got a holiday to research within an inch of its life. šŸ˜‚ So we’ve started talking about our big ā€œI beat cancerā€ trip instead. We have no idea where it will be yet, but the thought of booking something completely ridiculous and wonderful is helping us both.

I’m also thinking about picking my Greek back up. If I’m going to spend this much time at home, I should probably come out of it able to say more than hello, thank you and where’s the wine. šŸ‡¬šŸ‡·šŸ˜‚

And it’s not only the bigger things helping. The check-ins from my sons, daughter-in-law, friends, clients and everyone who has taken the time to message have meant so much too. Even a simple ā€œHow are you today?ā€ can make a real difference, especially on the quieter days.

There have also been some really lovely moments with people I don’t even know.

A lady commented on my last post to say she was having her first chemotherapy that week. Afterwards, she came back and told me my photo had been in her head while she was there. I still can’t quite believe something I posted helped somebody else feel a little less frightened.

Then, during my own first treatment, another lady who had already been having chemotherapy for over a year saw how scared I was. Her husband came over and handed me a bracelet with the words

ā€œDon’t let the hard days win.ā€

And yes, of course I cried.

My second round is tomorrow. I’d be lying if I said I wasn’t nervous, but getting through the first one has made the next one feel slightly less unknown.

So for now, I’m holding onto the holiday plans, the Greek lessons, the kindness of strangers, the messages from my family and friends, and the thought that every round gets me closer to that ridiculous blowout trip.

Round two tomorrow. Let’s do this. šŸ¤

20/07/2026

Life, Unedited — One round down

Last Monday, I shared the news that I’d been diagnosed with cancer and that The Glow Edit would be taking a pause while I started chemotherapy.

The weeks leading up to it had been a blur of MRIs, CT scans, blood tests, doctors’ appointments and meetings with my oncologist. Everything felt surreal, almost as though it was all happening to someone else.

Then the day of my first chemotherapy arrived, and suddenly it didn’t feel surreal anymore.

Before I even sat in the chair, I burst into tears. I felt completely overwhelmed by it all. The whole situation felt so alien to me because I’m normally the one who keeps going, sorts things out and just gets on with it.

My husband kept telling me, ā€œYou can do this. You’re going to get through it.ā€ He has been amazing through every part of this, and somehow I managed to pull myself together, sit in that chair and begin.

Although I did find myself wondering whether they’d think I was high maintenance if I asked to bring my new fully electric olive-green treatment bed in for the next round. šŸ˜‚

Now, one week later, my first round is done.

And honestly, it wasn’t as awful as I had built it up to be in my head. I know the effects can build as treatment goes on and that every round could be different, so I’m not getting ahead of myself. But for now, I’m grateful that this first one has been more manageable than I feared.

I’m also very aware that although I’m the one going through this physically, Rich and the rest of my family are going through it emotionally too. Cancer doesn’t just affect the person having the treatment. It affects everyone who loves them.

The messages, cards, gifts and kindness I’ve received have meant more than I can say. I haven’t managed to reply to everyone yet, but I have read every message, and knowing how many people are behind me has genuinely helped.

I’m taking the wins where I can, and getting through that first round feels like a pretty big one.

One round down. One step closer. šŸ¤

P.S. Cancer or no cancer, I’m still going to remind you all to wear your SPF in this heat ā˜€ļøšŸ˜‚

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