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in Health, Lifestyle &middot May 16, 2023

Can a Low Histamine Diet Help Those with (Certain) Chronic Illness Conditions?

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in Health, Lifestyle &middot May 16, 2023

Can a Low Histamine Diet Help Those with (Certain) Chronic Illness Conditions?

While I’m recovering from surgery, several other health bloggers are stepping in. Please enjoy this guest post from Claire of Through the Fibro Fog!

If people ask me whether I follow a specific diet for my chronic conditions, the reply to my answer is usually ‘a what diet?’. You see, I follow a low histamine diet, which isn’t very commonly known. You won’t see it in a magazine, or symbols for it on food packaging or a restaurant menu.

But as I have mast cell activation syndrome (MCAS), the low histamine diet is a big part of the measures I utilise to manage my condition and symptoms. So let’s talk about a low histamine diet and what it entails.

What is Mast Cell Activation Syndrome?

Mast cell activation syndrome is a condition where ‘chemicals called mast cell mediators are released too frequently or abundantly and/or in response to triggers that are not typically considered to be harmful, for example; foods or chemicals in the environment’ (Mast Cell Action).

Symptoms of MCAS can vary quite widely in individuals, with some experiencing gut issues, others headaches, flushing, itching, brain fog, nausea and at the more severe end of the spectrum, anaphylaxis.

It can be quite difficult to get a diagnosis of MCAS, at least where I live. It’s not a commonly known condition in society, and often not by doctors either. In the UK there are no NICE guidelines for the condition, meaning that gaining a diagnosis or treatment is very difficult. Sadly, some doctors deny MCAS exists, or say that it is rare and/or over-diagnosed.

How is MCAS diagnosed?

MCAS is typically treated by either an immunologist or allergist, although I have also heard of people being diagnosed by a rheumatologist or dermatologist that have a special interest in the condition.

As there isn’t an ‘agreed upon’ way to diagnose MCAS where I live, it seems to happen in different ways through different doctors. So I’ll speak about my experience, with the doctors that I saw.

The first doctor I saw, referred me for some (very expensive!) private tests that measured my histamine levels as well as other factors. We also measured my allergic response to about 20 common allergens such as dust mites and various foods, tested for dermatographism and did a tryptase test to rule out another condition called mastocytosis.

He also asked me a LOT of questions about my symptoms, when they started, triggers I noticed and so forth. I then took antihistamines for around a month to see my response to them. After the test results showed high histamine levels, the antihistamines had helped a little and with my clinical history, he diagnosed me with MCAS.

My current doctor, knowing that I had already been diagnosed, took a detailed clinical history, looked through my test results and diagnosed me also.

Mast Cell Action has a helpful guide to the typical MCAS diagnostic process that is worth a read.

What are the treatments for MCAS?

Common treatment for MCAS are antihistamines, mast cell stabilisers and, for some, supplements such as vitamin C and quercetin.

Different treatments work for different people, so you will likely need to work with your doctor to find the best treatment options for you. It can take a while to figure this out, often with some trial and error, and changing medications and doses.

What is a Low Histamine Diet?

A low histamine diet aims to reduce the amount of histamine being ingested through food. It’s often suggested for people with mast cell disorders, as well as histamine intolerance and sometimes also for conditions such as eczema, urticaria and migraine.

This diet limits higher histamine foods such as tomatoes, spinach, avocado and others, and focuses on fresh lower histamine foods. Personally, I was advised to use the Swiss Interest Group Histamine Intolerance guide by several doctors and a dietician. It gives the histamine ‘rating’ of dozens of different foods, and so you can see which ones are suitable and those you may wish to avoid. I would suggest asking a doctor or dietician for their suggestion on the histamine list they advise you to follow. I’ve seen some very strange suggestions for low histamine foods on some sites!

Can a low histamine diet help reduce symptoms?

As with many chronic illness conditions, we all respond differently to medications, diets and other lifestyle measures. I know of people who are able to manage their MCAS with diet and supplements alone, while others, including myself, need to take medication alongside the diet.

For me, it’s definitely a big piece of my treatment plan. I’ve come to learn the foods that trigger my mast cells the most (figs and alcohol are a no-go for me!), as well as happily learn that my stomach issues calm considerably when I stick to the diet.

It’s also the case that some people seem able to ‘add in’ medium histamine foods over time, as their MCAS becomes better managed through other treatments.

How do you start a low histamine diet?

It can be tricky to start the diet as it can seem so complicated in the beginning! I know I was quite lost for a while, but it led me to being creative in the kitchen and going on to share low histamine recipes on my website.

I still remember walking out of my doctor’s appointment and wondering what on earth I could eat! But seeing a dietician was really helpful, as well as following some practical tips that I’ve detailed in my ebook How to Get Started on a Low Histamine Diet.

Practical Tips for a Low Histamine Diet

Focus on the foods you can eat. It’s so easy to get caught up on the ‘forbidden’ foods on any diet, but this only leads us to feel negatively about it. Instead, make a list of all the foods you can have and will enjoy making meals with!

Break it down into categories if it is helpful. So the proteins you can have such as meats, low histamine cheeses, then starches such as quinoa, rice and potatoes, then vegetables, fruits, low histamine herbs and spices, low histamine teas and even fun mocktails. You’ll notice the list is quite long!

Figure out some easy meals. When time is tight it’s easy to just grab anything to eat. Instead, come up with some super simple meals that use food you usually have in the fridge or pantry. It will help prevent temptation to opt for a high histamine take-out!

Have snacks to hand. Whether it’s fresh fruit, suitable nuts and seeds or perhaps some energy balls, make sure to have something you can grab if hunger pangs strike!

Take your own food. I know it doesn’t seem much fun, but often taking your own prepared food when visiting friends or having an afternoon out is much easier. It’s sometimes very tricky to find fresh suitable food in cafes and it’s better to have your own than to get hungry!

Summary

Following a low histamine diet is something to ask your doctor or dietician about if you have a mast cell disorder or histamine intolerance. Whether it is alongside medications or perhaps with supplements too, it can be helpful for many with certain chronic illness conditions. It may feel tough to begin with, but you will soon get the hang of it and come to enjoy tasty and fun meals!

Claire smiles for the camera. She's a blond woman wearing a hounds tooth coat and glasses on top of her head.

My name is Claire and I live in London, UK. I live with a number of chronic illness conditions including mast cell activation syndrome, Ehlers-Danlos Syndrome, Dysautonomia and Fibromyalgia. Part of managing my condition is to follow a low histamine diet and you can find tasty recipes that I share on my website throughthefibrofog.com and on Instagram @lowhistaminekitchen.

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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Dos and don'ts for when someone in your life is di Dos and don'ts for when someone in your life is diagnosed with autoimmune arthritis! What are some that you would add?⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: "So someone you know was diagnosed with Autoimmune Arthritis". Under the Do column (indicated with a green checkmark) is:⁣
"As how they feel about it⁣
Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
Under the don't don't column (indicated with an x in a red circle) is:⁣
"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
Assume nothing about their lives has changed⁣
Conflate autoimmune arthritis with osteoarthritis⁣
Pass your cold to an immunosuppressed person".⁣
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Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

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Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

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Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

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There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣⁣

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