Tag: stoma
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It’s Not A Competition And We Can Wear White!
This is something I wrote yesterday on my Facebook page after seeing this post and the responses. I’m not sure whether this post was written in a celebratory manner or not but there were lots of derogatory comments about Sam Faiers and ‘how ill’ she is. Now I don’t agree with all she has said…
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The Spoonie Mummy Reviews – Phew!
Hello lovelies! I hope you are all having a good start to the week, I didn’t sleep very well but pushing through and getting some jobs done. So pleased to see the sunshine and it’s set to be a lovely weather week! I was added on Twitter by Phew! a couple of weeks ago. Take…
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The Spoonie Mummy Reviews – Stoma Style
Since the weather has started improving I’ve had some issues with underneath my stoma bag getting sweaty, especially when I wear high waisted trousers. This makes me uncomfortable and even though it’s not smelly it is unpleasant to feel ‘damp’ underneath my bag and I worry it could cause issues with the bag sticking to…
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The Spoonie Mummy Reviews – Bullen Healthcare Delivery Company
So I wrote this post over a week ago and then didn’t save it properly – doh! So here we go again! Today my recommendation is for my stoma supplies delivery company – Bullen Healthcare. I previously used another company which was the one I was ‘given’ by my stoma nurse when I left hospital. …
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Stoma Mail
When I had first had my operation one of the most amazing things was the support I received from people in the IBD and Ostomy communities. From the visit from wonderful Lauren from Purple Wings, to mailed gifts from far and wide to so many messages from people checking up on me – it all…
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My Stoma Bag Changing Routine
Tonight I thought I would share my stoma bag changing routine with you! I change my bag every evening after my shower. Some people choose to leave their bag on longer and change once every 3 to 4 days. It’s personal preference and what you skin can cope with as this varies from person to…
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Not Every Disability Is Visible
There has been a big push for these signs to be displayed on all disabled toilets recently but it sadly appears not everywhere has caught up and awareness, even amongst the disabled community is lacking. People with Crohns and Ulcerative Colitis often need to make multiple bathroom trips a day. They suffer severe diarrhoea episodes…
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Well This Wasn’t Part Of The Plan!
One minute you think you just need a day of rest…The next you are being admitted 🙈 Tonight I’m spending the night in hospital on IV steroids, fluids, pain meds and anti sickness awaiting gastro and rheumatology doctors to come sort me out on a proper medication regime in the morning to get this flare…
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The Spoonie Mummy 