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One Woman’s Incredible Story of a Chronic Allergic Reaction to Latex

Another great post from itchylittleworld.com – Natural remedies for eczema to soothe your itchy little world..

Last week, we received a truly incredible story from Renee, a long-time sufferer of eczema with a chronic allergic reaction to latex. She thought she had been avoiding latex for years, but discovered she’d unknowingly been exposing her body to latex in two hidden ways. Her story is quite shocking! See for yourself.

“I’m 60 years old.  When I worked in an OB/GYN lab in my 20s, there were no nitrile gloves, only rubber.  I became allergic to latex and so learned to stay away from rubber products, even supposedly latex-free elastics, and bromeliads (cross reactive with latex).  In my early 40s I began to have joint pain and skin rashes.  The joint pain was so bad. There were nights where I had to stop on the way to the restroom and just breathe, to try to let the pain ease a bit, before continuing on.  Eventually, my breathing became an issue as well and I was diagnosed with Reactive Airway Disease and exercise-induced asthma.  The joint pains were never definitively diagnosed and I went on the usual merry-go-round of diagnoses, e.g. lupus, fibromyalgia, rheumatoid arthritis, etc.  But then suddenly, in my early 50s, the problems disappeared.  The joint pain left, the breathing was no longer a problem, and my skin improved.  I didn’t understand why, but I was so grateful.

Latex Allergy4

In my late 50s, my husband was diagnosed with a brain tumor. 2016 was full of stress and sadness. My skin problems returned with a vengeance and I found I could not eat many foods that were rich in hevein and its cousins.  Hevein is the protein responsible for latex allergy.  If I ate coconut, palm oil, nuts, etc, the eczema patches flared and oozed.  The itching was non-stop, in spite of a daily regimen of antihistamines.  It was torture.  Everyone said “Stress!” and I thought it was as well, until the symptoms got even worse after my husband passed.  I was only able to eat 17 things and realized I had graduated to a full latex food allergy.  Any other food made my eczema and itching flare.  There were patches of infected skin all over my body.

A few weeks after the funeral, I had a molar pulled.  The oral surgeon showed it to me, saying yes, there had been a hairline fracture just like a previous molar he had pulled when I was in my 50s.  The tooth that he showed me had pink stuff in the root canals and I asked what it was.  He said, “Oh, it’s a resin from a tree called gutta percha.  It’s used to fill in the empty canals after the tooth’s roots are removed in a root canal job.”  I looked at that gummy resin and asked if it might be related to the rubber tree?  The oral surgeon suddenly looked really shaken and went to his computer.  Sure enough, gutta percha is related to the rubber tree.  I was being poisoned by my own tooth?  Incredible.

So looking back, my first autoimmunity started after my first root canal and resolved after the tooth was pulled, and now my second bout of autoimmunity started after the second root canal and would resolve just as quickly?  Sure enough, by that evening my inflamed skin and itching were about 1/2 of what they had been.  But even so, my eczema did not fully resolve and I was not able to add any foods back.  I thought okay there must be something else inside of me that is overstimulating my immune system.  The more I thought about it, the more I suspected a trans-urethral mesh, the “Sparc sling” that had been put in during my hysterectomy in 2004.  It’s the one you see on late-night TV, with lawyers asking if you’d like to join a class-action lawsuit against the manufacturers.  I had also suffered some of the symptoms they said on TV but it was the suspected autoimmunity that bothered me the most.

So on October 9th of this year, during abdominal surgery, the surgeon removed the mesh.  She was able to get it out totally, fortunately.  The rest of my skin began to clear on the operating table – seriously. The head OR nurse had been watching the eczema patches on my arm and chest because of the fear of my reactivity to their tapes, adhesives, etc.  Those things, especially the “inert ingredients” are all partially sourced from coconut and palm oils, and they were concerned of anaphylaxis.  Since I had told them that the patches would flare bright red if I were reacting to something, they were using those patches as their ‘canary in the mine shaft’.  After they wheeled me into PACU and I came out of anesthesia, the head nurse said, “Mrs. McMurray, look at your arm!”  It was totally clear.

Latex Allergy

The next day, a hospital official came to my room and asked to see the arm and my chest.  Both were totally clear.  Then the surgeon sent her Nurse Practitioner the day after that – it was still clear.  Everyone said the same thing – that in all of their years of working on patients, they had never seen an allergic reaction, especially something as tenacious as eczema, clear so quickly.

I am home now, three weeks later, and am a little bit red.  No eczema, but just a tinge of redness and a small amount of itching.  This is due to the corset I must wear.  Try as I might, I can’t stop the elastic bits from touching my skin.  But let’s put this in perspective – when that mesh and gutta percha were in my body, elastic sent me into absolute misery.  My skin would become red and weepy.  The sores itched like crazy, usually for 24 hours per day.  At night I’d wake up in respiratory distress because the swelling would reach my neck.  I slept with a rescue kit.  A little bit of redness and mild itching is nothing.  I am so, so happy.  I have to wear this corset for two more weeks and then I can take it off for good.  Then, after a few months, maybe I will start to experiment with slowly adding foods back.

Latex Allergy 3

I feel like I have a future now.  Frankly, when I was in the middle of the misery, I could not see me lasting 30 more years like that.  I did not want to live with that misery. Life is good. There is hope.”

Today, Renee’s skin is clear and healthy. She’s working every day to introduce foods back into her diet, but still experiences hives here and there from negative reactions. Although a nuisance, as she states, they are in no way as intolerable as her chronic eczema was. She also does not need to take as many antihistamines as she used to. By sharing her story, Renee hopes that she can help someone else suffering from a latex allergy.

 

For ideas to soothe your skin, start here for eczema relief!

 

Do you suffer from eczema as an allergic reaction to latex? We want to hear from you in the comments below!

One Woman’s Incredible Story of a Chronic Allergic Reaction to Latex appeared first on itchylittleworld.com. Come read more about natural remedies for eczema!

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Caring for a child with eczema: Jasper’s story

Looking after a child with severe eczema can be exhausting for parents as well as the child. There’s so much to consider, environment, clothes, weather, treatments, financial implications – the list goes on. Sorrel Ronan faces a relentless battle every day to keep her son’s skin healthy and pain-free.  She has kindly shared her story with the British Skin Foundation to help raise awareness of the impact the condition can have on both children and their families.

Jasper very clearly had dry skin since birth which was treated with olive oil as advised by health professionals. It wasn’t until around two months old that I noticed the coin sized patches were not going away, even after he moved on to stronger medications.

For four years we pretty much never detoured from the circle we were traveling around. Jasper’s eczema worsened so we went to the doctors. We’d be prescribed a new cream, the cream didn’t work and his skin became infected. Next we’d be prescribed antibiotics and wet wraps to treat the infection. Around and around we went… we were on first name basis with all the receptionists!

You name it, Jasper, now six years old, has tried every cream possible for his age. Creams that themselves have turned his skin red raw, stained the bedding and ruined clothes. And that’s just the prescribed treatments. I’ve spent hundreds over the years buying each and every ‘miracle’ cream and/or oil.

That’s the thing with eczema – someone always has a friend or family member who swears by a certain cream. There is so much out there that it’s very hard sifting through all of the ingredients to see which ones can actively help contain a flare up. The only respite he has ever experienced was one of the many times he was prescribed Prednisone.

Every single day we have to consider ‘How will what we are doing today affect Jasper’s skin?’

Can he play that game because he may get to hot? Who can he sit near in case strong scents irritate him? Will he sweat and scratch if he doesn’t get fresh air? Will an adult be watching him, and I mean really watching him so he wasn’t secretly scratching away his skin? Will there be a new trigger to add to the list? The mental checklist is never ending.

Starting school introduced a whole new batch of issues for Jasper and I believe the biggest one was how his eczema affected him emotionally. Children pointed and stared for a while, but I taught my son to explain that it was eczema and as children do, their minds moved on. The adults in the playground were a different story, with one man declaring in front of Jasper and I that his skin looked like road rash.

We see the dermatologist every three months or so. On his last visit Jasper’s skin was the best it’s ever been in his life. This is due to a combination of being moved on to Protopics, alongside me having two weeks off work so I could cream him almost hourly. It was also probably the sunniest two weeks he’s ever experienced, so shorts and sunshine helped.  

As soon as the cold weather set in I began to see his skin worsen each day. Nothing I do prevents his skin from deteriorating. I’m currently saving up to buy a special washing machine, one I read about online as it helped another family with their child’s eczema. Her story is very similar to Jasper’s, down to him having a server house dust mite allergy.

As well as the pain that eczema causes Jasper, it also has a huge impact on us financially. I feel the guilt that comes with me being unable to afford private care for him, the air purifiers, DermaSilks and all of the fancy bedding. I buy cheap and often, I just throw bedding and uniforms away weekly.

Sometimes I feel guilty when I think it is just eczema and things could be so much worse… but then I’m angered when people who do not live with this daily refer to it as ‘just eczema’. Unfortunately, we are yet to find the ‘right’ combination of creams to help with his eczema, and as I’m told, he’ll probably grow out of it. But that does not help right now.

The best way I have found to explain life of being a parent of eczema is this; just visualise a character, usually a comical one, moving to fetch an item up from the floor, only to kick it further away each time. That is life with eczema.

At the British Skin Foundation we believe that research is the key to fighting skin disease. We’re the only UK charity dedicated to raising money for all types of skin disease, including eczema. Our unwavering commitment to funding quality research means we won’t stop until we’ve found cures for common skin problems like eczema and acne, through to potential killers like malignant melanoma. To date we’ve raised £15 million to fund projects since 1996. For more information about eczema, visit the British Skin Foundation here.

Are you caring for a child who has a skin condition? British Skin Foundation experts will be answering your questions in a unique one-day clinic on Wednesday 18th January. Submit questions from Monday 16th January – more information here.

talkhealth Blog

Eczema from an Indian perspective- Our daughter’s story

Our lovely customers are spread out around the globe, which always serves to remind me that there are people suffering from eczema all around the world.  Today we hear from one of our amazingly brave mums in India, Anindita.  Her story of how their family has united to help cope with their daughter’s eczema is heartbreaking but also incredibly inspirational.

This is our daughter’s story of her ongoing struggle with severe eczema over the past few years. We have survived some very tough and uncertain times especially in the last couple of years. However, in spite of all the trauma and pain we have faced, we have come through it all with the help of invaluable support from close family and friends and her doctors. Most importantly, our daughter’s spirit remains intact and whoever interacts with her cannot help but notice her positive outlook and her sunny smile. This is what keeps us going, especially me, since I spearhead our family’s efforts to bring her eczema under control with the help of my extremely supportive husband who is also a doting father to his darling daughter.

I have captured our entire journey from the beginning in details in my blog “eczema-anindianperspective.com” through various posts. Here I have encapsulated our story for Gail Palmer’s blog at her gracious invitation. I have been purchasing products for eczema on her website EverythingForEczema.com for some time now and have found it very useful to be able to find various products under one roof.

Aiyana

Our daughter Aiyana was born on the American Independence Day, 4th July, 2006 in Mumbai, India (where we reside) after a completely hassle free pregnancy. She was a happy, healthy baby and until she was 1 year old we did not have any inkling about how our lives would change forever because of eczema (Atopic Dermatitis) in the years to come.

In India at that time eczema was uncommon and awareness was very poor and even had I came across anyone with this skin condition, I wouldn’t have even realised it. When Aiyana was about 6 months old I had to get back to full time work. I weaned her off my milk  and introduced cow’s milk as is the custom in India (again very few people had allergies to dairy or may not have even be aware whether they were allergic to dairy and dairy products). However, by the time she was one year old we realised that her skin was mostly rough all over and which never completely went away no matter how much we took care of her skin. Her pediatrician diagnosed her with Atopic Dermatitis and we took her to a dermatologist who confirmed the same. Thus started our journey with eczema.

How it all began

In the first few years till Aiyana was about 5 years, her eczema was mostly under control with moisturizers and minimal topical application. It all changed when we went to Rajasthan (a northern state in India) for a religious occasion in October 2011 for a few days. Since Rajasthan is mostly a desert with a very dry climate, her eczema worsened. However, even after we came back to a tropical climate like in Mumbai, her eczema did not let up and her skin condition went downhill from there in spite of all our efforts. When she reached a state of erythroderma (extreme shedding of skin with red exposed skin all over the body due to constant itching) in July 2012, we had no choice but start her on oral steroids (prednisolone). Aiyana was taken off the oral steroids and started on an immunosuppressive drug, cyclosporine which had a limited impact and once it was stopped in early 2013, she had be put back on oral steroids since her eczema was out of control. By this time we had tried various treatment options with varied success like Narrow band UVB, topical steroids and immunomodulators and were already following elaborate eczema safe skin care and bathing routines for her.

Our daughter’s struggle for survival

We decided to take her to see an experienced pediatric dermatologist at Great Ormond Street Hospital for Children in London during the summer of 2013. Since eczema is much more common in UK we hoped that experience of the doctors there would be able to help us control her eczema. However we soon came to realise that ultimately one has limited control of the outcomes in one’s life no matter how many precautions we take and all our planning. The dermatologist that we visited did all the requisite tests that need to be done before starting a patient on the immunosuppressive medication, Azathioprine, since one of the serious and sometimes life threatening side effects of this can be “bone marrow suppression” where the bone marrow simply shuts down and stops producing red and white blood cells. This is what we feared and is precisely what happened with our daughter though the medication was started only after her tests proved to be completely in the normal range. She was admitted to the Intensive Care Unit of a premiere hospital in Mumbai with a life threatening infection since her bone marrow had stopped producing white blood cells completely and could not fight any infection. However, our brave daughter fought back with the help of her doctors, the hospital staff and our family and friends who came and donated blood and platelets whenever required. After a nerve wracking 2 weeks she was finally declared to be out of danger. I have captured our experience and learning in my blog (“eczema-anindianperspective.com”) in the post – http://eczema-anindianperspective.com/2013/10/27/the-tough-get-going-part-2/

This traumatic experience has brought our family closer and I can see in my daughter a strength and maturity much beyond her age and which helps her to cope with this condition on a daily basis. I find that I am inspired by my daughter to continue to look for a better way of controlling her eczema and help her lead a normal life.

Our life today

Today Aiyana is on the immunosuppressive medication Methotrexate after having been on another immunosuppressive medication, Cyclosporine and the oral steroid, Prednisolone (alternatively as well as together at times) to keep her eczema under control. In the past few years we have made radical changes in our lifestyle right from skin care and bathing routines to detergent free clothes and dish washing amongst others. We have tried various products like moisturisers, creams, therapeutic clothing which have helped to some extent but we are still far from bringing Aiyana’s eczema under control.

Anindita and her daughter Aiyana

However, my role like any other mother is one of a never ending search for a better and healthier life for my children and my family. I have been doing a lot of research on the effects of diet and eczema and have only now come across one that I wanted to try on her by an Australian Nutritionist, Karen Fischer. I have started Aiyana on diet a couple of weeks back and we have a long way to go yet. This is where we are at the moment.

Be happy for this moment, this moment is your life

And in the end, this is what matters. How well we lived our life, how well we loved, how often we counted our blessings along the way; how well we learned to accept the things we simply cannot change and faced our most difficult moments. This is the lesson I strive to teach my children, one lesson that I am myself learning every day of my life.



 

 

 

 

Everything For Eczema

Sharing an Asthma Success Story from Canada

I still regularly hear from people who experience asthma improvements from implementing the SolveEczema site strategies.  I  would like to share a letter I received a year ago from Julie Leung, a mom in Canada who implemented SolveEczema.org strategies to solve her children’s eczema, and with whom I have been corresponding.  She describes the benefit to her own asthma as an adult.  I’ve heard this a lot, the benefits even to those who don’t have eczema, particularly to asthma and skin quality.  I thought her description was very powerful.

Baby with asthma inhaler

“Baby In Hospital” by Sura Nualpradid Freedigitalphotos.net

Even though people breathe in a great deal of detergent in “dust” these days because the dust in most home indoor environments comes largely from hair, skin cells, lint, I have always downplayed the potential benefits to asthma and other lung conditions pending research validation, and because I do not believe environmental detergents (as defined on my site) are the underlying cause of asthma, but an amplifier, abnormally influencing the membrane and the normal function of the immune system (for the reasons discussed on SolveEczema.org).  Additionally, unlike with eczema, there is  no way to give people simple GRAS (generally regarded as safe) recommendations that provide the kind of direct feedback that people with eczema experience when they properly implement SolveEczema strategies.  Until there are studies, it’s much harder to convince people to do what is necessary if they don’t have the immediate feedback of those with eczema.  Nevertheless, because so many people describe their improvements, I feel it’s important to share what is possible.

First, the caveats:

Photo by Arvind Balaraman Freedigitalphotos.com

Photo by Arvind Balaraman Freedigitalphotos.net

I am posting this to help people who are proactive and looking for better answers in their own health journeys.  It is not intended in any way as medical advice (as everyone who reads my site knows, I am not a doctor), nor intended to replace the relationship between doctor and patient.  In fact, please only read further if you have a good relationship with a doctor managing your asthma.  Implementing the strategies from SolveEczema.org is not trivial and requires understanding a very different perspective.  Things can go wrong, too.  A relationship with a physician is essential.  Implementing the strategies may help, but given the range of contributors to asthma, I do not want anyone to think I am suggesting a replacement for sound medical advice, follow up, and care.  Asthma medications can save lives.  Implementing the site strategies for asthma takes time, on the order of months, and unfortunately can be all too quickly reversed because of modern environmental influences that are sometimes out of people’s control.  Do NOT make changes to care based on a website (mine or anyone else’s) without thoroughly understanding and consulting with your physician.  Only make changes per SolveEczema if you’re willing to understand and do it safely, with your doctor in the loop.

Here is the letter [story and personal photos from Julie Leung, except where noted, all rights reserved, used with permission].  Many thanks to Julie for writing and being willing to share.  I would add that in terms of what Julie did, described below, in pushing herself to see how much her lungs had improved — that’s for information and is a “Do not try this at home” FYI only!  She is a very detail-oriented, highly analytical person with a science background, was (and is) actively in asthma medical care and management, with a history of excellent physical fitness and those adventure sports.  I recommend against readers “testing” improvements that way!:

Dear AJ,

In addition to the successes we’ve had with our children’s eczema, I wanted to share the surprisingly positive impact on my long-standing asthma.  I hope my testimony, so to speak, might help someone else.

When my husband and I began implementing the framework given on your site, I was on a year long maternity leave from work after the birth of our daughter and was spending most of my time in our detergent-free home.  By January of 2013, I discovered that my asthma had gone away completely and it seemed correlated to the detergent removal in our home.

Stop Asthma by Stuart Miles Freedigitalphotos.net

Stop Asthma by Stuart Miles Freedigitalphotos.net

From what I had already read on your site, my asthma disappearing was not an altogether unexpected result, but the extent of the improvement was wholly astonishing, and felt nearly miraculous.  I later returned to work and therefore to regular daily detergent exposure outside my home, and the resulting return of my asthma has convinced me of the significant impact that detergents have on my asthma.  What it also showed me was that I can have control over my well-being in a way I never would have thought possible before reading your site.

I’ve had asthma since I was a teenager, and in my adulthood, it came “under control” through regular use of steroid inhalers. Consistent with widely-accepted asthma management protocol, I was told that need of a “quick response” inhaler (like Ventolin) more than a few times a week meant my asthma was “out of control” and needed to be quieted by increasing the frequency and/or dosage of my steroid inhaler.

You’d pointed out to me that “steroid fears” are well-documented in the medical literature, and I found myself reflected in those profiles — I have always felt uneasy about taking so much steroid.  Over the years, I’ve constantly tried to use as little as possible, or wean myself off them completely.  Off, or on an inappropriately low dosage of, the drugs, my asthma is fine until I get a cold or exercise above my typical intensity. Then, inevitably suffering from constant wheezing that isn’t relieved by my “quick response” inhaler, I begrudgingly ramp up my steroid usage and maintain this dosage for at least 2 weeks, until my asthma once again comes under control.

When I found your site, we implemented the changes in our household to help our children, but I considered that I might also benefit from them.  I stopped taking my steroid inhalers, almost subconsciously, at the same time we started detergent removal from our home.  It is important to note that there was a period of about 9 months where I was no longer regularly exposed to detergents because I was spending almost all my time in my home because I was on maternity leave and also trying to minimize my baby’s exposure to detergents while problem-solving her eczema.

Within 4 months of starting detergent removal, I started to feel that I was perhaps not experiencing the same depth or sensitivity of asthma as I did prior. I started to tell a few people tentatively, always clarifying that I still thought I had asthma, but it seemed to be better. I seemed more resistant to triggers, didn’t wheeze as easily, or it took more physical exertion to have the asthma show up; when it did, it didn’t linger as long, and didn’t seem to need the short-acting inhaler to resolve.

Snowshoeing Kananaskis - Mtn scene7 months after starting detergent removal, I was invited on a snowshoeing trip in the mountains. The trip was in an area in which I used to cross-country ski frequently a number of years ago, and so my body was generally familiar with the terrain, conditions and weather.  Back when I was cross-country skiing regularly, I was exceptionally fit and this seemed to also help mitigate the asthma, raising the threshold of physical exertion before wheezing.  However, I always got asthma while skiing, and I always had to stop and take a puff or two of my short-acting inhaler, typically within 5 minutes of starting to cross-country ski, and often again later on in my 4-6 hour workout.  At the time of the snowshoeing trip, I had every reason to expect to be wheezy.  Not only had I become relatively out of shape, but at this point I hadn’t taken any inhalers for at least 6 months.

Snowshoeing Kananaskis - signsI brought my inhaler along just in case, but I was really curious to see whether I’d be asthmatic or not.  After the initial steps, getting into the groove, I listened to my body, tentatively, half expecting to need my inhaler.  No wheezing, not too much tightness in the chest.  So far so good.  I kept on.  And on.  And on. 2.5 hours into the trip, I suddenly realized, that despite climbing up and down a canyon, breaking through undisturbed snow at times, and talking while walking, I hadn’t needed my inhaler.

Snowshoeing Kananaskis - walking 2At the point of my no-asthma discovery, everyone on the trip was tired, but I had lots of energy because I was so excited!  I wanted to try to “incite” the asthma by pushing myself to the limits of physical exertion. I didn’t think I would have many other chances to “test” the condition of my asthma. I nearly ran up a 90 foot incline to the top of a dam, so fast that it was a few minutes before anyone else in our party caught up to me after I stopped. I experienced no wheezing! I could not remember the last time I exercised hard, started breathing hard, and did not feel the familiar tightening of my chest and wheezing coming on. I was elated!

Less than a month after that first trip, I went on another snoeshowing trip in the mountains where the level of activity was closer to what I’d regularly done when younger.  4 hours of constant movement and some chatting with my companions through the mountain landscape in cold weather yielded no wheezing whatsoever.  Again, I was floored.

Less than a month after that trip, my maternity leave ended and I returned to work and into a detergent-filled environment.  Within 4 days of returning to work, I ran for the bus for 15 seconds and had the most severe asthma attack I’d experienced in over a year:  the familiar sharp, stabbing pain in my chest, the wheezing and compressed lung capacity, and the taste of blood in my lungs — all symptoms typical of my asthma attacks.

As you’ve pointed out to me during problem-solving for my children, scientists often test for causation by removing the stimulus they hypothesize is causing an issue, then reintroducing the stimulus.  To show causation, it’s not enough that the issue resolves when the stimulus is removed; the issue needs to return when the stimulus is re-introduced.  As I reflect, I realize that’s precisely what I’ve inadvertently tested — when detergent are absent, my asthma disappears; re-introduce detergents, my asthma re-appears.

When I returned to work, I was in a detergent-filled environment for about 10-12 hours a day, 5 days a week.  I eventually needed my steroid inhalers to control my asthma again, but only needed about a quarter of my previous dose for control.  Over time, I ratcheted my dose down and used the steroid inhaler so infrequently that I was not considered to have my asthma under “drug control”.  Eventually, my asthma settled to a place where it was definitely worse than while I was on maternity leave, but better than the symptoms I’d had my entire life. Overall, compared to before detergent removal, it took more or longer physical exertion or exposure to allergens for my asthma to show up, the symptoms were not as severe when it did show up, and it required less drug to control.

In the summer of 2014, I went for spirometry testing.  At the time, I was using next to no drug and was feeling some frequent, general chest tightness, as I had since returning to work.  The respiratory therapist took 3 different measurements.  Surprisingly, she indicated that the numbers from all tests were very good and said that if she saw the numbers alone, without knowledge of my clinical history of long-term asthma, she would think that the patient did not have asthma!  In her report to my doctor, she indicated,  “Asthma is under control”, despite the fact that she and I both agreed I wasn’t taking enough steroid to consider my asthma as under control from drugs!  The respirologist who reviewed my spirometry results seemed to question whether the asthma diagnosis was even correct, something that had never happened before despite decades of treatment.

I know that I’m still an asthma sufferer, and, with the “right” conditions (such as long enough exposure to animals I’m allergic to, or if I’m in an really detergent-y environment for a long enough time), I will “express” my asthma.  But, I feel also that the clearing of detergents and detergent-laden dusts in my home environment has allowed my lungs to heal in a way that has significantly increased my thresholds to reacting in my lungs, much like it has for my daughter on her skin.  And, my results, coupled with observations I’ve made about my son, strongly indicate that I may also have delayed or perhaps even avoided the onset of asthma, or, at the very least, potentially reduced its severity if it does develop, in my children.

I hope that my story encourages those that are considering detergent removal or those who have already done so and are hard at work problem-solving for their families.  For as depressing as it is that our world is now inundated with chemicals that may have caused such a great degree of unnecessary sickness and suffering, it is hopeful that there is still something we can do about it.

-Julie Leung

 

To read more about Julie Leung’s allergy journey, or to find the list of products she uses in Canada, please see:   http://allergyjourney.com

Happy Holidays — Best Wishes for a Healthy, Eczema-free (and Asthma-free) New Year!

A.J. Lumsdaine
SolveEczema.org

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