When the gut is damaged

I’ve explained what happens in a healthy gut .  Now it’s time to discuss what happens when our microbial gut lining is damaged.  The microbial lining of our gut performs so many important functions that when it is damaged there is a lot that can go wrong.

  1. Without protection from the microbial lining the walls of the gut are open to attack from anything that comes along e.g viruses, funguses, bacteria, parasites, toxins.
  2. These “invaders” can then enter gut cells and cause inflammation of the gut wall, leading to diarrhoea or constipation.
  3. The gut wall becomes malnourished because the “good” bacteria are no longer present to digest food for the gut lining.
  4. The gut cell renewal process becomes slower, the new cells that are produced tend to be less healthy and without protection from the bacterial lining they become abnormal.
  5. The gut becomes unable to digest and absorb food properly, leading to mal-absorption, nutritional deficiencies and food intolerances.
  6. Fibre (which in a healthy gut is beneficial) is not broken down by the good bacteria and provides a habitat for pathogenic bacteria and aggravates inflammation in the gut wall.
  7. The immune system is compromised.  In people with damaged gut flora there are less lymphocytes (immune system cells).
  8. Our gut becomes “leaky” and unscreened molecules can enter the bloodstream, travel around our body and cause damage and symptoms in other organs.  There is a good explanation of leaky gut and how it affects us here, I especially like the diagrams.  In a nutshell it can affect the liver, the immune system, cause inflammation (leading to pain), brain fog, lowered immune system and more.

In summary the damaged gut lining does not just affect our digestion, but can cause lots of other problems all round the body. Once again thank you to Dr Natasha Campbell-Mcbride for her book Gut and Psychology Syndrome, which helped me to understand what happens in our gut.

A Healthy Gut

This post is going to get a bit technical about the biology of our guts.  I will attempt to explain what goes on in a healthy gut. My next post will explain what happens when our gut is not working properly (most people with CFS/ME have digestive problems – often diagnosed as Irritable Bowel Syndrome).  I share this information because I think it will help you to understand why I am following the diet that I am.

I credit Dr Natasha Campbell-McBride and her excellent book Gut and Psychology Syndrome for my understanding of this topic.  She is a practising doctor and her book is thoroughly researched, and includes a 17 page list of “selected” references.  Her explanations of what goes on in the gut and how this links to the brain were enlightening to me.

Microbes

Our gut is inhabited by millions of microbes, this is a symbiotic relationship where neither party can live without the other. Gut flora can be divided into 3 main types:

  1. Essential or Beneficial Flora – the most numerous in a healthy individual and the most important group
  2. Opportunistic Flora – in a healthy person their numbers are limited and tightly controlled by the beneficial bacteria
  3. Transitional Flora -generally ingested with food.  In a healthy gut these pass through without doing any harm, but if the beneficial bacteria is damaged they can cause disease.

Natural Barrier

The whole length of our digestive tract is coated with bacteria, providing a natural barrier against undigested food, toxins, parasites and pathenogenic micro organisms we ingest.  If this protective barrier gets damaged, the gut wall suffers.

Our bacterial barrier can produce anti-biotic, anti-viral and anti-fungal like substances and they can engage the immune system to fight invaders.  They also produce acid ensuring the pH near the wall of the gut is very uncomfortable for “bad” microbes.

Our indigenous gut flora is also good at neutralizing the toxins produced by pathogenic microbes and that we ingest with food.

Digestion and Absorption

The healthy flora on the gut wall are designed to take an active role in digestion and absorption.  They can digest proteins, ferment carbohydrates and break down lipids (fats) and fibre.  By products of bacterial activity in the gut are very important in transporting minerals, vitamins, water, gases and many other nutrients through the gut wall into the bloodstream.

Providing Nourishment

Healthy gut flora provide a major source of energy and nourishment for the cells lining the digestive tract.  The bacteria digest the food converting it into useful, nourishing substances for the gut lining.  It is estimated that the gut lining gets 60-70% of its energy from bacterial activity.

Our bacteria also produce various nutrients and vitamins, namely vitamin K, pantothenic acid, folic acid. Vitamins B1, B2, B3, B6 and B12, as well as some amino acids.

Renewal of Cells

Cells in the gut lining have to work very hard digesting food, and hence need to be young and in good shape.  The gut is constantly producing new cells and shedding old cells in a process of renewal.

Fibre

Fibre cannot be digested by a human gut without the help of beneficial bacteria.  In a healthy gut fibre is broken down by bacteria to provide nutrients which feed the gut wall and the rest of the body.  They also activate the fibre to take part in water and elecrolytes metabolism, recyle bile acids and cholesterol and other stuff.

Phew!

If you’ve made it this far – congratulations, especially if you have CFS/ME.  I normally try and keep my posts quite short so they’re not too taxing for those with brain fog, but every so often I feel the need to write a more in depth post.

As you can see our guts (and the bacteria residing there) provide many essential functions, so if we want to improve our health then they are a key part of the equation.  In my next post I will attempt to explain what happens when our gut is damaged.

Increasing or Decreasing?

During my recovery I have made several major changes in lifestyle.  Most of these have been done gradually, as when you have very little energy it’s hard to change anything.

I have been reflecting on how I have made these changes and realised that when I’m successful I focus on what I am increasing or moving towards, not what I am decreasing or moving away from.  Here’s a couple of examples to illustrate what I mean:

Increase rest and decrease activity

I focused on increasing my rest by agreeing a rest schedule with my Occupational Therapist and over the coming weeks my focus was on ensuring I rested at the times we had agreed.  To do this I had to stop whatever my activity was at that time and go and rest (at that time I used to lie on my bed to rest).  This naturally meant I decreased my activity, but I didn’t think about that aspect.

Increase vegetables and decrease processed food

I have made many changes to my diet.  You can view my foods to eat more of and foods to eat less of lists. Whist there does need to be some awareness of what you are trying not to eat it is much better to focus on adding in the foods you want to increase.Since we have a finite appetite this will naturally lead to a decrease in other foods (the processed stuff we want to move away from).

With this focus I can think about eating the foods that nourish my body and help it to heal, which makes me feel good about myself, rather than focusing on the foods I can’t eat and feeling deprived and negative about the changes.

I personally don’t ban any foods, I haven’t been diagnosed with a food allergy/intolerance.  So therefore if I want to eat a certain food I can. However, the more I stick to the foods that are good for me, the better I feel and the less I want to eat the foods that I’m trying to avoid.

If you’re struggling to make a change try focusing on the positive aspect of the change – know what you are moving towards and focus on that rather than what you are moving away from.

Alcohol

This post was inspired by a glass of wine on Saturday night – only my second alcoholic drink in nearly two years.

Why I Don’t Drink Alcohol

Since I got CFS/ME  in January 2012 I have avoided alcohol almost entirely.

For the first few months of illness I felt dizzy and ill most of the time, and I had no desire to add to that with a hangover.  Once I got my dizziness under control and was pacing better I decided to try a small amount of wine.  So one evening in August 2012 when my kids were staying with my sister I experimented and had one half glass.

From that experiment I discovered I was alcohol intolerant!  The next day I had the worst hangover ever, as if I’d drunk 2 bottles of wine instead of half a glass. I felt like I’d been poisoned.

That experience was enough to stop my trying alcohol again until now.

How the Body Processes Alcohol

I have picked out some highlights (relevent to CFS/ME) of what happens during alcohol metabolism from this article.

  • Alcohol is absorbed into the bloodstream through the small intestine.
  • It travels to the liver where it is converted to energy.  Whilst the liver is metabolising the alcohol it is unable to carry out other functions.
  • The liver can process 1/2 oz alcohol per hour.  Excess alcohol flows to other parts of the body.
  • Alcohol in the heart causes you to pump less blood and the blood vessels relax, causing a lowering of blood pressure.
  • Alcohol is a sedative. When it reaches your brain it slows the transmission of impulses between nerve cells that control your ability to think and move.
  • Alcohol reduces your brain’s production of anti-diuretic hormones, which keep you from making too much urine. You may lose lots of liquid, vitamins and minerals.

 What Does This Mean For Me?

  • Tests I did with my nutrtionist indicated my liver is not getting rid of toxins as it should, but is recirculating them around my body: this is probably why a small amount of alcohol had such a massive impact on me.
  • I am already eating extra salt to counteract low blood pressure, thus alcohol lowering my blood pressure is not something I want.
  • I already have brain fog, therefore I don’t want the sedative effect of alcohol dulling me further.
  • I take vitamin and mineral supplements and  I don’t want to waste them by peeing them out at a faster rate than normal.

It’s clear that the effects of alcohol are not going to help me feel better.

What happened after my drink on Saturday?

I’m pleased to report that I felt OK after my wine on Saturday night.  I think this could be because my sauna is helping me to detox, and hence my liver is better able to process the alcohol than it was.

What will my attitude to alcohol be going forward?  

It’s on my list of foods to eat less of and I intend to avoid it almost entirely, because it’s not going to help me recover and it may hinder recovery.   However, on very special occasions, if I want a drink I won’t be scared of how I’ll feel the next day, I’ll be able to imbibe if I want to.

What’s your experience of drinking alcohol and CFS/ME?

 

link fixed

I noticed that a link to my page about the stop process was broken.  Sorry about that.  I’ve fixed it now.

If you find any other links that aren’t working then please let me know by leaving a comment on the relevant post or emailing me at eat4meblog@gmail.com.

 

Sleep and brain detoxification

This morning I heard a story on the news about sleep being a time when the brain detoxifies and I wondered if there is a connection between this study and the brain fog we get with ME/CFS.

This is purely my own speculation based on observations of my brain fog.  My brain fog improved gradually as my sleep improved (after I began treating my adrenal fatigue). Perhaps this is because now I’m able to sleep better my brain has more time to detoxify itself, and hence everything works better.

Another possible reason for brain fog is mitochondrial failure.  Perhaps our brain cells simply can’t make enough energy to operate properly.

Whatever the reason behind my brain fog, I’m glad it’s receded sufficiently for me to be able to write this blog.  I’m thankful every day that my health is improving.

A quick way to increase the vegetable content of any meal

In my post Foods to eat more of, I said that I am aiming for 1/3 protein to 2/3 carbohydrates for every meal, that carbohydrates should be in the form of vegetables as much as possible and that I’m trying to eat plenty of green, leafy vegetables.

For a long time I was reliant on other people cooking meals (my family still cook 4 nights out of 7), and my family usually don’t provide such a high proportion of vegetables with a meal.

Often I have dragged myself to the table from where I have been lying (sofa or bed) to discover a meal that did not match my ideal.  I’d like to stress here that I am always grateful for a meal prepared by someone else, and I certainly don’t want to criticise whoever has prepared it or suggest that their efforts aren’t appreciated.  So I need to increase the vegetable content without creating a fuss.

My solution to this is to always keep a bag of ready washed green leaves in the fridge.  This could be spinach, lettuce, watercress, rocket or other green leaves that can be eaten without cooking.  Then I simply add a handful or two to my plate.  I also try and keep a jar of homemade salad dressing (olive oil, lemon juice, garlic, herbs and celtic sea salt) to make the salad a bit more interesting.

One extra tip if you’re going to try this; darker green leaves have more nutritional value than paler leaves, so don’t stick to iceberg lettuce, experiment with other darker green leaves.

Other helpful stuff

You may not have noticed that, as well as this blog, I have some other pages on my site.

Under the heading Other Helpful Stuff. You can currently find pages about:

I am sharing my experience of what has helped me in the hope it will help others.  I will be adding to this over the coming weeks with information about

  • Meditation
  • Epsom Salt Baths
  • Pacing
  • Doing activities I enjoy
  • Yoga and Qi Gong

Tip: Please don’t try and read all of this in one go.  Take your time, it will still be there tomorrow.

If there are other topics you would like me to write about please leave a comment below.

Bone Broth

I’ve already mentioned in Feeding hungry kids (and husbands) that a popular food in our house has been ready made soups from the chiller section of the supermarket.  I used to have a bowl of soup nearly every lunchtime. These were a life saver when I was too weak to cook.  However, now I’m improving I am managing to make more home made stocks and soups, although I still make use of ready made soups when I’ve run out of home made and I’m low on energy. I’ve been reading a lot about the benefits of bone broth.  It seems to be a bit of a super food.  Here’s some of the claims:

  • helps heal the gut
  • increase immunity
  • reduce joint pain in athletes
  • may improve sleep quality
  • helps the liver with detoxification
  • it’s a good source of magnesium, which I’ve found helpful in reducing restless legs and leg pain

If you want to research this further there here are some articles I found helpful:

As a CFS sufferer bone broth sounds like something I should be eating more of. I like the idea of perpetual soup.  I may try this next week and see how I get on.  I’m not sure my family will take kindly to drinking broth, but I will try it. I have made a couple of batches of chicken stock recently. I’ve used it in home made soups and various slow cooker recipes.  I still have a litre or so left in my freezer which I’m going to use in some leek and potato soup. Here’s how I make chicken stock: Ingredients

  • The remains of a chicken (carcass, skin etc.)
  • 1-2 bay leaves
  • 1-2 carrots
  • 1-2 celery sticks
  • 1 onion – peeled and halved
  • 3 peppercorns
  • celtic sea salt
  • herbs – usually thyme or rosemary (fresh or dried)

Put chicken carcass, skin and any other bits left when we’ve eaten the chicken into the slow cooker.  Add the other ingredients, cover with water to the capacity of the slow cooker.  Cook for approx 8 hours. Cool and drain the stock.  Keep in the fridge for approx 5 days or in the freezer for longer.

A new approach from the NHS?

I just came across this excellent article  by Nancy Blake entitled a Radical Care Pathway for CFS/ME.

I believe this approach would make a huge difference to patient outcomes. There are far too many people being told to keep pushing, when the best course of action would be to rest.

I hope the NHS takes this on board and treatment of CFS/ME patients improves.