Here's How You Treat Long Covid | Lessons From MCAS - Dr Tina Peers

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  • เผยแพร่เมื่อ 8 ม.ค. 2025

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  • @MP-py7pt
    @MP-py7pt 4 ปีที่แล้ว +325

    Should be up for an award in investigative journalism as well as public health!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +14

      Haha, thank you!

    • @alexhey8277
      @alexhey8277 4 ปีที่แล้ว

      @@RUNDMC1 Do you have any website as a source to recommend?

    • @eleanorcoleman284
      @eleanorcoleman284 4 ปีที่แล้ว +7

      Thank you for doing this. It’s difficult to deal with long covid symptoms and be treated like you’re anxious or crazy. You provide a glimpse of hope for people like me.

    • @markchristensen9783
      @markchristensen9783 3 ปีที่แล้ว

      @@RUNDMC1 important question . My issues are primarily body aches . Is MCAS protocol primarily only applicable to
      People with respiratory issues ? I’m taking the supplements but for last few days went back to high histamine foods and it’s not affecting me negatively . Having said that , if it’s not a good idea , how long does it take to get bad symptoms again if high histamine
      Foods are reintroduced. It’s been 3 days and not feeling worse .. any feedback is greatly appreciated!!

    • @truthseeker6688
      @truthseeker6688 3 ปีที่แล้ว +2

      long covid is a leaky gut syndrome. A doctor in pakistan is treating people long covid by prescribing them proton pump inhobitor like pantaprazole, eatung honey and yougurt in morning, eating raw onion and garlic with rice veggies, avoiding gluten, sugar, fast food, using olive oil etc. And people are healing in about 1 month of doing this

  • @lacisz
    @lacisz 4 ปีที่แล้ว +235

    Hey Gez, I know you are hearing it all the time, but your work is essential. You are doing what governments should do - collecting scientific data and making it palatable for all of us. Your way of presenting is objective and trustworthy. I'm also in the club, but after 8 months, I'm using my running shoes again. The brain fog is still persistent, but I'm hopeful. There are some clear minutes daily which wasn't true a few months before. Keep hangin' on, we need you. Thank you.

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +20

      Hey, thank you :) And congrats on getting those running shoes on - I’m eagerly awaiting the day I can do the same thing.

    • @christinechin1909
      @christinechin1909 3 ปีที่แล้ว

      💯 % agree 👍

    • @detectivewiggles
      @detectivewiggles 3 ปีที่แล้ว +2

      To eliminate brain fog, make sure you're not taking synthetic D.

    • @lacisz
      @lacisz 3 ปีที่แล้ว +3

      @Will Gmail Hey Will. Thanks for your question. It was a long journey, I was constantly monitoring my symptoms, stopped running and other sports, gained a few kilograms :) Physically I'm 100%, but the brain fog still persists. Strangely it's worse when I'm passive. I'm about 65-70% of my old self. A few more years to go :) How about you?

    • @PATHAN_writes19
      @PATHAN_writes19 2 ปีที่แล้ว

      @@lacisz How are you now ?? Hope you feel better and get your normal life back ???

  • @sinnombre-wy5fv
    @sinnombre-wy5fv ปีที่แล้ว +14

    Thank you for this video. I am at the end of my rope here with 2 yrs of long covid and vids like these keep me going.

  • @janealbinson7190
    @janealbinson7190 2 ปีที่แล้ว +16

    I have had ME/CFS for 14 years. I’m aware of the similarity between Long Covid and ME and when I heard Dr Peers talking about MCAS the symptoms were almost exactly those I suffer from. Thank you for your work and for this very useful video. I’ll be following the recommendations and reporting back.

    • @kenziemackmusic
      @kenziemackmusic 2 ปีที่แล้ว

      common conditions miss diagnosed MCAS x

    • @ebaldwin-charles9804
      @ebaldwin-charles9804 2 ปีที่แล้ว

      Hi @janealbinson7190 any update? Thanks so much

    • @charlieb9144
      @charlieb9144 ปีที่แล้ว +1

      Hi @Jane Albinson - did you follow this and has any worked? I've been diagnosed with ME since 2012 but had it years before. Has anything worked for you? I'm so fed up of the fatigue. I'm currently trying nega dosing B1 (Elliot overton yt and Dr Eric Berg.) To see if that's a piece of the puzzle. Hope you're doing ok

    • @celestine.love88
      @celestine.love88 ปีที่แล้ว

      ​@@charlieb9144hi, is B1 works for you?

  • @krg9942
    @krg9942 2 ปีที่แล้ว +19

    I followed this regime and I feel so much better! THANK YOU!
    After my first night time Benadryl, I felt 75% better. After a week, I feel 90% better with my energy!
    Before, I was so exhausted, I went from the bed to the couch for over 2 years.
    Gez, you and your research saved my life!
    Forever grateful,
    Kim.
    Update 9/16/22:
    After learning that benadryl is super bad for your brain, I switched to Allegra, unfortunately it only helps about 60%. At this point anything is still appreciated, but I went back to bed / couch, unless I need to struggle along in a task.
    I have added in Nasalcrom nose spray & Alaway eye drops, as they are mast cell stabilizers.
    Desperately trying to get back into life.

    • @renovatingspaces7067
      @renovatingspaces7067 2 ปีที่แล้ว

      I take 1 chewable children benadryl and seems to enough! Sometimes 2.

    • @RunningWithSauce
      @RunningWithSauce 2 ปีที่แล้ว +3

      Hey KRG, I'm a systemic mastocytosis patient. We have this same problem for years. What is prescribed is TWO antihistamines for us. Whats called an H1 and an H2. It takes time to figure out the right combination for you. I'm currently taking Famotindine 20mg every 12 hours and Xyzal 5mg every 12 hours as needed. NSAIDS are triggers for many of us, so I stay away from them, but many also take a baby aspirin with this combination. Hope that helps. Benadryl is reserved as a "rescue med" only for a really bad flare up or before any invasive procedures like surgery.
      I hope that helps

    • @pattijesinoski1958
      @pattijesinoski1958 2 ปีที่แล้ว

      Sadly, long term use of benadryl can cause long term constipation.

    • @pattijesinoski1958
      @pattijesinoski1958 2 ปีที่แล้ว

      Taking allerga above suggested dosage by manufacturer can cause tachycardia, sleep deprevation, and heart palpitations. I had patients using toxic dosages.

    • @RunningWithSauce
      @RunningWithSauce 2 ปีที่แล้ว +1

      @@pattijesinoski1958 i take up to 12 times the recommended dose of antihistamines. This is my prescription from doctors because I have a very rare incurable disease called systemic mastocytosis. It causes the same cytokine storms that covid has only I get them constantly. I have zero issues. I get blood work every 3 months plus a dexa and PET scan to be sure. Zyrtec or Xyzal plus Pepcid up to 4 times a day. No side effects at all.

  • @scsu11iv
    @scsu11iv 3 ปีที่แล้ว +55

    Gez - this entire series is totally amazing and has helped me get back onto my feet after suffering for over 6 months with long-COVID, including getting blown-off by several doctors. Can I send you some money or something? I mean - this work is absolutely fantastic! Please keep up the great work - you are truly serving humanity and you work is greatly appreciated!

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +42

      No need to send money, just get better - that’s all I want for all of us!

    • @celestine.love88
      @celestine.love88 2 ปีที่แล้ว +1

      how is your progress now?

    • @GlamandFabQueenTV
      @GlamandFabQueenTV 2 ปีที่แล้ว +2

      Pls share what you did.
      What supplements you took?
      How much mg a day?
      What food to avoid etc
      Thanks

    • @scsu11iv
      @scsu11iv 2 ปีที่แล้ว +2

      @@GlamandFabQueenTV I did the vitamin stack for NAD+ deficiency. It's in one of Gez's videos. For me, the nicotinic acid was the key. I've actually been increasing the dosage of that lately, as it truly helps with my fatigue after physical activity.

    • @marisademore468
      @marisademore468 2 ปีที่แล้ว +2

      @@scsu11iv What is the name of the video please?

  • @a.g.9919
    @a.g.9919 4 ปีที่แล้ว +21

    @RUN-DMC I had post viral fatigue or ME in the early 90's for 2 years full time, and then relapses, pre internet and i had everything - from shortness of breath to brain fog, diarrhoea, insomnia and crippling exhaustion.Yes and very poor tolerance to exercise. Any exercise would set me back for weeks apart from very gentle walking if i had the energy. Big meals would also set me back for weeks, i would ache all over for days after a big meal. When i finally found a book in a library explaining about post viral, chronic fatigue, i cried with relief just to know I was not alone, but trying to convince a doctor was something else entirely. Also everyone around me thought i was making it up because i always looked so well.
    I tried exclusion diets, and very strict regimes and whilst they helped the game changer for me was total fasting and acceptance. People talk of acceptance but somehow that really does allow the body to heal.It's like you have to tell your own body ' I know i am ill and very tired, and i accept that, I give in, I will not fight against it, and i will be better in the future' And fasting helps very quickly, well it did for me. One supplement really helped me too, and that was Q10. I would even say that with a very good diet that was the only one i needed. But certainly I did try all sorts of vitamins and supplements. I did not find anti - histamine foods the culprit. Avocado, tomato etc, these things are fine. And white rice was very healing for me. Heavy oils and raw onion was bad for me. But the main thing was to have very little food. To fast. And when eating to eat very slowly and to learn to stop before being full, and then eat more if needed after it was properly digested. And if i felt a bad bout of exhaustion etc coming on - to fully fast. I know its boring but so better than being unwell. I highly recommend when you can (when we are allowed) going to thailand and doing a 7 day fast and having some colonics. I swear this will really help you heal. It's a miracle (well it was for me) Another thing very good for ME or Post Viral - is cold showers and a sauna followed by cold water plunge pool - i think it has been proven to regenerate the immune system (also was good for me)

    • @kevinagee5085
      @kevinagee5085 3 ปีที่แล้ว +1

      has the viral fatigue went away since then?

    • @janne2744
      @janne2744 2 หลายเดือนก่อน

      Cold showers😱

    • @Texasgirlinacrazyworld
      @Texasgirlinacrazyworld หลายเดือนก่อน

      Cold plunge actually puts the body into Fight or Flight lol

  • @latestlindsey5620
    @latestlindsey5620 4 ปีที่แล้ว +57

    My doctor told me that quote "my husband and I do not look like people who have mast cell syndrome" and he does nothing for us, thank God for your videos! Since I started treated us, my rashes went away, the chronic fatigue went away, and my flair-ups are a lot less! I really am grateful your sharing this and I've been telling everyone I meet with long covid to look into mast cell syndrome.

    • @latestlindsey5620
      @latestlindsey5620 4 ปีที่แล้ว +13

      @Elizabeth Fondse it was sort of a weird white peeling rash all over my arm. I ended up using milkweed from a plant and it took it away, but I heard it can have a reverse effect for different people. I basically followed her advice, low histamine diet, Quercetin, zinc, vitamin B and vitamin C and I'm on a 0 histamine probiotic and I'm finally healing. 😊 I also did a 2 week cleanse and it worked wonders. For the first time in 13 months, I can drink coffee again!

    • @sonofherne
      @sonofherne 3 ปีที่แล้ว +9

      I don't have LC but my health was ruined by a terrible virus 18 years ago. Very similar symptoms. One single dr decided to try giving me H1 and H2 blockers for Mast Cell. Since then, my fatigue has lifted enough to give me a far greater quality of life. Not perfect but I don't need to sleep every afternoon anymore. My brain fog is less, my skin rashes are gone.

    • @NoesKicker
      @NoesKicker 3 ปีที่แล้ว +2

      @@latestlindsey5620 YOOOO Congrats! I still drink coffee even though I can tell its a trigger for me. I really need to stop or at least get my health back in order first lol

    • @latestlindsey5620
      @latestlindsey5620 3 ปีที่แล้ว +1

      @@NoesKicker thanks so much! I know it sucks but now I'm back to 5 cups a day lmao, you'll get there 😂😂

    • @joeorler4097
      @joeorler4097 3 ปีที่แล้ว +3

      Get a new Dr

  • @meirwilenkin9218
    @meirwilenkin9218 4 ปีที่แล้ว +66

    You’ve been so incredibly helpful to many of us suffering from this. Thank you thank you thank you

  • @tinker3962
    @tinker3962 4 ปีที่แล้ว +100

    Brilliant analysis. Finally a coherent post infection strategy.Thank you so much for sharing this

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +5

      Pleasure Tristin!

    • @sleepsmartsmashstress740
      @sleepsmartsmashstress740 4 ปีที่แล้ว +1

      There is no single perfect post infection strategy Humans are a not homogenous cluster so there are subgroups and outliars . Even if an approach works for most it may not work for a quarter to half of the population. Tailoring is required. Rules of thumb to not work on all ten digits as only two of them are thumbs

    • @tinker3962
      @tinker3962 4 ปีที่แล้ว +3

      @@sleepsmartsmashstress740 You are your own laboratory. At birth no one came with an owner's manual. However, we do learn through the shared experiences with each other. In undertaking a healing journey, a great deal of therapeutic insight can be gained through the personal testimonies of others that have sorted out things that worked for them.I value greatly the efforts of others in bringing health to those around them.

  • @Asdfghjklzxcvb-u5p
    @Asdfghjklzxcvb-u5p 9 หลายเดือนก่อน +15

    I do not understand why all doctors 4 years into this are not on the same page? I wish I had seen this video two years ago.

    • @tacocat8608
      @tacocat8608 8 หลายเดือนก่อน

      Right? I’ve been saying the same thing!

    • @stevenjames5419
      @stevenjames5419 5 หลายเดือนก่อน

      Because doctors have been threatened and if they say the wrong thing they can lose their license

    • @MegaLeoben
      @MegaLeoben 2 หลายเดือนก่อน

      Doctors arent scientists... duh. they follow procedure.

  • @oldArmyVet
    @oldArmyVet 2 ปีที่แล้ว +68

    I had long covid, I used copious amounts of vitamin c, pineapple juice, lemon, honey, cinnamon, plus everyday I made a tumeric, milk,and black pepper drink in the morning. I pushed myself everyday, walk until I couldn't walk anymore, rest repeat. I'm now in better shape than I was before I got long covid.

    • @naturespleasantries
      @naturespleasantries ปีที่แล้ว

      What we’re your symptoms

    • @oldArmyVet
      @oldArmyVet ปีที่แล้ว +3

      Shortness of breath, fatigue, weak, loss of smell, taste, joint pain, brain fog wich I still have that symptom and still have some smell deficit.

    • @downtoearth1982
      @downtoearth1982 ปีที่แล้ว

      Hi how are you doing nowadays and did you keep yourself on any antihistamines.H1 and H2 blockers

    • @oldArmyVet
      @oldArmyVet ปีที่แล้ว

      @@downtoearth1982 doing pretty good, still get winded randomly. No , I just kept the same regiment as above

    • @nancymccall5209
      @nancymccall5209 9 หลายเดือนก่อน

      @@oldArmyVet 3:59

  • @brittanymlanders
    @brittanymlanders 5 หลายเดือนก่อน +3

    This was so validating to hear… everything I’ve been experiencing was stayed so eloquently & simply. Makes me feel relief that I am not “crazy” or whatever.

  • @teresa4957
    @teresa4957 3 ปีที่แล้ว +45

    I'm so tired of feeling terrible. So grateful to hear what some of the triggers are for long covid as well as what vitamins can address my symptoms. It's exhausting to not feel good all the time. Thanks for your information and expertise.

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +4

      That’s ok - I know how you feel Teresa. Best of luck with your recovery.

    • @KathleenHanrahan-p1u
      @KathleenHanrahan-p1u 9 หลายเดือนก่อน

      I’m the same 4 years no one can understand how bad it is 🙏

  • @LauraPazzaglia
    @LauraPazzaglia 2 ปีที่แล้ว +48

    This video was EXTREMELY helpful! My post-exercise long-covid symptoms were worsening (fatigue, muscle aches, weakness febrile pains) week after week and I couldn't figure out why. This video made it clear. I was reducing my hi-dose Vitamin C that I had been taking during COVID, and fresh tomatoes just came into season and I was gorging on those every day, twice a day - the absolute opposite of what is recommended here (and I was feeling it!). Going to re-up my Vitamin C, double my Vitamin B dosage (I have MTHFR gene mutation) and add Quercetin. I am already taking the other supplements but right after watching this video I also ran out to my terrace, stripped down, and got 15 mins of sun top and then bottom to increase Vitamin D production. I am so relieved to have found the reason I was getting worse and look forward to improving!!!! I was really scared. THANK YOU!!! Ciao from Italy, L

    • @Aaaaaalex09
      @Aaaaaalex09 ปีที่แล้ว +3

      How are you tiday Laura 9 months later??

  • @MR-hr6pp
    @MR-hr6pp 9 หลายเดือนก่อน +9

    I successfully improved my post COVID immune response with a water fast. On the second day migraines occurred which disappeared after drinking a small glass of distilled water as mast cells burst consequently. At least in my case the symptoms improved tremendously after water fasting for three days and it had a sustainable effect. I know there are so many different remedies being praised on the internet what makes people sigh and resign, but this is what helped me speeding up the recovery process. I was struck by the coronavirus two times in 2023 and still struggle with the consequences. Maybe this is helpful to at least someone, so I just wanted to share this.

    • @tacocat8608
      @tacocat8608 8 หลายเดือนก่อน

      Can you tell me exactly how to conduct a successful three day water fast? I was literally thinking this is something I need to try, just earlier today. 🙏🏼

    • @MR-hr6pp
      @MR-hr6pp 8 หลายเดือนก่อน

      @@tacocat8608 Don’t eat but drink water instead. My body told me with intense feelings of hunger when to quit. When I felt weak I did push ups because this stabilized my cardiovascular system. You need to drink plenty of water. I drank about 4-5 liters per day. A pinch of salt without additives a few times per day did also help me stabilize. It also helped me with headaches. When they got heavy on day two and three I had a small glass of distilled water to ease the pain. The distilled water destroys mast cells in your blood which build histamine what is responsible for your headaches during the fast. But be careful with the amount you take because distilled water can be dangerous when consumed in large quantity.

  • @dedesunbeam9361
    @dedesunbeam9361 4 ปีที่แล้ว +18

    This video may well have changed my life. As soon as I saw it my partner and I started to follow the advice. We are both long-haulers (since March/April) and both have mild asthma, bad allergies, and he has rheumatoid arthritis. He developed covid toes/fingers which were diagnosed by our doctor as eczema and successfully treated with a topical cream.
    We are changing our diet and buying the supplements. I can't begin to tell you now important this video was for us. I think even if it's not a perfect cure, it will improve our health. Of all the media sources on L-H Covid, you are the single one who's helped us. Please keep posting - I look for a new video from you every day.

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +3

      Hi Dede, gosh I’m so pleased to hear it’s helped but do wait on improvement in symptoms before you offer me any credit! And if you subscribe you don’t have to look every day 😊
      Best of luck with your recovery.

  • @funghouls5498
    @funghouls5498 3 หลายเดือนก่อน +3

    For the past few months, I have been experiencing fatigue, lightheadedness, tinnitus, and lately, heart arrhythmias, and palpitations. It got to the point where after working out I felt like I was having a heart attack, but with no pain just extremely hard to breathe and very rapid heart rate so I rushed to the hospital twice, and they could find no problems with my heart . I was sent to a cardiologist for observation over the course of a month and they also could find no heart problems so I was dumbfounded until I found out about POTS/long Covid, histamine intolerance.
    This is what I needed today. Thank you so much for doing your research. I realize this is from three years ago, but it is relevant to me today as I got Covid in December 2023 and I have all the symptoms of MCAS, histamine intolerance, Long Covid. Incidentally, Dr. Sanjay Gupta Has videos on this as well and he’s using a saline IV solution to help clear out histamines in people with POTS.

    • @RUNDMC1
      @RUNDMC1  3 หลายเดือนก่อน +1

      I’m assuming you’ve been told this already, but lay off the working out for a bit!

    • @funghouls5498
      @funghouls5498 3 หลายเดือนก่อน +1

      @@RUNDMC1 yes. Thank you.

  • @mariarooney6262
    @mariarooney6262 2 ปีที่แล้ว +8

    Unbelievable. I never heard of long COVID. I just went to the doctor today and he said I have it, with all the symptoms I have. This video is excellent. Thank you. I already do the diet and vitamins but I eat alot of Avacados and bananas so I will stop them and do the rest of the protocol. The best health to all who have this and hoping you will be well sooner than you think. ❤️

  • @novaaahd4834
    @novaaahd4834 3 ปีที่แล้ว +39

    I had covid in October with few symptoms and was nothing more than a bad cold, then I got worse with headaches, heart palpatation, body twitches, chest pain, fatigue ,anxiety and depression.I had a severe headache for 3 months after which led to me having a brain MRI but everything was normal, it does get better, im 5 months down the line and am a lot better but still got a bit more to go👍🏻

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +6

      Glad to hear you’re recovering!

    • @aminagundes6234
      @aminagundes6234 3 ปีที่แล้ว +5

      Happy to hear that you are recovering

    • @caelyndisanti5595
      @caelyndisanti5595 2 ปีที่แล้ว +5

      Did you follow a low histamine diet or what did you do that helped you get better? I am suffering with daily headaches everyday for going on 3 months now and am thinking of starting a LH diet.

    • @lukesmith3283
      @lukesmith3283 2 ปีที่แล้ว +4

      Hi Novaaa how are you doing?

    • @jadedavis6961
      @jadedavis6961 2 ปีที่แล้ว +8

      I know exactly how your feeling I’ve been going through the same exact symptoms including internal tremors. My headaches have improved and I no longer have palpitations. We will get through this!

  • @santoshingle3989
    @santoshingle3989 4 ปีที่แล้ว +20

    This guy deserve noble prize, what a useful information

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +1

      Haha, thank you Santosh!

    • @2000disneyland
      @2000disneyland 2 ปีที่แล้ว

      I agree! I was close to giving up until I found this channel. His research & information have given me hope.

  • @ysbyttybedbug
    @ysbyttybedbug 4 ปีที่แล้ว +18

    In some ways, this is good news in that it may provide a way forward, but I have to say, my heart sank when that list of supplements/over the counter meds came up. The problem is, many, if not most, people with a chronic illness end up on low incomes. All those supplements & antihistamines are therefore not an affordable option.

    • @shiningoutlight
      @shiningoutlight 4 ปีที่แล้ว +1

      I am low income and I prioritize. Many of these supplements are cheap.

    • @alicequayle4625
      @alicequayle4625 4 ปีที่แล้ว +2

      They should really be available on prescription.

    • @carolenmarch-williams7417
      @carolenmarch-williams7417 4 ปีที่แล้ว +1

      Piping Rock are an online company in US who do the cheapest best quality for your money. I use to use other more expensive UK based companies until l discovered this . Look at their prices, cheaper than others.

    • @heide-raquelfuss5580
      @heide-raquelfuss5580 4 ปีที่แล้ว +2

      @@alicequayle4625 most doctors would not be willing to prescribe them. Because insurance would make it more difficult to get them in the first place.
      Doctors would only prescribe them if you have tested you need them. And there you probably will fail too. Because their tests are also ecpensive. So the doctor would not test you. Because again the insurance does not want to pay it. The medical system together with insurance companies and pharma and share holders and investesters are complicated issues. People do not understand this topics yet.

    • @qingdaogrrl
      @qingdaogrrl 3 หลายเดือนก่อน

      first treat anxiety/depression / calming vagus nerve and limbic system. the other stuff is just fluff. if all i could get was RX meds - then singulair or xolair and ativan or klonopin would be my go to. LDN and ketotifen (and or cromonlyn) are nice to haves. luteolin and anti histamines (try to get them RX so insurance pays instead of otc out of pocket) - but doing anything you can to calm your nervous system / mental health is the most effective part of all of this. and it's not for forever. once it clicks, your body takes over and heals. it doesn't get rid of igE allergies, but most of the sensitivities caused by stress = gone. (in my experience)

  • @omarbradford6130
    @omarbradford6130 4 ปีที่แล้ว +32

    Thank you so much Tina and RUNDMC. I've been experiencing long covid symptoms for around 7 months and this series as well as this video in particular has given me a lot of hope.

    • @edayenii
      @edayenii 4 ปีที่แล้ว +1

      Did you follow their suggestions? How are you feeling?

    • @Ma1efcent
      @Ma1efcent 3 ปีที่แล้ว +1

      How are you doing Omar?

    • @frantapolak
      @frantapolak 3 ปีที่แล้ว

      Yes, how are you doing? :)

    • @fearless6947
      @fearless6947 2 ปีที่แล้ว

      hello?

  • @evanmaxwell4649
    @evanmaxwell4649 4 ปีที่แล้ว +15

    Thank you so much for posting this!!! I’ve had debilitating long hauler covid for almost six months! The brain fog is INSANE!!

    • @drew2fast489
      @drew2fast489 4 ปีที่แล้ว

      I'm sorry, man. I know that has to be tough.

    • @merrick51
      @merrick51 3 ปีที่แล้ว +1

      Yeah it’s completely paralyzing

    • @LordVeroeven
      @LordVeroeven 3 ปีที่แล้ว +1

      What’s up Evan - So I just recently nearly passed from Covid Delta 2 SARS 2, or whatever they want to call it.
      Anyways, I am now in recovery phase, but some things I’m dealing with are Confusion, Irritability, Anger, getting worked up easily and my hands / head / body will start sort of shaking, maybe like nervousness, etc.
      How long did the fog last?
      I call it Covid Confusion / Feeling Lethargic..
      I’ve never been sick before, so this has all been a culture shock for me..
      Thanks, Brother

    • @PATHAN_writes19
      @PATHAN_writes19 2 ปีที่แล้ว

      @@LordVeroeven how are you now ?? Did you recover fully and get your normal life back ?

    • @PATHAN_writes19
      @PATHAN_writes19 2 ปีที่แล้ว

      Did you feel any improvement ?

  • @carolenmarch-williams7417
    @carolenmarch-williams7417 4 ปีที่แล้ว +21

    Very interesting. Yet another excellently produced educative film on Long Covid, sighting MCAS as the probable major underlying culprit , with very accessible advice on how to manage it via diet and supplements. Hopefully, this advice will be a major breakthrough for many. Thank you so much for doing the research to elucidate this for Long Haulers but also for those of us that have EDS

  • @kaylabryson1932
    @kaylabryson1932 3 ปีที่แล้ว +20

    My son is a year long Covid sufferer. He’s on a strict low histamine diet and doing supplements. He is still struggling …. He’s found the answers trial and error after his MD just brushed him off as anxiety problem.

    • @ezzovonachalm9815
      @ezzovonachalm9815 ปีที่แล้ว +3

      kaylabrison
      anxiety is the normal reaction to the postcov syndrome and its bunch of symptoms. A medic who diagnoses PCS as a manifestation of anxiety should be obliged to restitue his medical diplome and go back to the medical faculty to renew his / her medical diplome.

  • @jondavies1593
    @jondavies1593 4 ปีที่แล้ว +16

    Literally have nearly all these symptoms. GP is absolutely adamant theres nothing wrong!

    • @jzinser-mandala9117
      @jzinser-mandala9117 4 ปีที่แล้ว +11

      My doctor is less than helpful. Decided I had sleep apnea though I have no symptoms for that. I had COVID before the recognition and so, no positive test months later. Testing was rare for some time anyway. Without a positive test, but most of the symptoms, I am treated like a hypochondriac. That attitude certainly doesn’t help my determination to recover.

    • @jondavies1593
      @jondavies1593 4 ปีที่แล้ว +11

      @@jzinser-mandala9117 I've had blood tests, ecgs and chest xrays, all have come back absolutely clear yet I'm still getting bad headaches, keep going light headed, stomach ache , ribs ache and chest aches and get short or breath easily, along with being constantly tired. GP says theres too many symptoms to diagnose me with anything!

    • @christiangranqvist2350
      @christiangranqvist2350 4 ปีที่แล้ว +6

      Jon Davies Seems like the doctors are leaving the battlefield on walkover. I guess some other professions will have to take up the slack. A lot of money in this if one would have a protocol for recovery.

    • @melanieberlier8487
      @melanieberlier8487 4 ปีที่แล้ว +2

      I went undiagnosed until my late forties. There are some wonderful supportive groups on Facebook and www.TMS.org (the mastocytosis society) is a wealth of information and lists of doctors who work with us mast cell patients. This is how I finally got help that put me into remission. I still have flares and need to take extra care but I’ve been able to have a mostly normal life.

    • @jamiedorn4105
      @jamiedorn4105 4 ปีที่แล้ว +3

      @@jondavies1593 I too have had rib aches/ chest aches along with shortness of breath etc. My pulminologist diagnosed the rib and sternum pain as costochondritus. It can be triggered by respiratory viruses or harsh coughing. If you look it up on you tube there are stretches that if done consistently should help along with anti- inflammatory supplements like turmeric.

  • @cliffolson3229
    @cliffolson3229 4 ปีที่แล้ว +9

    The symptoms you explain are so similar to the ones I have had for the last 10 years after recovering from alcohol induced pancreatitis,it's unreal.The fatigue,itching,brain fog,stomach,rapid pulse,.....I was diagnosed with Fibromyalgia but have always thought it much more to it than that.Thank you so much for this video.

    • @Tinyteacher1111
      @Tinyteacher1111 2 ปีที่แล้ว

      Dr. Frid in NY claims that fibromyalgia is actually a symptom of something larger. I believe her. I have it, and I didn’t get it until I got breast implants, which are so toxic inside the body, I got sicker and sicker with autoimmune diseases, mold toxicity (saline), and infections. I lost so much, I’ll never recover my family, friends, relationships, money, etc. 🥲

    • @charlieb9144
      @charlieb9144 ปีที่แล้ว

      Hi, hope you're well now. Alcohol really depletes B1 thiamine - which causes fibro symptoms. If you still need help check out Elliot overton on TH-cam he talks all about high doses of B1 also Dr Eric Berg has a few good videos on it. Wish you well

  • @tonymack66
    @tonymack66 4 ปีที่แล้ว +69

    Maybe it was coincidental, but I started to feel consistently better after starting to eat more fresh fruit on a daily basis; I had been unwell with long Covid symptoms for 4 months up until that point.
    All in all it took me six months to get my fitness levels back up to where I was prior to being unwell, that is, from the end of March to the end of September this year.
    I wish all long Covid sufferers an eventual recovery and soon !!!! Peace.

    • @petinapowers2869
      @petinapowers2869 4 ปีที่แล้ว +4

      I am happy for you. Seriously. I had a timeline for building my health back. But, it is not working. I have tried several paths. Right now, it seems, I have to focus on my physical activity level or my cognitive activity level. I am going with the cognitive level for now. However, over winter break I am going to experiment more with my physical activity level.

    • @tonymack66
      @tonymack66 4 ปีที่แล้ว +10

      @@petinapowers2869 I roadwalk every day up to 10 miles a day and this I could not do anywhere near a few months ago when I was unwell; even mild exertion would set me back almost a week every time.
      So, with regards to physical activity I say take it easy and don't push yourself too hard. Good luck.

    • @lacisz
      @lacisz 4 ปีที่แล้ว +8

      It's good to hear, that you are better. For me, It was almost 8 months to get back to running (5km, daily). But the "brain fog" is not lifted. I still feel if I'm away from my life. I just wonder, will it go away?

    • @petinapowers2869
      @petinapowers2869 4 ปีที่แล้ว +8

      @@tonymack66 It is a lovely day in north Texas. I just finished a short walk. One block. That is all I can manage. Thank you for giving me hope.

    • @petinapowers2869
      @petinapowers2869 4 ปีที่แล้ว +5

      @@lacisz Lacisz. I am the opposite. My brain fog is less frequent. I can mentally multi-task at times. I am still disorganized though. That is not normal for me. My physical activity is the primary issue. So, perhaps one area recovers first, and the other later? Also, congratulations on your physical recovery!

  • @miguelnunez2623
    @miguelnunez2623 2 ปีที่แล้ว +6

    Had mild covid in January then in February I got pots symptoms and shortness of breath . And couldn't exercise . I would get short of breath and weird anxiety after trying to exercise even lightly. Fast foward to this may and I decided to take benadryl cause I got shortness of breath after eating food. Took it cause I heard it was good for anxiety and it helped me breathe ALOT better . She's definitely spot on. This is a mast cell issue

    • @felipejotz7054
      @felipejotz7054 2 ปีที่แล้ว

      How are you doing today, Miguel?

  • @michellemoore7053
    @michellemoore7053 4 ปีที่แล้ว +18

    This was really helpful! Thank you. I was fortunate to stumble on MCAS as a possibility in late April and strictly followed a low histamine diet (and vitamin/antihistamine routine) for 6 months. As a former tea addict I feel for you :). I went 6 months without a cup of tea, but have finally reintroduced 1 cup a day in November (major victory.) Good luck!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +1

      Thank you Michelle!

    • @ApprendreSansEcole
      @ApprendreSansEcole 4 ปีที่แล้ว +1

      Do you feel completely recovered ?

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +1

      Apprendre Sans Ecole No, I’m a long way from that!

    • @michellemoore7053
      @michellemoore7053 4 ปีที่แล้ว +5

      @@ApprendreSansEcole I am really close. Just very minor things left.

    • @sharonproctor4079
      @sharonproctor4079 4 ปีที่แล้ว

      Why no tea?

  • @joannarichards6245
    @joannarichards6245 ปีที่แล้ว +1

    This was so so helpful. My symptoms had improved until I stopped taking the vitamins and I feel like I’m back to stage one and I couldn’t remember the regimen. Thanks so much for doing all the work you have compiling this resource, I always trust what is here amongst all the endless information. X

  • @Anamaria-ew8lh
    @Anamaria-ew8lh 4 ปีที่แล้ว +17

    Thank you again for the most important research for us, the long haulers! Hope we get better, soon!

    • @jaisarmiento1188
      @jaisarmiento1188 4 ปีที่แล้ว

      What are you issues?

    • @Anamaria-ew8lh
      @Anamaria-ew8lh 4 ปีที่แล้ว +1

      @@jaisarmiento1188 At 8 months after Covid, I still have troubles with fatigue, chest tighteness and, sometimes, digestive issues.

  • @AndyConwaySinger
    @AndyConwaySinger 2 ปีที่แล้ว +15

    I've had literally every symptom on this list. Some have gone away, some have went and come back. So shortness of breath and fatigue, gastric issues have been the ones that are lingering the last 2 years. I'm taking PPIS for GERD (Post Covid) and antihistamine. I'm also trying a low histamine diet. Sick of it. Agony. Also I'm 35 and was very fit before covid.

    • @RUNDMC1
      @RUNDMC1  2 ปีที่แล้ว +4

      Know how you feel Andy!

    • @christopherm6725
      @christopherm6725 2 ปีที่แล้ว +2

      Yep same Andy! I was healthy before except for some anxiety issues. Fatigue is brutal. Heavy eyes, muscle issues. It’s awful. Praying for healing for u

  • @ryancparker
    @ryancparker 3 ปีที่แล้ว +17

    I was suffering from long Covid. Going on a low histamine diet with vitamin D, C and Zinc supplements worked wonders for me. I felt better every single day until after a week all my symptoms were completely gone. Thank you!

    • @samanthar5123
      @samanthar5123 3 ปีที่แล้ว

      What were your symptoms

    • @ryancparker
      @ryancparker 3 ปีที่แล้ว +3

      @@samanthar5123 chest pain, numbness in my left arm, tightness in my shoulder, nausea, diarrhea, and just generally feeling like hot garbage every day

    • @andrewjones3826
      @andrewjones3826 3 ปีที่แล้ว

      Did you eat any meat?

    • @ryancparker
      @ryancparker 3 ปีที่แล้ว +2

      @@andrewjones3826 my primary meal every day has consisted of eggs and broccoli cooked in olive oil with an orange on the side. I’ve started eating some chicken breast and apples as well. I’ve been experimenting with other foods to mixed results. Peanut butter and tomato soup are off limits, but pizza surprisingly seemed okay.
      Alcohol is off limits. One of my worst nights during long covid was when I got home after drinking five beers. At the time I had no idea why I felt so horrible.
      Before I went on a strict antihistamine diet I was eating a banana every morning along with tomatoes, avocados, spinach, whole wheat, and sliced chicken breast unaware that they were high in histamine or that histamine could affect my body the way it did.
      Something else to note is that I had an allergic reaction to the J&J vaccine as well. The side effects were very similar to what I experienced from long covid and lasted about five months.

    • @andrewjones3826
      @andrewjones3826 3 ปีที่แล้ว +4

      @@ryancparker glad for you. I'm only 4 weeks in but I know I'm not shifting it.
      Been on low Hist diet for 3 days and the vit stack. Feeling better I think but still have moment I feel like death for an hour.
      I too was pounding down the spinach and avos, plus bread.
      Hopefully in time I'll feel normal

  • @JamieGerig
    @JamieGerig 2 ปีที่แล้ว +3

    i have been researching my nightmare symptoms for 8 months now... and in 5 minutes this video has nailed it... thank you so much!

    • @celestine.love88
      @celestine.love88 2 ปีที่แล้ว

      how is your progress now?

    • @LongCOVIDAdvocator
      @LongCOVIDAdvocator 2 ปีที่แล้ว +1

      I know for a fact I have long COVID. I've had repeated wet dreams and nightmares every night. I've never had it before in my life. Covid really did me dirty.

    • @19grand
      @19grand 2 ปีที่แล้ว

      How you doing now?

  • @drclareharley
    @drclareharley 4 ปีที่แล้ว +11

    We have two 9 month long haulers in the family, this is incredibly helpful and high quality info, thank you so much!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +2

      That’s alright! Got some very good data on the efficacy of the treatment too to show in my next film

    • @TheBushRanger.
      @TheBushRanger. 2 ปีที่แล้ว

      How are they now Clare?

  • @wematter4870
    @wematter4870 2 ปีที่แล้ว +2

    I became better by cutting wheat , coffee , spinach , I take multivitamins with minerals , vit D , zinc
    Spring is my favourite season
    The worst symptoms were anxiety , palpitations, mood swings , tinnitus , arthritis, GI problems .
    When I am under its spell , I fast , then I feel much better .
    I had long covid , same symptoms but more debilitating .
    I think now I had these symptoms all my life , and managed them by fasting , or cutting food I felt affected me badly , supplements.
    Thank you for this eye opening video

  • @InnerLantern7
    @InnerLantern7 4 ปีที่แล้ว +3

    I'm an MCAS/Ehlers-Danlos patient. My MCAS is FORTUNATELY well managed now, but it took a long time and lots of suffering to get the treatment right. Thank you to my great immunologist, biweekly Dupixent injections, quercetin, vitamins C&D, H1 & H2 blockers, famotidine, and taking precautions before eating/drinking that might trigger my mast cells.

  • @jdragyn720
    @jdragyn720 4 ปีที่แล้ว +7

    WOW. I am the person with the MCAS before the COVID. I got COVID in March, was super sick, got a bit better, then worse again. Repeat x 2. Started finally feeling better, until 2-3 weeks ago, started low grade fever with worsening of cough. Cannot express how fatigued I am. I have Fibro, MCAS, Eh-Los Danlos, Hashimoto's etc... Yeah, having the MCAS helped, because I was already on meds. Harder, because all my symptoms were to the Nth degree. I identified with everything she said- totally hit the spot. Would like to add Mangosteen power is a Mast cell stabilizer, and so is marijuana. I use both daily. I am getting better, just the 2 step forward, 1 back is, well, adding to fatigue. It will get better. Slow and sure. Just wanted to let you know I hear you- and I needed to hear you.
    thank you all- JAFO

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว

      Great to hear that JAFO :)

    • @2000disneyland
      @2000disneyland 2 ปีที่แล้ว +1

      Thank you for your post, including the marijuana bit. I have access to it, but didn’t know if it would help. I’m willing to try, along with the other protocols. I’ve been to the point of giving up, but this channel has given me hope.

  • @merrynhopkins1162
    @merrynhopkins1162 ปีที่แล้ว +4

    Thank you Gez
    I’m a long hauler in Australia - treating myself watching and reading as much as I can
    You both have given me hope
    There’s absolutely no long covid understanding or MCAS here even at the clinics - the UK and northern hemisphere countries are so far ahead !!!
    Many thanks
    Merryn

    • @RUNDMC1
      @RUNDMC1  ปีที่แล้ว

      Best of luck to you Merryn!

    • @BrandonGreenShow
      @BrandonGreenShow ปีที่แล้ว

      be careful who you tell your symptoms to in Australia... These MTHFR' Doctors wouldnt know what a MTHFR was if it hit them in the head!
      th-cam.com/video/rFkVEBRfdys/w-d-xo.html - getting taken to Psyche ward
      th-cam.com/video/6DmBaPeGdio/w-d-xo.html - Dont go telling your crazy symptoms to just anybody

    • @briechilli4496
      @briechilli4496 ปีที่แล้ว

      How are you now ? I am in Australia too 😢

  • @jessicam807
    @jessicam807 4 ปีที่แล้ว +50

    Thanks for your hard work! I noticed a difference in some of my neuro symptoms following a low-histamine diet so I'm sticking to it. But I'm really worried about the virus lingering in our bodies, in my case this is month 8 and the cough came back. GP has no clue about it. I think it's pretty obvious at this point that we need massive research about viral persistence ASAP.

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +12

      Agreed.

    • @headfullofmusic422
      @headfullofmusic422 3 ปีที่แล้ว

      how are you doing now? are you feeling like your normal self again? and could you share some anti histamine recipes?

    • @jessicam807
      @jessicam807 3 ปีที่แล้ว +3

      @@headfullofmusic422 hello! I am feeling much better since I started taking Famotidine (h2 blocker), honestly I am a really lazy and bad cook, I just eat simple things like chicken and steak, potatoes, I can manage to include tomatoe a few times a week. That's pretty much it. Cereals or porridge for breakfast.
      I also stopped coffee and tea 100%, which was super hard but I feel the difference.
      I still have some symptoms but I reached a point where I am able to work/clean/have a pseudo normal life.

    • @teddybearroosevelt1847
      @teddybearroosevelt1847 3 ปีที่แล้ว

      @@jessicam807 So tomato is high histamine. You may wanna avoid it altogether if you wanna alleviate your symptoms

    • @ikyathay2998
      @ikyathay2998 3 ปีที่แล้ว

      I'm trying to follow it. But I'm already underweight. So I don't know where this will go

  • @jzinser-mandala9117
    @jzinser-mandala9117 4 ปีที่แล้ว +12

    Wow. This was really helpful.I have been eating some things I thought were really good for me, but are not. And, no tea for now. Your podcasts have been more helpful than many others..or even my doctor. Thank you!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +3

      It’s a pleasure.

  • @caroliner2029
    @caroliner2029 3 ปีที่แล้ว +9

    Thank you!
    Thank you!
    Thank you!
    I have a chronic mast cell activation syndrome from the first dose of AZ "vaccine" which I lined up for seven weeks ago.
    Brain fog, fatigue, lightheadedness, headache, eye pain, swelling and itchiness, nausea, neck stiffness and pain, and tingling in my face, tingling in my arms to fingers.

  • @amyjoon4687
    @amyjoon4687 3 ปีที่แล้ว +5

    Thank you for this ibfo!! Altho, if your MCAS has salicylate triggers, watch the quercetin. And im so grateful for this information. I've been watching long covid triggering mast cell issues and since covid, I'm now ragingly reactive to salicylates. And my quercetin was giving me raging nerve pain. You are an ANGEL!!!

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว

      I’m glad you’re getting on top of it Amy!

    • @tuulalarson2625
      @tuulalarson2625 ปีที่แล้ว

      I´m salicylate sensitive, plus I´m diagnosed with histamine intolerance by my allergy doctor. I have had covid for 8 months now and my main symptom right now is vertigo. I walk like a penguin. When my covid started, I had a huge histamine release with itchy rash on the inside of my arms and on my back. Recently, I bought the enzyme DAO, diamine oxidase (made of kidneys from pigs), and I noticed an improvement after only one day! After five days the itchy rash was gone! Then I tested what happened without DAO and the itchy rash came back. And then I started to take three pills DAO per day again and the itchy rash disappeared again. Now I´m trying to find cheaper replacements for DAO.

    • @hc6747
      @hc6747 5 หลายเดือนก่อน

      Hi, I know this was years ago, but what did you use instead of quercetin? Or did you just follow the rest of the protocol and leave out quercetin? I also suspect salicylate intolerance. Thank you!

  • @janicemaceachern1004
    @janicemaceachern1004 3 ปีที่แล้ว +5

    This makes so much sense to me. I always believed there were a few common denominators that were stirring up so much misery in my life.

  • @kaylacarpenter272
    @kaylacarpenter272 2 ปีที่แล้ว +7

    I have MCAS from black mold poisoning and Lyme. I was at the best I've been in years, then got Covid. Recovered great, but then MCAS came back with a vengeance. Suicide fuel. Haven't slept in days. Already had severe insomnia. Not even a bar if xan knocks me out after this Covid MCAS.

    • @marycolhenry
      @marycolhenry 11 หลายเดือนก่อน

      So how do you no mold caused the mcas and it wasn’t your nervous system.😊

  • @sputster
    @sputster 4 ปีที่แล้ว +9

    Finally, there is a light at the end of the tunnel! Been sick with covid since March 2020 and I showed this to my doctor!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +1

      Best of luck with your recovery!

    • @myopinonz
      @myopinonz 3 ปีที่แล้ว +1

      Yes, I had it as well since March, I get extreme fatigue, bit the main issue is I can't catch my breath, I feel chest crushing tightness as if I ran a marathon and I just got moving!!

    • @manindermanku8667
      @manindermanku8667 3 ปีที่แล้ว

      @@myopinonz how are you how is your breathing do you feel breathless when you walk around or when you even sitting down

    • @manindermanku8667
      @manindermanku8667 3 ปีที่แล้ว

      Sputster how are you feeling now I am also suffering from nearly four months

    • @sputster
      @sputster 3 ปีที่แล้ว

      @@manindermanku8667 I used to do cardio twice a week and weights three times a week. Today I feel far from how I used to be. I have days where I can run with no issues and other days where I can't even go up the stairs without being out of breath. I have started the intake of antihistamines to confirm what they say in the video. It might not work for everyone, but I am no doctor.

  • @EmuEmi
    @EmuEmi 2 ปีที่แล้ว +3

    Thank you so much for this video. 7 months in and am miserable. I’ve lost so much weight because of the mcas symptoms. Hoping to recover and get my life back

  • @marshapple
    @marshapple 4 ปีที่แล้ว +20

    I believe vitamins C and D, zinc, melatonin has help me a bit. However, it was after I received electrolytes via IV fluid, did my extreme fatigue became more manageable. The dizziness lingered for a bit but I never stopped taking my vitamins, melatonin, drink a lot of fluids, and eat more fruits. Now, I am alot better eventhough sometimes I still feel a little unwell. Thank you for the info.

    • @jeanettevalencia1975
      @jeanettevalencia1975 4 ปีที่แล้ว

      How long were you struggling with severe fatigue prior the IV fluid?

    • @marshapple
      @marshapple 4 ปีที่แล้ว +2

      @@jeanettevalencia1975 15days before the IV. I am still fatigue, though not at bad as when I was positive for covid. I wouldn't call it severe since I wasn't hospitalized

    • @shrutipandey2
      @shrutipandey2 3 ปีที่แล้ว

      Howr are you now

    • @marshapple
      @marshapple 3 ปีที่แล้ว +1

      @@shrutipandey2 i am doinf great. Thanks

    • @imsocheeky1220
      @imsocheeky1220 3 ปีที่แล้ว

      Hello are you doing better ?

  • @michelleg4895
    @michelleg4895 4 ปีที่แล้ว +10

    Nice one Gez. As always, articulate, succinct and full of information. Thanks!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +2

      Thanks Michelle!

  • @Whistlewalk
    @Whistlewalk 2 ปีที่แล้ว +2

    Thank you so much!! I've been feeling so abandoned. I'll be on this tomorrow for sure.

  • @kimberlysullivan2187
    @kimberlysullivan2187 4 ปีที่แล้ว +10

    My daughter is an elite athlete with long COVID symptoms. She can't get back to her normal workouts and is having all sorts of issues. She has been on niacin 2 weeks and is seeing a lot of improvement.

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +4

      Really good to hear that. She’s going to have to be careful about getting back to workouts though - even easy ones.

    • @rootsandvulture
      @rootsandvulture 3 ปีที่แล้ว

      Please could you tell me how.many mg of Niacin she took?

    • @kimberlysullivan2187
      @kimberlysullivan2187 3 ปีที่แล้ว

      @@rootsandvulture I don't recall the dose now. I think we found the information from this page though on what people were taking.

    • @AlejandroLopez-rs6qt
      @AlejandroLopez-rs6qt 2 ปีที่แล้ว

      @@RUNDMC1 wdym ?

    • @katherineb9815
      @katherineb9815 2 ปีที่แล้ว

      Niacinamide or niacin? How much? Can you recommend a brand?

  • @TALKCalgary
    @TALKCalgary 2 ปีที่แล้ว +2

    This has to be some of the most informative information I've come across throughout this entire pandemic. So refreshing to to know that there are still a few people capable of thinking outside of the box and not just regurgitating government propaganda.

  • @cindyritmeester
    @cindyritmeester 4 ปีที่แล้ว +6

    I am a Covid long-hauler and have flare-ups with pain in lungs, pain in joints, pain in spleen and occasional eye infection. A friend of mine who works in the medical sector says my symptoms and triggers of long Covid remind her of an auto-immune disease. I was perfectly healthy before Covid, working out etc. I am looking at natural medicine now for possible support

  • @visamedic
    @visamedic 5 หลายเดือนก่อน +1

    I got COVID during the Delta wave in 2021. I attribute me catching it to a lapse in the preventive protocol I had put myself on, combined with added stress and a lot of extra shifts. I was taking NAC, Vit D, Vit C, Niacin (every other day) and Turmeric. I ended up in the ICU for 10 days. When released I was on O2 for an additional 3-4 months. I was unable to return to work for 11 months. I’ve dealt with Long COVID since. The tachycardia and the extreme SOB has lessened. I pushed myself with higher elevations while I was out. I still have issues with any exertion. I still have issues with elevations over 7000’, and any exertion over 8000’ is very hard to recover from. I actually keep a few of those oxygen cans in my truck just in case. I’ve found that Turmeric and Glycine have helped. I am going to add back in NAC and vitamin D as well as the rest of my original protocol because I firmly believe something much bigger is coming.

  • @alisonreed4408
    @alisonreed4408 4 ปีที่แล้ว +8

    This is brilliant as always Gez, thank you! One thing that wasn't so clear in regards to MCAS - is it a lifelong management? I know the partial answer was that once the mast cells are replaced in 6 months they can be less sensitive, but wasn't quite clear if that means they would no longer need to be managed..

  • @brittanykidd1336
    @brittanykidd1336 4 ปีที่แล้ว +6

    Really appreciate what you’re doing!! Thank you for keeping our hope alive!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว

      Thanks Brittany!

  • @nomebear
    @nomebear 4 ปีที่แล้ว +6

    I have directed my physician to view your interview with Dr. Tina Peers. This video answered so many questions.

  • @nomorel7884
    @nomorel7884 3 ปีที่แล้ว +5

    Hallelujah for this interview!!!!!!!! Finally someone that is saying what I have been thinking all a long with my 5 years of ME/CFS Dr Peers you are a godsend

  • @BarryOGrady
    @BarryOGrady 3 ปีที่แล้ว +8

    Thanks again, Gez. Great video. Three months with Long Covid (and have asthma since childhood). Fatigue is the main thing. Hits me at about 4pm every day and the legs have that feeling you get when you've got lactic acid built up after a series of uphill sprints. Tina is right - I go for a walk, and the next day I am wiped. Anyway, I will give this three/four step plan a go. You need a rack for your nice marathon medals! Can't wait to be back up training for one ...

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +3

      Thanks Barry - Tina is right, you have to really reduce the amount you’re trying to do. And yes those running medals are a mess, I ought to sort them out!

    • @captmorgan2063
      @captmorgan2063 3 ปีที่แล้ว

      Barry how are you doing now?

    • @BarryOGrady
      @BarryOGrady 3 ปีที่แล้ว +3

      @@captmorgan2063 Thanks for asking. Still fatigued with sore muscles and the ankle and hip joints are sore each evening. Got ultrasounds (to check heart), X-ray (lungs) and bloods twice, nothing showing. Going to long covid clinic next week. Paying, coz you'd need a detective to find any long covid services in the public side. Regarding work, I have v understanding staff, so they are taking work off me :-) and have a lot of good projects going on with great people, so lots to distract me. Wiped every evening so bed at 9ish.. (not that I sleep). Am running - but no marathon in 2021 (real or virtual). Hopeful! And aware there are others who are a lot worse, so not complaining!

    • @captmorgan2063
      @captmorgan2063 3 ปีที่แล้ว +2

      @@BarryOGrady hate to hear that but keep the positive attitude I'm going through the same thing I am 9 months post covid still can't work out and dealing with mcast histamine like issues

    • @BarryOGrady
      @BarryOGrady 3 ปีที่แล้ว +3

      @@captmorgan2063 You able to get help? As per Gez's suggestion to me, I took it real handy and upped my running v v gradually. Now and then I crash for a few days by overdoing it, though. Yeah, stay positive. I have continued on the Vit D and C and then a generic every-vitamin tablet each day.

  • @carmenwheatley5376
    @carmenwheatley5376 4 ปีที่แล้ว +9

    With MCAS you need to work on damping down the sympathetic nervous system. Low dose naltrexone and intensive breathing exercises, together with gentle exercise like Qi Gong, can work wonders. Cobalamin is essential because it is a key regulator of the immune system and directly impacts on mast cells.

  • @rosalindmartin4469
    @rosalindmartin4469 4 ปีที่แล้ว +8

    Well done, Sir. Thank you.
    Walk tall, as is said in Jamaica👍

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +1

      Thanks Rosalind :)

  • @gillianbradbeer4752
    @gillianbradbeer4752 4 ปีที่แล้ว +6

    Another great video, thank you so much Gez, your videos have helped me so much these past 8 months. I really don’t know how you’re managing it!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว

      Thanks Gillian! Hope you’re seeing some recovery.

  • @cealy6669
    @cealy6669 4 ปีที่แล้ว +4

    Thank you for this work that you are doing. I find your information more helpful, information, and cutting edge than what is shared via most media platforms.

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว

      Pleasure - glad you’ve found it helpful!

  • @micheleclark59
    @micheleclark59 2 ปีที่แล้ว +1

    I’ve had fibromyalgia for 15 years, in speaking to my sister who Has Long Covid, a Loud bell went off in my head. When she made it to the rheumatologist BINGO, She developed fibromyalgia. My point being if you HAVE a crappy chronic illness that runs in your family, (Also 2 1st cousins, total 5 of us with it) Covid tends to stress your body enough for it to surface.

  • @matthewhenry4729
    @matthewhenry4729 3 ปีที่แล้ว +3

    THANK YOU for your research. You sir, have helped me alot along my journey to recovery as a Long Covid patient. Keep up the good work!...

  • @danmarquez3971
    @danmarquez3971 4 ปีที่แล้ว +27

    Interesting!! Great tips, too! Chilis and red onions allegedly help stabilize mast cells. (Interestingly, they are loaded with quercetin). Regarding the low histamine diet, I think the low-histamine plant diet rocks. A problem with meat, fish, eggs, and dairy is that they allegedly increase TMAO via the gut flora. TMAO reportedly increases inflammation, which calls to question the validity of the low-histamine cookbooks that promote animals products. (If you got bit by a lone star tick, meat can potentially give you anaphylactic shock !) If you have Type 2 diabetes or are prone to Type 1 diabetes, better follow PCRM guidelines! Despite all this, I do take the listed supplements (D3, zinc, etc.) and drink mineralized water (not sparkling) to keep kidney pH up. (COVID flourishes rapidly at pH 6...).

    • @mariakristinahawl1640
      @mariakristinahawl1640 3 ปีที่แล้ว +4

      Would've been easier to follow this without all of the abbreviations.

  • @stephieg
    @stephieg 3 ปีที่แล้ว +4

    This totally makes sense. I have long covid and was diagnosed with MCAS about a year after I got covid. Also have had autoimmune diseases and allergies for years although my immunologist says my immune system is very peculiar and based on biopsy results and so on my autoimmune dieases are not tied to my MCAS - he says it is almost like I have two different immune systems.

    • @EmuEmi
      @EmuEmi 2 ปีที่แล้ว

      Did you try the low histamine diet? Did it help?

  • @al-zd1zh
    @al-zd1zh 4 ปีที่แล้ว +2

    Really appreciate your personal drive & commitment to supporting long Covid recovery. Living with this bizarre menu for 8 months now. Rest & pace aid basic functions. Does anyone know of a blood test - private or otherwise - to support the mast theory. Great work & admire you dealing with fatigue but delivering your much needed videos.

    • @alicequayle4625
      @alicequayle4625 4 ปีที่แล้ว +2

      I think Tina Peers might mention someone that does tests on her website.

  • @sabinecohen8369
    @sabinecohen8369 4 ปีที่แล้ว +17

    So that explains why Famotine -taking covid patients had better out come than PPI-taking covid patients who developed severe covid:. The mass cells were somewhat inhibited producing histamine by Famotines' competition for H2 receptor sites.

    • @jaisarmiento1188
      @jaisarmiento1188 4 ปีที่แล้ว +1

      I still have prescription,Should we start taking famotine?

    • @starlinguk
      @starlinguk 4 ปีที่แล้ว +2

      I take it (I've had long Covid since March). It does nothing whatsoever. I'm going to stop, it's not worth the money. Tbh, a lot of the MCAS symptoms don't sound familiar at all. Oh, I take cetirizine as well, was already taking it before I got ill. It helps a bit with the rashes but that's it.

  • @MrsMac3099
    @MrsMac3099 2 ปีที่แล้ว +1

    What an eye opener. I have delt with this for 4 months now. Doctors didn't know what is wrong. I have been miserable, fatigue is so bad , hives, itchy all over. Idk if I have new food allergies, or the lip swelling is involved. They had me on prednisolone, antihistamines for H1, and H2. I am going to try the diet and supplements. I did have HSP as a child , and different food allergies that come and go, bad fall allergies, with severe migraines.

    • @RUNDMC1
      @RUNDMC1  2 ปีที่แล้ว +1

      Wishing you the best in your recovery!

    • @MrsMac3099
      @MrsMac3099 2 ปีที่แล้ว

      @@RUNDMC1 thank you so much. The last couple days I have taken Zyrtec, pepcid, and ate low histamine foods and taken my vitamins. I feel almost like myself. Still drained, but better. Thank you again for all of these videos !!!! I do have one condition that I don't think other people in your study have. Spinal cord injury, nerve damage. l5-S1 and other complications that go along with that.

  • @lillimay5
    @lillimay5 4 ปีที่แล้ว +6

    I cannot thank you enough. My doctors who even know MCAS couldn’t figure out why I wasn’t responding to my normal meds after my illness

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +4

      Hope that this helps you - my symptoms have definitely been improving since changing diet and taking supplements

    • @MrLuca18
      @MrLuca18 4 ปีที่แล้ว +1

      @@RUNDMC1 what diet you on and supplements

  • @nancyblake1679
    @nancyblake1679 4 ปีที่แล้ว +2

    No mention of ME/CFS, yet ‘fatigue’ is a major symptom. (ME/CFS fatigue is more correctly described as ‘muscle failure after minimal exertion’. And the IOM Committee reporting on ME/CFS went further..’the central characteristic of this disease is that exertion of any type - physical, cognitive or emotional - may adversely affect many systems ....’. Exertion can do multisystem damage.). ME/CFS , like polio, occurs after a viral infection. Covid is a viral infection, although from a different family.
    It is typical of ME/CFS patients that the previous life-style was a high exertion one...atheletes, marathonners, back-packers - and those involved in physically demanding care roles - women with small children, or looking after elderly or disabled family members. I suspect that this will be found true of many long-haul covid sufferers...it is notable that they tend to be younger, fit individuals whose actual illness may have been apparently mild.
    Melvin Ramsay, Infectious Diseases consultant at the Royal Free who treated and recorded patients from the 1955 outbreak, concluded that complete rest from the inception gave the best prognosis, and many patients at that time (also from the 1932 Los Angeles outbreak) fully recovered. He recommended six months of complete rest, and even now there is an occasional patient reporting full recovery fromME/CFS after a brave GP told them to just go home and rest for six months.
    One interesting piece of research would be to study whether long-haul covid was more likely to occur in patients who tried to maintain an active life-style during and after their illness. And whether a relatively lengthy period of convalescence focusing on conserving energy would be more helpful than attempts at ‘rehabilitation’...encouraging increases in activity, and even exercise..
    ME/CFS does include immune system disorders...either over- or under-activity. Many patients ‘catch everything that’s going’, and are sicker than most when they do. Others, (I am one of them) suffer a more or less permanent state of immune activation (a bit of exertion brings on a sore throat...hard to offer a psychoanalytic explanation for that!) but almost never get sick, or only mildly, when the usual run of colds or ‘sickness and diarrhoea’ are going around. The continued immune activity, and the fact that the illness fluctuates in relation to exertion throughout its very long course: activity continues to bring on relapse; concentrated rest continues to create some level of improvement - suggests that there is some level of viral potential hiding away..possibly in muscle fibre.
    People with ME/CFS tend to have discovered for themselves many of the supplements you suggest, which again seems to point to common features.
    Finally, I was struck by your remark that mast cells are renewed in six months. It quite possible that this is nothing more than a coincidence, but could the six months of rest prescribed by Ramsay have permitted the active mast cells finally to overcome whatever element of pathogen still remaining, and to have produced new cells no longer overstimulated by that, so able to function normally? That would be a complete recovery.

  • @ivocx2228
    @ivocx2228 4 ปีที่แล้ว +6

    Thanks to your info and the long covid FB group, where I learned about it, I managed to move from lying flat on my back for whole day to functioning almost normaly within months. I am able to do long walks again :-). Another thing that worked for me was fasting. I used to fast 2 days a week before Covid and as soon as I switched to low histamine diet and started to feel better, my body kinda required it again. What I find interesting is that in the days when I fast, I can push myself physicaly without negative effects the next day. This is how I was building my stamina: normal days taking things very easy, fasting days exercising more (within limits, after spending 2,5 months in bed, even a brisk walk is an exercise). Perhaps this may help with your running.. BIG THANKS for your tremendous work!

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +2

      So glad to hear you’re recovering! Fasting does seem to work for a lot of people

  • @JenDez-2017
    @JenDez-2017 ปีที่แล้ว +2

    I would REALLY like to talk to Dr Peers. I'm not even half way through this video and she's hitting everything on my checklist. She even mentioned exercise intolerance. As an elementary student, I'd get a swollen throat filled with mucus and heart beating out of my chest (I was not an obese child). I was the fastest child in my class, for short distances only. The longer the distance, the more intolerable. I was eventually diagnosed with "Asthma", but my doctor said it was really "Exercise Induced Bronchial Spasms". Also, pre-covid, my lips would swell up with odd reactions to normal things, like to COLD (I was eating ice cream and was playing with it as a 3-4 year old, just cupping my lips around it), my lips were noticeably swollen for 2-3 hours afterward - enough for my uncle to make fun of me. I also had lip swelling after playing the "watch your mouth" game where you put a plastic dental appliance in your mouth and try to say words on a card. Same thing, my lips were swollen for hours afterward. I was also hospitalized with Anaphylactic shock for 3 days after a medicine reaction. Just lots and lots of scenarios like that over the years.
    Once having Covid, my entire system is haywire!!! Doctors here in the NW United States don't know what to do with me. They discharged me from the Cardiac Rehab clinic because they could see that my exercise threshold was declining and they diagnosed me with Post Exertional Malaise. I've also been diagnosed with POTS after experiencing PVCs, racing heartrate, dizziness, loss of balance, etc . . . They also suspect MCAS. I've also been found to have a soft tissue lesion, my hormone cycles are now extremely painful. The muscle and joint pain can be intolerable. But no one knows how to treat this.

    • @revelation12_1
      @revelation12_1 ปีที่แล้ว

      How are you doing now? ❤

    • @JenDez-2017
      @JenDez-2017 ปีที่แล้ว

      @@revelation12_1 I was eventually dismissed with Long Covid and bedridden. I could only talk through gasps. After a month in bed, I began getting up, but pacing and doing only essential things (showers were only 1xper week) otherwise strength gives out completely. I got into a groove and was able to cope with a seated walker and could sit when I felt syncope coming. Now I'm walking a bit without my walker. It's been over a year and 3 months since I had Covid.

  • @larasita11
    @larasita11 4 ปีที่แล้ว +8

    Wonderful information, thank you!
    Great questions, so good to be starting to hear some answers from practioners who have actually been trying to find treatments. We know they are out there and having successes... we need to hear their results and their voices!
    Love all your videos! Top go-to channel for fresh thinking during all these days.

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว

      Thank you! Hope you’re doing ok :)

  • @richardbriseno3032
    @richardbriseno3032 4 ปีที่แล้ว +1

    Long Hauler syndrome, otherwise known as ME/CFS, MCAS, Dysautonomia, Post Viral Fatigue Syndrome, Yuppie Flu, etc. is due to the virus persisting in the brain, Neurons and Glial cells. This prevents the immune system from clearing the infection completely. As a result, the histamine alarm remains ON and Histamine buckets stay full or near full causing symptoms that do not go away and vary with time. Watch her mention persistent infection at 12:15. I know about post viral illness because I got sick in April 2005 and still remain sick to this day with a stomach flu virus, Im awaiting antiviral development due out soon. Ive participated in 3 clinical trials out of Columbia, Ithaca and the NIH. Im glad to see this illness is getting much attention now, hopefully a cure will come soon. Ive been told its all in my head, be glad im not suffering from a "Real" illness, Eat better, take vitamins, etc.

  • @DeadlyCyanide1
    @DeadlyCyanide1 4 ปีที่แล้ว +3

    I am eds, mcas and pots I can't thank you enough for this. This is the best ever and I learned somethings as well

    • @RUNDMC1
      @RUNDMC1  4 ปีที่แล้ว +2

      Thanks Amanda, I really hope it makes a difference for you!

    • @DeadlyCyanide1
      @DeadlyCyanide1 4 ปีที่แล้ว

      @@RUNDMC1 thank you me too

    • @josephinethornton3823
      @josephinethornton3823 4 ปีที่แล้ว +1

      The trifecta! I too have the trifecta and am here for this man's work. Both SO and I got Covid-19 and it's been fascinating to see the way it's been affecting us differently.
      He's experiencing dysautonomia for the first time, and mine is WILDLY out of control, as is my mast cell. I often wake up with parts of my face swollen, which is shocking to see in the mirror.
      SO notices the chest tightness right before he leaves for work (he was bedridden for 3 months, and it's 6 months he's upright since then. He can work, but that's all the energy he has, and back to bed until work again). I suspect his chest pain right before work is due to the stress of trying to get ready for work, rushing to try not to be late, etc, and the stress of it causes a mast cell reaction.

    • @DeadlyCyanide1
      @DeadlyCyanide1 4 ปีที่แล้ว

      @@josephinethornton3823 if you're mast cells are going out of whack you might not be on the right protocol and if you're not on a protocol you must be you have to find the right doctor to get you on the right protocol everybody is different so different protocols for different people it's all about trial and error in the beginning . If you don't have a Mast Cell Doctor please get one and the pots need to be taken care of by a cardiologist first and then a neurologist afterward if everything is okay with cardiology.

  • @paulp1372
    @paulp1372 2 ปีที่แล้ว +1

    I absolutely relate to the 'getting of histamine high foods' . When Long Covid hit me hard for three months from early January 2022 - it was straight after a slightly binge based Christmas period - of increased dairy, meats and alcohol

  • @alexhey8277
    @alexhey8277 4 ปีที่แล้ว +11

    This is so helpful. It mirrors all my post covid problems, as a allergic ridden person in bloom.

    • @2000disneyland
      @2000disneyland 2 ปีที่แล้ว +1

      Allergies plague me too, which seems to contribute to Long Covid symptoms.

  • @ShayneWolfe
    @ShayneWolfe 3 ปีที่แล้ว +1

    I got diagnosed with Menieres Disease a few weeks after getting sick with what I thought was a common cold around the time that the first lock downs happened for Covid (Early 2020). I was getting vertigo 1-2 times a week, and was dizzy almost 24/7. I had to quit flight training, completely change my life, etc. It sucked. Doctors bascially said good luck to me and offered no real options. I was on my own. Nearly 2 years later, I'm almost vertigo free. I've only had 2 episodes this whole year, no more ear fullness, no more hearing loss, very little tinnitus.
    My theory now is that I actually had covid when I was sick in early 2020, and my long haul symptoms closley resembled menieres disease.

    • @CaliHummel
      @CaliHummel 2 ปีที่แล้ว +1

      %100 cause this is me. What did you do to help?

    • @ShayneWolfe
      @ShayneWolfe 2 ปีที่แล้ว +1

      @@CaliHummel Check out the John of Ohio regimen (google it). Like I said, I'm not sure if I just had long covid or if the regime is what helped...maybe a culmination of them both?

  • @David-uf8ex
    @David-uf8ex 4 ปีที่แล้ว +14

    What a great video very helpful 👍🏻 Thank you

  • @GR1MMDJ
    @GR1MMDJ 2 ปีที่แล้ว +2

    I’m so glad I found this channel. Thank you for all your information and encouragement. I had a question if anyone knows if coffee / caffeine is ok to drink. I feel like it enhances my mood in the morning but sometimes seems to trigger some symptoms after.

    • @RUNDMC1
      @RUNDMC1  2 ปีที่แล้ว

      Different for everyone - but can certainly be a trigger for some. You can mitigate with antihistamines to some degree

  • @DeirdreSM
    @DeirdreSM 4 ปีที่แล้ว +5

    Looking at the low histamine diet…that's already what I'd been doing for the most part, though I do like my legumes. This could explain why I feel better when I'm taking antihistamines regardless of whether I have active "allergy" symptoms or not.

  • @petinapowers2869
    @petinapowers2869 4 ปีที่แล้ว +2

    RUN-DMC, MCAS as a part of the problem makes sense. I brought this up to my PCP (GP) and he just brushed the idea it off. (Honestly, as most of you know, it is exhausting to work and study, much less be your own monitoring device and specialist.) I cook with chilies on a daily basis, but I also eat bananas and citrus on a daily basis. So, maybe they were counteracting each other. On another note, I believe my recent episodes with hypersomnia were triggered by increased activity. The upside is that every time I emerge from one of these episodes I improve cognitively. I am still disorganized though, and out of breath after a block or so of walking.

  • @sabinecohen8369
    @sabinecohen8369 4 ปีที่แล้ว +13

    Recovering from covid and found I felt better next day taking Famotine h.s. Gonna try an anti histamine diet. Thank You!!

    • @shiningoutlight
      @shiningoutlight 4 ปีที่แล้ว

      true

    • @MrLuca18
      @MrLuca18 4 ปีที่แล้ว +2

      I took antihistamines made me feel worst

    • @joeorler4097
      @joeorler4097 3 ปีที่แล้ว

      @@MrLuca18 Same here they made me extremely anxious POST covid

  • @judygmiller
    @judygmiller 3 ปีที่แล้ว +2

    I followed the suggestions and my long covid symptoms lifted 95% across 2+ weeks. I didn't know about low histamine diet and needed very simple due to brain fog, so I just ate fresh cooked beef 2x a day while I studied. Now trying one new food a day. But I feel great!

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +1

      Very glad to hear it!

    • @judymiller5154
      @judymiller5154 3 ปีที่แล้ว

      @@RUNDMC1 surprising benefit - the bedtime tachycardia I've suffered in clusters for years and was quite constant in past 6 months has disappeared suddenly with the low histamine approach! I was told by a doc 30 yrs ago my heart is fine, avoid alcohol (only trigger mentioned) and learn to live with it. May God abundantly bless you for all your effort helping us and bring you total healing! ❤🙏❤

    • @jamesmurphy8676
      @jamesmurphy8676 7 หลายเดือนก่อน +1

      @@judymiller5154hi Judy how long did you do it for please reply. Hope you’re still better

  • @MaxPlaysFIFA
    @MaxPlaysFIFA 3 ปีที่แล้ว +10

    Hi gez
    So everything atm is pointing towards MCAS being my issue. Eating alot of chocolate seems to trigger it for example and the niacin is helping a lot, I’ve also been taking h1s , so I’m now going to ask my doctor for a H2 and a mast cell stabiliser, is it recommended to take all of these at once?

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +3

      Yes I would do. Good luck with it Eoin!

    • @MaxPlaysFIFA
      @MaxPlaysFIFA 3 ปีที่แล้ว +5

      @@RUNDMC1 thanks gez, your research and work on this deserves huge recognition, once again. thankyou!

    • @EdHunteR87
      @EdHunteR87 3 ปีที่แล้ว +3

      Hello Eoin, how much Niacin do you take daily ?

    • @michaelday5605
      @michaelday5605 3 ปีที่แล้ว +3

      Check covid19criticalcare.com/covid-19-protocols/i-recover-protocol/ for dosages of h1/h2 and mast cell stabilizers

    • @mikecarey1990
      @mikecarey1990 3 ปีที่แล้ว

      More medical nonsense. Deal with the cause instead of treating the symptoms with drugs. Wake up! Drugs do not fix anything.

  • @lynnehill652
    @lynnehill652 8 หลายเดือนก่อน +1

    I've had long covid for 2 1/2 years, with all the usual symptoms. Breathing and heart palpitations are the worst symptoms, but I also had severe fatigue until I discovered the amino acid, glycine. I take a spoonful three times a day in warm water. It has been the only thing that has helped me. I still am out of breath and I take metoprolol for my heart, but my energy is much better.

  • @aoifel77
    @aoifel77 4 ปีที่แล้ว +10

    This was amazing 👏 thank you so much for all your videos and research. I had Covid in March & was on treatment for Lyme disease just prior to contracting it. This information is gold to me xx

    • @truthtriumphant5503
      @truthtriumphant5503 4 ปีที่แล้ว +1

      Hi fellow Lymie!!! I hope you are recovering well from both...but, seeing how you are on a site for long haulers...seems like you are having overlapping issues too...Have you noticed how much the symptoms overlap? I'm new to the site and am exciting about learn too : )

    • @aoifel77
      @aoifel77 4 ปีที่แล้ว +3

      @@truthtriumphant5503 Hi Debra, the symptoms definitely overlap like fatigue and joint and muscle pains but the lung pain and breathlessness are unique for me to Covid after effects. I'm 9 months post Covid & post Lyme treatment. Still struggling a lot some days but definitely improving. Wishing you healing & health x

    • @truthtriumphant5503
      @truthtriumphant5503 4 ปีที่แล้ว +1

      @@aoifel77 ...I don't know what route you are taking in getting the Lyme into remission. But, some of the things that have really helped me are bi-weekly coffee enemas (to get the built-up toxins out that cause a lot of the pain and to increase the glutathione levels 700%)...I use ozone insufflation afterward. Have been doing them for over 4 years now...and it really does help. Hubby and I also use a Rife machine and infrared sauna...along with a boatload of vitamins/minerals. One thing that helped when I was bedridden with fatigue was Meyer's cocktail IVs...I had to use a roller walker if I went more than from the bed to the couch. Since so many of the symptoms seem to overlap...and like with Lyme...so many people have different symptoms that can be caused by so many different personal issues in the body. This COVID long haulers is going to be very difficult to treat in a modern medical environment. Hubby and I were sick for 1 month with a fever with COVID and two more months of severe fatigue...I'm sure if we had not been detoxing with the Lyme...it would have killed us. I hope you get to feeling much better and thank you for replying : ). How long were you sick with Lyme before being diagnosed?

    • @aoifel77
      @aoifel77 4 ปีที่แล้ว +2

      @@truthtriumphant5503 oh wow thanks so much for all the information. I've not tried most of those things but have read about them and would love too. I did antibiotics for 5 months, then herbals.. I take a ton of supplements and sea swim, do Yoga & breath work, Salt baths, CBD oil, I honestly think Lyme is under control with me now bar a few flare ups. The Covid long haulers symptoms are hard though and much like Lyme very hard to get help from traditional doctors. I'm on Instagram if you use it might be easier to chat. My ig is Efaphotography11 xxx

    • @truthtriumphant5503
      @truthtriumphant5503 4 ปีที่แล้ว +2

      @@aoifel77 You are welcome...I use to be on a lot of Lyme groups when I was really sick and unable to function. My experience with traditional doctors is not good and because of that ...I no longer trust a pill or an ill : ). The symptoms of COVID are probably like Lyme and has multiply issues going on than just a virus. The virus is just showing where the problems are. For me to get better I had to have all of my amalgams and root canals removed...when I did the MS/Alzheimers/dementia symptoms went away. When I started the coffee enemas ...the Fibro pain went away...when I started high dose vitamins (like with the Meyers Cocktail) ...my energy got a lot better. You are probably young by your pic and not as toxic as a 66 year old...that makes a difference. I am sure we would have died from COVID had we not been dealing with Lyme for all of these years...correcting what was causing our immune system to falter. It concerns me for those with COVID long haulers ...if they rely on traditional medicine..they probably will never truly get better. See, I think the makers of Lyme and COVID are the same..bioweapon has too many things in common. Did you ever go down that rabbit hole? If not check out Plum Island. Stay well..and check out www.drjaydavidson.com He was my Lyme doctor and has a lot of good videos/articles that are very interesting and helpful.

  • @kd2533
    @kd2533 ปีที่แล้ว

    Her protocol has helped me immensely with long covid from both the virus itself and the shots,, EDS and MCAS. I'm grateful.

  • @oliverneech3950
    @oliverneech3950 4 ปีที่แล้ว +4

    Thank you for all of your videos. You truly are an awesome guy!

  • @minituremarvels
    @minituremarvels 2 ปีที่แล้ว +2

    I made a comment a while back on experimenting with water fasting to combat my Long Covid. I was suffering with debilitating fatigue and PEM that would leave me unable to do the laundry. Breathlessness, the lot. Life felt on hold for the best part of a year. I did a 3 day water fast (with salt/electrolytes), and can now happily say my condition is cured. Resolved 95% within a week of the fast, brief minor recurrence of very mild fatigue for a few days here and there, now 100% gone. Just a case of rebuilding strength and cardio now. Can do full strength training sessions as per pre Covid, no PEM to speak of. I’d highly recommend people to try this, with proper research and advice from a doctor. Any questions, I’ll do my best to help. May everyone recover as fast as possible. Cheers 🙂

    • @abdielmata
      @abdielmata 2 ปีที่แล้ว +1

      Great you recovered! I’m on my second bout with Covid and second bout with Long Hauler symptoms. Have your symptoms come back since then, did you follow an antihistamine diet and did you take any supplements?

    • @minituremarvels
      @minituremarvels 2 ปีที่แล้ว +2

      @@abdielmata I feel really lucky to have recovered with this method! No, I have not had any relapse since March when I did the fast. Waited this long before posting as I wanted to be sure it wasn't just a temporary fix. Just did a heavy gym session last night, no PEM to speak of. I didn't undertake the antihistamine diet. The other things I did were acupuncture, niacin (which helped a bit), and meditation.

    • @cryptocurrency2312
      @cryptocurrency2312 2 ปีที่แล้ว +1

      @@minituremarvels what supplements/vitamins/medications you took while fasting?

    • @minituremarvels
      @minituremarvels 2 ปีที่แล้ว +1

      @@cryptocurrency2312 Nothing other than the essential electrolytes; salt (sodium chloride), magnesium, potassium (be very careful with this as you can overdose!), and calcium. Electrolytes are essential when fasting as you can easily become imbalanced and start getting symptoms that will force you to end the fast without them.

    • @abdielmata
      @abdielmata 2 ปีที่แล้ว +2

      @@minituremarvels thank you! I’ve seen your testimony comment on several videos. On day 3 and going for 7! If I feel good, I may keep going. My muscles don’t hurt as much anymore, but the fatigue is still there.

  • @sabinecohen8369
    @sabinecohen8369 4 ปีที่แล้ว +31

    I have mild Raynaud's and some OA. I think anyone prone to autoimmune disorders will be prone to long haul covid.

    • @llathem2212
      @llathem2212 4 ปีที่แล้ว +1

      Yep. Correct, I have lupus and 10 months later I got better in August, but am now worse. I think it’s bc I had food allergies prior to COVID.

    • @wicksandsticks
      @wicksandsticks 3 ปีที่แล้ว

      I’ve always had post viral fatigue after having bad viruses (mono and the flu). Now I have long covid. Rheumatoid Arthritis runs in my family as well so I suppose I’m prone to autoimmune disorders. Maybe that has something to do with why I always get post viral syndrome. Immune system attack. I’m not a doctor but this is all very interesting.

  • @pattijesinoski1958
    @pattijesinoski1958 2 ปีที่แล้ว +1

    as a pharmacist, i am against valium(dependency) and toxic SSRI'S for treatment. Many elderly end up with tons of longterm toxic results of SSRI, including chronic diarrhea leading to dehydration, sleep issues,

  • @tamzidmafiz6259
    @tamzidmafiz6259 4 ปีที่แล้ว +7

    Excellent interview and content!!! Thank you both very much :)

  • @ApprendreSansEcole
    @ApprendreSansEcole 4 ปีที่แล้ว +18

    Thank you so much for this very informative video. I’m glad dr Peers mentioned viral persistance as a possibility, but what would she recommend to fight the virus in that case ? Also, people have made a link between mold toxicity and MCAS. I would be interested in her take on that.

    • @katiehettinger7857
      @katiehettinger7857 4 ปีที่แล้ว +4

      Thanks for bring up mold sensitivity, this has been a long term problem for me and it make so much sense. ;)

    • @sheilaloya8900
      @sheilaloya8900 3 ปีที่แล้ว

      There's a number of studies showing high causal link to EMF/ELF radiation (wifi/microwaves/5g etc)

    • @grossy25
      @grossy25 2 ปีที่แล้ว +2

      Two excellent points! Mold toxicity and EMFS from cellphones wifis laptops Bluetooth cell towers triggers MCAS. MOLD+EMFS= MCAS

  • @teddybearroosevelt1847
    @teddybearroosevelt1847 3 ปีที่แล้ว +3

    It seems that taking N Acetyl Cysteine, which is the precursor to the antioxidant glutathione, as well as glutathione itself has significantly improved my condition.
    Anyone else who has this experience?
    Let’s spread the word!

    • @RUNDMC1
      @RUNDMC1  3 ปีที่แล้ว +2

      Great to hear it!

  • @carolreilly5458
    @carolreilly5458 2 ปีที่แล้ว +2

    Thanks for this. Explains the symptoms I'm having before and after covid. Will try your recommendations and hopefully will improve.