CFS

Health Anxiety - What it's like to live with

Health Anxiety

Health Anxiety – it’s something I mentioned in my last post and boy is it making life almost impossible to live right now. It’s just relentless. And the worst thing? When you’re this anxious for this long, you start getting even more physical symptoms. And what does my brain do with those? Decides I must be ill, poisoned, or dying of something. I literally have no idea what symptoms I’m experiencing are even real now and which ones are either being created by my psyche, my stress response (those ones are real) and which I’m just imagining due to being so sensitive to every single movement, noise or feeling in my body. I can’t even express how all-consuming this is. It’s like nothing else I’ve ever experienced and it’s terrifying.

Every single sensation is now worrying me, am I hungry or is it a stomach tumour? Is my appetite lower than usual? Does that mean I’ve got cancer or is it just that I’m so stressed my appetite has been suppressed? Why can’t I go to the toilet? Am I under-nourished? Sick? Or has my digestion shut down because of my stress response. My heart rate seems a bit high even though I’ve taken my beta-blockers, maybe they’re not working anymore, maybe something else is wrong. Have I eaten the wrong stuff? Is sugar causing it? When did I last eat sugar? It can’t be sugar, I’ve not had any today, maybe it’s adrenaline as I’ve not actually eaten anything yet. My downstairs bits feel funny. I don’t remember that happening before. I don’t remember being able to feel there before. Maybe it’s just a random twinge. Why am I getting repeating random twinges there? Maybe it’s cancer? Would I even know? What if it is? How will I get treatment? I’ve still not had my smear test that was due two years ago because I can’t face going to the doctors, my anxiety just won’t let me. I know I need to go, I know that finding there are changes is so much better than leaving it and them possibly developing into cancer and yet the thought of even trying to make the appointment makes me feel physically sick and my stomach ties itself in knots. I just can’t do it at the moment. I get a pain in my mouth and I’m convinced it must be an abscess, a rotten tooth or that I’ll need a filling. I religiously brush my teeth and realise I’m probably brushing them too hard and causing the pain because I’m so worried about needing dental work. My ears feel weird or I get a slight pain and I’m sure I must be getting an ear infection again. I sneeze or have a slight sore throat and I’m instantly sure I’m getting a cold or flu and that I’ll get really ill with it. Any sort of pain or weird sensation is instantly focussed on, fixated upon and blown out of all proportion. No matter how logical I try to be, no matter how many statistics I bombard myself with to try and make myself see sense, it just doesn’t work. Even when the sensations or symptoms go away, my brain just fixates on the next one. It’s so consuming that I can’t do many activities now because I just can’t focus on them, I’m too busy being convinced that I’m going to get really ill or die. I’m not even scared of dying, if I drop dead tomorrow, I’m kind of ok with that, but I’m absolutely scared senseless of suffering. I’ve felt this way for as long as I can remember. I’ve had a lot of health problems for the latter two thirds of my life, none of them have been serious or life-threatening, but all have involved a lot of aches and pains and never feeling “well”. These conditions have also meant that when I get regular viruses or infections I’m hit much harder by them and get more severely ill and suffer for longer than regular people do. For some reason, I’ve managed to develop a huge fear of suffering that has been increasing for years and made me very frightened to be around other people who are ill firstly because I hate seeing suffering and secondly because of the risk of being infected by them. The only type of illness and suffering I don’t have an issue being around is mental illness which is why I managed to work successfully in mental health and in a hospital no less.

Back to now though. This health anxiety is just crippling. I can’t face going to the doctors to have any of my fears allayed and I often wonder if that would even help because I swear that at the first sign of a new symptom I’d be back at square one again. I’m also so scared that they’d find something that I then have no idea how to cope with treatment for, it hardly even seems worth getting investigated if I then can’t get treated for whatever hideous thing it might be. And I realise just how unlikely it is that there’s anything wrong with me, but still, the worries are constantly there. Today I found out that the most common cancer in women under the age of 33 is cervical. Oh joy! I also know from research that almost all of the female cancers, at least those affecting the lower half of the body, have very few noticeable symptoms and that those I may experience are remarkably similar to IBS symptoms which I also suffer badly from, especially when my anxiety is this bad. I can’t tell you how useful that is when trying to talk yourself down from being convinced you’ve got every disease under the sun. I’m sure that half of the symptoms I’m now experiencing are because I’m focusing so much on my body that I’m getting phantom symptoms from sending too much of my attention to those areas. It’s just doing me in. I’m sick of feeling so on edge, sick of feeling so out of control, sick of feeling like I’m going mad and sick of being convinced that I’m going to die some horrible, slow, painful death. I just want my brain to calm down, chill out and focus on something a bit less morbid than my own death or illness.

Anyone who thinks anxiety is a walk in the park clearly hasn’t visited this particular park which is currently frequented by wolves, big cats, and a whole heap of horrid diseases trying to kill me off at every turn. I have such a strong urge to give up, to stop even trying and to just give in. I don’t even know why I feel like that, I know it wouldn’t help. But I’m so tired. So tired of the thoughts, the constant stream of worries and then symptoms and the desire to research it but knowing that’ll almost certainly make me feel worse. I’m tired of fighting, of dreaming about it, of never being free. I’m tired of all of it. It’s been almost 4 years of fighting with my own head, fighting against each and every new worry that comes up, trying to adapt to every change, to every loss. Having health anxiety and worrying that I might lose even more functioning on top of all of that is nigh on impossible to cope with and means that I spend a lot of each day on the verge of crying because I feel like I’m falling apart. Part of me knows that this will probably pass, or at least ease off, just like a lot of the worries I’ve had throughout this period of illness. But I also know that the anxiety is becoming more and more ingrained and it feels like it’s taking a bigger hold with each passing month. It scares me so much. I don’t want this to become who I am. I have always been determined to be separate from my illnesses, to have them but not to be them. I’m not sure how much longer I’ll be able to say that of the anxiety. It feels so intrinsically linked to who I am now. Most of the time I can differentiate between thoughts from the condition and thoughts of my own but when the thoughts from my condition are so overwhelmingly frequent, so loud and so awful, it’s hard to know where my own thoughts begin because there seem to be so few of them now, there simply isn’t room for anything much other than health anxiety and the occasional worry about going outside.

After my last post I’d hoped to be back to reviewing quite soon. I hoped that expressing how I’d been feeling would help it lessen and in some ways it has, I definitely feel less alone but sadly my health anxiety has just ramped up and up, day after day. My mum came to visit for the weekend and we had a lovely time and I managed to go out with her on two days and take lots of photographs and do lots of walking outside seeing loads of nature and very few people (my idea of perfect!). But still, even while I was out, I was getting twinges, random stabbing pains, wondering if I’d need mum to take me to the hospital. I’m at the point where I’m so frightened that I’m asking people random, really personal questions to find out if what I’m experiencing is normal or likely to be the cause of my premature death. I hate what this is turning me into. My social phobia is ramping up because I know I’m becoming obsessive about this and I’m terrified I’ll bore people or alienate myself from the few people remaining in my life. But I know that I can’t keep this inside as it feels like it’s eating me alive.

I’m not really sure where this post has gone or where it’s ended up. As usual, it feels like a rambling mess and I’m hoping I’ve pulled it miraculously out of the bag and written something at least partially coherent. I’m guessing it’s a heap of negativity and for that I’m sorry but I also can’t even begin to sugarcoat this and I always promised I would never do that, that I’d tell my story, tell the story of so many of us with mental illness, warts and all, with all the worst bits left in. So if this has left you feeling bleak or despondent then I guess that gives you a snapshot into what it’s like to be inside my head, to live a few minutes in my life and I can assure you that it’s infinitely worse when there’s no cause, no end in sight and no tab to close. I hope that sooner than I think, I’ll be feeling a bit brighter, a bit more hopeful and a little less plagued and that I’ll be back with some more positive posts that at least end on a lighter note. I’ll try to edit my photos from the weekend down enough that I won’t bore you all to tears with shot after shot of the same deer or ducks, that’s about the only task I’m managing to do whilst this poorly and I’m still sticking to my showering every day routine. Everything else is pretty much out of reach but I’ll try to get back on with my small tasks project and see if I can achieve a little more than showering and deleting photos. Writing this has been a bit helpful and some of the physical symptoms have eased off a bit which will hopefully sink in to my anxious brain as proof that they’re stress-induced. Huge hugs to all of you who are feeling this way or even just a little bit this way, you’re all warriors to fight this fight every day and I hope it gets easier for us all soon, we damn well deserve it!

Confidence Crisis

Lovely readers, I’m so sorry for the radio silence this year, it’s certainly not been intentional and I’m working hard to try and get myself back in a position where I can be blogging and reviewing again because I miss it and I miss you guys! I’ve had a lot of stuff going on in my personal life and change never does me much good, especially when multiple things are having to be dealt with at once. It’s also a really rough time of year for me, I’m never well at this time of year so it’s unsurprising that I’m so badly affected currently. I thought it was going to last just a couple of weeks and I did manage to write and share a review in early January but since then my confidence has completely deserted me, my words have disappeared and my motivation has been non-existent. None of that is conducive to blogging. I did manage to record and share a couple of videos which can be found here, but that’s pretty much it. I’ve not even been doing anything that’s not blogging. I’ve just been spectacularly unproductive. In some ways, I wish I’d realised how long this would last and just written off blogging for the last 6 weeks and got on with something fun or at least distracting. Instead, I’ve spent the whole time spending way too much time asleep and in bed, scrolling through Facebook aimlessly and watching crappy television for more hours than I care to remember or admit! My flat is dirty and untidy, I’m not showering often enough, I keep missing meals and the thoughts going through my head are much darker than usual and very much swirling around the I can’t be bothered and what’s the point sort of level. My focus is completely gone, my memory is dire and I just don’t know where the last 6 weeks have gone, I can count on one hand the number of meaningful or useful activities I’ve done in that time, even when I really start lowering my standards of what classes as productive, I’ve done next to nothing for weeks!

Throughout this time, I thought I was doing a pretty good job of covering up how much I was struggling. It turns out, I’m not half the actress I think I am. Though the flipside of that is that it’s quite comforting to realise that even when you don’t tell your boyfriend of 6 years that you’re feeling crappy, he can work it out from your subtle behaviour changes (including less nagging about cleaning and tidying). I always put off telling people that I’m worse or struggling more as I’ve previously documented on this blog. I hate admitting it to myself, let alone anyone else and it doesn’t properly sink in with me until other people around me know about it and then it’s a real wake up call. I tend to wait weeks, partially to be sure, and also because I spend that time in denial, before telling anyone but telling them usually leads to at least getting a bit more help to drag myself out of the pit I’ve inadvertently ended up in. I never learn though and always leave it ages before telling anyone or properly asking for help. Normally, my depression is pretty under control, it still sneaks in whenever it can, I still get horrible dark thoughts creeping in regularly but I’m able to dismiss them and get on with being productive and busy and that generally drowns it out. Recently though, that’s not the case, the depression has really ramped up in intensity and it’s crushed my confidence, my motivation and drive and has also made me unbelievably tired and pessimistic, which isn’t like me. On top of this, my anxiety is just on fire! For a while I’ve been noticing that as soon as one worry lessens, it gets replaced by another. This isn’t something I’m consciously doing and it’s currently something I have absolutely no control over but as soon as one thing becomes easier, less worrying, or goes away, another worry comes straight on in behind it and replaces its space. All of the things I was told by my psychiatrist, by therapists and that I learnt in my psychology degree, aren’t working. I was always a huge proponent of the idea of systematic desensitisation, the idea that the more you do a specific thing, the less it will make you anxious and the more used to it you’ll get. The theory is all completely sound, the research backs it up, but my experience is absolutely not showing it to work. No matter how many times I visit my family or don’t get food poisoning or don’t get an IBS attack when I’m out, I never consistently feel better about being in those situations again. I go through phases of things being a bit easier and then much harder but these seem to come and go like the weather with no rhyme or reason and no logic or pattern that I can decipher at all. No matter how much CBT I try to use I just don’t calm down or get over the thoughts. I’m a very logical person, I know the likelihood of my worries coming true (at least the ones I’m aware of rather than the residual feeling of fear for no reason that I so often experience now) but knowing these things won’t happen doesn’t stop me feeling intense anxiety each and every time I have to do something that my brain has decided is anxiety-provoking. I make no medical sense and no one around me, me included, has any idea why I’m like this or what to do to make it better. I was told a few years ago by my psychiatrist that I needed to stay outside for at least 6 hours for my anxiety to calm down and that then being outside would get easier. I’ve done this a number of times since then, in various places and with varying levels of success and yet I’m still severely agoraphobic, unable to even take my bins outside most days and suffering IBS attacks and extreme anxiety about going to places locally that I’ve known my whole life. It’s just doing my head in.

To top all of that off, my brain has decided to become hugely worried about germs and food poisoning. My mind is honestly a living hell right now. My brain is almost constantly fixated on worrying about getting ill with a virus or getting food poisoning. I’ve even considered going vegetarian (not an option long-term as my diet is very limited already due to dislike of a lot of foods and many vegetables being IBS trigger foods) so that I don’t have to keep worrying about meat being off. My partner is an ex-chef, we both know a lot about food storage, prep and just doing a good old sniff test, and yet my brain just can’t switch off these worries and once it’s decided that something is a “risk”, it just obsesses and even causes me physical symptoms because I spend so many hours worrying. Sometimes I just can’t eat the food because I’m so worried about it making me ill even though I logically know it’s absolutely fine. I’m pretty sure that part of the reason I’m so scared of getting ill is because I’m worried about getting so ill that I’ll need medical treatment and that invariably involves leaving the house. I’m increasingly worried about getting a serious health problem that I currently can’t imagine being able to receive treatment for because going out is so difficult for me. No doctor will just drug me up to the eyeballs on Diazepam for the foreseeable future while I get whatever fictitious disease my brain conjures up treated or cured. I hope that if I ever did get a serious illness the fear of it being left untreated would take over the fear of going out and getting treatment and that I’d be able to go and deal with it but part of me thinks that’s just wishful thinking and isn’t exactly likely. I hope I’ll never have to find out but I spend a huge amount of my time at the moment worrying about getting all sorts of conditions and diseases and trying to work out how I’d deal with it without just imploding.

So that’s where I’ve been at since December. I’ve realised that doing nothing and sitting around feeling sorry for myself isn’t working or helping at all; not that it’s really been a choice but still, it’s not helpful. So I’m trying my best to do little tasks that are productive and make me feel better in the hopes that they might spur me on to do bigger and better things and if not, well at least the small tasks I’ve done are done. I started earlier in the week by turning my mattress because for the last few weeks I’ve been getting backache and my tummy has felt twisted when lying on my side in bed, turning the mattress has really helped. I also changed my bedding at the same time. It took me an hour to do all of this and I had to change the duvet cover the following night because I was exhausted but I now have clean sheets and a comfy bed again and this also meant I had to clear up the things that were being dumped on my bed and also that I’ve made myself shower every day so I’m not getting my sheets dirty quicker than necessary. Some days these showers have been 2 hours before I go to bed but still, I have at least showered every day for 4, possibly 5 days, I forget when I started this. I’ve also done 3 lots of laundry, one each night when Joe’s gone off to work his night shifts and put those up and taken the previous day’s load down so it can be replaced with wet stuff. Yesterday I was feeling really low and rubbish and completely unmotivated but my head was just buzzing from too much screentime and I felt like I was going mad, eventually I got so fed up that I went and did some washing up and then hoovered most of the flat while Joe cooked dinner. There are still thick layers of dust on any above-floor surfaces and I’m sure there are other grim discoveries to make that I’m currently just trying to ignore but my floors are mostly clean, my bed is welcoming, my laundry is done and I’ve been clean for a few days in a row. Given how dreadful and unproductive I’ve been feeling, that’s pretty huge progress really and more in 4 days than I’ve managed in over 6 weeks! I’m really trying to make this stick and hope that even though my mental state is completely crap currently, at least my surroundings won’t be so bad and won’t be making me worse anymore. I’m hoping that I might even be able to slowly work through some reviews and finally start getting back on track with that because I’m dreadfully behind and don’t want to just give up like this.

So yes, that’s where I’m at. Not a good place to be at all and I’ve got no idea when the anxiety might start shifting or the depression easing off a bit but I’m hoping that my goal of doing a small task or two a day is at least achievable (possibly with help and encouragement from Joe) and will start making me see the difference I can make to my surroundings and stop me feeling quite so useless and unmotivated. I’m hoping the confidence might journey back to me after that!

P.S Apologies if none of this made sense, seemed to change writing style throughout (it was written in a few goes rather than all at once like I usually write) or doesn’t sound like me normally. I don’t write well when I’m this ill and I’m too distracted to be able to properly edit or read through it to check it makes sense so this is raw and as it came to me. Future posts are unlikely to be like this so please don’t desert the blog just based on this post, I felt I needed to get all of this out and explain to you all what’s been happening for me but it’s far from the standard I would normally hope to produce, I hope you understand.

Confidence and Capability – Video Post

Not feeling confident has a huge impact on every aspect of your life and in this video I discuss how difficult it is to do most things when you don’t feel confident or capable and worry about everything too much – this is why I’ve only managed to do one video and review in the last 6 weeks which I hope will change soon!

Christmas Tree Time Lapse 2017

Christmas Tree Decorating Time Lapse 2017 – Video Post

As some of you know, I’m well known for my obsession with Christmas and in particular, Christmas decorations, my partner and I decorated the tree together this year and recorded a time lapse video of the process. Please do check us out building and decorating it at 64x speed, Merry Christmas!

Photography for Agoraphobia: Photobook 1 – Video Post

I suffer from severe agoraphobia which has left me virtually housebound since March 2014, photography helps me to go out a bit more often, for longer, and keeps me calmer and here I show a flick through of the first of four photobooks that I’ve made of my best photos this year.

How to Talk to Someone Who’s Feeling Suicidal – Video Post

Knowing what to say to someone who’s feeling suicidal can be really difficult but saying something rather than nothing could be the difference between that person being able to seek help or remaining feeling alone and worthless. Here, I talk about what helps, what doesn’t, the difference you could make and the thoughts and feelings that go alongside feeling suicidal because of mental or physical illness.

Unsolicited Advice – Video Post

Unsolicited Advice is something many of us with mental illness and long-term physical illness experience and at best it’s an irritant, at worst, it can be damaging and harmful. As a sufferer of Depression, Generalised Anxiety Disorder, Social Phobia and Agoraphobia, amongst other conditions, I receive a lot of “advice” that’s not asked for, nor wanted, and some of this has been possibly dangerous if I didn’t have the knowledge that I do.

A Day with Depression – Video Post

Living with mental illness brings many different types of days, today my depression has really taken over and rather than cover it up and film on a different day, I thought I’d show you, warts and all, what it’s like to live with and how it affects me and so many others.

Hello! My First Video in Front of the Camera!

Hello lovelies, friends and family have been suggesting to me for the last 3.5 years to do Vlogs and I’ve never felt confident enough or had any particular desire to do it so I’ve always stuck to just blogging. However, I’m getting a bit bored currently and really want to branch out and get my voice heard just that little bit more and video posts seemed like the best way of doing this and after a fabulous pep talk on the phone with a Uni friend today, I decided to bite the bullet and record something. It was meant to be 2 minutes of me just saying Hi, but it turned into something a lot longer and a bit more informative. Please do give it a watch and let me know what you think of it. I’m hoping to use these videos to expand more on my blog posts, to reach a wider audience and to help you see the face behind mental illness and invisible conditions.  The link to the post about Trichotillomania that I mention in the video can be found here.

Seasonal Affective Disorder (SAD) What it's like to live with. Click through to read more!

Seasonal Affective Disorder (SAD) – What it’s like to live with

I originally wrote this post in October last year (2016) and never got round to posting it, therefore all of the dates and amounts of time are wrong by a year. I haven’t yet written a review of the lightbox that I mention in it but briefly, it definitely helps me, it’s not a cure but it’s significantly better than not using one and it definitely helps with my daytime sleepiness and feeling low and unmotivated, it’s still really tough going but it really takes the edge off and makes things easier.

As winter approaches, a large number of people around the world start to get a sense of dread. The nights start drawing in, it gets colder, darker, cloudier and rainier, and your mood starts to lower. For most people this time of year isn’t a problem, many are looking forward to Halloween, Thanksgiving, Hannukah or Christmas, the changing colours of the leaves, Bonfire Night etc. I look forward to the festivals I celebrate amongst those but mostly, I feel dread and this year it’s been particularly early and particularly pronounced. Most people have heard of Seasonal Affective Disorder (SAD), most of us have heard of someone we know having it and most of us aren’t exactly sympathetic about it. I’ll freely admit that as a long-term (10 years and counting) sufferer of depression, I didn’t have a lot of sympathy for people who only felt low for 3 months of the year when I got a jolly helping of it all year round. It sounded a bit like an excuse from people who didn’t like getting out of bed on a cold morning and didn’t fancy venturing out during the darker days. Oh how wrong I was! Despite having depression for a decade, I’ve never been particularly affected by the weather. I was always worse at Christmas but I’m as sure as I can be that this was due to family pressure, coursework deadlines and exam dates looming rather than anything to do with the light levels or temperature outside. I know this because come the middle to end of January, my depression would ease up just a little and I’d be back to muddling along as best as I possibly could. I also remember often being worse during any school/college holidays because I had to spend more time with my family and had less distraction and structure so weather and light levels really didn’t seem to be playing a part.

I happily went about thinking that SAD was a bit of a wishy-washy diagnosis for people who were a bit more sleepy in winter until I got ill and became housebound with my anxiety disorders 2.5 years ago. I’m now approaching my 3rd Winter of being predominantly indoors and I can safely say I’m dreading it. While I’m not diagnosed with SAD, it’s obvious to me and anyone around me that I have it now. This year it’s started kicking in earlier than ever, I’m normally safe until early to mid October but I’m already over 3 weeks in to feeling sleepy, drained and generally crap and this is unlikely to let up until February or even March. For those in any doubt, and for my cocky, accidentally judgemental younger self, SAD is not just feeling a bit sleepy. For me, it involves being barely able to wake up in the morning, even with my usual alarm, and usual amount of sleep, it’s being so painfully tired that I literally can’t face getting up and have to go back to sleep for a bit. It’s being cold. All the time. It’s also being awake for under 3 hours and then being so tired that I’m unable to stay awake and ending up falling asleep sat up and no amount of food, drink, or needing to go to the toilet will stave it off for long. It’s also like someone comes along and stuffs a huge bag of cotton wool inside my head that doesn’t shift for at least 3 months. Everything takes longer. It’s harder to think, harder to concentrate, harder to motivate myself to do, well anything! I also crave certain foods which I never crave the rest of the year, I just want to stuff my face with carbs, sugar, and high fat food, probably in the hopes of hibernating or giving myself energy to actually feel properly awake for once. My body just stops producing heat so that it doesn’t matter how many layers I wear or just how close to looking like the Michelin man I get, I’m producing no heat so the layers just keep in the cold. My feet go blue, as do my hands, my joints seize up and I ache. I find sitting up a struggle because I’m so tired but sleeping doesn’t help, I never feel any better so I just lose hours of my day to napping and get nothing done because I feel so groggy. Then the depression kicks you hard. Everything is so much harder and you start wondering what the point of doing any of it is. I know that I’ll be lucky if I get through half of the short list of tasks I’ve set myself each day which means each day I fail. Each day my to-do list gets longer because I’m so unproductive. Nothing helps, not eating, not sleeping, not drinking, not forcing myself to get things done. It’s relentless!

As you can imagine, I’m very keen to discover anything that might help with alleviating any or all of the symptoms. Sadly, most of the treatments for SAD are the same as for depression and are therefore things that I’ve already tried and that either haven’t worked, or have made me significantly worse so it’s not looking overly hopeful for my feeling better any time soon. The NHS website recommends being outside as much as possible (not particularly possible for me), sitting near windows (I do this as much as possible), regular exercise (again, not especially easy for me) and trying to avoid stress (yeah right!). More medical treatments include medication which I react very badly to, therapy that I’ve previously had and that there are months long waiting lists for and light therapy which has mixed evidence regarding its effectiveness so there aren’t any ideal options!

I hope my description of how it affects me will help other disbelievers to realise how debilitating it can be and that it’s a condition that has a long list of symptoms that are really difficult to deal with, I’ve certainly had my eyes opened after suffering from it for the past 2 years and entering my third! Various members of my family now also suffer badly in the Winter and while none of us are diagnosed, again, it’s very clear that they have SAD too. My mum very kindly bought me a light box which is recommended for the treatment (not cure) of SAD and I’m now using it, as is my boyfriend, and two other family members have them too. I’m tentatively optimistic about it as it definitely seems to be helping me and I will write a full review in a few weeks’ time once we’ve all had a longer chance to use it and decide if it’s the light or external factors that may be helping us. All 4 of us have very different symptoms, diagnoses and lives, as well as being different ages and genders so we should be a pretty good cross-section of people to test it. I’ll report back soon. If anyone is interested in reading more or testing out a lightbox themselves then below is a link to the one we’re all trying out as it’s one that’s cheaper than most while still being approved as effective and having great reviews. I have no affiliation with the company and will be (as always) providing a full and totally honest review, the link below is an affiliate link which means that a small percentage of any sales made through it will be paid to me and help towards the running of my blog, I never promote items that I don’t believe in and would never give false hope to sufferers of what I know, from my own lived experience, to be hugely debilitating conditions. If you get one then please do let me know how you get on with it and whether it helps you!

Amazon UK – Lightbox 10,000 Lux