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The stigmatization of people living with a visible difference I have a fairly unusual circumstance in that my symptoms oscillate dramatically from day to day. I can experience days as a “normal person” and then days when I look anything but.  The way in which my appearance varies so wildly can make maintaining emotional and psychological homeostasis very difficult. How am I supposed to remain balanced when my physical symptoms are all over the place? There is an obvious benefit of this in that there are days when the stars align and I get to experience life without the crushing weight of insecurity on my shoulders. Sometimes this lines up miraculously, for example on my wedding day, other days not so much. This inconsistency creates a perpetual cycle of fear as to when I will spend the next day crippled with pain and embarrassment in how I look. It’s very difficult to settle into “my normal” when I don’t really know what that is for me. An interesting perspective this has given me is an insight into just how deeply stigmatized we are as those living with a visible difference as I’ve experienced both sides of the coin many times. The stark contrast in the way I’m treated day to day when I look “normal” is pretty shocking. When my skin is flaring I often start each interaction with somebody new at a disadvantage/on the back foot. I have to make considerable effort to win them over and to get them to treat me as they would anyone else. During a particularly bad flair I remember a college teacher physically recoiling from me as I dared to get too close. The opposite is true when my symptoms are clear. Not only does life feel infinitely easier as my cognition isn’t being taken up by pain, discomfort, insecurity, itch, lack of sleep but the way in which I’m treated is noticeably more friendly and welcoming. Of course this is not every interaction I have, the world is full of wonderful people who are able to see past peoples appearances however unfortunately even one negative interaction can have a devastating effect, and I assure you it’s regularly more than one.  Unconscious bias is a complex concept as none of us want to be accused of something we’re not consciously doing. However as difficult as it is I do believe it’s something we should all reflect on as conscious or unconscious the damage that can be caused is horrendous. This is why it takes me an extended period of time to trust people, let my guard down and be my authentic self, something shared by many in the visible difference community. This can easily make us more isolated, insular and plays into what can be the all encompassing negative experience of life with a visible difference.

After a recent holiday to Santorini I found myself looking back over photos and worrying that I was becoming part of the problem. We all feel the draw to get that photo where everything looks great and perfect. I thought I’d do a post to demonstrate that this certainly isn’t the case. As always the camera doesn't properly show the extent but I can assure you it was looking (and feeling) angry. We all want to be seen to be living that dream life, perhaps AD sufferers even more than others. We’ve been made to feel worthless all too many times and there’s a desire to “prove people wrong”. I’ve certainly, up until recently, only ever wanted to hide my condition and not be open about it for obvious reasons. Something I love about the Tiktok generation is their commitment to authenticity and the celebration of differences. I find this quite inspiring and I hope it’s the start of an important societal shift in that we don’t feel so ashamed of anything that doesn’t make us “normal”.

In my opinion turning up to the hospital and letting yourself be swept along by the system is a recipe for disaster. Rightly or wrongly there are a lot of steps which can make things a lot more comfortable and effective. Advocacy This is without doubt the most important piece of advice I can give you. If you are too unwell or unable to advocate effectively for yourself then you need to have someone to advocate for you. The system is flawed and unfortunately the “squeaky wheel” gets the best care. Noone will know your needs like your close friends and family, they have to speak up for you and push. It feels very unBritish to make a fuss but this is often the only way to get things done. Food and supplies The food is dreadful, I’m sorry but it is. I certainly wasn’t expecting michelin starred grub but I think the dinner being a jacket potato every single night is a joke. You need people to bring you supplies or you might find yourself going crazy. Be ready for a calm but firm fight You unfortunately need to psychologically prepare yourself to push and fight for what you need. It’s almost unavoidable. Us AD suffered will be very used to that. Doctors appointments The doctors always come round outside of visiting hours, if you’re family, in my opinion, ignore the visiting hours and make sure you’re there for these appointments. Have your questions prepared as you never really know when they’re going to show up. Notes Write notes of everything; medication times, questions for the doctors etc.  Don’t take the health care providers word as gospel We often can feel uncomfortable challenging the professionals however, as in every industry, the professional can regularly get things wrong. This happened multiple times throughout my stay; wrong medications, incorrect information, having a necessary surgery cancelled, so be prepared to challenge the medical advice.

The eternal tightrope of “naive to tin foil hat”. My time in hospital recently hammered home an uncomfortable truth, something which seems to permeate all areas of life but is especially obvious in healthcare. That is the importance of a healthy scepticism to authority.  Over the last few years, heavily assisted by the internet, the levels of total nonsense information we all encounter has gone through the roof. A seeming disregard by far too many to science and generally everything which pulled us out of the dark ages. However the answer to this, in my opinion, is not a slavish obedience to anyone wearing a stethoscope around their neck/with letters after their name etc. Afterall It was not that long ago that some doctors walked onto our TV screens, stared at us in the eyes and told us the health benefits of smoking.  The boring truth, as in all areas of life, is somewhere in the middle and we must lean on science and the experts while feeling no discomfort in challenging authority and trusting our instincts. I witnessed time and time again mistakes and poor information during my time in hospital. I certainly don’t believe this was from a place of malice however if this hadn't been challenged the negative outcome for me would have been the same.  When you’re feeling unwell it feels all too easy to handover to the experts entirely and sit back and relax. Unfortunately unless you have advocates around you 24/7 we simply don’t have that luxury.  From an AD perspective I was like almost anyone in the UK, in that we believe our route for any kind of complex health condition is as follows; GP, referral to specialist, see the specialist, if they can’t help you’re more or less at the end of the road. This is simply not the case. After years of seeing a local dermatologist and being told I was at the end of the road I then did my research and went to a London specialist who said I hadn’t even “scratched the surface”. They then proceeded to treatments and medications I’d never been offered after decades of suffering with my condition. I did learn something fairly recently which blew my mind after speaking to a doctor who is heavily involved in skin condition research. He said that in order to prescribe the latest ground breaking skin treatment, dermatologists have to keep up and keep themselves educated which many simply do not. They therefore may be telling their patients that they’re essentially out of ideas simply because they themselves have not kept themselves up to date with the latest treatments. On the other side of the equation a lot of us feel a sense of desperation which can make us vulnerable to the snake oil salesman as “it probably won’t work but I can’t take the chance in case it does”. Which I fully understand and empathise with and I myself have spent plenty of money on what was ultimately nonsense.  To summarise; we all need a “healthy” level of scepticism and what exactly this equates to is almost impossible to define. Lean heavily on science and the professionals but don’t ignore that voice/your own instincts when you know something isn’t right.

That club consists of members who keep failing on systemic treatments. Dupilumab was supposed to be the miracle (and for many it is and continues to be). However I’ve now tried Dupilumab, Tralokinumab (although I was only on this for a month and needed to jump on to something more fast acting), Abroctinib and will now be going on to Upadacitinib. While at my last Guy’s appointment I was enrolled into the “Genetic analysis of eczema subtypes” study which as the title suggests is researching the genetic components of the condition and how it might better be treated. For instance in my case, whether there’s something which can show that someone similar to me would respond better to one systemic over another. Meaning a patient can go directly onto what they will respond best with.  It involves an initial batch of appointments and then an appointment around every 6 months which will line up with my usual Guy’s appointments. Travel is reimbursed, although this can take around 2 months. Which I do think is disappointing as people are already donating their time.  There’s also optional skin biopsies which is essentially where a 6mm core of your skin is taken for analysis. The biopsy appointments are paid at £60 per appointment and they would ideally like for me to have 5. They do require a few stitches, take some time to heal and can leave a small scar. Just to make you aware if you’ve never had one, they're not pleasant and its almost like a minor surgery.  Although it’s a significant time commitment I feel it’s important to do so to help push forward Eczema research. However the primary reason I say all this is not to pat myself on the back but to highlight that there are a huge number of organisations/hospitals/charities etc who could really benefit from the help/insight/experience of an AD sufferer or carer.  Due to regulation, outreach can sometimes be difficult so if you reach out to them first it opens the door for them to be able to use you. It’s just something to consider as this was how I originally started my work with Sanofi which led to so many other really inspiring opportunities. I’m soon to start work as an ambassador for Changing Faces, on the advisory panel for Eczema Outreach Support and a PIP panel member for NICE.

After years of avoiding it I finally took the plunge and started weekly therapy sessions. After the difficulty of the first session where everything came pouring out I immediately felt a benefit. Just the act of sitting in a quiet room for an hour with nothing to do other than to talk about what's on my mind felt very peaceful. As we all know the mental health aspect of chronic skin conditions is where the real danger lies. We can’t ignore the profound effects it causes. A clear way to address this is through therapy, I would at the very least suggest giving it a try as I know it doesn’t seem to benefit everyone.  It often feels almost as if the counsellor is facilitating a conversation with yourself, this then leads you to coming to conclusions all on your own about the best ways forward etc. I thought I’d share a few things that I have found helpful:As skin condition sufferers we regularly have to deal with the catch 22 of someone making an off hand remark about our appearance. Thereby shining a light on the thing we are most insecure about. In that moment I’m instantly plunged into a feeling of almost fight or flight due to the feeling of humiliation. In this same instant I have to analyse the situation and decide how best to respond. I for one usually just want the situation to be over as quickly as possible especially the more eyes this tactless comment has attracted my way. This tied with the fact the comment often doesn’t come from a place of malice and not working to embarrass the person who said it results in me often just laughing it off. Something which my counsellor said which I quite liked was “someone needs to be embarrassed in that situation, why does it always have to be you?” Another key aspect of this is I don’t want to appear overly sensitive. A comment about someone's face being red for most normal healthy people is quite harmless banter. However, due to another suggestion from my therapist, to counteract this I try to take a step back from the situation and judge it as if it was someone I loved with the skin condition and someone has just made that comment to them. This makes my response feel so much more clearer as I would be far less tolerant if for example my wife deeply suffered with this condition and someone made a tactless comment towards her. Ultimately for me to just laugh it off to get out of the situation is the coward's way out. If the person isn’t being malicious and they have to feel slightly embarrassed when I explain to them the situation then so be it. If it is malicious then it’s so much easier to hit back.  Something else I have greatly benefitted from is mindfulness, this is wonderful in theory but can be difficult in reality. I like to think of it as your thoughts are like cars driving along a busy motorway. You are not on the road, you're simply standing to the side observing the road. To take that second and observe my thoughts from a more objective outside perspective rather than from inside the emotion of those thoughts can feel very liberating when you get it right.

Another one bites the dust/all hail prednisolone Another ground breaking systemic treatment, another “failure”. At least this time I’m well within the Guy's and St Thomas' dermatology system so I know my path to the next step should be much quicker and more painless. After around 6 months on Abroticitib a Jaks inhibitor (brand name Cibinqo by Pfizer), with initially strong results, the effect began to wear off. Slowly at first and then rapidly. It wasn’t quite as miraculous as Dupilumab at the start but I’d have been very happy if those results had stuck around.  I immediately paid for a private GP appointment for £40 to get a prescription of Prednisolone. If you can’t get into your NHS GP and you’re in the position to, don’t muck around, get the private appointment. £40 to get the help you need is a small price to pay. Should you have to? Of course not, but the situation is what it is and when you feel like you’re being eaten alive the priority is not the fairness of the situation, the priority is to get you out of pain. There’s loads of different ones, Dr Online, push doctor, tap GP, I tend to do the rounds on all of them and see who’s got the earliest appointment. I made sure to not hold back on how much I was struggling psychologically. There’s a time for a tough upper lip but it is not when you’re in front of a HCP. It ultimately makes their job much easier if they’re able to say that prescribing you a certain medication is an absolute necessity due to the damage your skin is having on your mental health. My word Prednisolone is magic stuff. It’s given me a reset/relief that I needed desperately and allowed time for the real medication to kick in. I understand the negative side effects (decreased bone density etc) but when you feel like you’ve been dunked in a vat of acid and you haven’t slept properly in weeks I’ll take those side effects thank you very much. I completely understand that HCP’s have to stress the dangers of Pred in order for it to be taken responsibly. However it can be a bit frustrating when you have no option but to take a potentially harmful medication and you’re constantly reminded how you “shouldn’t really be on it”. This is another reason why it’s important to hammer home the point that this is not optional, as otherwise they may resist giving it to you. Pre pred: Post pred (4 days later): Fortunately I was able to attend Guy's as a walk in a few days later and I immediately felt in good hands. You can never underestimate how vital it is to an AD sufferer when they’re at their lowest to feel like they’re talking to a HCP who is fully empathetic to the situation and grasps the urgency.  Although there does seem to still be some bureaucracy in terms of actually getting the medication in patients hands. Again I can fully appreciate these are serious medications and protocols need to be followed. However you’re dealing with patients who are psychologically on their knees with every day being a challenge to get through. I therefore do think there could be room for improvement here. Especially with the positive effects of Pred being on a timer before you have to up the dose and put yourself at greater risk. I’ve got a call with Guys tomorrow so hopefully I’ll have an update on my first delivery of my next medication; Upadacitinib.

A few things to be grateful for It wasn’t all doom and gloom from my time in hospital, as flawed and stretched as the NHS is there’s still so much to be grateful for. Here are my examples: Walking out of a 10 day hospital stay without having one thought on any financial impact (beyond the lost days at work) is something we take for granted in the UK. In many parts of the world, including many developed ones, there are people one hospital bill away from poverty. I do love to be part of a system that when you’re sick you don’t have to deal with the added stress/strain of any financial pressures. There are doctors, nurses, HCP’s within the system who are wonderful, caring people who must be very resilient to not be completely worn down by a system so stretched. It was such a breath of fresh air whenever I felt under the care of someone who seemed to genuinely be concerned about my welfare. Towards the end of my stay I had to have an epidural blood patch and the surgical team couldn't have been more kind and professional.  Basic protocol seemed to be followed very religiously, my blood pressure etc was taken very routinely and I felt like staff often had clear systems that they implemented well. Every room I was in was always kept pretty immaculately clean, from the bins being changed every day to the bedding being changed whenever it was requested. Cleanliness never felt like an issue.

A fairly eye opening experience I recently had a ten day stint in hospital due to a CSF leak/intracranial hypotension. In layman's terms the fluid around my brain was leaking causing my brain to drop in my head. I’m planning on doing three posts about this experience; pros, cons and some (hopefully useful) advice. Starting with the cons. I feel like the NHS is a symbol of national pride and so it often feels as if it’s unacceptable to discuss any kind of flaws in the system. However some of the care I received/witnessed was concerning to say the least. Of course there were some wonderful health care providers and I understand that many of the issues are simply a lack of resources. However this doesn’t change the fact that without adequate advocacy, time spent within an NHS hospital is now something which fills me with dread. Please see below a few of the examples of my time in hospital: I was held in A and E for around 24 hours before I was transferred to a ward. The main symptoms I experienced was excruciating pain while sitting or standing. I was abruptly awoken on the second day, a bowl of cereal put in my hands, sat bolt up right and left in around 5 seconds flat. The pain and nausea from being sat up was immediate and extreme. I pressed the nurse call button but nobody came for around 15 minutes, the whole time I was in agony, I then started to shout for help, still nobody came. Eventually by chance a nurse came past and helped lay my bed flat, this was probably around 20 minutes after I pressed the help button. This was something I witnessed from multiple patients on multiple occasions. Call buttons not being answered and patients having to shout for help for extended periods of time.  As anyone with AD knows our treatment routine is incredibly important, a daily shower then followed by the application of moisturisers etc is essential in managing our condition. When coming up to the 24 hour mark in A and E I made it clear that I would need to have access to a shower soon. This was met with resistance and involved a significant amount of pushing to make it happen. It frankly felt like the usual dismissive attitudes we all face as skin condition sufferers and the imbalance of perception towards the care needs of some conditions compared to others. Also, I was placed in a side room in A and E as I initially had suspected Meningitis however I would of course have to leave this room to go to the toilet. This meant that multiple times I was walking (or more like stumbling) through a packed A and E with what could have been a highly contagious and dangerous virus.  Again, my main symptoms were excruciating pain while sitting up and an extreme sensitivity to light and yet very regularly a health care provider would walk into my room immediately turn on all the lights and attempt to sit me up.  There were also numerous instances where pressure was applied to do what was easiest for staff rather than what my care needs were at the time. As an example, as mentioned, I was vomiting and in horrific pain if I was sitting up or standing but they would always try to get me to go to appointments in a wheelchair rather than on a trolley. If you're on your own and feeling awful it's all too easy to give in to this pressure. It also makes you feel very uncomfortable, as if you’re just making a fuss. In the first ward I was in I was being woken roughly every hour throughout the night. I of course appreciate that sometimes there's no getting around it, for example medications or blood pressure checks etc. However I was having blood tests at 4:30am every day, had someone come in at around 1am to check the stock of a little tupperware box in the room and had someone shout from the doorway at around 2am "Do you have a cannula?!". Leading on from this it was rare I felt any compassion, empathy or just general human interaction. It all felt very cold and clinical.  Something which I also find quite concerning is that visiting hours are always after the doctors have done their rounds. Often patients are very unwell and it makes sense for the family to be there to support and make sure the right questions are being asked. Considering the pressure placed on A and E due to a lack of available beds in the wards I felt like the system moved very slowly from within the wards. I could have easily been out of hospital a good few days earlier, with my bed freed up for another patient if there was a bit more urgency in providing the necessary treatment/procedures.  I understand that the NHS is stretched but in my opinion this doesn't change the fact that it is either fit for purpose or it's not. I don't wish to get political but I do hope that Labour use their large majority to do what is necessary to reform. The primary concern I have is for those without a support network and without the ability to effectively advocate for themselves. My brother has autism and I now know that if he was to ever be in hospital someone would need to be with him every minute of the day.  It certainly wasn’t all doom and gloom and there is still much to be grateful for having access to the NHS which I’ll cover in my next blog followed by some advice which I think can really help make the experience that bit easier. Spoiler alert: have someone who can bring you some different meals from time to time!

Apologies for the gap in my posts/going off topic for this one Obviously my blog is supposed to be AD related however I thought it was worth sharing my experience over the last few weeks. I'm still feeling pretty ropey so I'm going to keep it brief: It started with a very weird headache, not your usual banging but more like an intense pressure sensation. It was also significantly better laid down than sitting or standing up. I also had quite severe pain in my neck and back. After two days of the symptoms increasing rapidly we called 111 and it was recommended I go to A and E as they suspected I had Meningitis. I then spent the next 24 hours in A and E while they tried to find me a bed. After getting to the ward I had a lumber puncture which involved me being in the fetal position while a doctor inserted a big old needle in my spine to take and then test some of my spinal fluid. This showed that it wasn't meningitis but my MRI results showed it was a CerebroSpinal Fluid leak which then caused intracranial hypotension. This is where there is a tear in the dura surrounding the fluid in your spine/brain which then causes the fluid to leak out. This drop of pressure caused my brain to drop in my head. I then had an epdural blood patch which invovled once again laying in the fetal position while a nurse took blood from my hand which was then passed over to a doctor who injected it into my spine. This is supposed to help "patch" the tear in the dura. I have to say this is the first time in my life I've felt that I might be in a bit of trouble (besides the mental health risks from AD). I have never felt so sick and in pain. There was a point that if I was upright at all I would be throwing up. One small mercy was that my skin held up for some bizare reason. But this did cause further complications as I needed to have my daily shower to maintain this but being on my feet felt impossible. I'd literally have to lay down multiple times to reset and go again over the course of a 5 minute shower. Since getting home I do feel like I'm slowly on the mend, mornings are difficult but after an hour or so the pain in my head subsides and is around 75% better. However I do have quite significant double vision which is quite debilatating. Bed rest is supposed to be very important for the healing process but it's frustrating having to stay laid down all day even if I can be relatively productive with my laptop. While we all know the NHS can be a mixed bag I have to say some of the things I saw/experienced were scary. I continue to be incredibly lucky in that I had my Mum and my wife there with me the whole way through. It's terrifying the thought of being in that situation and not having people to advocate for me.

An amazing service by an amazing organisation Do you remember those times when you were going out and your Mum would tell you to take a coat, you wouldn’t and then would not only immediately regret it but would outright refuse to admit you were cold? Well this is one of those situations however I’m going to be mature enough to admit….Mum was right.  She has been telling me to try this for years and because I’m a stupid bloke and didn’t want to go down the route of “make-up” I shied away from it. However, after some recent work with Changing Faces I once again came across their Skin Camouflage service and thought it was time to give it a go. https://www.andyandad.com/post/my-blog-post-with-changing-faces I felt like a bit of a fraud going in as this service helps some of the most courageous individuals in our society. For example, people who have acquired severe burns or scarring, who have not only overcome a life-changing event but also have to handle life with a visible difference afterwards. However, my practitioner couldn’t have been more lovely from start to finish and the information was all very manageable.  My skin has been reasonably good recently so I didn’t think it would make too much difference but when I was shown the mirror it immediately gave me a lump in my throat. It made a VERY big difference and it certainly didn’t look like I was covered in make-up. I see this as another tool in the toolbox for when I need it. It’s so reassuring to know I have this option. Social events in the calendar can be so daunting as I just never know what condition I’m going to wake up in and I believe the anxiety alone from this lack of control can worsen my symptoms. However, having the Skin Camouflage products feels like I’ve been given an element of control and an option for if the worst happens and I do wake up with a flare. We went to our good friends (very hot) wedding a few days ago. This scenario would usually have been massively anxiety inducing as there was a lot of people I didn't know and my face would usually be very flushed. However just a light covering of skin camouflage kept the redness at bay and allowed me to enjoy the day with my beautiful wife. This is something that many take for granted but feels like such a gift to someone like me. At the end of my appointment, I was sent away with paperwork and guidance as to exactly what products I needed. I was told that this would be sent to my GP to be put on prescription, but these are at GP discretion and vary between health boards. As such I have to decide whether it’s worth the fight to try and achieve this. In my opinion many healthcare professionals still don’t truly appreciate the catastrophic emotional toll of visible conditions and the dangerous psychological impact they can have. This can create some push back and reluctance to provide what is needed. For example, my symptoms are highly photoaggravated and I therefore have to apply suncream multiple times per day. A letter was sent to my GP for this to be placed on repeat prescription by my consultant, but I know for a fact this won’t be done without applying significant pressure.  Nevertheless, I would strongly recommend this service to anyone. It doesn’t mean applying tons of make up to your face every day if you don't want to. It can simply be an option to have in your back pocket and I thought the results were pretty amazing. You can find more info below: https://www.changingfaces.org.uk/services-support/skin-camouflage-service/

Normally a title like that is for some glamorous beauty influencer but that’s not quite the angle I’m coming from! So if you’re anything like me when I’m following someone online looking for answers whether that’s for the gym/investing etc I’m always keen to know exactly what that person is doing. Of course everyone has different circumstances and what’s best for them and what works for me may very well not work for you blah blah blah! However this is currently what I’m doing to keep things in control, and for the last few weeks things have been fairly reasonable: Zerodouble gel This is my moisturiser which I also use as a shower gel. When I first went to St Johns Dermtology in London one of the first thing they did was trial me on all different types of moisturiersrs and this seemed to be the best. Anyone with AD, Eczema, Psoriasis etc will know that a good moisturiser is your foundation and is absolutely essential. I was using Epaderm for a long time but I found this way too thick whereas zerodouble is a good level. You can also get it off Amazon for when I mess up my repeat presceiption/the pharmacy isnt able to get hold of it for any reason. I put this on all over during and after my shower and then again all over before bed. Polytar Scalp Shampoo I wash my hair with this everyday and I am lucky to have very little scalp issues. When I was younger and more recently during my crazy flares this wasn’t the case so it’s nice to have this largely under control. Something I used in this past when things weren’t under control was Betacap, this can sting a bit but I found it to really help. Betnovate RD This is a cream I use before bed on my face, it’s a light steroid so not a long term solution and I’m currently down to using this 3 times per week with the aim of using only once per week. Over the last few years I keep waking up with my face being red and sore, despite a fresh pillow case every night, hypoallergenic pillows etc. This certainly seems to help with this, as does Daktakort. Abrocitnib Jaks Inhibator The main medication I take is a tablet once per day called Abrocitnib which is made by Pfizer. The National Eczema Society has a great article all about this explaining how it works etc. Ive been taking this for around 3 months and so far so good. Neck down in particular things are very much in control. This does require blood monitoring but the pro is that it is a daily tablet rather than a weekly/biweekly injection like some of the other equivalent treatments. https://eczema.org/information-and-advice/treatments-for-eczema/abrocitinib/ Protopic Ointment I apply this after the shower on my face and leave it for around 30 minutes before wiping it off as I find it doesn't soak in and it can clog my pores and give me some nasty spots. This is an immunosuppressant medication which helps to calm the inflammation on my face. La Roche-Posay suncream After my last appoinment at Guy's hospital the consultant believe that I needed to be more proactive with suncream as my symptoms did look photo aggravated. They suggested I apply this every four hours no matter the time of year. Fexofenadine The “Atopic” in Atopic dermatitis means a sensitivity to allergens and I find taking one of these helps quite significantly. This allergen sensitivity has led to issues with my eyes and general hay fever symptoms. Fexofenadine does seem to control these symptoms quite well. Aciclovir tablets Unfortunately my eye related issues have caused what was essentrially a cold sore on my eye a few times which has left scarring and impacted my vision. Aciclovir helps reduce the likelihood of this happening again in the future. Hylonight/Hyloforte/Opatanol/Ikervis Eyes issues are obviously not directly skin related but a side effect of the medications I've taken and again my sensitivity to allergens. This is what I take eye drop/ointment wise, for the last few years this has kept my eyes completely under control. For the longest time my eye issues were constant and debilatating, the only way to calm them down was to sleep it off. Nowdays Opatanol first thing in the morning, followed by Ikervis shortly after, Hylonight before bed and Hylorfore used if and when seems to have done the job. Nasacort Nasal Spray My nose was blocked every single night before I started using this (along with a nose strip) and I believe it really helps me sleep. Mirvaso I go into a bit more detail about my experience with Mirvaso on a previous blog post, however I’ve found this to be an excellent emergency tool for when my face is extremely flushed. https://www.andyandad.com/post/my-experience-with-mirvaso I wouldn't be surprised if I've missed something and there's also other medications/treatments which I don't use on a regular basis. If you have any questions about your own routine or mine please feel free to drop me an email!