The interviewer was soooo disruptive! She didn't allow the doctor to finish his thoughts, and she continuously interrupted him with her "empty" interjections of "ok", "ah" "uh-huh" and laughter. With all due respect, it was annoying! 😤 Let the guest talk! In an interview with a lot of technical information, the ongoing interruption is not conducive to the flow and impacts the transmission of the information to the audience.
Yes, I'm an ex interview er as a job ....her interruptions were tragic because I desperately wanted to hear him speak. I have MCAS and needed to learn from him
I have had Mcas for at least 20 years, have seen multiple specialists. Taking histamine meds since 2016 but they no longer work and I cannot find a dr that knows what to do for my constant itching skinand inflammation.. Clinics and hospitals are all chaotic so finding help is almost impossible. Even my pcp is not available most times. Too busy
In EXACT same boat! I’ve resorted to researching on my own. Which is taking forever but will hopefully be worth it in the end. The challenge is getting the appropriate testing performed...& then of course sourcing rx drugs later. First I’ll see how far I can get with OTC meds & supplements. I’m also looking into gene testing to see if I have any mutations that are driving the constellation of health problems I’ve had for decades. Only to be told “I’m fine & it’s all in my head”. Sound familiar?! 🙄 Seeking Health is a good company to check into, they have some mast cell supps that are helping some already.
Was pre med, now retired educator, HS, college, 31years, now 31/2 yrs, long cov, w pre existing conditions, long Lyme., celiac, autoimmune, ,gut dysbiosis. some days barely functional.. researched all this for 3years😮.Dr T is brilliant!put it all together in common sense, clear, precise info💕..we desperately need integrated approach as done as indicated here, I see 11 Drs who treat 11 body parts 😢..THANK YOU💞
Pretty sure this is what I have, yet I get told I only have edema and uticaria. So sick of the terrible system. Also had exacxtly that, a car accident and after that have come down with all different reactions, and mostly after eating. Yet they tell me it has nothing to do with food even though ive got my IGG tested and turns out i am intolerant to diary, gluten and eggs and few other things. However I also get reactions when its not any of those 3, especially sulphites but the rest I don't know. Can't handle most perfume smell, smoke etc. So tired most of the time, and already have chronic pain. This whole thing is awful and not getting anywhere with the doctors is extremely tough.
Hi Doc. Where in London or UK I can visit a specialist for mast cells please?! I’ve been in very bad condition for years, and having many symptoms of MCAS. No any docs.know what to do with me anymore or how to treat me😞 and I’m getting worse year by year.
I love her passion and love for this genius. Please keep important interviews coming. I really think spike proteins correlates with other viruses and germs for long COVID. Also harmed and caused inflamed blood vessels.
I JUST DON’T CARE ANYMORE. I will not seek out medical care any longer to try to figure out what is wrong with me and I don’t have the credit cards to do it anyway. Over 30 years of being sick. I’m done. We should be hospitalized until a diagnosis is made.
How are IgG reactions related to MC activity? My daughter had 5 anaphylactic shocks last year and then we have been in and out of the ER many times. Avoiding triggers on IgG has stopped her from going to the ER. Also she’s taking H1, H2 and leukotrine inhibitors. Symptoms are respiratory, gastric, neurological and skin related. Where can we get in Florida someone who can help us with diagnosis? Thank you.
I would like to know the answer to that question to I’m in Florida. I even saw immunologist at Jon Hopkins and Tampa. Mine is viral related I had a black mold exposure. I Lyme disease in 2002 which it has reactivated that Epstein bar and settle mega virus I react everything food sense and it’s causing me neurological issues. I can’t find anybody to help me around here. I don’t know what to do.
I had testing and showed extremely high prostaglandin d2 at 550. I experience severe stomach pain and bloating when eating, then severe nervousness and anxiety with racing thoughts. All triggered by eating. Also have eosinophilic esophogitius. Does this qualify as mcas. And can the high prostaglandin explain my symptoms.
Far too many times, the interviewer seems to get in the way of the presentation. They do not give added value to the interview...just let the guy talk...he usually has a specific talk about all his research.
I would like to know if there is a food or a diet that is beneficial for long term treatment of MCAS. I have been diagnosed with MCAS. My immunologist put me on the low histamine diet. I did not find it sustainable and it even caused me to have issues with my nails and hair. I decided to come off it while still avoiding my food triggers. I would like to know if the whole food diet would be better at treating MCAS?
My goodness, the interviewer is irritating. Just can't stop interrupting. We are an intelligent audience, we don't need her to rephrase, or hype and highlight. How did the Doctor even regain his train of thought after all of her interruptions every few seconds. I unfortunately had to pass up finishing listening.
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Dear you are interviewing the master in MCAS pleaseeeee let him talk.
He is brilliant but this was difficult to listen to bc she kept interrupting
I always enjoy Dr. Theoharides. What a gem of a human being! So intelligent and compassionate!
We agree!
The interviewer was soooo disruptive! She didn't allow the doctor to finish his thoughts, and she continuously interrupted him with her "empty" interjections of "ok", "ah" "uh-huh" and laughter. With all due respect, it was annoying! 😤 Let the guest talk! In an interview with a lot of technical information, the ongoing interruption is not conducive to the flow and impacts the transmission of the information to the audience.
Yes, yes, YES! 😁
Yes, I'm an ex interview er as a job ....her interruptions were tragic because I desperately wanted to hear him speak. I have MCAS and needed to learn from him
Wish the dr's mic was turned up a bit...he speaks softly. But lady speaks quite loudly so her mic could be turned down.
Girl. Please let him talk. You have a great podcast but relax and let him speak ❤
I wish she would have let him finish his connection of hypothalamus, to amgdala to micro glial. She needs to shut up and let him finish!
Great doctor, just wish the interviewer would have allowed him to speak more. Too many interruptions, making it difficult to follow him.
I have had Mcas for at least 20 years, have seen multiple specialists. Taking histamine meds since 2016 but they no longer work and I cannot find a dr that knows what to do for my constant itching skinand inflammation.. Clinics and hospitals are all chaotic so finding help is almost impossible. Even my pcp is not available most times. Too busy
How do ww find a doctor? I am trying to get diagnosed. Does this doctor not see patients?
In EXACT same boat! I’ve resorted to researching on my own. Which is taking forever but will hopefully be worth it in the end. The challenge is getting the appropriate testing performed...& then of course sourcing rx drugs later. First I’ll see how far I can get with OTC meds & supplements. I’m also looking into gene testing to see if I have any mutations that are driving the constellation of health problems I’ve had for decades. Only to be told “I’m fine & it’s all in my head”. Sound familiar?! 🙄 Seeking Health is a good company to check into, they have some mast cell supps that are helping some already.
Was pre med, now retired educator, HS, college, 31years, now 31/2 yrs, long cov, w pre existing conditions, long Lyme., celiac, autoimmune, ,gut dysbiosis. some days barely functional.. researched all this for 3years😮.Dr T is brilliant!put it all together in common sense, clear, precise info💕..we desperately need integrated approach as done as indicated here, I see 11 Drs who treat 11 body parts 😢..THANK YOU💞
Pretty sure this is what I have, yet I get told I only have edema and uticaria. So sick of the terrible system. Also had exacxtly that, a car accident and after that have come down with all different reactions, and mostly after eating. Yet they tell me it has nothing to do with food even though ive got my IGG tested and turns out i am intolerant to diary, gluten and eggs and few other things. However I also get reactions when its not any of those 3, especially sulphites but the rest I don't know. Can't handle most perfume smell, smoke etc. So tired most of the time, and already have chronic pain. This whole thing is awful and not getting anywhere with the doctors is extremely tough.
Hi Doc. Where in London or UK I can visit a specialist for mast cells please?! I’ve been in very bad condition for years, and having many symptoms of MCAS. No any docs.know what to do with me anymore or how to treat me😞 and I’m getting worse year by year.
I love her passion and love for this genius. Please keep important interviews coming. I really think spike proteins correlates with other viruses and germs for long COVID. Also harmed and caused inflamed blood vessels.
covid triggers/reactivates EBV, e.g...has this to do -somehow -with mast cells?
I JUST DON’T CARE ANYMORE. I will not seek out medical care any longer to try to figure out what is wrong with me and I don’t have the credit cards to do it anyway. Over 30 years of being sick. I’m done. We should be hospitalized until a diagnosis is made.
Let him talk she interrupts.. annoying
A truly amazing and enlightening talk! Thanks very much for providing this very relevant information to patients and providers‼️
Beautiful explanation! I appreciate your knowledge. God bless!
Glad it was helpful!
Brilliant ❤😮
You are amazing ❤😊 you saved my life sir
How are IgG reactions related to MC activity? My daughter had 5 anaphylactic shocks last year and then we have been in and out of the ER many times. Avoiding triggers on IgG has stopped her from going to the ER. Also she’s taking H1, H2 and leukotrine inhibitors. Symptoms are respiratory, gastric, neurological and skin related. Where can we get in Florida someone who can help us with diagnosis? Thank you.
I would like to know the answer to that question to I’m in Florida. I even saw immunologist at Jon Hopkins and Tampa. Mine is viral related I had a black mold exposure. I Lyme disease in 2002 which it has reactivated that Epstein bar and settle mega virus I react everything food sense and it’s causing me neurological issues. I can’t find anybody to help me around here. I don’t know what to do.
Thank you for hope!
Thank you.
I had testing and showed extremely high prostaglandin d2 at 550. I experience severe stomach pain and bloating when eating, then severe nervousness and anxiety with racing thoughts. All triggered by eating. Also have eosinophilic esophogitius. Does this qualify as mcas. And can the high prostaglandin explain my symptoms.
Far too many times, the interviewer seems to get in the way of the presentation. They do not give added value to the interview...just let the guy talk...he usually has a specific talk about all his research.
Her mic being 10x louder than his doesn’t help the situation. Can barely hear the poor guy
he is great! she is obnoxious. my god lady, it's not about you!
Yes! Yes! Yes! Ok! GO ON YESSS YEAH RIGHT? YES!
maybe low copper too much zinc
24:34 😳🤯🧐💯
I would like to know if there is a food or a diet that is beneficial for long term treatment of MCAS. I have been diagnosed with MCAS. My immunologist put me on the low histamine diet. I did not find it sustainable and it even caused me to have issues with my nails and hair. I decided to come off it while still avoiding my food triggers. I would like to know if the whole food diet would be better at treating MCAS?
I have had the most benefits from the autoimmune protocol. It focuses on nutrient density while removing common triggers.
My goodness, the interviewer is irritating. Just can't stop interrupting. We are an intelligent audience, we don't need her to rephrase, or hype and highlight. How did the Doctor even regain his train of thought after all of her interruptions every few seconds. I unfortunately had to pass up finishing listening.
Agree the interviewer was disruptive- talks way too much and over the doc- please get another interviewer
Can’t stand that women disrupting the doctor! This isn’t about her!
She talks too much
She said herself she was excited 😆
She was a not relevant disruption@@ruthgoldflam-un4cw
Too annoying to watch 😢
Too annoying.
Maybe do her own interviews
next time don't ever let her host the interview, she is annoying