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Don’t let dry skin spoil your little one’s adventures: tips & solutions for winter

 Over 1 in 5 children have eczema or a dry skin condition. Winter is often worse with wind-chill, cold, and central heating triggering flare ups. The associated itching, irritation and poor sleep can really spoil little ones fun, so dry skin treatment for children, Epaderm Junior, has a few tips to help.

  1. Wrap up! Hands and the back of the neck are particularly vulnerable to drying out, so cotton gloves and scarves are an essential skincare kit – as well as keeping them snug during adventures.
  2. Hydrate – A cold drink is less appetising, so many children drink less in winter. Keeping them hydrated can help their skin, so try warming up drinks like apple juice to make them enticing.
  3. Apply emollients – Some moisturisers can contribute to skin dryness. Oil-rich emollients such as Epaderm Junior help stop water from leaving the skin which is great during winter. The ointment is a thick effective barrier, often used at night, where the cream is absorbed easily for use during the day.
  4. Avoid washing – Many children would be delighted, but we don’t mean avoid bath time altogether! Hot water and soap can also dry children’s skin. Try replacing soap with Epaderm Junior Ointment, it won’t foam up, but cleans and helps lock moisture into the skin at bath time too.

To find out more about Epaderm Junior, read our product reviews here.

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Allergy testing reminds me how little I know about medicine

Yesterday my daughter V went in for what has become a yearly ritual: her specific IgE blood test. She bravely went in after listening to the previous patient scream for 20 minutes. She yelped when she was stuck, but gritted it out while the nurse drew four vials of blood.

Four vials seems like a lot. My wife, who is a veterinarian, says she only takes one vial to test dogs for multiple allergens.

The process reminds me how little I know about medicine in practice.

IgE is a type of antibody, a Y-shaped molecule with sticky ends that recognizes allergens and triggers inflammation. Kaiser Permanente, our HMO, uses the ELISA test to measure IgE levels, instead of RAST, which has been abandoned since 2010 because it involves using radioactive material.

The first result came back as “IgE, QN    368    Standard range 0 – 75    U/mL”

“U” is for “unit.” How many antibodies in a unit? I have no idea. The internet is no help here. 368 U/ml, from what I can tell, is her measure of total IgE, all the antibodies of this type she has circulating in her blood.

So that means V’s IgE is five times the maximum normal limit. That’s typical for someone with atopy.

We’re still waiting for the specific results. I wouldn’t put it past Kaiser to waste at least one vial doing the wrong test, and then tell us we need to come in and give more blood.

Last year, among other things, V tested positive for IgE against milk, with 7.8 U/mL. I find it remarkable that her titer of antibodies to milk is 10% of the maximum number of antibodies that a “normal” person should have against everything.

V has eczema and mild asthma. Positive IgE tests are no guarantee of allergy, but we know she’s allergic to milk, since she vomits every time we give it to her. (Our son has no allergies and my wife and I have accidentally switched the kids’ glasses at lunch. Oops.)

She also has consistently tested positive for peanut and walnut allergy (and beef!), though there are as yet no incidents where she’s eaten some and had a reaction. We’re just trying to keep tabs on her allergies as she grows up, hoping, of course, that they will go away—but also fearing that she could develop a life-threatening allergy.
End Eczema

Supreme Court gene patent decision means little for eczema research

Following last week’s decision by the US Supreme Court that human genes cannot be patented, I’d say nothing has changed for eczema patients.

What I mean is that it makes little difference to eczema therapies now or in the future whether companies can obtain US patents on human genes.

I see two major issues: moral and commercial. Morally, I feel it’s a great triumph that even the famously conservative justices of the Supreme Court—who we really expected to side with big bucks, as they seem reliably to do—unanimously affirmed that nobody can own naturally-occurring human DNA. No company can own a piece of my genetic heritage.

Commercially, the issue is intellectual property. I work in biotech, and every day I hear about how it’s crucial for companies to control their IP. No investor is going to back a company that can obviously be sued in the future or that is developing a product that could instantly be copied by a competitor without penalty.

The loser in the decision was Myriad Genetics, which owned the US patent on BRCA1 and BRCA2, two human genes in which mutations increase one’s chances of getting breast cancer. (From what I can tell, Myriad had patents on the normal genes as well as common cancer-linked mutations.) Myriad had exclusive rights to DNA tests that could determine whether patients had mutations. Now many other companies are developing similar tests, and the competition will drive down the price of the tests.

That’s great if you want to get tested for breast cancer. But what does it mean for companies that are developing diagnostic tests for other conditions? These companies may abandon their efforts. Or the companies may never get started.

At least that is what one commercially-minded person whose views I respect tells me.

The Faster Cures blog, conversely, makes the point that patenting DNA could, and has, led to R&D on diseases being blocked by legal obstruction. Lilly, apparently, spent eight years fighting Harvard, MIT and others over the rights to one particular gene, NF-kB. Presumably lots of money got spent that might have gone to actual research instead of lawyers.

But for a gene patent to be useful, there must first of all be a strong link between genetics and disease. Eczema, despite being known to have a strong genetic component, has not been definitively linked to genes except in the case of filaggrin. There are a few mutations that seem to correspond to particularly severe eczema but they don’t occur in many people.

In any case, the sequence of filaggrin was made public in 2006 so the point is moot—once made public, an invention can’t be patented. (I searched the US Patent and Trademark Office database and didn’t see anything.)

Also a diagnostic test is only useful if it gives you information you can act on. There’s no point telling an adult that they have severe eczema, because they already know that. And if parents learn that their child is at risk—not guaranteed—of developing eczema, what can they do to prevent it?

Not much that I know of.

Diagnostics aside, how might a gene patent be useful?

Many drugs or biotherapies being developed affect how genes are regulated—how the process of turning their information into protein is amplified or damped. Perhaps owning a gene patent would let you control work that other people are doing to regulate that gene. We’ll never know now! What is certain, though, is that if you had a gene patent and lots of money, you could probably intimidate other companies by threatening them with expensive legal action.

I don’t think enough is known about eczema at this point that a gene patent would have been a factor. Look at the existing therapies and the few in the pipeline (such as Anacor’s). They are all either anti-inflammatories or calcineurin inhibitors. They don’t affect genes directly.

Researchers are starting to put together useful models of how itch signals get transmitted from the skin to the brain. For itch, we wouldn’t be interested in a diagnostic, but we would like to have a therapy. It’s conceivable that one or two genes may turn out to be key, and we might want drugs to regulate them. But gene patents would not be necessary for scientists or companies to do that work.

In short: last week’s Supreme Court decision, while morally important and laudable, will have little effect on the field of eczema research and therapy.
End Eczema

Our little Rainbow

I have fond memories from my childhood of my time as a Brownie and Girl Guide…

 

Drinking my first cup of tea at Brownie camp, first time away from my mum and dad (a whole 3 miles down the road), being a sixer, the honour of carrying the flag for our unit at church parade, doing a reading in church, trips to the pantomime, indoor marshmallow toasting with candles (probably not allowed these days), bonfires, playing ‘murder in the dark’ – always a favourite as we could do lots of screaming when we ‘died’ – as well as other games and making new friends I didn’t go to school with.  I’m glad they’ve updated the uniform now though, the brown culottes were particularly awful!

 

I remember when Rainbows was introduced – a section of the girl guiding movement for younger girls aged 5-7.  As Ella reached school age, I put her name down for our local Rainbow group.  I was keen for her to experience being a part of the guiding community and to have an extra opportunity to be included, to learn, to grow and to have lots of fun in the process.

 

I was very open with them on her application what she could do and what she would need help with but did worry that they may not be able to accommodate her needs.  I even offered to get involved as a leader if necessary so that they would have additional adult support if that was what was needed.

 

After nearly a year on the waiting list I got a call to say she could start in April after the Easter break.  I had a long discussion with the leader who called me and explained about Ella using makaton, that she was still not toilet trained and that she needed close supervision.

 

After bombarding them with all that information, we went along to her first session at Rainbows.  I took her in, offered to stay and was told as long as I’d left a contact number I could go but if I wanted to stay then that was fine too.  And with that, the Rainbows had now formed two lines and Ella happily sailed passed me, following her peers with a wave saying;
‘goodbye mummy, see you later’ 

So, decision made for me, I left her to it. And that’s as hard as sending her to Rainbows has been, unlike a lot of other activities we have signed her up for or tried to include her in before.  No EHCP’s to sort, no IEP, meetings to be had, no funding or 1:1 support to be found. No conditions on how and when she can take part.  The onus on inclusion and giving Ella the supervision she needs has been taken on 100% by the Rainbows team and not passed back to me as is so often the case.
The leaders ensure she is safe and supervised and able to get involved in whatever activities they are doing. The guiding movement has a commitment to be accessible to all and it’s been fantastic to see that ethos of inclusion working well in practice.  It proves to me that inclusion can happen and can work as so often we come up against barriers and challenges to allow Ella to take part and be included with her peers.
Every week they do a craft activity and we all know how much Ella loves her art and crafts. Every Tuesday she comes home proudly clutching a project related to whatever topic they are doing covered in wet glue/sequins/feathers/wet paint/drawings.  One week we even got her first ever independent, legible attempt at her name:
 
 
This week at the annual Rainbow, Brownie and Guide ‘Bonween’ party, Ella along with several other little girls made her Rainbow Promise.  We have been practising the promise over the last few weeks and have learnt the Makaton version too to help Ella commit it to memory better.  She was a little bit overwhelmed by all the people and what was expected of her on the night but she did a fab job considering and I am super proud!
Here is the picture of her with her trefoil badge getting a welcome handshake:



I was very impressed to find the Makaton version of all the guiding promises available on their website (another sign of their commitment to inclusion and being accessible to all):


I am sure Ella will continue to enjoy being a Rainbow and in a couple of years she will hopefully move up and become a Brownie.

I’ve kept my Brownie sash all these years, covered in the badges I earned (including m Highway badge), which six I belonged to (I was an Imp), my pack name, promise badges and my shiny silver trefoil badge.  Once Ella graduates to Brownies I’ll be able to show her my badges and I look forward to helping her to earn some of her own too.
Our little Rainbow xx

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Baby Eczema Care – Information & Tips For Caring For Your Little One

Eczema is a very frustrating condition for anyone to have but when it’s your child suffering, you really want a cure! Unfortunately, there is no real cure for eczema and all cases are a little different, so it’s very hard to find the right things to use to actually relive the irritation. Avoiding the use of a steroid cream is important for most parents.

From our research, eczema could really stem from environmental toxins – so here are a list of things to consider:

It’s really important to avoid any highly fragranced products around your eczema sufferer 
Laundry detergent – use fragrance free and made for sensitive skin, use it for all of your laundry ( bedding, clothes, the whole household) 
Personal fragrances – if you or any member of your household wears perfume –  it can contribute to and possibly bring on flare ups
Cleaning supplies – use simple things to clean your household such as vinegar and water in a spray bottle/ baking soda and water for hard to clean things. (commercial brands tend to have tons of  fragrance and again can bring on irritation) 
Try to keep your baby off of your carpets/hardwood floors – dust can aggravate the skin so try laying a blanket down washed in fragrance free detergent when the baby is playing on the floor
Family pets can also have dander that may also contribute
Try to keep an even temperature in your house – extremes can cause flare-ups
Having a humidifier in the baby’s room will aid in the dryness

If you have exhausted all these methods around your home, you may want to have a good look your little one’s diet. It appears that many eczema sufferers have reactions and flare-ups to things such as dairy (milk, cheese, yogurt, etc..) wheat (bread, pastas, etc..) and highly acidic foods (eggs, chicken, dairy, etc..) This of course requires diligence and a process of elimination as to what foods bring the flare-ups on. Luckily these days there are many options for gluten free and lactose free items as an alternative. 

Keep in mind there is no real cure and all cases of eczema are different. The common thread is that they all need to be dealt with in a gentle and soothing manner by keeping the area clean and well moisturized with a natural baby skin care cream. 

Tawna Hill is the Founder of Tawna Hill Baby – Natural Baby Care. A mother who only wanted to use the purest ingredients to soften and soothe her baby’s delicate skin, after dealing with a life altering illness while she was pregnant. Tawna Hill Baby donates 25 cents from the sale of each product to the search for a cure. 

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