Histamine Intolerances - What is Mast Cell Disorder?
Histamine Intolerance, Mast Cell Activation Syndrome, Mast Cell Disorder Affects Almost Everyone to varying degrees. So why is no one talking about it? And what is the solution? MCAS is also commonly referred to as a type of Mast Cell Activation Disorder (MCAD).
Let’s start with “what’s a mast cell?”
Unless you’re a medical professional you’ve probably never heard of them. And honestly very few medical professionals even are aware of the serious implications that mast cell disorders are causing on an epidemic scale. Mast cells are best known for releasing histamine and being a key player in serious allergic reactions… like someone having anaphylaxis from bee stings or peanuts, or an asthma attack triggered by something like smoke.
Mast cells are a part of the immune system and play a vital role in detecting and responding to foreign substances throughout the body, though the details are still poorly understood. These little cells are activated and actually explode (fancier term- degranulate) to release a huge variety of chemicals, presumably depending on what activated them. These chemicals are used to mediate other reactions and many other things yet to be discovered; this is why you’ll often hear these released chemicals referred to as mediators. One thing they do seem to know- mast cells promote inflammation and cell proliferation for wound healing.
Mast cells are born from stem cells in the bone barrow. They’re prolific, being found in most tissues throughout the body, especially those close to the outside environment, including the lungs, gastrointestinal tract and skin… They’re even found in close contact with neurons, but the exact purpose is still a mystery under research.
What is MCAS?
This is what happens when mast cells aren’t working properly. For some reason (not yet known) these cells are releasing chemicals when they shouldn’t, resulting in a list of unpleasant symptoms. It’s speculated that maybe mast cells could be altered genetically, maybe as a part of a connective tissue problem, or perhaps that MCAS is even autoimmune in nature for some, or maybe MCAS can be tied into neurological dysfunction somehow. The fact is experts do not know, but these researchers are working on it. Research is revealing a complex and still mysterious relationship between the immune and nervous systems. Read more in this review article about The Significance of Conversation between Mast Cells and Nerves. Also important to know is that MCAS is NOT the same as mastocytosis. MCAS is essentially having a normal amount of mast cells that aren’t working correctly, whereas mastocytosis involves a problem of too many mast cells thanks to a cell proliferating out of control (akin to cancer).
Mast Cells & Dysautonomia
This fantastic paper Postural orthostatic tachycardia syndrome and the potential role of mast cell activation by leading experts summarizes the latest understanding (December 2018). This fantastic talk also delves into misbehaving mast cells presenting as MCAS including their relationship to dysautonomia, with Dr. Andrew White & Dr. Jonathan Bernstein. Lots of fresh, easy-to-understand information here.
Watch mast cells degranulate… Symptoms
These are common symptoms I often hear about. There is also a lot of overlap with POTS symptoms. Symptoms vary by person. For some, the condition can be mild, while for others completely debilitating. For a very thorough listing of common symptoms see journal article Characterization of Mast Cell Activation Syndrome.
Mental: Anxiety, Brain fog- difficulty concentrating & recalling words/facts/memories, Depression, Mood swings, Panic attacks, Irritability, feelings of Dread, Test/Performance Anxiety.
Gastrointestinal: Abdominal Pain, Constipation, Cramping, Diarrhea, Nausea
Dermatological: Chronically dry skin, Flushing, Foliculitis, Hives, Itching, Pale skin, Rashes, Dermatographia (skin writing- raised warm red welts from scratches)
Respiratory: Chronic congestion, Coughing, Nasal stuffiness, Wheezing, Difficulty breathing deeply
Cardiovascular: Heart palpitations, Dizziness, Fainting, Near-fainting, Lightheadedness, Low blood pressure, High blood pressure
Vision: Blurred vision, Dry irritated eyes, Red eyes, Watery eyes
Auditory: Sound sensitivity, Tinnitus
Pain: Headaches, Migraines, Joint pain, Chest pain, (Abdominal pain), Back Pain, Joint Pain
Migraines / Headaches: Headaches, migraines
Other: Weight gain and retention despite low calorie intake and exercise, Slow time to heal wounds, Acute sense of smell
Anaphylaxis: If too many mediators are spilt into your system, you may also experience anaphylaxis, which primarily includes: difficulty breathing, itchy hives, flushing or pale skin, feeling of warmth, weak and rapid pulse, nausea, vomiting, diarrhea, dizziness and fainting.
Anecdotally, those who react immediately after exposure to a trigger are called “shockers,” and those that react later are called “leakers.”
These common triggers are things that can cause symptoms, or just make those symptoms so much worse. This is not a full list of triggers just a few common triggers.
- Nutrient Sensitivities (ie: vitamins, minerals amino acids)
- Foods Sensitivities (specific to client)
- Emotional and physical stress
- Hot or cold temperatures
- NSAIDS (non-steroidal anti-inflammatory drugs), antibiotics, and other
- Skin friction or pressure
- Strong scents or smells (even from perfumes or essential oils)
- Bug bites
What’s it really like to have MCAS?
- New fears. Things that you used to take for granted now become a source of fear. Exerting yourself too much, eating the wrong food, getting too emotional, or getting too warm can all end up sending you to the ER.
- Limited exertion. You can essentially be allergic to exercise. A few hours after a strenuous workout I have a delayed allergic like response that presents like anaphylaxis (this makes me a “leaker”). Yes, it’s weird. My heart rate goes through the roof. I feel like I’m dying. I get uncontrollable shake/shivers, vomiting, nausea and go ghost white. All just from a session at the gym. Other people with MCAS get their symptoms during or right after exercise. They can get hives, dizziness and have trouble breathing along with other awful symptoms.
- Limited diet. Many with MCAS will react to certain foods, and the list can become long. Even simple ingredients like sugar or MSG from your favorite Chinese food can trigger symptoms. Alcohol is also a major trigger for MCAS affected people.
- At the mercy of the air. A whiff of someone’s perfume or cologne can be a trigger. This can make going out into the world difficult, because you can’t control the air. The best you can do is wear something like a Vogmask. Forget going to the local home store with the heavy odors of fertilizer and paints. As a healthy person I hardly registered smells, and a waft from someone drenched in cologne was a mere annoyance, but for someone with MCAS this can ruin their entire day. Imagine turning the dial up on the list of symptoms above from just breathing some fragrant air.
- No warm weather. Hot or cold temperatures are a common trigger for MCAS. That makes going outside difficult! “Hot temperature” for me is above 75℉. Not exactly a lot of wiggle room. After standing in warm weather a few minutes I find it incredibly difficult to stand, my heart rate will shoot up and I’ll have to sit or lay down or else I’ll pass out. That’s accompanied by nausea. It’s like getting hit in the gut with the flu just from trying to be in beautiful beach weather… and I love the beach.
- Leaving the house requires bravery. The price to pay for exposure to triggers is high, because you can end up feeling very bad for hours or days. Amazing all people with MCAS don’t just become agoraphobic hermits. After your symptoms have been triggered, you can’t just stop the “trigger” and feel ok. You can’t stop exercising, or get away from fumes and immediately rebound. This is because the mast cells have dumped their chemicals into your system and it takes time to process and eliminate them. Even after acute symptoms like swelling or nausea subside, good chance you’ll be exhausted and fatigued for days as your body recovers from the toxic dump of your mast cells.
- You’re less reliable. Some days may be drastically better or worse than others, often times for no knowable reason. This makes planning social and professional engagements a huge challenge, if not impossible. Can you make that presentation? Can you even make it to the movies or that coffee joint? Having an unreliable body changes and strains almost all your social relationships. Your true friends and family will adjust and help, and others will fall away from your life. You experience loss, anger, and maybe even shame.
- Anxiety for attacks. Going anywhere can cause anxiety, especially given all the potential triggers that can cause a life shaking event. You probably battle a justified and logical anxiety, and constantly plan the worst case. Trying to be safe is a struggle. Do I have all my emergency meds? Where’s the closest ER/Urgent Care? Where are the bathrooms? Will I be safe if I need to lay down or use an EpiPen? These are not the questions of a hypochondriac. Knowing these things makes you safer. Attacks happen and can’t be reliably prevented at all times. They come on quickly, with little to no time to get out of a store or social situation. The best you can do is reduce your exposure to triggers, while balancing the need to live life.
- …Then having an attack. You experience attacks that are scary and incredibly socially awkward. An attack doesn’t have to be full blown anaphylaxis. You can have a cluster of intense awful symptoms that disable you. We all have them. The unpredictability of them amplifies their awfulness. My scary attacks involve my heart rate shooting up, which comes with a sense of doom in itself. Then, feeling a wave of dizziness, I start shaking, shivering and chattering uncontrollably. I know this means to lay down ASAP or my body will pass out and do it for me. Sometimes there’s nausea and vomiting. If the attack escalates, I often feel the overwhelming need to empty my bladder, then maybe my bowels. How am I supposed to use the toilet when I can’t even stand? I take emergency meds, sometimes I can get there myself, sometimes I get carried, and at my absolute worst- bedpans like a 90-year-old (in private thank sweet baby goodness). I feel like I’m dying, though I never do.
- Losing or downgrading your career. Working a full-time job can be hard, if not impossible. You may have to reduce your work schedule and lose career advancement, if not let go of your career entirely. And if you’re able to keep your career, you’ll probably be working MUCH harder than those healthy counterparts around you. I had to leave my full-time job as a professional mechanical engineer, creating a huge loss of financial independence and identity. Healthy people having a taste of this condition would call in for a sick day and get to the hospital.
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