Skip to main content

Stoma jumble sale

Not having a Stoma anymore means that I have lots of medical products at home that I no longer require. (It still sounds very strange to be able to say that I don't have a Stoma- not sure how long it will take to get used to it!)

I wasn't really sure what I was going to do with all but thought I would worry about that in the coming weeks. 

Anyway, I was chatting to the lady in the bed next to me who was saying that her Stoma supply company didn't supply very good wipes (for cleaning the Stoma site when changing the bag). She liked the ones that I had so I told her I had a lot at home. 

I said that I could get my parents to bring all my supplies in and she could rummage through the bag 

And that's exactly what she did. 


My parents thought it was hilarious how excited she got about a new product shed never used and how animatedly we talked about all the item. Mum said it was like a Stoma jumble sale!

And the good news is that the Stoma nurse has taken the items she didn't use or want. She will send them to a charity that dispatch them to third world countries where some people have to resort to using crisp packets as Stoma bags because they can't afford to buy the proper stuff. 

So everyone's a winner- happy days. 

NB x

Comments

Popular posts from this blog

The spoon theory

Have you heard of 'The Spoon Theory'? No? Neither had I before I got ill. Why would I have? I didn't spend my time trawling through the internet in search of lotions and potions and pills that might just make me feel a little bit better,  because I was well. I was out living life and having fun.  Don't get me wrong. I'm not saying that I don't have fun any more. I just have less of it, with fewer people and without the aid of alcohol!  The spoon theory was written by Christine Miserandino and she asks that when you reference the theory you add a link to her website, so here it is:  http://www.butyoudontlooksick.com/articles/written-by-christine/the-spoon-theory/ I  saw this tonight on Facebook and thought was a brilliant visual to help you understand the 'theory' (and my life) a bit better.  That really is what it's like having a chronic illness. But the trouble is you never know how many spoons you have when you wake up. My  body likes to play trick...

Home today?

The antibiotics have finished now and last night my Hickman line was used for the first time. So far it seems to be working fine and if the doctors are happy with it when they do the rounds later this morning I will be able to go home. Today! Yay! Of course I'm excited to perhaps be going home but I'm also relieved as my poor veins have just about had it. I never really have any decent veins in my hands and arms and the few that can be used have been well and truely pricked to death. It's got so bad that I'm now having cannulas put in my feet. And yes, it did hurt.  Hopefully later I will be packing my bag and going home to Hubby and the kids.Unfortunately everyone is at work today so if, no, when I get discharged later I will have to make my own way home. Nottingham has a really good transport system, including a tram stop at the hospital but I don't think I'm up to using public transport today. I'm going to splash out on a cab that will take me door to doo...

Swimming fail

I was discharged from hospital on Friday afternoon and within a few hours of being home I was out taking Big Girl to her netball training session. I didn’t feel great but Hubby had a load of work to do so I thought if I did the netball run it would take the pressure off him. Usually after dropping Big Girl off I go to my sisters house as she only lives 5 minutes from where netball training takes place but this week both her and her husband were out so I resorted to wandering the local retail park. I was hopeful that I would be able to get some Christmas presents as I haven’t bought a single thing yet but I just couldn’t get into the mood for shopping. I think being tired and in pain didn’t really help so in the end I went back to the car and sat and watched Netflix.  Driving home that evening the pain got worse and by the time we arrived home I was in agony. I crawled up the stairs and into bed hugging the sick bowl. Part of me was wondering if I would end up having to go back into...