Could you be one of the 17 percent?
The often undiagnosed condition that makes people vulnerable to spike protein damage, and what you can do about it. Plus, don’t miss our Q&A next Friday!
Do you have Mast Cell Activation Syndrome, or MCAS? Most people have no idea whether they do or don’t – and yet it’s implicated in a whole host of conditions that really mess up people’s quality of life: IBS, chronic fatigue, fibromyalgia, and yes, long Covid and vaccine damage.
What’s so extraordinary is that as many as 17% of us have it – and yet few doctors even know about it. Fortunately, there’s one doctor who is something of an expert on MCAS – and she joins me this Sunday for a Tess Talks I really think all of us would benefit from hearing.
Dr Tina Peers is a Consultant in Contraception and Reproductive health, with a special interest in menopause, and more recently in MCAS and histamine intolerance. During Covid, Tina became an authority in treating long Covid, and opened a long Covid clinic in November 2020. She has also contributed to developing the FLCCC protocols that have helped countless people around the world prevent, treat and recover from Covid-19.
In our conversation, Dr Peers explains what MCAS is and why it leads to so many conditions that medicine struggles to treat. She shares her personal story about how she became an expert on MCAS, and how she saw very early on that it had serious implications for long Covid. Today, she is also treating people injured from the Covid-19 vaccines – and has some truly uplifting success stories on this that are a tonic to hear.
Dr Peers also offers clear, practical guidelines on things we can all do to help the body detox from the damaging effects of spike protein – whether that’s from Covid or the Covid-19 vaccines. It’s a conversation that’s uplifting, informative and healing. I hope you can tune in, this Sunday.
Next week, we have something altogether new…
Ask me a question next Friday!
One of the unexpected joys of launching this Substack has been the wonderful community of readers who share their views, advice, experiences and more in the comments. I learn a lot from you!
As mentioned previously, I’m holding our first Substack event next week: a session for paid Substack subscribers to ask me any burning questions over Zoom, and I will do my best to answer them.
It’s going to be on Friday, 25th November at 7pm London time, so please save the date. You’ll be able to submit questions live in the chat, but if you already know what you’d like to ask me, please let me know now via email.
Thank you!
I’m throwing the kitchen sink at my vac iniury and doing multiple protocols with lots of functional medicine added in the mix. I am pretty sure I have MCAS. Leave it to me to be “special”
I was diagnosed with MCAS ten years ago. It’s quite manageable once you realize what’s going on. When COVID hit and the vax became available I already knew I’d never take it. I can’t tolerate any vaccines. And this one was certainly had a giant red flag.
I’d also be interested to know if people with the MTHFR mutation are more vulnerable to spike damage?