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Severe Eczema Teenager

155 replies

GlitteryUnicornSparkles · 04/04/2025 20:50

I’m hoping someone may be able to offer some advice. Apologies if it’s long I’m just trying to give an accurate picture.

My son has just turned 16. He has a history of asthma (though he seems to be growing out of this) and a long list of allergies.

For many years he’s struggled with heat related itchiness on his hands and feet / ankles such as after a hot bath or shower, or getting too hot in bed (I have the same issue, with my legs), Dr said its quite common and theres a name for it I can’t remember and its not really a concern.

2 years ago he suddenly developed what was diagnosed as eczema on his hands, they were very dry and itchy, his fingers were splitting when he moved them and he was covered in cuts and had removed all the skin up the outsides from scratching. We tried every cream on the market to no avail. Dr’s prescribed emollients to leave on overnight which helped a bit but overtime this extended to his arms. Again the Dr’s tried different creams just reiterating he needs to be using at least 4 times a day including during school which he struggled with a little.

He then started to complain his face and neck were starting to feel dry & irritated, he was told he could use the emollient on his face so he was putting that on at night. We then got a notification that they were changing the brand of emollient but did not say it couldn’t be used on his face. Nothing was helping his arms at this point and he was cut to ribbons, they tried a steroid cream (which states not to use on broken skin on the leaflet) but it made him sting so badly he wouldn’t use it. One night he got hot, the emollient creams were runny and ran / got wiped into his eyes, he had a pretty bad reaction and he rubbed away 8/9 of the 11 layers of his corneas and ended up in A&E having to have anaesthetic eye drops put in every 20-30 minutes due to screaming with pain. He was then referred to an ophthalmologist and had to have drops in his eyes for several months. Whilst he was in A&E he was so irritated and clawing it his skin and bleeding everywhere that a Dr came & prescribed him oral steroids, antibiotics because they said his arms were infected and told him to take piriton on top of his normal antihistamines that he takes for his allergies to help with the itch. They made such a difference but of course as soon as he finished the very short course it all just flared back up. The Dr text to say the new emollient was not safe for use on the face and changed the emollient back!. Prescribed more creams.

He then started with issues on his legs. A dozen trips back and forth to the GP we just keep getting told ‘use them more’. He’s tried steroid creams at low dose that do not help at higher doses sting. He then developed the eczema down his sides. The GPs were of little help. Eventually they referred him to a dermatologist (exactly 12 months ago now).

Over the summer months his skin did improve quite a bit which helped him cope a little.

Come autumn / winter it’s just gone downhill rapidly. He shaved his legs because he thought it would help get the creams on better. After more antibiotics for infection, another dose of oral steroids and multiple weeks of topical steroid things were much improved, until of course he had to stop the steroids again, even though he weaned down strengths. We keep getting turned down for repeat prescriptions of standard cream too because he’s ‘using too much cream’ its a bloody battle to get enough.

At this point he was getting upset because some days he physically could not shower for the pain and wouldn’t leave the house without showering. Sometimes the irritation is so bad he’s punching walls out of frustration. He’s had a tonne of time off school. He’s doing guitar and engineering at GCSE, two subjects he loves but heavily involve using hands which he struggles to do. He was / is barely sleeping so was / is constantly tired and was put on prescription strength / addictive antihistamines to try help with the itching and to help him sleep but they did nothing. The GP wrote an exopodite letter to the Dermatologist in December.

In Feb my mum paid for him to see a private dermatologist who prescribed the tiniest tubes of Protopic given the size of area to use twice a day, however he’s been told he needs to cover up and stay out of the sun because the cream increases the risk of cancer - awesome just as we are heading towards summer. Its done nothing and his skin is getting worse.

We are now at a point where it’s literally his whole body. At home he won’t wear clothes because he says it hurts when they touch or rub against his skin. Some days the thought of showering makes him upset because it hurts so much. He barely leaves his room for this reason and has missed a tonne of school due to the same. He’s not only sore but very self conscious of how bad his face & hands look. He no longer goes out socialising with friends, doesn’t want to attend prom etc. He just sits in his room covering himself in creams when hes not in school. He’s perpetually in a bad mood because he's sore, irritated and tired which makes homelife stressful as does everything he touches being covered in greasy slime. I’m constantly having to walk round wiping everything he’s touched.

He showers once a day, he uses very cool / cold water. He uses prescription shower cream. He’s on antihistamines. We’ve replaced his bed, mattress, duvet and pillows and they are all anti-allergy & have anti-allergy protectors. The emollients make his bedding disgusting and thick with slime so he washes / changes sheets every few days. Everything is washed at 60 degrees c. We tried changing to non-bio washing tabs and removing fabric softener of any kind hes only getting worse. It’s having a massive impact on us both mentally as well as him physically.

We finally have an appointment with an NHS dermatologist in 3 weeks. I’m worried that all they are going to do is prescribe more bloody creams and turn us away.

Has anyone found something that actually helps or can advise on things to discuss with the dermatologist because this last two years has been pretty awful. He’s had other health issues on top of this so its all just getting a bit too much.

Sorry if I’ve rambled. Thank you if you made it to the end.

OP posts:
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Ihatelittlefriendsusan · 25/07/2025 00:07

Thats awful.

Ring the secretary for the consultant and explain, ime they are far more reasonable than the receptionist team!

Sending hugs my lovely

GlitteryUnicornSparkles · 25/07/2025 10:03

Ihatelittlefriendsusan · 25/07/2025 00:07

Thats awful.

Ring the secretary for the consultant and explain, ime they are far more reasonable than the receptionist team!

Sending hugs my lovely

Its the secretary I’ve spoken to.

OP posts:
Ihatelittlefriendsusan · 25/07/2025 12:06

Oh crap.

In which case PALs might be able to help, but if not just keep calling them. They absolutely have the ability to swap him to a different clinic, its exactly the same service just usually a different day...we get swapped all the time depending on availability when dd needs her 12 week bloods for the methotrexate.

ADX · 25/07/2025 13:29

Hi Glittery

am so so sorry your son is going through this
I have experience the same with my son and it is totally heartbreaking to not be able to remove their pain .

I could scream about a the hoops you need to jump and recall all of o well t

I often think that Drs etc don’t quite get how much of their lives are affected by this. It has put my sons life on hold when it happens and this time he has been out of work for over 2 years and counting

my son has always had eczema and flare ups increasing in severity over the yrs( he is an adult now)

where his got as bad as you describe your sons as being he was eventually (after a 15 month nhs dermatologist appointment wait) proscribed cyclosporine. It required regular bloods tests(think re liver) but it did work and results started to show within about 3 weeks. I hope this works for you son too .
as a parent the pain felt to see your child go through this is immense and many tears have been shed .

the treatment kept my sons eczema at bay for about 6 years
unfortunately it is back and not responding to immune suppressants this time.
we have the added complication that as he is a POC his skin colour has been completely changed from the eczema and he has lost his hair too. He has been on opioids painkillers for over a yr now.

this thread has given a few ideas and suggestions to make to dermatologists.

I wish for your son’s condition to be successfully treated with his cyclosporine as ours was. The relief when something does work is immense. It’s a long journey for which I send my best wishes for you all.

seoda24 · 25/07/2025 13:41

So sorry to hear you are going through this - your poor son . Cyclosporine worked wonders for me and I definitely could see the positive results within 3 weeks . Here’s hoping for a positive and speedy outcome for your son . Most debilitating…

BigOldBlobsy · 25/07/2025 16:25

Poor thing , I’ve been there. The only thing that helped me and my daughter;

Weaning off steroid creams gradually as these were thinning the skin (has taken years and my skin is very much ‘normal’ and under control now)

MooGoo creams (check ingredients for you)

Antihistamines - Fexofenadine, Promethazine and Hydroxyzine Hydrochloride although not sure if they prescribe this anymore

no soap powder - switched to soap nuts instead natural and low irritant

no shower gels - used oat baths (just oats in a pair of old tights and lukewarm bath each night until controlled)

GlitteryUnicornSparkles · 16/08/2025 19:58

So another long update for anyone following and interested.

As per an earlier post, my son started the cyclosporin, 100mg in the morning and 25mg at night. He was only given a 3 week prescription but they couldn’t actually fit him in for his follow up for 4 weeks time and only by double booking us, meaning he took it for 3 weeks then had a week off. During which time we replaced his entire wardrobe with 100% cotton only clothes as advised.

Since finishing school for the summer (meaning he can sit with his clothes off in his room frequently reapplying creams and taking to slapping himself to try and avoid scratching himself) he was already starting to look physically better before finally starting to take the cyclosporin though was still feeling and was clearly still highly irritated. During the later end of the 3 weeks on the cyclosporin and after a few days away on holiday where he’d spent quite a bit of time out in the sunshine paddleboarding, I personally noticed he didn’t seem to be slapping himself as much and he did visibly look quite a bit better though he says he didn’t feel it had really made much difference especially irritation wise!?

Today was the 4 week follow up following a week off the cyclosporin having only taken 3 weeks worth prior. The good news was that his blood results had indicated that the treatment was working and the drug was reducing the inflammation markers and his organs were coping fine.

The bad news is that she also decided to request an immunoglobulin test, something that hasn’t been done before and we were not aware of being requested. His serum levels have come back through the roof, which she is now concerned could potentially indicate he has some sort of syndrome or even cancer and his immune system could already be compromised. As a result of this she is no longer willing to prescribe immune suppressants until these things can be ruled out. She is now referring him on to a specialist haematologist for investigations and potentially also an immunotherapist. I have no idea how long these referrals will take to come through but in the meantime she has prescribed topical steroids which he is reluctant to use, and told him to use organic extra virgin olive oil on his skin as it has anti-inflammatory properties. She will follow up with us in 6-8 weeks to see how things are going.

This is a really disappointing result, he’s only 2 weeks off starting college and we were really hoping we’d have seen some real results by then, up until this week the majority of his summer holidays have pretty much been wasted hiding away in his room except for the few hours a week he goes out to do his part-time job. I’m really worried that once he starts college and isn’t able to apply his creams as frequently as he has been doing along with a turn in the weather as we head into autumn that he is just going to go back into a downwards spiral.

I was a bit sidelined today as its not what we were expecting so I didn’t think to ask, which I’m now kicking myself for (hindsight is a wonderful thing) but when we go back again in 6-8 weeks, I’m going to ask about the Dupixent again as an alternative treatment since this isn’t an immune suppressant and doesn’t require regular blood tests.

OP posts:
Ihatelittlefriendsusan · 17/08/2025 07:03

Oh god @GlitteryUnicornSparkles what a curve ball!

I really hope it is just a weird blip on his tests and nothing serious! But please keep us posted.

If his skin is healing from the cyclosporin then hopefully the steroids wont sting as much and might help ease things. Which ones has she given him?

Mynewnameis · 18/08/2025 13:39

Sorry to hear this op.
Hope things can move quickly

bunnyapple4 · 19/08/2025 08:49

Dr Aron was the only thing that ‘cured’ my eczema, cured as in the sense that it is now 99% gone and I just use the cream as and when it starts to flare.

I suffered for 35 years, I was covered head to foot, ended up in topical steroid withdrawal but within 2 weeks of using the cream it was like I had never had eczema. Also it has completely sorted my daughter’s eczema. Wish I had known about it far far sooner, it’s been literally a lifesaver.

Hazlenuts2016 · 19/08/2025 10:06

bunnyapple4 · 19/08/2025 08:49

Dr Aron was the only thing that ‘cured’ my eczema, cured as in the sense that it is now 99% gone and I just use the cream as and when it starts to flare.

I suffered for 35 years, I was covered head to foot, ended up in topical steroid withdrawal but within 2 weeks of using the cream it was like I had never had eczema. Also it has completely sorted my daughter’s eczema. Wish I had known about it far far sooner, it’s been literally a lifesaver.

If this is a sales post, I don't think this is the right time or place.

bunnyapple4 · 19/08/2025 15:51

It’s not a sales post in the slightest. I was trying to help, and recommend something that changed mine and my daughter’s lives in relation to eczema.

Hazlenuts2016 · 19/08/2025 17:13

bunnyapple4 · 19/08/2025 15:51

It’s not a sales post in the slightest. I was trying to help, and recommend something that changed mine and my daughter’s lives in relation to eczema.

Happy to be corrected. Am just always cautious of private treatments, particularly when someone is already under NHS care and there could be contraindications. However, glad you and your daughter found something that worked for you.

Passthecake30 · 19/08/2025 17:25

Hi OP, you said previously that he was resistant to changing dairy in his diet but it might be worth a go, for a few months. My dd is definitely sensitive to dairy, as are a lot of people with excema. It didn’t show up on blood tests (she’s allergic to dust mites and pollen).
Do you have an air filter with dehumidifier in his room?

bunnyapple4 · 19/08/2025 17:30

@Hazlenuts2016Thank you. I admit when I first heard of it I thought it was a gimmick, however I was desperate (to the point where my skin was so bad I couldn’t tolerate wearing clothes, and all the NHS would do was prescribe stronger and stronger steroid creams - which lead to TSW, which just perpetuated the problem), however after two weeks of using the cream (which is a mix of a base moisteriser with small quantity of antibiotic cream and steroid) it was like I had never had eczema in the first place. As I said, I only use it now and again if I feel a flare up is coming, and it has worked for my daughter’s eczema as well. She calls it ‘magic cream’.

TheGirlattheBack · 19/08/2025 18:10

RampantIvy · 05/04/2025 22:32

I agree with this. After extensive testing, the dermatologist discovered that DD was allergic to glucosides (found in most shampoos) and triethanolamines (found in shampoos, creams (many of which are eczema treatments) and detergents.

DD now uses Epaderm for moisturiser and a solid var of shampoo from Holland and Barrett and has been eczema free for several months.

I have eczema and I’m also really allergic to the prescription emollient creams you get for eczema. Took years to work out why my eczema was getting worse and worse - it was a vicious cycle or worsening eczema - more cream - worsening eczema. Does your son feel his eczema gets more itchy when the creams are applied?

After cutting out all of the prescription creams it’s mostly cleared up. I use Dove soap and CeraVe moisturisers. The reparative hand cream works a treat when I have a flare up.

coxesorangepippin · 19/08/2025 19:26

To be fair I have heard of Dr. Arun mentioned before on the eczema threads

DelilahMy · 19/08/2025 19:48

My heart goes out to him.

I had chronic eczema in childhood, am now in my 50’s. It settled down when I was 8 years old after a week in Spain in the sunshine and sea water.

At times throughout my life, however, I still occasionally get flare ups. This summer I’ve had an unusually angry flare up over my entire body. I suspect hormone related but who knows?

I can only tell you what has worked for me over the years. In my experience doctors do not help, you just learn how to manage it. Dermatology might be more help than a GP.

How I get on top of flare ups:

Steroids, steroids, steroids. I do not fear them and the alternative suffering is worse. I have managed to quell this summers flare up with Betnovate that I have purchased online. I cannot be bothered to waste time in pain waiting to see my GP and then them not prescribing anything useful.

I am allergic to most emollients the GPs prescribe. Oilatum, Doublebase etc. - all bloody awful and make it worse.

When skin is really bad, I use nothing but steroid. The skin is so sensitive at that point that it will react to everything that goes on it, exacerbating the situation.

I use laundry balls for washing clothes, no detergent.

Salt in bath is good.

I get on okay with Aveeno in the bath and shower. Childs Farm bath stuff and moisturiser is fine for me.

Sunbeds help. Or being out in the sun, sea water is great.

But mostly just use steroid cream only until it’s under control. Shower using something very mild, pat skin dry, steroid - and nothing but steroid for as long as it takes to clear it. Then taper slowly off.

I have used steroid cream for years and my skin hasn't thinned, by the way.

Allergy testing, had it all done and it is of no help to me.

Good luck, I hope he is more comfortable soon.

DelilahMy · 19/08/2025 19:51

Just read tour update today, OP. All the best with the test results .

Cherrycola4 · 19/08/2025 19:59

Cut out washing powder/liquid completely. It’s really helped my eczema. I just wash my clothes without any detergent, they smell fine.

Eczema creams can make me itch more. Oilatum Bath additive, loads of it, helps.

Sending him my best wishes.

DelilahMy · 19/08/2025 20:16

I forgot to list 1 antihistamine at night and in the morning if needed (Cetirizine by far the best).

DelilahMy · 19/08/2025 20:18

coxesorangepippin · 19/08/2025 19:26

To be fair I have heard of Dr. Arun mentioned before on the eczema threads

There’s a Facebook group UK Eczema Support that’s useful.

Hazlenuts2016 · 19/08/2025 21:26

@GlitteryUnicornSparkles I really wish him all the best with his next set of blood test results and hope that you find a stress free treatment that works well for him soon.

GlitteryUnicornSparkles · 20/08/2025 06:15

DelilahMy · 19/08/2025 20:18

There’s a Facebook group UK Eczema Support that’s useful.

I’ve just joined this. 😊

OP posts:
GlitteryUnicornSparkles · 20/08/2025 06:19

DelilahMy · 19/08/2025 20:16

I forgot to list 1 antihistamine at night and in the morning if needed (Cetirizine by far the best).

He was already on Cetirizine, they’ve changed him over to 180mg of Fenofexadine twice a day.

OP posts: