Langsung ke konten utama

N:Rem sleep mattress topper tablet system- sponsored post

I have been given this product as part of a product review through the Chronic Illness Bloggers (http://chronicillnessbloggers.com/chronic-illness-bloggers/) network. Although the product was a gift, all opinions in this review remain my own and I was in no way influenced by the company.

When I got the email through offering me the opportunity to receive the N:Rem sleep system comfort changing mattress topper (https://nremsleepsystem.co.uk/topper/to review, I was intrigued. It's an interesting product and concept, and not one I'd come across previously.

It's a mattress topper but comes in pieces/tablets with differing levels of softness, so you can put these together in an order that suits you. Each piece is made of reflex foam of varying densities. You get 2 super soft, 1 soft, 1 medium, and 1 firm (easily identified by their colour), which together will cover the length of the bed. The idea is that you can use the softer ones for painful areas, and firmer ones for areas needing greater support. You can re-order them whenever you need to (if a different area becomes particularly painful), and if you share your bed, a partner can have their own set on their side of the bed, with an order that suits them and their body. It gives you options and flexibility. With chronic pain, things change, and it can be a case of trial and error to find what works for you, so this flexibility appealed.

I get a lot of hip and rib pain in particular, so this was an idea that really appealed to me. The thought that I might be able to reduce pressure on body parts that are particularly painful was enticing. Anyone who deals with chronic pain will know that getting comfortable in bed is a huge struggle. Painsomnia (inability to sleep due to pain) is a problem many of us face on a regular basis. My hopes were therefore high, although, having lived with pain for many years, I knew I also needed to remain realistic.

When I opened the box, the smell of foam was quite strong (as you'd expect), so I left them to air for a while before use. This did go after a few days.

You place the different density tablets on top of your existing mattress. For those of you who are fellow wheelchair users, it's worth considering the fact that this obviously raises the height of the bed, so could affect transfers- it's 12cm deep, so not a huge change, but enough to notice- this could obviously be a help or a hindrance, depending on individual situation, just felt it was worth noting.

My mum put them on my bed, with a single fitted sheet around them- this did tend to make them buckle and pop up to begin with, but once she'd managed to get them flat, they did stay flat, and they've not moved at all since then. It's worth considering the fact that the extra height may cause issues with your usual bedding due to the added depth, but there are ways around it. I believe when you actually buy the product, you get a cover to place the foam tablets within too.

My bed was comfortable before, but I can certainly feel the difference. It's much squidgier (for want of a better word!). I have them ordered (from head to toe): firm, super soft, super soft, medium, soft. I get a lot of horrendous pain in my hips and ribs in particular, and this order has suited me really well. I haven't tried other orders (yet), because I haven't felt the need.



I have been feeling more comfortable, and although I do still sit up with my light on for a while when I go to bed each night (until my meds kick in), I don't think I've been kept awake specifically by pain, or certainly only rarely, since having the topper on! The very disturbed nights I have had (because of sleep reversal type problems or anxiety etc), I've been quite comfortable lying in bed. I turn the light off once I feel sleepy, and fairly soon fall to sleep, which is particularly helpful given that lying with my light off, waiting to fall asleep, can be a difficult time for me for various reasons. The shorter that time is, the better!!

When I wake in the morning, I do still sometimes have some joints I need to pop back into position, as has been the case for a long time, and I am still in pain, but my pain isn't through the roof. I can wake up and lie in the same position for a while without my pain getting too awful. That's a big thing for me. It's really nice to start the day without my pain already continuously at an unbearable level.

The extra height has made wheelchair-bed transfers more difficult for me, but I've found the topper beneficial enough that it won't be coming back off!

Is it the cure for my chronic pain? No- it was never going to be. But it DOES mean I can now sleep quite restfully without aggravating my pain, and feel fairly comfortable lying in bed in the morning, which is fabulous!

For further information about the product, please see their website: https://nremsleepsystem.co.uk/topper/ It's not a cheap product, but you can get a free trial to see whether it suits you, and there's the option of a £1 per night payment plan too. I'd say it's definitely worth a look and taking up the free trial if pain or discomfort is causing you real difficulties with your sleep!

If you have a product you'd like me to review, please contact me on Jess.cfs.blog@gmail.com - I'll only ever provide a full and honest review, but if it's a good product, that's nothing to fear 😉

Komentar

Postingan populer dari blog ini

Update 23/2/17 - ISTDP/mental health, my flat and physio etc

Just an update.. Physically, I'm doing fairly well. My hand coordination is mostly a lot better (unless I'm startled or post-seizure). I'm walking quite a bit now- I'm using 2 crutches and can only do very short distances, but the amount I can do is actually quite functional and useful now. I'm still supervised when walking but I don't need someone glued to my side anymore. I still use my wheelchairs quite a lot, but I'm often using my crutches as much in the house now. I've even had a few occasions where I've left the house completely without my wheelchair (only out to the car on the drive and then in from the car a very short way, but for me that's massive!). It shows a physical step forward, but also means I get some mental space away from the constant presence of my wheelchair too. Yes, my wheelchair is enabling, but to an extent it's also symbolic of a phase of my life that has been pretty horrific, so some space sometimes is very ni...

NHS: Junior doctors strike

This is a bit of an essay, but I just want to have my say. I'm in the UK and we are lucky enough to have a National Health Service. The NHS means a lot to me as a patient. I have a lot of chronic conditions- the NHS has done a lot for me over the years, and if the government runs the NHS into the ground (which seems to be its intention), an insurance company wouldn't want to take me on. It'd be an inconvenience for many healthy people, but an absolute disaster for the thousands of people like me. I am totally in support of the junior doctors strike. The team of junior doctors were incredible while I was in hospital. Some of them were always there each day when we were woken up, and still there when we were settling down into bed each night, including over weekends. The team of junior doctors took all the bloods, were on all the ward rounds, discussed diagnoses with family members, supervised students, made life-saving decisions, re-assessed patients whenever a new symptom e...

Time to break my silence: my new symptoms, diagnoses and challenges..

Advanced warning - this post is long ! Fellow fatigued people in particular- you may not want to read all at once! In the past I've shared all my medical battles and worries on here very openly. In the past, things have gone quiet only when I was too ill to write, too busy to, or there was little change so little to share. This time it's been a bit different. My long silence hasn't really been entirely for any of those reasons. The truth is that I needed some time and space to process things and understand things privately. When I received my first chronic illness diagnosis, it was many months before I talked openly about it with anyone; this time I was having to have daily discussions with doctors for months and was having to communicate with lots of different people fairly constantly. I couldn't, and didn't want to, hide my illness in the same way as I did back in 2010, but there were certain elements that I didn't want to share publicly/openly. I wanted the p...