Dr Castells interview: lifestyle changes DO work for mast cell/histamine disorders

Young sports woman with barbell.

Many of you will read the title of this post and think “D’oh! Of course lifestyle changes work for mast cell/histamine disorders!”

But would you believe that out of eight world renowned mast cell experts at the European Mastocytosis Conference patient Q & A session in London last week, none of them appeared to acknowledge that lifestyle and diet play a part in either the progression, regression or management of mast cell activation, mastocytosis, systemic mastocytosis and by extension (I would think), histamine intolerance (if indeed they believed it exists). (Click through to my FAQ to learn how mast cells, histamine intolerance and allergies are related). 

And that dear friends is why I believe I seriously lucked out in first being diagnosed with histamine intolerance rather than mast cell activation. Why? Because it was impressed upon me that diet was the key to controlling symptoms. I was however eventually also told it wasn’t all about food – something I chose to ignore till my symptoms didn’t really resolve on the standard low histamine diet. (They got better at first but soon with each food I eliminated from my diet I grew sicker and sicker.)

But that’s old news.

Coming up with the recipes for my high nutrient antihistamine and anti-inflammatory books gave me my life back, and as regular readers know, I’m now actually in the best health of my life!

The new news is that one of the world’s most respected mast cell experts, Dr Mariana Castells, was kind enough to grant me an interview. The even better news is that she believes, (wholeheartedly I might add), that lifestyle changes – exercise, diet and stress relief can cause a remission of mast cell symptoms. She told me a wonderful story (not unlike my own) in which a patient with systemic mastocytosis who wasn’t seeing the improvement she wanted from meds, chucked it all in: changed her life, diet, started exercising and traveling. She came back years later to relate to Castells that her symptoms were in remission and that she no longer took any meds for her systemic mastocytosis. This is not an isolated case. I’ll soon begin featuring recovery stories sent in by readers of this blog and also those of friends.

For those of you who don’t know, English is not Dr Castells’ mother tongue – she’s Spanish.

“In terms of systemic mastocytosis, and some with cutaneous mastocytosis, the most important things is to think about changing the lifestyle and the two most important pieces of the lifestyle are the exercise and the diet – interchangeably I mean, not one over the other,” Dr Castells.

She went on to cover something very close to my heart: that nutrition, rather any particular one type of diet is the critical component.

“The diet is critical and there is no single diet, so there are diets that will be good for a patient or not so good, grains, fruits, vegetables, any of that with antioxidants are tremendously good for patients – fats are not so good, said Dr Castells. 

Surprised to hear me agree with her? While I credit diet with helping me heal, it wasn’t the low histamine diet that did so, but rather the very high nutrient diet I adopted just over a year ago. I believe that a diet rich in natural antihistamines helped me reach where I am now, though I concede that simply replacing the low nutrient foods with nutritionally excellent foods, be they antihistamine foods or not, has upped my intake of hundreds of phytonutrients that support my body as a whole. Throw in the placebo effect, because I’ve convinced myself it’s why I’m healing, and we’re cooking.

It’s so important to remember, as I say over and over, histamine is only ONE of many inflammatory elements released by mast cells (I’m shocked that some people don’t even know that histamine is already stored in our bodies!) and as such we’re better off eating any kind of diet does not cause inflammation in our bodies, regardless of what it is.

I didn’t have time to ask a follow up on the fats point – but I’m not really surprised she said that. And please, let’s be honest with ourselves. You may think you do ok with Chocolate Chunk Cookie Dough ice cream for breakfast, lunch and dinner, but we know better right?

And couch potatoes, time to get those sneaks on!

Dr Castells says that it’s important to “maintain a healthy lifestyle, which is at least 30-45 minutes of exercise per day like brisk walking, not running but jogging, swimming, and even dancing. I actually have patients who dance Zumba, it’s pretty heavy duty in decreasing calories, so those are the lifestyle changes that a patient with systemic mastocytosis needs to make in order to improve the quality of their life.”

But I’m too exhausted all the time? Can’t you just give me more meds instead?

“Fatigue doesn’t respond well to all the medications we use, even the more sophisticated ones – fatigue only responds to changes you make to your tissues through exercising or changes you make to your intestinal absorption by changing what you eat,” says Dr Castells.

I know many of us are scared to exercise. I know I was. This doesn’t mean you should run out and take a one hour aerobics class but rather that incremental steps may help train mast cells, giving more energy to build up to a routine that will in turn generate more energy.

Castells’ 20 years of seeing mastocytosis patients has shown her that if a patient comes to her with symptoms, and a digestive tract loaded with mast cells, it may well be time to completely change their approach to diet and exercise – because a clean break and a change in perspective could just be what the doctor ordered (sorry, couldn’t resist).

Interestingly the analogy Dr Castells used is one I often do myself – cancer induced inflammation, saying that genetic markers/similarities exist: “There is a tremendous inflammatory component. In cancer it’s harder to get that inflammatory component in check, but in mastocytosis, just by educating the mast cells to a certain level of activity, tremendously reduces that inflammatory component,” she said.

Yoga is an excellent inflammation busting exercise, there’s even a few studies on yogic pranayama breathing shown to lower histamine in particular.

Dr Castells recipe for health?

“My recipe, not as a physician, but as someone who has followed patients with mastocytosis over about 20 something years, and seeing it’s kind of evidence based, not published, but evidence based, the patients in which I have been most successful in treating are patients who make changes in exercise and diet, and need a few medications here and there. They’ll need protection with an epi pen, in case of anaphylactic events, they may still have days in which things are different, but the need for medications is lowered, the quality of life is dramatically increased and overall the disease in the great majority of patients is very stable,” she said. 

Don’t miss part two of this interview where we cover:

1. The role of stress in mast cell disorders

2. How mast cell disorders can be misdiagnosed as psychiatric

3. The importance of managing your environment

4. How a positive attitude impacts prognosis

5. Why medication won’t help fatigue (and what you can do about it)

You’ll also find out the best kinds of exercise for histamine intolerance in my post here. 

Please don’t forget antihistamine, pain killing foods can still hurt us, so please always check with your doctor before adding new foods to your diet. 

 

69 responses to “Dr Castells interview: lifestyle changes DO work for mast cell/histamine disorders”

  1. PC Avatar
    PC

    Hi, do you know if peppermint tea is anti histamine or high histamine?

  2. Vivian Avatar
    Vivian

    Great interview. Thanks Yasmina! I feel like we’re on to something as these very knowledgeable & experienced doctors are speaking up about the condition.

  3. thelowhistaminechef Avatar

    Thank you Vivian! YES! Absolutely – I feel re-invigorated and doubly determined to continue tweaking every lifestyle change I can make. Thanks for posting.

  4. thelowhistaminechef Avatar

    Hi there, it is supposed to be an antihistamine, but some people react to it…as with all things, it’s very individual.

  5. Tina Avatar
    Tina

    Thank you so much, Yasmina. I’m a graduate student with a young child and I’m struggling with a whole host of new symptoms. Your posts are good reminders about the importance of daily consistency in exercise, nutrition, sleep, and stress management. (Not ironically my research is in aging and cognition, specifically stress and sleep!)

  6. thelowhistaminechef Avatar

    Hi Tina, I’m glad the posts are hitting home for you. I need reminders myself – that’s why I started the blog initially – as a motivator. Lol that’s brilliant. Please share your research if you come across anything of interest and good luck with the studies!

  7. Audrey Walker Avatar
    Audrey Walker

    Thanks so much for sharing this! I find that ginger and the herb stinging nettles help me a great deal.

  8. Sarah Avatar
    Sarah

    Thanks Yasmina! Great information that fills me with hope!

  9. Tina Avatar
    Tina

    Will do.

    I just purchased the IF Tracker App this morning. I’m SHOCKED as to how my overall daily eating is actually inflammatory. Today I’m going to make some adjustments so that my overall IF rating is positive. Oi!

  10. thelowhistaminechef Avatar

    Hi Audrey, ginger helps me too! And turmeric 🙂 Thanks for reading.

  11. thelowhistaminechef Avatar

    I’m not sure how I feel about that IF thing. I’m not satisfied that their info is accurate. There are so many factors that make a food inflammatory and I think they get it wrong a lot of the time…

  12. thelowhistaminechef Avatar

    My pleasure, thanks for reading Sarah! That’s exactly what it did for me 🙂

  13. Lara Alexandra Avatar
    Lara Alexandra

    Hi Yasmina, I was diagnosed with chronic urticaria/angioedema almost 2 years ago and it is most likely autoimmune. The best case I can hope for is a “spontaneous remission.” I’ve been following your blog for a while since histamine is definitely an issue for me and purchased your latest cookbook (it is great!). Anyway, I just wanted to let you know you are basically my hero through this thing. It is incredibly frightening when your health changes drastically so suddenly and you don’t know what is happening to you. Your blog has provided me with a lot of comfort through this and I’m incredibly grateful.

  14. bbblues Avatar
    bbblues

    I’m familiar with a number of MCAS/SM patients whose debilitating fatigue was medicated by Dr. Castells with substantial success.

    I don’t want to discount how vital exercise and dietary measures can be. I hope there’s no suggestion that these are necessarily a panacea — no blaming those of us whose medical condition remains atrocious. If vigorous exercise, healthy diet, Yoga-type breathing/stretching/imaging, etc. could successfully “control” my systemic mast cell (“activation”) disease and other afflictions, I would never have become sick to begin with. I would be the picture of health, as I long was and expected to remain for many decades. I benefitted enormously from such measures. Doctors have marveled at my determined resilience, unflagging hopes, exceptional pain tolerance, etc. Alas, I have suffered a series of devastating medical setbacks despite these measures, despite my endless efforts to expedite a breakthrough with my medical condition, with my treatment. Including aggressive off-label Xolair treatment Dr. Castells impressively secured authorization for, recognizing my doctors and I had pretty much exhausted all other available measures, including scores of medications, other agents, other measures as touted here.

  15. Hayden Barnes-Turnidge Avatar
    Hayden Barnes-Turnidge

    Great interview! I am really happy to hear there is a doctor who would recognize the connections between diet and exercise. I was initially diagnosed with a histamine intolerance, but now my doctors are looking into MCAD. I found Dr. Castells comment about fat interesting because when I lower the fat content in my food I tend to feel so much better! I was wondering if you have found that to be true or have found any interesting research involving that? It really seems to make a big difference in how I feel.

  16. Fiona Stryjak-Smith Avatar
    Fiona Stryjak-Smith

    I swear, the only thing that has kept me out of a wheelchair, with my 6+ years of Systemic Masto & POTS is Yoga and walking. I’ve recently added small jaunts on my trike down the backlane when no other humans are about. I have anaphylaxis about once a week or once every 2 weeks if I’m lucky, but I use meditative breathing to stave off reactions so that I’m no longer having several per week. I mean, I still end up needing ambulances and emerg. but not near the frequency of before. I have hopes it will go down to NIL and eventually an epipen WILL expire. 😀

    Also, despite the serious fatigue and pain I’m in, I’m diving headlong into an anti-inflammatory approach to my diet now (which you’re helping me with!) Each one of us IS different and what I’ve figured out, through trial and error, is I don’t do well on fats (Paleo) but DO need adequate protein BUT seriously feel SOOOOO much body pain if I eat meat. Recently, I did a MTHFR gene testing thingy and discovered that I’m positive for a bunch of MTHFR genes that, for me specifically, create an AMMONIA intolerance. So when I eat meat, I don’t break it down efficiently and over time, ammonia builds up in my joints, tissue and blood causing inflammation, pain, etc. SO…I am now vegetarian.

    I want OFF these meds. I saw my Immunologist this past Monday. She needed my weight for a test we were doing. I said to her that when I first started seeing her, years ago, I weighed literally 80 lbs less. She said she was sorry, it’s the drugs I’m on. I said I don’t buy it. There are people on these drugs that don’t pile it on like this. She said it’s like food, some people have metabolism’s that can deal with the foods/drugs and some don’t. She said she knew when they put me on the meds that this would likely happen, ESPECIALLY because I’m so anaphylactic and require so many steroids. I said I would never have taken them if I’d known. She said she knows, that’s why they didn’t tell me. But it’s ‘fat or dead’. I don’t like those choices. So I keep fighting. I keep trying.

    So IF there’s a way to do this disease with diet and exercise and lifestyle..I’m ALL over it.

    I have cut out the stress in my life.

    I have started my Masters degree this September, which makes me happy despite the challenges it brings (doing it by distance ed. as I can’t really leave my house.) Doing things to make our souls happy is important…whatever it is.

    I got the probiotics you talked about. I think healing my gut is the next logical step. Literally EVERYTHING I put in it turns to vomit or diarrhoea the minute it hits my tract, which isn’t a good sign. I see a Gastroenterologist this month but meh, what’s he gonna do? Scope me and tell me I have mast cells or eosinophils in there? so what??? So, between diet, juicing and probiotics, I’m hoping I see some difference.

    I take the least amount of drugs that I can live with, and am constantly testing to see if I can live with less.

    ALso, because I’m still recovering from Addisons/Adrenal failure, I need to eat at regular intervals and have no appetite at all. So I keep a timer. it dings, I prep food and nosh. I don’t always eat it all but I try. Enough of this ‘starving fat’ malarky.

    And water. HYDRATE, HYDRATE, HYDRATE.

    Oh and SLEEP. I no longer need sleeping pills and am only having like maybe ONE night a week of insomnia as opposed to weeks of it and then collapsing in a heap of exhaustion and brain fog.

    Taking the steps, small ones, or the leaps, where they are, in the journey to wellness are immense.

    I think what you offer people is wonderful Yasmina! I don’t really have the energy to do this kind of research, even though I need it, so THANK YOU!!!!

  17. Jill Fremont Avatar
    Jill Fremont

    Thank goodness Dr. Joneja will stick her neck out and acknowledge diet. I’ve seen two mast cell specialist in the last month and neither would admit to any sort of diet modifications being helpful which leaves you at the mercy of meds and the docs. I’m so happy as the acknowledgement of this empowers those of us who will watch what we put into our mouths! Great info. Thanks!

  18. Jill Fremont Avatar
    Jill Fremont

    oops, sorry, i meant Dr. Castells! I had Dr. Joneja’s last interview on my brain 🙂

  19. Ann Avatar
    Ann

    Would love to get some specifics on how the vitamins you’re taking work. I’m catching up with you on realizing I have to eat better than low histamine.
    What do these do?

    Twinlab quercetin and vitamin c (both mast cell stabilisers/antihistamines)

    Source Naturals Mangosteen (mast cell stabiliser & helps with high prostaglandins)

    Spatone iron supplement (basically just iron rich mineral water)

    Viridian Nutrition digestive enzymes (occasionally)

    Carlson Vitamin K2 (soy free)

  20. Tracy Knupp Avatar
    Tracy Knupp

    Yasmina- Thank you for seeking out the truth and having the courage to advocate for a healthy lifestyle and diet as a means to healing for SM/MCAD. I’m new to this process but I have found that my Dr’s appreciate research info I bring to my appts. I will certainly bring this interview with me when I see my Immunologist next week. It was your site that led me to look into histamine intolerance/MCAD/MCAS as the cause of symptoms. Your site is inspiring!

  21. Anne Berry DeRuiter Avatar
    Anne Berry DeRuiter

    I’d like to hear more about the fat angle as well. I discovered my histamine problem when I tried a low carb/high fat diet and felt really lousy. I haven’t determined if the fat is the problem or I’m reacting to too many nuts (or both) but I agree with Hayden that I feel much better after eating a salad than after eating something high fat.

  22. thelowhistaminechef Avatar

    Hi there, it’s SO incredibly sweet of you to take the time to leave this message. I’m very glad the blog has been of use to you – that’s why I began sharing my story in the first place 🙂 I don’t see why we shouldn’t hope for the best – I believe remission is possible!

  23. thelowhistaminechef Avatar

    Hi there, at no point in our interview did Castells say that meds are not the first line of treatment, nor that they are not effective in treating mast cell disorders. On the contrary, she was sharing that in 20 years of treating patients she has observed that those who made lifestyle changes (in addition to meds) had the best prognosis overall. I also do not say in the post, or anywhere on this site, that I believe we brought on these conditions by our personal choices. I do believe that in MY case but I cannot speak for others. In my case it wasn’t diet/exercise so much as completely disregarding the massive amount of stress that working in war zones caused me. To the point where I acknowledged I suffered some kind of PTSD, but still I refused to accept the role of stress in my declining health. Even if we have lived the most virtuous life imaginable I believe it’s still reasonable to assume that the chemicals in our food as well as what our mothers consumed during pregnancy, the hormones found in tap water etc, are more likely to blame than a lack of exercise. There’s little point in playing the blame game I believe – I keep my eye on the goal. I’m terribly sorry that you fell ill despite looking after yourself so well for all those years. Truly I am. I’m just trying to spread a little hope. If people try a little harder with diet and exercise, even if there’s no progress on the mast cell front, at the very least their body may become stronger overall. There’s no harm in that.

  24. thelowhistaminechef Avatar

    Hi there, see I actually find the opposite to be true! As I always say, we’re very different. I’m not talking about deep fried foods or ice cream here, but rather that I felt a decline in my overall health when I completely restricted fats in my diet. When I added olive and coconut oil back to my diet I felt so much better. Having researched it I discovered that medium chain fatty acids as found in those oils cause a spike in the histamine lowering diamine oxidase enzyme, in addition to their both possessing significant anti-inflammatory properties. What i had been told by the person who initially diagnosed me with histamine intolerance is that histamine is often stored in fat. So that might be why animal fat bothers. But generally fat is inflammatory and that may be what she was talking about. Hope that helps!

  25. thelowhistaminechef Avatar

    Thanks so much! I’m glad you enjoyed it. If you read the comment below (sorry was working my way up!) my answer is there.

  26. thelowhistaminechef Avatar

    YES!! I’m so glad to hear of your amazing progress! Every time we speak you’re getting better. You started in such an incredibly difficult place with all the allergies and anaphylaxis but of course this is mega news 🙂 I KNOW you can do it.

  27. thelowhistaminechef Avatar

    You’re very welcome! Thanks for reading 🙂

  28. Anne Berry DeRuiter Avatar
    Anne Berry DeRuiter

    EVERYTHING you’ve written has helped! BTW, if someone wants one of your books in hard copy, they can print it out and take it to an office supply store and get it bound. Voila, book.

  29. thelowhistaminechef Avatar

    Hi Ann,

    The Twinlab Q&C – they are both mast cell stabilisers, meaning that they prevent the mast cell from releasing histamine to start with. I find this more beneficial than using H1 and H2 receptor blockers that only prevent the histamine, already in the blood stream, from causing a worse reaction. Start at the course I say!

    Mangosteen: mast cell stabiliser, prostaglandin inhibitor. PDG is another inflammatory element leaked by unstable mast cells. I always say that it’s a mistake to focus on just the histamine. Mangosteen also helps with IgE type reactions.

    Spatone: yup. That’s what it is. I don’t eat meat, just a bit of lamb so I need to keep my iron up. This is the only iron I somewhat tolerate.

    Viridian enzymes: I have low dao so I assume that my other enzymes are likely to be low so I’ll sometimes take a couple of these to help my body digest challenging foods (not that I do that often).

    K2 – many of us have low bone density. It’s typical of mast cell disorders. This K2 is soy free (and free of all other allergens). K2 has been shown to be more effective than many forms of calcium at building quality bone.

  30. thelowhistaminechef Avatar

    Thanks Tracy, that’s so sweet of you to say 🙂 Thank you for reading and taking the time to post such a lovely message. Best of luck with the appointment, please let me know what happens!

  31. thelowhistaminechef Avatar

    🙂 So sweet! YES! Great idea thank you.

  32. Natalie Avatar
    Natalie

    So is high intensity exercise not something that someone with mastocytosis or histamine intolerance should be doing? I noticed recommendations are walking, yoga etc. I crossfit 3x a week and some days it makes me so dizzy, weak and tired I can barely finish a workout. It feels like I’m regressing in terms of strength, especially during estrogen peaks and during allergy seasons.

  33. Tracy Knupp Avatar
    Tracy Knupp

    Yasmina- I have a confirmed diagnosis of MCAD/Systemic Mastocytosis from a Dr. at National Jewish Hospital Immunuology Dept in Denver, CO. He agrees that the low histamine diet will be beneficial along with the Cromolyn Sodium treatment. I have agreed to the medication along with a prescription strength H1/H2 blocker and Leukotriene inhibitor for the next two months. I made the apple/blueberry/giner desert this weekend and served it over frozen almond milk and then used the excess on the waffles I made from your recipe. All I can say is Hip Hip Hooray!!!!!! both recipes are DIVINE and will become staples in my diet. It helped me feel normal again to have good food to eat and to not have reactions from eating it!!!! The second best part is that my husband loved it too. I have been cooking two different meals for him and I for years which takes up a lot of my time. I’m looking forward to only cooking one healthy and satisfying meal/desert etc. that we can both enjoy. Thank you again. PS. I ordered the Anti Cookbook this weekend. I’m looking forweard to trying every recipe!

  34. Kari Avatar
    Kari

    I agree that diet has made a huge difference (even though my docs didn’t think it would!). I’m curious about the exercise part, though, as any kind of physical stress/exertion (picking up one of my kids, standing for more than a minute or two, crouching down, etc.) sets me into an anaphylactoid reaction and can land me in the ER. I have systemic masto – maybe it’s different for those with MCAS/histamine intolerance?

  35. thelowhistaminechef Avatar

    Hi Natalie, Dr Castells says some people do Zumba! That’s very cardio. In my case running makes me feel like hell, kickboxing not so great (but not horrible), and yoga used to make me shake like a leaf and come down with a migraine. But recently I completed my first 90 minute full primary series ashtanga class in three years (!!) and felt INCREDIBLE after. I have been slowly increasing my exercise while working on keeping my heart/stress under control. I’m planning to write up a post about it.

  36. thelowhistaminechef Avatar

    Hi Kari, I don’t think it is different. I’m prone to anaphylaxis too. Castells told me, while we chatted before the interview, that she has SM patients who travel, exercise, some even who manage to do it meds free, because of their lifestyle (stress, exercise and diet) changes. I think it takes time, and we musn’t push ourselves. When I did I ended up in big trouble. It has taken me three years to get where I am now…please see my answer to someone else below…

  37. Natalie Avatar
    Natalie

    Thanks! I talked to my crossfit trainers and I’ve scaled way back on the aerobic activity and just do weight training mostly and its helping already! I love yoga and i think I need to include it more in my schedule again

  38. RepublicAnn Avatar
    RepublicAnn

    The more docs I see, the more I realize it’s their livelihood and of course they think their way to treat is best. Do you think a Ford dealer is going to suggest you buy a Chrysler? Most of the MDs suggest a prescription is a must. I had an allergist who watched me swell up and sent me to the ER from his office tell me their was no such thing as food intolerance. I have been daily prescription free for 3 years. Had taken a few anti-histamines in the past few years and tylenol for cramps, but have gotten rid of those as well in the past few months with diet change and adding quercetin and green juice.

    Yasmina, thanks for all the great info. You seem to have the most similar health history to me that I’ve found and I’m following your recovery in the same manner.

  39. Maddie Avatar
    Maddie

    Hi, Where is part 2 of this interview? Can you provide a link?

  40. Lindsay Avatar
    Lindsay

    Thanks for this! I would love to read and share an article that is solely (or mostly) about the role of stress in mast cell disorders. Looking up part 2 now, but think the topic of stress could be it’s own article.

  41. Lindsay Avatar
    Lindsay

    Thanks for this! I would love to read and share an article that is solely (or mostly) about the role of stress in mast cell disorders. Looking up part 2 now, but think the topic of stress could be it’s own article.

  42. Lise Avatar
    Lise

    I’m sort of a newbie here, and to my MCAD dx, but when I first got it I did a google search on EMF and mast cell activation and there was research going back almost 2 decades showing mast cell activation from exposure to computer and tv use. I have been experimenting with this for a few years now, and especially since moving and having less wifi neighbors, turning off my wifi and using ethernet cable, turning of circuit breakers at night, I’mm doing better. Still a long way to go, but now I have the brain power and strength to implement the diet and exercise I was unable to do much but vegetate before. I’m just saying, in our current electronic and frequency saturated environment, if you are unable to get results, maybe you might look into this aspect. Good luck

  43. Lise Avatar
    Lise

    I’m sort of a newbie here, and to my MCAD dx, but when I first got it I did a google search on EMF and mast cell activation and there was research going back almost 2 decades showing mast cell activation from exposure to computer and tv use. I have been experimenting with this for a few years now, and especially since moving and having less wifi neighbors, turning off my wifi and using ethernet cable, turning of circuit breakers at night, I’mm doing better. Still a long way to go, but now I have the brain power and strength to implement the diet and exercise I was unable to do much but vegetate before. I’m just saying, in our current electronic and frequency saturated environment, if you are unable to get results, maybe you might look into this aspect. Good luck

  44. Jordan Avatar
    Jordan

    Thanks Yasmina! So grateful for the information and motivation! Best, Jordan

  45. Jordan Avatar
    Jordan

    Thanks Yasmina! So grateful for the information and motivation! Best, Jordan

  46. Loren Avatar
    Loren

    FATS can be life saving. It totally depends upon the person. Every individual is incredibly unique, and will do better with different foods.

    There is substantial evidence that a ketogenic diet can reverse mast cell diseases and autoimmune diseases.

    http://www.ncbi.nlm.nih.gov/pubmed/25302070

    Although I think the key is prolonged periods of trigger avoidance, which seems to help heal the individual and clear up the responseas to triggers.

    Yasmina, I like your blog, but you can’t apply what worked for you to everyone. This is a disease of individuality. I think if you frequently interviewed people who have overcome this disease in a different way then your own, it would add substantial value – and add wisdom to your understanding of this disease.

  47. Loren Avatar
    Loren

    FATS can be life saving. It totally depends upon the person. Every individual is incredibly unique, and will do better with different foods.

    There is substantial evidence that a ketogenic diet can reverse mast cell diseases and autoimmune diseases.

    http://www.ncbi.nlm.nih.gov/pubmed/25302070

    Although I think the key is prolonged periods of trigger avoidance, which seems to help heal the individual and clear up the responseas to triggers.

    Yasmina, I like your blog, but you can’t apply what worked for you to everyone. This is a disease of individuality. I think if you frequently interviewed people who have overcome this disease in a different way then your own, it would add substantial value – and add wisdom to your understanding of this disease.

  48. thelowhistaminechef Avatar

    Hi love: “fat’s are not so good, said Dr. Castells.” She’s not telling people not to eat them, just that they’re not so good (in her opinion) as others. Her full quote: “The diet is critical and there is no single diet, so there are diets that will be good for a patient or not so good, grains, fruits, vegetables, any of that with antioxidants are tremendously good for patients.” So, she herself is saying that it’s not a one size all fits approach, something I do say quite a bit in most of my posts. This blog is about my healing, how I achieved it, in case there are others who have either not had the results they would have wished with other approaches or are just interested in how I managed to go from bed bound to eating what I want and living meds free in just a few years. I speak about that which has worked for me, that which has failed, but what I don’t do is speak of things I haven’t personally tried. I don’t believe the ketogenic diet to be a health one as practised faithfully. I do believe there is a healthier way to do it, but again, it’s not something I would do myself, so not something I would talk about on my blog. I’m sure there are people out there with histamine/mast cell disorders who are exploring this diet, and they will write about it (if they aren’t already). For the most part they will discuss their success with this approach, rather than speaking about others they haven’t tried. I’m sure there’s more ways than one to skin a cat (sorry vegans/PETA folk), and the great thing about living in this modern age is that there’s a blog covering each and every one of these ways to do so. I need a better analogy but you know what I mean 😉 Dr. Fuhrman doesn’t believe in fats, so people who also don’t believe fats are great will be into his stuff. If they decide it’s not working for them they might soon head over to Chris Kresser and go for Paleo. I’m just one talking head, sharing one particular viewpoint, that a balanced diet high in nutrients works not just for mast cell disorders, but for running your body successfully no matter the issue. If people are looking for an all round approach to mast cell disorders there’s any number of excellent blogs who blog about the entire issue. This is the low histamine chef, so I blog the recipes that have helped me heal xo

  49. thelowhistaminechef Avatar

    Hi love! Thanks for reading and taking the time to post 🙂

  50. thelowhistaminechef Avatar

    Hi love! Thanks for reading and taking the time to post 🙂

  51. thelowhistaminechef Avatar

    Hi love, you’re right. I just know that most aren’t ready to commit to a life of meditation and yoga, so telling them that stress causes these issues is just going to make them more stressed and miserable. So I just talk about it in various posts 🙂

  52. thelowhistaminechef Avatar

    Hi love, you’re right. I just know that most aren’t ready to commit to a life of meditation and yoga, so telling them that stress causes these issues is just going to make them more stressed and miserable. So I just talk about it in various posts 🙂

  53. thelowhistaminechef Avatar

    Hi love, it’s in the post.

  54. thelowhistaminechef Avatar

    Hi love, it’s in the post.

  55. thelowhistaminechef Avatar

    I’m so sorry to hear of your similar experiences love. I’m very happy to hear that these changes are bringing you relief.

  56. thelowhistaminechef Avatar

    I’m so sorry to hear of your similar experiences love. I’m very happy to hear that these changes are bringing you relief.

  57. Jessica Avatar
    Jessica

    Kari, can you say more about anaphylactoid reaction caused by physical movement or stress? Is there a place I can read more about this? My husband gets something like this and I want to understand it. (he can’t stand up for more than 10 minutes, if there is a loud noise near him, his nervous system goes haywire, etc.) He wants to do physical exercise, but even 5 minutes of walking causes him hours of pain.

  58. Jessica Avatar
    Jessica

    Kari, can you say more about anaphylactoid reaction caused by physical movement or stress? Is there a place I can read more about this? My husband gets something like this and I want to understand it. (he can’t stand up for more than 10 minutes, if there is a loud noise near him, his nervous system goes haywire, etc.) He wants to do physical exercise, but even 5 minutes of walking causes him hours of pain.

  59. Shelley Avatar
    Shelley

    So, are you saying we need to not worry about histamine foods and just eat a diet high in nutrient rich foods? Is that what worked for you? Can you tell me which books I need to buy to get started. Is there one that will give me the whole picture?

  60. Shelley Avatar
    Shelley

    So, are you saying we need to not worry about histamine foods and just eat a diet high in nutrient rich foods? Is that what worked for you? Can you tell me which books I need to buy to get started. Is there one that will give me the whole picture?

  61. Jack Cowie Avatar
    Jack Cowie

    I co-direct a non-profit for people living with multiple sclerosis. 9 weeks ago I was diagnosed with Mast Cell Activation Syndrome. Because of my work in MS, I had a light speed understanding of MCAS and Mastocytosis. In MY OPINION, what is most important to understand is the role of prostaglandin (PD2) on histemic reaction. An individual with normal histamine levels, can be tremendously affected if their own histamine prostaglandin reaction is virulent. I believe ENTIRELY that the treatment for every person is PERSONAL! No two people will react the same to the same triggers nor will they have the same reactions to histamine laden foods.
    At a recent support group meeting I learned (so gratefully) that with MCAS or mastocytosis, that every day is different from another, and what we react to today will not affect us tomorrow. Treatments seem the same.
    What I believe I have also discovered, is that MCAS is the precursor, and possibly the cause, of all autoimmune disorders. They all have an inflammatory response. The differing degrees of affectation are a result of the prostaglandin/histamine affectation. Why one person presents with MS, vs. ALS, vs. Parkinson’s, vs. Alzheimer’s, vs. Crohns, vs. Colitis, vs. IRB is the small differentials in DNA that dictate differences each person’s vulnerability.
    Just my opinion, I could be wrong.

  62. Jack Cowie Avatar
    Jack Cowie

    I co-direct a non-profit for people living with multiple sclerosis. 9 weeks ago I was diagnosed with Mast Cell Activation Syndrome. Because of my work in MS, I had a light speed understanding of MCAS and Mastocytosis. In MY OPINION, what is most important to understand is the role of prostaglandin (PD2) on histemic reaction. An individual with normal histamine levels, can be tremendously affected if their own histamine prostaglandin reaction is virulent. I believe ENTIRELY that the treatment for every person is PERSONAL! No two people will react the same to the same triggers nor will they have the same reactions to histamine laden foods.
    At a recent support group meeting I learned (so gratefully) that with MCAS or mastocytosis, that every day is different from another, and what we react to today will not affect us tomorrow. Treatments seem the same.
    What I believe I have also discovered, is that MCAS is the precursor, and possibly the cause, of all autoimmune disorders. They all have an inflammatory response. The differing degrees of affectation are a result of the prostaglandin/histamine affectation. Why one person presents with MS, vs. ALS, vs. Parkinson’s, vs. Alzheimer’s, vs. Crohns, vs. Colitis, vs. IRB is the small differentials in DNA that dictate differences each person’s vulnerability.
    Just my opinion, I could be wrong.

  63. Stefanie Avatar
    Stefanie

    HiHelp , I really don’t know where to go….I feel my two boys 4 and 5 may have , mast cell…..so what do I do? Where do I go for a diagnosis…or help….we have been in and out of Emergency rooms and been to many docs…and no one ever knows what’s wrong. I found mast cell from all their symptoms….pediatrian has never even heard of it. Where do I go? We are doing every elimination diet possible and they are so very very sick…its activated every few months and they have urination and fever now, flushing, gut issues, crazy phenol and histamine reactions to food. Anger, fatigue, aches, uncontrollable laughter, crying, purple circles under their eyes. Im watching them distuct befor my eyes, they are just babies…please tell me what kind of Doctor I need to see?

  64. disqus_6DbrMJ2WvJ Avatar
    disqus_6DbrMJ2WvJ

    Hi Fiona, Where did you get all of the testing done to take you to a clear diagnosis? Thanks! – Julie

  65. disqus_6DbrMJ2WvJ Avatar
    disqus_6DbrMJ2WvJ

    Hi Fiona, Where did you get all of the testing done to take you to a clear diagnosis? Thanks! – Julie

  66. don b Avatar
    don b

    I will attest to the diet and exercise. I have been of of daily antihistamines, ranitidine and nalcrom for over a year now and relate it to diet adjustments and daily exercise. Still take Benadryl and epi pens when attacks come, but their severity and frequency has greatly diminished.

  67. don b Avatar
    don b

    I will attest to the diet and exercise. I have been of of daily antihistamines, ranitidine and nalcrom for over a year now and relate it to diet adjustments and daily exercise. Still take Benadryl and epi pens when attacks come, but their severity and frequency has greatly diminished.

  68. Namaste Avatar
    Namaste

    What can you do when you have severe spinal problems and can’t excercise

  69. Namaste Avatar
    Namaste

    What can you do when you have severe spinal problems and can’t excercise

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Welcome!

Yasmina was an award-winning broadcast journalist with a decade of experience covering war zones for CNN and the BBC. She devoted her journalism skills to researching and writing about histamine. Click here to learn about her. Each post is carefully and fully referenced with the latest scientific research. Not sure where to start? Here’s a four week meal plan and overall Histamine Reset.


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