Learn with Comfizz
Stoma Tips

January 20th is #GetToKnowYourCustomersDay. As a long-standing Comfizz customer myself, I’m sure you have read by now how much I love Comfizz products. In this post, I wanted to talk to other Comfizz customers, get to know a bit about them & what their favourite Comfizz product is & why. Thank you to those of you who reached out to me over on Instagram to get involved in this blog post.

I wanted to start the year off by sharing a few of my 2021 outfits with you & tips on stoma fashion. You can view many more outfits, as well as mind & body tips and so much more over on my Instagram. 

Because Comfizz supportwear come in different levels, there is a product level perfect for varying levels of activity. I wear level 1(light support) as you can find here most days under my outfits. This gives me that added peace of mind that my abdomen is more supported as I go about my day to day life.

Hi lovelies! It's Amy here, or as some of you may know me, ibdwarriorprincess on Instagram.  I hope you all enjoyed Halloween (if you celebrate). I decked our house out with some decorations, we had a pumpkin carving night & really enjoyed it!  Now the weather is getting colder, it can be handy to be aware of the ways that it can affect having an ileostomy, especially when it comes to your equipment and skin etc for your bag to adhere to. Before I get started, I'd like to just remind you that this isn't medical advice. This post is drawn from my own experiences of living with an ileostomy & my own research.  Warm output I'll start with this...

October was a very special time for me as I entered my first 10K race in Cardiff, South Wales. Whatever possessed me to do it you ask? How many of you who are reading this with a chronic illness have found they can’t be as active as they once were? For me it was like a light switch was flicked and I couldn’t do anything without being in pain anymore. Its debilitating, demoralising and can lead you down a dark path mentally with the mental health benefits you loose over night. My health journey has been quite the fair ground ride. Born with Hirschsprungs Disease, multiple surgeries, 3 stomas and having a child which has the same yet more severely,...

I’m back again guys following a lovely holiday with my family! We have always stayed in the UK since we had our baby ostomate now 5 years old, so current circumstances haven’t made any difference to us choosing to visit the beautiful Exmouth in Devon. Despite a few wet days at the start, parts of the UK entered a heatwave with temperatures entering late 20s/early 30s. This was my first holiday as an ostomate, but going on staycations for five years with my little one Jake meant you would think there wouldn’t be many surprises. I felt pretty organised with the only difference being myself to care for during bag leaks, hoping that Jakes stoma didn’t feel left out and...

I started blogging about having a little one with a stoma in 2016. I used Instagram as a platform to share my story in the hope of helping in the way many had for me by sharing the highs and the lows of having a baby with Hirschsprungs Disease. The bowel disease which affects 1 in 5000 babies a year in the UK, is caused by the nerve cells in the intestines needed to move stool along into the rectum for toileting (known as ganglion cells) not being present. This causes the body unable to remove its own waste, with the tummy starting to distend and very little to no poo being passed. Surgery is essential with bowel washouts required...

Men's Health Week has nearly come to an end (14th - 20th June). Obviously from my blog posts here with Comfizz, you read a lot about how life is for me as a female with IBD and a stoma. It's widely known that women often seem to be a lot more forthcoming in talking our their struggles & experiences in general, let alone with something so personal, so it's been really nice to hear from Neil, Andy, Lee, Sean & Keith about their experiences. Thank you so much guys for being so open & sharing your stories & tips.