Skip to main content

Cath-dry dressing trial

I ordered some CathDry dressings at the start of the year with the plan to start going swimming again but my recent hospital stay meant that I never actually got round to using them. I’ve been packing stuff for my holiday and when I was sorting through all the medical stuff I need to take I came across them. The house we are staying in for the first week has its own pool and last year I had to sit on the side watching everyone else having fun in the water. So I decided to pack the CathDry dressings incase I decide I want to go in. 

But because I’ve never actually used one before I thought it would be a good idea to have a trial run at home. So this morning I put one on and jumped in the shower. I was still hooked up to my feed so had to feed the giving set wire back out of the dressing so I wasn’t expecting it to be watertight… but it was! I was only in the shower for 10 minutes but when I got out my Hickman line was completely dry! 


(Yes, I’m aware it looks like a condom for my line 🤣🤣)

One thing I like about these dressings is that they have a moisture detector. So if water gets past the adhesive the ring changes colour from white to red. This makes sure you know when you need to get out of the water before your line gets wet and potentially bugs get in. 

I’m not sure if I will go in the pool or the sea while I’m away but the thing is that this year is the first year in 8 years that I actually have a choice. One of the worst things about this illness is that it takes away your choices and often dictates what your able to do (or not do). So to be given the choice back is empowering. I just want to say thank you to Kim at FEAR (Face Everything And Rise) because it was through her website that I learnt about CathDry dressings. Watching her use them gave me the encouragement to order some and hopefully I will get back into the water soon. If anyone is thinking about trying them you can get a free sample through the website and then they’re available on NHS prescription. 


Comments

Popular posts from this blog

New car smell

After everything that’s happened over the last 5 weeks not many days have been good days but today was. I will write a blog post about everything that happened but that’s for another day!  Today I went to pick up my new motability car and got to breathe in that new car smell. I am now the proud lease holder of this lovely Volvo XC40.  To be honest, part of me wasn’t sure whether to write a blog post about getting the new car with everything that’s been going on with the disability benefit reforms. There’s been so much written about motability cars on social media but a lot of it is misinformation and hate and that made me nervous to write this post. But I figured that most people reading it are friends and family and understand my need for the car. But for those that don’t let me explain a bit about how the motability scheme works.  I am lucky enough (or unlucky enough depending on how you look at it) to claim PIP- personal independence payment. This benefit is designed t...

The germs have got me 🦠

Being on azathioprine, influximab and prednisone is helping to control this recent Crohns flare up. But unfortunately they work by wiping out my immune system making me more susceptible to all the bugs doing the rounds. I refuse to stay at home and be held hostage by these meds though- for me they are there to give me my life back, not to make me a prisoner in my own house, so the inevitable has happened and I’ve got a cold.  ‘It’s only a cold’ you might think, but with no immune system to fight it off this cold has made me pretty poorly. Yesterday I couldn’t get out of bed and felt so, so ill. I was coughing and struggling to breathe so I’m pretty sure I’ve got a chest infection too. But I can’t confirm that because apparently even being immunocompromised with a suspected chest infection is not enough to see a GP these days!  I spoke to the receptionist at the GP surgery this morning who told me that all the urgent appointments for today were gone (and this was at 8.25am, aft...

Disability benefits cuts

So in Rachel Reeves spring statement earlier this week it was confirmed that there will be massive changes to the benefits system including the way that PIP is assessed and changes to the health element of Universal credit.  As someone who is receipt of both PIP and ESA disability benefits I find this whole situation…  🔲 terrifying  🔲 baffling  🔲 rage inducing  🔲 disgusting  🔲 [all of the above] I honestly cannot believe that a LABOUR government is looking to balance the books of the country by taking money from some of the poorest and most vulnerable in our society. This is the sort of thing I would have expected the Tories to do but when I voted Labour I honestly thought that not only would they look after and protect the neediest but they would actually make things in our society better and fairer. How wrong I was. Looks like I’m going to have to get some ‘Fuck Labour’ merch to go along with my ‘Fuck the Tories’ stuff I already own!  Now I do b...