Itchy eczema allergic toddler - not settling after 6 months. Ideas? (long)

So my DS was a very VERY itchy baby, diagnosed with exczema at 8 weeks and has never stopped having it to some degree. He spent his first 6 months wearing mittens/socks on his hands cos he would just scratch himself to pieces. At 10 months he was diagnosed with allergies to egg and treenuts (he'd never been given them directly, only exposure was through BM). Once I changed my diet, the itching and the eczema settled BRILLIANTLY. He also drank better and "snuffled" less.

Then last Sep (just before his 3rd B'day) he started repeatedly waking at night, scratching, crying, very distressed. (and this is a kid who was always a cruisy happy sleeper - EVEN as an itchy baby!) We saw the GP, we moved up our annual skin pr ick test, and we ended up having to put him on Zyrtec around the clock. The allergy paed that we said advised us that there were no new allergies (very uncommon to get them apparently) and that sometimes something just sets them off, keep him on Zyrtec 24/7 for 3-6 months until it had settled. We also had been using phenergan AS WELL when needed (bathing a toddler at 1am who is howlingly itchy just really doesn't get my rocks off for some odd reason). He also commented that the eczema was well controlled.

Last month I was STILL having trouble with him waking/crying/scratching - 5 mths down the track. Finally a BIG penny dropped and I realised how many of MY skincare products contained either macadamia oil, almond oil or shea butter (also a treenut). None of his did, but quite a lot of mine did... and they list them with the latin names, so you have to go googling to even find out it out!! :wall: so annoying given we'd had NO medico of any sort ever suggest to watch out for it, and I really don't understand how even baby and toddler products can include them but don't have to declare it! (anyway that's a separate rant from me!). So I've removed everything (yes that seems to include my lipstick - boo), and we've definitely had improvement. Yay. No more phenergan required, we just continued the zyrtec.

So this month, I've been trying to drop the zyrtec. But almost every attempt and suddenly I have a boy waking at night, scratching and crying. I made it to 4 days zyrtec-free last week. But then he woke 7 nights in a row. We're at the stage that we can try a food challenge with egg.... but of course I can't do it while he's on the zyrtec.

I went to my GP today who has her own very itchy boy and we're off to see a paediatric dermatologist on Mon (waiting list was till June, but got in on a cancellation WOOT!). This guy is apparently very good with allergies & digestive stuff too. My doc agreed that my normal allergist probably isn't going to have any further insight. As for me, well i think sometimes Dr Mum's solve more than Dr $$$'s do, so I'm trying to put on my thinking cap. Historically, this itching is just like what he had as a baby - which suggests to me the same culprits. It could be a food he's having is contaminated - as we do eat some commercial food and virtually everything says "may contain traces blah blah blah". I do try to cook a lot at home however as we have multiple food restrictions in the household.

Also, DH and I DO actually eat eggs and nuts ourselves (and tbh with my limitations from a nutritional perspective I really shouldn't be avoiding them)... but I've rearranged the pantry, we try to eat them at night when he's in bed, wash face, hands, clean teeth etc afterwards. Surely he couldn't be that sensitive that having them in the house would set him of? Could he be?

The other option is it's a sensitivity and not an allergy per se. So he's just a sensitive flower and I should cut some other common irritants from his diet and see what happens. Meh. Really not keen. Plus he's fed at FDC two days a week which makes it hard to control his diet. (And really I shouldn't get started, but i have restrictions, DH has restrictions and we're currently trialling DH on a diet for his vertigo... I don't think I can handle more diets honestly).

There's another thing, maybe it's the FDC food? So saying I think she's even more paranoid than i am - she won't give him foods that say "may contain traces" whereas I do!

Or i look for other sources of irritation - washing powder, chemical cleaners etc... I could change all that kinda stuff (which I haven't changed recently - and my DH rudely said I don't clean enough for it to be the cleaning solutions bwahahaha cheeky git), but honestly to me it seems more consistent with somethign that's going in him IYKWIM not outside him. I know that sounds silly when he's itching, but he has particularly itchy zones. Around the eyes, and back of the head in particular. Knees and legs cos he often has access (summer shorts).

Oh and my GP thinks in both our boys' case it is the eczema - but we're both told it's mild eczema, but we both have insanely itchy boys.

Anyway, that's my rant & rave. Love to hear any other ideas. Are other kids with "mild" eczema this itchy?
TIA for reading :)

I'm having "fun" with a 2 3/4 yr old whose itching is driving me insane as well. He's scratched raw elbows, behind knees and ankles. We've seen an pediatric allergist (sesame - mid reaction, egg white and dairy - very mild reaction) and that temporarily cleared it up along with a steroid cream. Eczema came back last Oct and hasn't gone so got a referral earlier this year to a dermatologist, several blood tests later and we're about to start a third type of steroid cream and be referred to a dietician, I'm kind of over it all. When we first saw the dermatologist we were told to put ds on a restricted diet without some things being explained why they were on the list but not others (eg ice cream was not allowed but other dairy products were) and to use a stronger steroid cream than we had been. The diet was supposed to last for a month as it was supposed to clear up DS's skin and then we'd be allowed to reintroduce foods back on slowly. Well ds skin didn't clear up totally in the 3 weeks we did it (including at CC) when we went back to see dermatologist but she said we could reintroduce foods again and it's gotten worse even with dropping back foods. DS ends up going around with crepe bandage on both elbows to stop him scratching at night - refreshed daily. Band-Aids are leaving welts on his skin if we try to cover the worst bits:wall:. His legs are now starting up as well - came home today from CC with crepe bandage tied around both ankles because he scratched so much that they were bleeding.

I soooo get you on the scratching thing. If ds could just leave it alone for 2-3 days it'd nearly be healed!

I've tried the eczema moo goo cream (nut oil based); tried hemp cream/oil from the body shop; tried sorbelene cream (ds has screamed when putting this on and we've tried different brands); tried other moisturizers.

Currently also trying a natural based moisturizing cream called mums secret - started that last night - friend recommended that - can send link to info on that one if you like in a pm later. That one at least smells nice and feels nice rubbing it in. Can't remember all the ingredients of that one but I know it's not nut based at all as I checked thinking I might send it to CC for them to put on during the day.

I would have tried the third steroid cream (this one also has an anti-fungal cream in it) but I only collected it from the hospital pharmacy this evening while DH was getting DS ready for bed & I was on my way out for tea. We'll start that one in the morning.

Apparently the dermatologist is referring us onto a dietician in a couple of weeks to see if we can work out if it's diet related.
I've ordered a new mattress for DS in case it's dust mites or something in the mattress- he has a second hand mattress on his bed - asked DH to sort that out and I was still waiting 2 weeks later so gave up and sorted that out today. Also need to work on washing his sheets more often :redface: as I'm not good at changing his sheets - old bendy mattress doesn't make sheet changing easy in the third trimester of pg and DH doesn't think to do it :rolleyes:

Oooh you poor thing! I think your poor DS's skin sounds worse than mine. And don't you love having to cut their nails just insanely short to minimise the damage? I still remember a confident father of 3 (when I was complaining about cutting the nails one day) offering to do it - and saying, oh but these nails don't need cutting. And I'm like "oh yes they do!" - it's enough for him to wake with a face covered in scabs and a blood-spotted sheet.

Interestingly we have a second-hand mattress too.... aaargh maybe I should go shopping. And oooh I remember the nuisance that changing bed linen was in 3rd tri! GL with that!

I also remember trialling moo goo eczema balm on him years ago... pre-diagnosis. Didn't even realise/notice that it had almond oil back then, but I didn't have to worry in those days! I actually did a few weeks trial - that on one side of his face and his "conventional" treatment (can't even remember what it was) on the other side. And the other side won (and was vastly cheaper), so I've not bothered with it since. We typically moisturise with Dermeze (which always has seemed to work the best for him) or Dermaveen and bathe in QV, all of which seems to work. I guess. i say that, but then I'm posting here, so it's not really working is it!

Interesting about the dietitian. I really hope they don't suggest that route to us... but should I say that when it could help? Seriously though it could just be my full time job managing to feed us all if we have to do another diet for him!! :wall:

Thanks for the info on the cream, I found it with some googling. It looks really good, and I like the combo of plant oils they've used. I did get really over buying lots of different creams when he was younger... but now I've had to shelve most of mine, it might be a good idea!

I found a vac packed single mattress for about $200 delivered on the oo .com (I think its .au too) site. It's supposed to help with allergies and only take 1-2 business days to deliver and about a day to reach normal size again. Hoping it's here by Tuesday (monday would be great) so ds can be in it by Wednesday night. Might mean its easier to change sheets too :crossfingers:

Hi hon, eczema can be really horrible. Cut out dairy, eggs and wheat from your diet if you are breastfeeding this is known to help. Nightshades can also irritate.

Poor little man. poor you too. Ive suffered terrible itchy skin/dermatis since my teenage years, on wednsday i brought mcarthers pawpaw liquid gold cream and my dry scaly patchs have gone
, i havent itched in bed since,. it does tingle when first applyed. Amazing cream, even relives my soar achy back. it was expensive at 60$, but well worth it.
i cant tell you if it contains nuts though. if you google it their is heaps of info and a facebook page full of testimonies.

Oh gosh belfie, i was going to come in and offer advice, but you have done and tried everything.
The 'best' moisturiser for my DS has turned out to be a natural colloidal oatmeal one. (Aveeno). So we do the colloidal creamy wash in the shower (pfft bath - not happening here!), and then the eczema cream and them the colloidal oatmeal moisturiser.
Also i bought a 100% silk duvet inner. Seems to help him not get too hot and irritated at night.
I know this all costs money and there are no guarantees it will work for your kids.
I'm sorry you have to deal with this. Sounds more than 'mild' to me.

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If ds could just leave it alone for 2-3 days it'd nearly be healed!

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The itch from eczema is so severe, it is virtually impossible to 'just leave it alone', even if you are right that not scratching will improve it. And the nature of eczema is such that even if you get one bout 'healed', it will generally come back anyway.

I was a child who's parents tried everything people are talking about here, with minimal success. I used to wake up in the mornings and the very first thing I would do is check my fingernails, to see how much blood there was under them, how badly I had damaged myself, every single day of my childhood. It wan't until I was in my teens that I became better at managing my eczema, through identifying, and therefore being able to avoid my triggers.

My triggers include woollen clothing and carpets, dust, dust mites, pets, saliva (even my own), grass, all soaps and detergents, the preservatives in many, many creams and lotions, (including hypoallergenic ones, specific eczema ones, and even in topical steroids which were prescribed for my eczema)! Most shampoos and conditioners cause a flare-up - which of course, is all over my body, because the shower rinses them off from the top, all way down. Hot water aggravates me. Anything oily, even olive oil or butter on my skin when I cook, let alone bio-oil and vitamin E capsules, etc, makes my skin inflamed and itchy. I don't use any creams with oils in them. I can eat oranges, lemons, tomatoes, papaya, pineapple, coconut cream, vinegar, but heaven forbid should they touch my skin. Honey, and anything with royal jelly in it. Alcohol swabs. Swimming pool chlorine. Most sunscreens. Sunburn. My own sweat. All the other sunscreens when combined with sweat. Oh, and stress. That's a biggie. As for my current flare-up, I'm hoping I'm not actually allergic to my own pregnancy hormones, but I'm going through a bad patch right now and I can't work out what it is from.

I have noticed that my eczema is worse when others around me complain their hayfever is flaring up, so I presume I'm also triggered by airborne pollens.

There are different elements to managing eczema: 1)Identifying the triggers and avoiding them, 2) treating the inevitable flare-ups (any rashy/ itchy patches at all, even if they are 'normal for your child', and 3) maintaining the skin barrier. All those moisturisers that we keep buying and trying and discarding, even the ones that 'worked a treat' for someone else, they just help to maintain the skin when it's already in good shape. They are not likely to help resolve the rashy patches, and for many of us, they just sting and therefore make us rub and itch, because they're getting into the raw patches and cracks. The patches will almost definitely need treating with steroids and/or other anti-inflammatory/immune-suppressing/anti-bacterial/anti-viral treatments. And they will keep coming back if you don't work out what the allergens and triggers are.

It is definitely worth trying getting bedding with mite-proof covers, and change the sheets regularly, for sibling on who's beds they might play, and for your own bed, if they ever creep in. Vacuum up play areas regularly. Borrow or buy a vacuum with a HEPA filter, and see if that helps. Don't 'dust' because then the allergens just get airborne and settle elsewhere. Use a damp cloth and wipe surfaces, instead, especially in their bedrooms and play areas. Those 'electrostatic dusters' are not as good as you'd like to think - a damp cloth is far more effective. Get rid of, or cover woollen carpets and rugs that they sit and roll around on, and try using a rug for playing on grass. Vacuum the couch regularly. Avoid room sprays, fabric softeners, perfumed washing powders. Try different washing powders, or soapnuts, or ecoballs (my choice). Do do this at low expense, borrow/swap a couple of doses of washing powder from every family you know, and monitor their skin. Watch out for eco-cycles on washing machines, because the low water use often doesn't rinse the soap out enough for us sensitive types. Rinse off well after swimming, and don't sit around in wet bathing suits.

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Surely he couldn't be that sensitive that having them in the house would set him of? Could he be?

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Possibly, but it's not likely. Playing with egg cartons, however, can be a trigger for some kids - I've heard of that. FDC may well use them for craft projects,even if you don't at home.

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Band-Aids are leaving welts on his skin if we try to cover the worst bits

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Adhesives are a common enough trigger, too. You could well make the bits around the bad bit, worse. For me, the adhesive doesn't cause a problem, but when it's removed, a few skin cells come off with it, and I think that tiny bit of damage to my skin barrier makes it likely I'll flare up there within a few hours.

Think carefully about any pets you have. Even if you'd like to think your child is not allergic to the animal (or have had skin ***** testing to show they are not allergic - the animal may still be a trigger), even if you think of your pet as 'part of the family', even if the animal is kept in a cage in another sibling's bedroom, even it it lives 'mostly outside'... You should be really, truly certain that your child has absolutely no reaction to your pet before you decide to keep it (the pet, not the child.) :) At other people's houses with animals, realise that removing the pet from the room the child is in will not stop the reaction, though it might help a little. To this day I will sit with a clean towel (not from the linen cupboard that their cat likes to sleep in!) on any furniture I sit on, and will change my clothes when I get home. And DP can't pat or cuddle animals, because just sitting in the car with him can make me worse afterwards.

Eczema itching is not just like having an annoying mozzie bite, it's an agony. It's torture. Doing anything that makes it worse is cruelty. If you haven't suffered it yourself, you have no idea.

And the things that come up positive on skin ***** testing or IgE blood tests are not the only allergens for your child, and things that are not allergens can still be triggers. I am not technically allergic to any of the foods I mentioned, and on an elimination diet as a child, my eczema got worse, not better, which confounded the dietician and dermatologist at the time!

Things that are 'all natural' are not necessarily better than synthetic. I can't even rest my palm on the woven natural fibre matting in my yoga class at the moment, but I'm fine on the rubbery mat.

If GP management of your child's problem is not enough to allow them to sleep well and function normally during the day, get referred to a paediatric dermatologist. Get skin***** testing, and/or blood IgE tests. Get referred to a dietician, and ask about elimination diets to help to identify any food triggers AND make sure they're still getting a balanced diet. Ask about skin-supportive supplements, like zinc. Ask about short courses of oral steroids to control flare-ups. Ask about pimecrolimus/tacrolimus instead of steroids (I don't know if they are an option for children.) Ask about wet wraps, and anti-bacterial baths to control staph populations on their skin. Ask about intermittent antifungal treatment. And keep on asking, over time. What's available and what's recommended keeps changing as more and more research is done in this field. And what works for your child now, may reduce in it's effectiveness down the track, and something else becomes more appropriate.

Get a copy of Prof Susan Prescott's recent book, 'The Allergy Epidemic', UWA publishing, 2011. It's very readable, and extremely interesting for any person with allergies or an allergic-type child, and includes the very latest research and theories, and will stand you in good stead when discussing issues with any kind of dr or specialist.

And as far as your children having 'mild eczema' goes, those who have posted here are clearly all trying to do their best to help, to find solutions and causes and treatments, and although no-one feels like they're doing everything, or being completely successful, imagine how much worse your child would be if you were doing nothing at all. Your child is probably only diagnosed with 'mild eczema' because you are doing stuff to stop it from being 'moderate' or 'severe'.

And finally, what works for one, will not always work for another. Everyone is different, with different triggers and treatments. But as hard as it can be to work out what the triggers are, and to find effective treatment, it's worth it to help your child feel normal, not have unattractive skin that makes them a target for bullying and unkindness, avoid the stronger medications where possible, sleep well and therefore have to opportunity to learn and concentrate and think clearly, instead of half their brain constantly being devoted to 'I shouldn't scratch that itch'... ultimately to be healthy.

Sorry that was so long. Obviously this is a topic that's of great personal interest to me, and I thought maybe an adult's perspective might be useful to the Mums of affected kids. If you get through it all, I hope it's useful. :)

Just another thought Belfie, check out GAPS as a means of healing eczema. Goodluck

I've thought about doing the gaps diet but I'm not sure how it would work with childcare thrown in the mix for 3 days a week - I need to read up more about it.


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Band-Aids are leaving welts on his skin if we try to cover the worst bits:wall:.

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Latex allergy? Regular band aids cause havoc here.

I've used the regular and sensitive bandaids (& not just the bandaud brand) and had reactions to both and paper tape when using that to hold non stick dressings over the latest raw patch.

Thanks for that insight pholi it helps to understand a but but it's just so frustrating watching it. I think what ds currently is reacting to is more like a fungal infection as its not presenting like his usual appearance of eczema. Rolled up our carpet mat in the lounge tonight and swept the floorboards under that - hoping that helps too.
Seriously starting to think I need to find out about wet wrapping too.

Great post Pholi!

If it's specific areas of his head, has he recently got a new hat? that might be different fabric? Also, with things like soap and shampoo, there is the possibility of becoming sensitized, in the sense that something that didn't used to cause a problem is now more of an issue after a few years of exposure. So an experiment may be worthwhile. We don't use soap on DS other than on his hands and bum - just water. It seems to do the trick anyway. DS is set off by sorbolene and dermeez, but OK with moogoo. We try and cover him up as much as possible to minimize sunscreen (so long cotton pants and long sleeved lightweight shirts).

And as far as the bandaids are concerned, have you tried cutifilm (from pharmacists) - it's expensive, but no reactions to it from either me or DS. Personally I find the rough edge of bandaids is what sets us off (as it seems to abrade the neighboring skin). The cutifilm is much thinner and softer, so less of an issue.

pimecromelis is available on special order prescription for eczema on the faces of kids - DS has it. It's very expensive, so keep it in the fridge do you don't have to throw it out 3 months after opening the tube!

My DS has very mild eczema - but when it flares he will scratch holes in himself like nothing on earth - and will use his toenails as much as his fingers!

Bella - any chance the dishes from the nuts are mingling with the rest of the dishes and cross contamination is happening there? Dishwashing isn't perfect at removing proteins. Can you keep the dishes separate and see if it helps?

(sorry for hijacking)
We're down to plain water for baths including washing hair. For a while there we had a sleep association (still do occasionally) with scratching the back of his head before being able to sleep :wall: but that's not bad at all. Arms are particularly bad around elbows - will rub them raw against the couch/sheets whatever - & ankles are a bit like that too. He didn't use to do that.
Ds used to have some very mild eczema on his face but that cleared up long ago and hasn't reappeared ever!
This time round it's coming up as little blisters and not the usual dry skin only so I suspect it's more than just the usual eczema.


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Most Awesome Advice Pholi. I really got a lot out of reading of your experiences and your advice. As a mother who has never suffered eczema, I never fully understood how my child suffered, but I agree it is important to try to do everything you can to try to relieve symptoms and find answers.

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And finally, what works for one, will not always work for another. Everyone is different, with different triggers and treatments.

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With this in mind, what worked for me and my DD was eliminating sulphites. DD started exhibiting symptoms at 2 months and got steadily worse until I figured a solution at about 10 months. She was reacting to the sulphites in my diet through breast milk and as soon as I started cutting them out I noticed a dramatic improvement. I was really lucky in that the answer came relatively easily and was limited to only one trigger. Apparently sulphites are a common trigger of eczema and asthma but we tend to overlook them as they are considered a 'safe' preservative.

DS's has always been the blisters, rather than dry skin (he's either symptom-free or a mess of blisters and scratches, but nothing in between). When the blisters happen we use elocon for a couple of days and they go away - but they rarely go away without the elocon.
Has he started something that makes him sweatier or more abraded - kindy sandpit for example?

Bella - has this period of recurring eczema coincided with xander becoming independently toilet trained? And is he washing his own hands - and maybe not rinsing very well, and then putting soap residue where it can irritate? Especially if FDC has non-eczema-friendly soap.

It was spring :lol: and this summer hasn't been it's normal self.


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Well we had an interesting appointment with the dermatologist today. NOW I think i get it.

I have a boy with food allergies, MILD eczema, PLUS chronic hives and dermatagraphia (I have this last one myself too). So that explains all the itching, and when the itching is bad enough, it exacerbates the eczema. And triggers-wise, well yes, he talked about all the usual stuff - overheating, environmental triggers but also explained that he might easily get worse due to a virus or a food sensitivity. He wasn't saying that we need to do an elimination diet per se, but suggested we keep an eye on the really acidic things, plus the sulfites, nitrates, nitrites, salicylates and amines (which I'm watching out for with hubby anyway). And interestingly my son will not eat pizza for love or money and I reckon it's the tomato paste. Plus he does tend to get a bit of eczema just under his bottom lip which is very indicative of something bothering him intolerance-wise. So I think I will definitely do some playing around with that. The dr also suggested a cotton mattress protector rather than rubber backed one, I'm going to try a different doona (the asthma foundation says feather is great but mightn't be good from a skin perspective).

So I'm thinking of either artificial type one (that sounds awful, but you know - those allergenic ones), cotton or bamboo... thoughts on that? I can't stand wool myself so I'm really disinclined to go near that. And my DD will need a doona soon enough anyway, so I don't mind buying a second one).

And the good old moisturise, moisturise, moisturise. And keep him on Zyrtec for as long as we have to - that the 3-6mths timeframe provided by my allergist has no real relevance. It makes the food challenges a bit trickier but fundamentally it makes me feel quite validated to keep him on it to keep him more comfortable. He said for every year he's taking it, he'll be 50% likely to have to do another year. So hopefully he'll grow out of it, but in the meantime he doesn't have to keep suffering as much with the itching. He's also upped the dose too. Interestingly he didn't think my lipstick or skin care products would be playing a part. Hmm I'm still not sure about that. And suggested that if we need an asthma preventer we should go for singulair as it both does that and is an antihistamine as well - might consider it for winter.

Kmn - kindy sandpit and soap residue could definitely be a factor, however he hasn't seemed to be that much worse since starting kindy this year (and toilet training was only in Jan) - he's been worse since sept last year at which point nothing really had changed (that I can remember!). RE the dishes, well we tend to eat things that are dish-independant IYKWIM (muesli bar etc) or I make things in my Thermomix but I nearly always (but not 100%!!!!) handwash dishes that I've cooked allergens in - so I might continue doing that. And oh... toenails! He's never done that one. Ouch!

Jackrose - I'm so glad you commented about the sulfites cos we know my DH doesn't do so well with them, so makes sense they could be a trigger... and TOTALLY agree with what you said about Pholi's comments, it was really informative.

Leckert - pls don't apologist for hijacking at all, if it helps us then that's fantastic. I wished I'd posted earlier because I've found the entire discussion very interesting, thought provoking and informative.

Lenny - where did you get hte silk duvet inner from? That's another interesting possibility for us.

Pholi - seriously I'm looking for the *bow down* emoticon, AWESOME post, thank you so much. IT's funny sometimes I've felt guilty, do I use the steroid creams too much, do I dose him on antihistamines too much. Felt totally validated that I AM trying to help minimise his suffering. It's funny he's such a cruisey little dude, a great sleeper - which is really a miracle for an itchy kid I think. This is a 3yo who happily puts himself to bed when he's tired! Or maybe he suffered so much he could deal with anything now?

Does anyone else find their kids get flared up massively in different places? I can't take him down to Tassie without him looking terrible (my family is there), so now I know, so I always just get preventative - full zyrtec and constant moisturising to keep it more controlled before it can flare up.

We're lucky in that we've not had to deal with wet wrapping or bandaids - he doesn't get that bad. And when he does scratch himself till he bleeds it's usually my sign to cut his nails so he can't damage himself too much. Ah, it's heartbreaking stuff isn't it. Well onwards & upwards. SEnding non-itchy vibes too all.

Well the anti fungal part of the cream seems to be working wonders here - arms are looking near normal and clear after 4 applications AND he's not scratched his elbows even though there's been no bandage on them as well :leap:
Still waiting on new mattress to be delivered. Have rolled up mat but DH wants one to put down still :wall: mainly for the new addition soon - I'm telling him a blanket/quilt will be fine and we don't need a new mat


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that's great Leckert! Let us know how you go with the mattress.

Kmn - just had another thought. Our kindy teacher has a child herself who is anaphylactic, so thus far she's been really great with allergy issues, so I think the soap is probably fine. Plus his hands haven't gotten any worse since starting (and he tends to get eczema on his thumb-sucking thumb - only place he's had infected eczema actually), so I think if it was a problem, we would have noticed.

Incidentally I was just looking at the eczema association of aus website and they don't recommend wool for bedding. They also say "Use non-biological soap powders and detergents." I don't understand what they mean by that?? Does it make sense to anyone else?

That's great you have some answers Belfie, It's really all trial and error. Regarding your products, I had to get dh to change everything he uses to natural products as I was reacting to everything he used including shaving cream. Also with the moisturising, I found that to be really helpful especially when I smothered on the cream and put a wet dressing over it (this was incredibly relieving for the itch as well), however my chines herbal medicine therapist said that my eczema is a 'damp' condition (as in it weeps) so keeping it dry is better than moisturising. I've been testing this the theory over the last couple of months but the jury is still out.

oh that's interesting. Would you still moisturise when wet? I know we've always tried to do that - the old "seal the damp skin" theory which does seem to help him.

Now i'm confused. The eczema foundation says:

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"The importance of house-dust mites has long been considered a factor for asthma sufferers, but for many years it was not appreciated that people with eczema could also be affected by the mites. However, more research has shown that for some people these little mites do trigger flare-ups of eczema.... Buy duvets and pillows that are made from man-made fibres rather than feathers."

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So they definitely think the dustmites in the bedding plays a part.

But the asthma foundation says:

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Feather bedding may be a better bedding option as it has substantially lower house dust mite allergen levels. Tightly woven (impermeable) covers should be used for mattresses, quilts and pillows but they must enclose the whole item for best effect.

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And that's the bit they both agree on - that the covers should be used. So I'm thinking I'll invest in some. I also need to fix my washing machine which has only washed on cold for quite some time lol.

And just some more detail from the national asthma foundation:

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What type of bedding is best?
For some time it was recommended that people who have asthma (or who are more likely to develop asthma) avoid feather bedding and choose synthetic materials (eg foam, polyester or dacron) as they withstand frequent washing. This is now not thought to be the case. ew studies have shown that not only does synthetic bedding have higher levels of house dust mites and their allergens than feather bedding, it may also increase the risk of infants developing wheeze.
This may be because the synthetic materials give off substances that irritate the airways and make them more susceptible to allergens. Again, this is an area where we have much to learn.
In the meantime, it seems sensible to use low allergen bedding for infants and children at high risk of allergy or asthma. Where possible, use encasings for mattresses, pillows and doonas, rather than plastic covers.
Low allergen bedding should be used. Feather bedding pillows and quilts have substantially lower mite allergen levels than synthetic bedding. The use of bulky items such as pillows and quilts (feather or synthetic) is not recommended for infants under 12 months because of the increased risk of SIDS.

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They mean that enzymes in soap powders can irritate some people, and also that sometimes plant-sourced ingredients can be more allergenic than chemical ones which can be purified so that they only contain the appropriate chemical.
We do OK with the omo sensitive stuff here - but we only put 1/4 of the recommended dose in each wash.

Bel all these chicks are such a help but i thought of something that may help as well is the Bosistos eucalyptus dust mite wash. My chemist sells it, it's a liquid laundry detergent that kills mites in linennand bedding and safeway sell the powder. I use it here as the euc kills germs, it's bio friendly etc.and didn't sentiment flare up Izzys eczema.

Got the silk inner from an online store called cocoon (?) i think. There are other retailers, but this was a Melb one.
It's light, and thin. We have it one our bed for eczema DH too. There is a but - you can't launder it.

I haven't personally tried this but I was interested in it because there has been some success with psoriasis which I suffer from. I dont have eczema but it was what the "posters child" (on another tip forum I am on) suffered from and many others tried it most I think with some success.

A tablespoon of molasses once a day. It has to be pure molasses which you can get from many health food shops or even some coles and woolies sell it. Be careful though as there is an sweet or and unsweet type. It doesnt matter which one but the unsweetened is very hard to get down.
The "poster" stirred it through a glass of chocolate milk for her daughter and said within a week it was gone and this was from been covered. A aboriginal elder had told her the tip and she was very skeptical but thought what have I got to loose I have tried everything?!

Many others also gave it a go and many of them couldnt thank her enough for such an easy solution to something they had been fighting with for years.

As I said I havent tried it but I have been on this other site for years and have discovered many useful and handy tips and ideas so I thought I would let you know.

This is all so hard & confusing. My DD3 was diagnosed with eczema at 5 weeks old & suffered a constant rash on her neck/chest right up til we moved to the other side of the country! I have not had to treat her eczema once since we moved to WA. We were in a humid coastal area before though. Its alot dryer here.

I stopped using washing powders etc straight away. Never really did, but I think a couple of her singlets mixed in with our washing & that triggered that first flare up. I never have used bath products on her, except goats milk. I used to just leave the cake in the bath so the water was white for her to soak in it. That was the only way to clear it up without cortisone cream. (I really didn't want to use cortisone on such a teeny tiny baby).

I now only use the Eco store products. I have no idea if it was them, or the move, or both, but her skin is amazing now :) It was not at the extreme extent of some of yours, except that first break out. & just that stubborn rash that she had for well over 12 months.

I also have an asthmatic allergic to mites & mould, so I really try to be strict on keeping them at bay.

Hi there belfie, I thought of you today when my hands were sore, inflamed/swollen and ITCHY!!! I soaked some oats and then put my hands in the mixture and it was heaven! I put the mix in the fridge and I have just done it again... The mix is even better cold. It really takes the redness out and the swelling and I can just move my hands so much more now. Just something for you to try :) Happy easter.

Either the hazel wood necklace (from all about amber) or the steroid cream being applied 2x day (stronger on than previous - thanks DH for not applying when getting ds1 dressed :wall: ) or the 3 quarters of a footy match (was happy there and not sooking for DH so wasn't going to take him out) soaking in Epsom salted bath seems to nearly have cleared up the eczema again!!!!
Ds1's face flared up due to a throat infection. His face hadn't flared up since we first cleared it up early on. Hoping that another Epsom salt bath tonight will help with the last bits behind his knees will have to try this again if it comes up again next spring.


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