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Covid-19 Vaccine side effects

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Thisistoomuch
(@margaret2022)
Very Active Member
Joined: 8 months ago
Posts: 216
 

Well I finally received my covid antibody levels and they’re at 954 u/ml. They are trending down. So it took like 5 months for it to go from 1927 to 954. I can’t wait for another 5 months to go by. I’m hoping once this gets out of my system things will improve. I wonder if it was even the vaccine the ophthalmologist I saw saidnhis wife had dizziness after her vaccine. I said finally someone who understands where I am coming from. And he also mentioned that it can be due to the chicken pox virus where it can attack the nerves. Then I thought of Justin bieber. So he’s a neuro ophthalmologist. He did do some tests with me and looked into my eyes said there was nothing wrong. Which is good. 
also he mentioned viruses can do things to the nerves and cause the nerve that connects to the eye and ear not send the right signals to the brain and cause sorts of symptoms. Good thing is no issues. I wasn’t sure what to take from that appointment. I am great full for nothing bad showing from the tests. But at the same time I guess I was hoping he would give me something. He did mention it sounded like vestibular neuritis. Then I mentioned prednisone he said no there was no need for prednisone. He told me to get back into my routine of things. To go out and give it time. Sorry all over the place with this post. I’m just glad I’m home now, it was a long trip.


   
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Asanders
(@asanders)
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Joined: 10 months ago
Posts: 51
 
Posted by: @ksharky13
Posted by: @asanders
Posted by: @ksharky13

Thanks for the detailed reply.  Glad to hear that you feel close to normal most of the time.  Also very glad to hear that your tinnitus resolved.  That gives me hope.  I'll have to look into the blood cupping you mention.  Were there any other things (supplements, etc.) that you think may have helped your tinnitus, or do you think it was just a matter of time while the inflammation reduced?  I know a lot of people on here have mentioned that they started to get better and then had a relapse (or two).  I guess that could be what I'm going through, but it's been 3+ months so it gets concerning that it could be permanent the longer it goes on. Anyway, thanks again for replying and sharing your experiences.  I hope you continue to get better and back to normal.

Actually other than tinnutus and dizziness nothing is resolved. I feel normal thanks to cortisone and tramadol. If I pass a single dose of cortisone all the inflammation comes back. So in reality nothing changed but I just dont feel the pain and symptoms as long as I am on cortisone.

tinnutis is totally gone tough. Most of my problems are in my lower body but every now and then I feel inflammation around my eyes and chin, and I have lip, tongue, and several face muscle twitches, and Trigeminal neuralgia but no tinnutus dizziness or headaches. I am pretty sure removing toxic blood behind my ears helped my tinnutus to resolve. I also used  Betahistine dihydrochloride and Trimetazidine dihydrochloride during the time I had tinnutus. Of course starting cortisone early was probably another factor that helped.

My problem with inflammation is that I feel it all around in my body but my CRP levels are within normal range so my doctors refuse to accept that I have an inflammation problem and I have no clue why my crp levels are not elevated even tough inflammation destroys my body. My rheomotologits insists that the pain I feel in my knees, shoulders and hips are not bone pain but probably nerve pain. 

My hemotologist thinks I dont have a blood clotting problem since D-dimer and other blood clotting related tests are normal. But I have abnormally high  neutrophils and leukocytes and low eisonophils. 

So still no diagnosis, no IVIG or another treatment by insurance. 

 

 

 

Quick question:  How many cupping sessions did you do before you noticed any improvement in your tinnitus?  Also, did you place a cup directly behind your ear on more on you neck?  I did my first session last night on my extremely sore shoulder and neck muscles.  Not sure how I could get a cup to stay right behind my ear, though.  I think the one session helped a little with my muscles, but not the tinnitus yet (as expected).  I definitely bruised, which my daughter (who is a physician and who did the cupping for me) said indicates a lot of inflammation (the darker the bruise, the more inflammation). Any information you can share would be greatly appreciated.  Thanks.

 I stopped taking Betahistine dihydrochloride after my tinnutus stopped. It was like 2-3 months total.

About cupping, I am not sure if dry cupping only without blood removal would work. I did not do it myself, there are doctors who do wet cupping with blood removal as a natural theuropatic therapy. They put the cups on specific points on your body, wait for the cups to fill, they cut the skin with needles or gilettes and let the toxicated blood out like a filter and wait a little more and than repeat. Acutally this is like acapuncture there are some exact points where the cups should be placed. For tinnutus my doctor placed two cups behind my ears close to my neck, and after the procedure showed me the contents of the cup, and it was nothing like blood. 

this is a research article abot migraines and wet cupping  but  the image shows exactly the place where my doctor had put the cups on my head. http://www.bmrat.org/index.php/BMRAT/article/view/521  

 or this

https://www.facebook.com/hijamahealthandherbs/photos/todays-client-suffering-from-tinnitus-disease-ringing-in-the-ear-treatment-/1105079636332573/?paipv=0&eav=AfZs2SgSeJZIe7vk6A_MC6esNWPMzFii3LmL66w6o6LteAS7pTpOijINBFH0YyGrX6Y&_rdr

I have done this 3 times up to now but I am planning to repeat every month (not ears but full body wet cupping) now as I feel a lot better afterwards. Again the procedure seems painful but you dont really feel any pain at all. At least I did not.

At first I was thinking like what is the difference of this from blood donation? When you donate your blood your body produces new fresh blood. But blood donation take the blood from your vessels, this procedure does not take blood from vessels but from between cells. And doctors tell me that it is a combinations of dead cells, toxins, chemicals, and other stuff between cells which blocks blood flow.

 

 

This post was modified 2 months ago 2 times by Asanders

   
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Michalalala
(@michalalala)
Active Member
Joined: 1 year ago
Posts: 9
 

@ladyd hi, i would love to hear how you’ve been? I probably experienced exactly the same thing as you have. I got my first VM attack not long after my vaccination. I had not idea what was going on and after couple of months of dizziness and tingling sensations my neurologist made me to undergo spinal tap to rule out MS, which was the worst thing that could ever happen to me. I got terrible headaches from the spinal tap, which would not go away so I got my first panic attack ever, which triggered severe balance issues, feeling similar to walking on marshmallows. This is were my PPPD started, I experience constant swaying etc. I just found out that PPPD is the actual name for my diagnosis so I was prescribed with SSRIs - this would be my first experience with medication of such kind, let’s see how this goes.

Have you had any success with any treatment?

take care <3

m.

 


   
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alia
 alia
(@sunrise)
Very Active Member
Joined: 11 months ago
Posts: 163
 

I would like to share a link about Nattokinase:

https://www.youtube.com/watch?v=3tqwqEqOBe4


   
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Tinnitus from Covid Vaccine
(@ksharky13)
Very Active Member
Joined: 9 months ago
Posts: 118
 

So has anyone on this forum developed tinnitus from the vaccine, had it resolve to a great degree over a few months, only to have a relapse a couple of months later, and then resolve again?  Mine is a constant high-pitched hiss or screech, much like you'd hear from an old fashioned TV set (some people on here have referred to it as the Moderna Hiss).  It's been a few months into my relapse and I'm starting to fear that it may be permanent.  I can't think of any other potential cause of my sudden tinnitus.  And while I'm going through an incredibly stressful period in my life, I'm not a huge believer in stress being a root cause of tinnitus.  If anyone has recovered from vaccine-induced tinnitus, please tell your story here.  Thank you.   


   
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AEjessie
(@aejessie)
New Member
Joined: 2 months ago
Posts: 1
 

I was searching for the benefits of castor oil the other day, and I read quite a lot of articles and wathced some videos, they all said that castor oil really did a lot of good. What do you think of this?


   
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Thisistoomuch
(@margaret2022)
Very Active Member
Joined: 8 months ago
Posts: 216
 
Posted by: @michalalala

@ladyd hi, i would love to hear how you’ve been? I probably experienced exactly the same thing as you have. I got my first VM attack not long after my vaccination. I had not idea what was going on and after couple of months of dizziness and tingling sensations my neurologist made me to undergo spinal tap to rule out MS, which was the worst thing that could ever happen to me. I got terrible headaches from the spinal tap, which would not go away so I got my first panic attack ever, which triggered severe balance issues, feeling similar to walking on marshmallows. This is were my PPPD started, I experience constant swaying etc. I just found out that PPPD is the actual name for my diagnosis so I was prescribed with SSRIs - this would be my first experience with medication of such kind, let’s see how this goes.

Have you had any success with any treatment?

take care <3

m.

 

My neurologist wanted me to get a spinal tap too but I refused because I had two c sections and those ruined my back for 5 years due to the epidural so now I probably have scarring on my spine why I had so much pain for 5 years after each c section. He also wanted to prescribe me olanzipine which he tells me to calm down my nervous system. So what caused your dizziness for him to prescribe and ssri what was their reason to prescribe it? I didn’t bother taking the medication I was afraid it would make my tinnitus in my head much worse seems like every time I go to a specialist I come back worse because I saw an ophthalmologist and I feel like I see dark spots because I was looking into his machine that has fricken bright lights. So I’m not sure what to do anymore I had so much tests already done by specialists or just scans such as MRIs ct scans neurology ophthalmology ENT hearing tests all normal but my left ear hearing remains very sensitive it was so bad I had to change the light led light bulbs in my house cuz of the humming it sends off I can’t sleep with my hubby anymore because he snores and it’s not even loud. I also have eye issues as well. Driving at night it feels worse it’s mainly my left eye only and left ear. I thought I needed like prism lenses cuz I was reading about that binoculars dysfunction and the neuro ophthalmologist I saw said my eyes were fine nothing wrong.  So I’m like wtf. It’s been 8 months now since Jan 10th 2022. The day my life was ruined. 


   
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Thisistoomuch
(@margaret2022)
Very Active Member
Joined: 8 months ago
Posts: 216
 
Posted by: @aejessie

I was searching for the benefits of castor oil the other day, and I read quite a lot of articles and wathced some videos, they all said that castor oil really did a lot of good. What do you think of this?

Black seed oil is another one. I was taking that for about 2 weeks I felt good but not sure if it was making a difference with my symptoms it was hard to say.


   
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Michalalala
(@michalalala)
Active Member
Joined: 1 year ago
Posts: 9
 

@margaret2022
Hi, I am sorry to hear you are suffering too. I have these symptoms since June 2021 after 2 Moderna vaccines. I enjoyed hell of a road with all kinds of specialists since them (mostly making me feel worse then helping with the issue). 

The ground for prescribing SSRIs is vestibular migraine and PPPD diagnose itself. In both cases SSRIs can help to calm down overreacting brain and nervous system. This is something that does not happen over night, it’s a long way run but I am determined to try it (not that I have that many options after 15months of suffering of various debilitating symptoms).

Hanging in there!

m.

This post was modified 2 months ago by Michalalala

   
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Kristin
(@kg1986)
Active Member
Joined: 11 months ago
Posts: 32
 

Hi Everyone, I used to post a ton in these forums when I first was going thru all my symptoms. Back in November of 2021 is when I started waking up w pins and needles in my arms which eventually turned into the biggest nightmare of my life.

-Numbness

-Muscle weakness

-Back spams

-Muscle twitching, internal tremors

-head aches, brain fog

-Shooting random nerve pain

-anxiety (thought for sure I had MS, ALS or a brain tumor.)

-nausea/GI issues

-Heart problems (pain) they put me on meds for pericarditis

 

This all started about 1-2 months after my second pfizer vx..some drs say its not that, but most of them say it could be and have no real answers besides "nerve inflammation"

 

Every day it would be something new...over time I saw so many drs, has MRIS, blood tests...couldnt figure anything out besides my IGG and EBV were high and my D was a little low and D dimer was high.

 

After a few months of a strict diet and lots of supplements I felt better, back to working out and being a mom again....then in March I got covid for the first known time and a lot of symptoms came flooding back..but again in time they got better. I would say I have been 80-90% better but never 100%

Recently I did start lifting heavier in my workout, but I work out 5-7 days a week and didnt think anything of it at the time. Then within a few days my back started feeling sore on the spine and radiating lower. It got so intense it was making me sick. I got an X ray-normal....Its been a little over a week and now I am feeling the pins and needles again, waking up feeling so strange and fuzzy, brain fog, my feet have the internal tremors again, some muscle twitching all over randomly and I feel just awful. Has anyone has trouble with back spasms? I did have a cold a few weeks ago, I almost wonder if everytime I get sick this is going to happen. I went to a new Dr Wednesday and told her everything. She said shes going to order another MRI with contrast since they did not last time. I am just so scared they are missing something that is happening to me, but then I try to tell myself this has been going on for a year now and its almost like flare ups, not a progressive condition. I still fear the worst (cancer obviously)...It would just be nice to hear from people that can understand my frustrations, really hard to someone who hasnt experienced this nightmare to fully grasp how awful its been.I am only 35 and has two babies under 3 and I just want to feel alive again.

 

KG

This post was modified 2 months ago by Kristin

   
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Thisistoomuch
(@margaret2022)
Very Active Member
Joined: 8 months ago
Posts: 216
 
Posted by: @asanders
Posted by: @ksharky13

I have to admit I am truly saddened by the severe drop-off of activity on this forum.  It was once a treasure trove of information, insights, and experiences from so many people suffering numerous adverse side effects from the Covid vaccines.  My symptoms seemed to have subsided after 3-4 months, but have spiked again and it's been another 4 months and I don't see any level of improvement.  While my biggest symptom/issue is tinnitus, I also have a constant mild (but still aggravating) headache, tight and sore shoulder and neck muscles, a slight dizziness feeling, and a brain fog/racing brain that is unnerving. 

I don't know if I'm just suffering from severe anxiety and depression coming out of the pandemic into a world that des not mirror what it was before Covid, or if it's truly related to the vaccine.  If it is anxiety/depression, I'm totally uncomfortable taking any kind of medicine (SSRI's can cause/worsen tinnitus, which I do not need).  I wish that folks who have had success / recovery would come back on here to tell their stories to give us hope.  I truly don't want to live the rest of my life feeling like this.  I feel like a different person than I was just over a year ago.  

you are right but that is one the reasons that the activity is less now. I guess everyone here tried all recommended drugs,supplements, treatments and there is nothing left to try, there is nothing left to write. 

after 15 months, I guess I am getting used to living with this thing. I still use 24 or 32 mg prednisolone everyday (16 mg morning 8 or 16 mg night)and If I try to decrease the dosage I immediately get worse.

I also started to use tramadol(ultram) and it changed my life. It is an opioid and it is the only pain killer that worked for my bone pain and pins/needles and heat attacks. I no longer feel constant pain but some brief attacks  thanks to tramadol. but it is a pain to get prescription because for some reason the doctors are so reluctant to prescribe(they think I might get addicted to it).   as long as it stops the pain who cares if I get addicted to it!! apparently my doctors do!!. theyt dont care about my pain, they dont care about how I struggle everyday but they do care if I get addicted to a painkiller....I dont know what to say. So if you have  bone pain and pin/needle type neuropaty you should try tramadol. I tried gabapentin , cymbalta, and several other painkillers before tramadol but they had like 0 effect. and the good thing is it has no side effects for me. cymbalta had so many side effects but no real effect at all. 

I also tried 10 day continous prolonged water fasting. I was planning to go at least 15 days but unfortunatly I had to stop becauase I  lost 8 kilos in 10 days (55 kilos) . I was already underweight to begin with  so I had to stop. I realized that I can go easily for 20 days or more. So now I am trying to gain weight and then I will try for a longer period.  I felt a lot better after fasting but it was not a cure. many sources about prolonged fasting state that for serious diseases like cancer, autoimmune diseases fasting period should be longer than 30 days and close to 40. I dont know if I can do 30 but I will retry as soon as I am over 75 kilos. (I am 65 kilos now so 10 more kilos left). As your body starts to starve, logically it starts to eat unused/unimportant cells, so the longer the fasting period, the more spike proteins should be removed. 

I am still thinking about getting apheresis but my conclusion is that it just gives some temporary relief (at most like 2/3 months for some and no change at all for some) and then everything comes back. so I am not sure if is worth it. 

I am lucky Tinnutus and dizziness not come back yet, I still remember the horrible days with nonstop tinnutus.  I am still not sure how I get rid of it but perhaps it was the blood cupping done at the back of my ears. They actually let the dirty blood full of with toxins jammed between the cells  behind your ear out of your body. so I guess it was how I get rid of tinnutus. it is also called hacamat. I know the procedure seems a little painful but I felt no pain and I was relieved. Now I do hacamat once per month on my back and legs to remove the dirty blood full of with spike proteins, I am pretty sure it helps a lot.

so most of the time my life is very close to normal but I am very worried about my dependence on cortisone. I dont have any short term cortisone side effects, but I am worried about long term side effects of it like osteoperosis/osteonecrosis.   I dont really care about tramadol since it seems to have no side effects other than addiction. I am very lucky it worked on me. 

 

 

Hi there how often were you taking the serc? I tried it in the beginning it did make me nauseous but I didn’t notice if it made a difference at the time when this was alll stated I think I was looking to be normal once again and when It didn’t then I gave up immediately on anything. Because what serc does is improve blood circulation to the ears…I’m wonder if the inflammation to the nerves in our inner ear parts are affected by this. And with improved blood flow can help restore the inflammation, I’m wondering and thinking. I wonder if that’s what happened in your case. And the cupping too makes sense of any heavy metals or toxins in that specific area. Cuz I’m a believer of acupuncture and cupping as acupuncture helped with my back problems. Cured it 95%. After years of suffering. Anyway yeah I was wondering about the dosing too like how much serc a day you were taking? and how often ?

 

 


   
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Dhalia
(@sweetie)
Active Member
Joined: 10 months ago
Posts: 12
 

A must watch

https://www.oraclefilms.com/safeandeffective


   
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Utkris
(@kristinriderre-com)
Active Member
Joined: 2 years ago
Posts: 3
 

After 18 months my son was finally diagnosed with POTS.  This is the first "diagnosis" he has had since getting sick.  I suspect there are more things to come, who knows.  He was told to take 6-8 grams of salt per day via salt pills and increase water intake.  Severe nausea and stomach pain since starting the salt pills. He's working up to a gallon of water a day.  This is all so awful.  

 


   
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Thisistoomuch
(@margaret2022)
Very Active Member
Joined: 8 months ago
Posts: 216
 
Posted by: @sweetie

A must watch

https://www.oraclefilms.com/safeandeffective

Oh my goodness. I am lost for words. I wish there was someone who would be held accountable for all of us. This sucks. These ppl are still suffering 

m


   
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Thisistoomuch
(@margaret2022)
Very Active Member
Joined: 8 months ago
Posts: 216
 
Posted by: @stars182

@margaret2022 Any improvement in your T?

No improvement. None what’s so ever. It’s actually getting worse. I’ll be 9 months in soon. And my anti body levels dropped 1000. Was 1927 in April checked sept 2nd they are 900’s. I’m not even sure if it’s related. I’m guessing this vaccine triggered an vestibular injury that’s probably why I felt the pain behind my head followed by that 3 second dizzy spell and now my brain can’t reset itself. Or if it’s inflammation. I’ve read prednisone didn’t do any good for some ppl. With their tinnitus. So I’m not sure anymore. Just hate these rough days. I wish someone could tell me what it is and what to do. Like ohh yeah it’s a nerve issue here take this. Or it’s a mitochondrial issue start on these herbals. Like I never met anyone that even offered to try this or I’ll refer you to this person. There has to be someone out there that knows what labs to test for and see what can be offered to help. I’m worried this tinnitus will get worse and it’ll ruin my life even more. I’m constantly telling people to keep it down at work or at home I feel like such a burden. I might as well stay home and quit my job. So I’m not making others feel miserable. When they’re around me. I just hate it. All I hear is this loud hiss. And my ears are so sensitive. It’s over and over. And every time I go to the doctor I always get worse. I’m not sure anymore. I just feel so beat. I notice too if I have a night of crying my sensitivity gets much worse it does eventually ease up it could take up to a week but it’s still there and still awful. How are you holding up. Also I have issues with my eyes where they feel like they don’t work together. It’s awful. It hurts me to yell. When I’m going grocery shopping too at the supermarket it’s overwhelming for my head and eyes and ears. It’s awful. I hate the government so much. I honestly don’t know if it’s even a vaccine injury because everyone tells me it’s not and I’m starting to believe them. I’m just a ball of mess and all over the place. I was never this type of person as well. This is not me it has changed me. I’m afraid for my marriage and my children. Not sure what this will do for my future. Some days I feel like quitting my nursing job. But I love my job I love my patients. And I love  my colleagues well most of them there’s the odd one or two that I think despise me but that’s their problem lol. Anyway my rant of the day.


   
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