what have people found helpful? and what are people doing to heal themselves?
i have found the MRI brain/spine and autoimmune tests helpful in ruling out other causes. i have been eating healthy and keeping active to heal. not taking any medications or supplements. not sure is time helping, or the healthier lifestyle
@hopetofeelbetter Thank you; I'll keep an eye out for the lower dose. I did great with it on Saturday; perhaps taking it two days in a row was too much for my system. I was shocked at how quickly it eliminated the pressure in the back of my head and I was hoping it was something I could continue using.
I may also try Nasalcrom - it's supposed to be a mast cell stabilizer (?), which several people have said helped on this forum!
@nodiagnosis Thank you. My provider suggested I try a CT if my symptoms didn't get better, but this was a month ago. When I go in to see her again, I will ask for an MRI.
@rainyday CT is likely more accessible and more cost effective, but there's a radiation dose involved and it won't provide any information on structures such as the nervous system. MRI is gold standard and with no radiation dose but is likely less accessible and more expensive if you are in a country where free healthcare is not accessible to you or you are without health insurance. A CT is worth having if that's all that's available to you - it's going to rule out most things! However, you should certainly see is an MRI available to you as your first port of call.
@nodiagnosis I will definitely try for the MRI. I'm in the U.S. and the cost of healthcare is through the roof. At this point, though, I'm willing to do or try anything.
Earlier you asked if anything has helped anyone on this forum - Vital Nutrients' BCQ supplement has helped me and it provides relief from the inflammation and odd nerve sensations I've been experiencing. It's costly (at $55 per bottle for 120 capsules), but it's been the only thing that has consistently provided relief.
I'm taking a multivitamin, CoQ10, and Vitamin D3 as well. I've found cutting inflammatory foods, dairy, and sugar has helped as well, if only marginally.
what have people found helpful? and what are people doing to heal themselves?
i have found the MRI brain/spine and autoimmune tests helpful in ruling out other causes. i have been eating healthy and keeping active to heal. not taking any medications or supplements. not sure is time helping, or the healthier lifestyle
Can I ask what autoimmune tests you are referring to? And I am assuming your results were normal?
As far as what I am doing and what is helpful, I'm still at the early phase (2 months) where I can't tell if its time that is helping or what I am attempting to do. I for sure notice that caffeine, alcohol, stress, and even exercise make my symptoms worse. I have been drinking excessive amounts of tea (decaffeinated) and taking vitamin C, D, and omega 3s. Its so challenging to tell what is actually helping because my symptoms fluctuate throughout the day.
Has anyone tried Flonase, Nasacort, or Nasalcrom for head pressure and brain fog?
I've seen all three suggested throughout this forum.
I tried Flonase on Saturday when I felt head pressure and brain fog coming on, and within 15 minutes, they were both gone. I was thrilled!
However, when I tried Flonase again on Sunday, I became extremely weak and fatigued 15 minutes afterwards. I didn't have the head pressure or brain fog, thankfully, but I felt severely physically sick - like one does with a nasty flu.
Now I'm wondering if it was just a coincidence or if the Flonase could have caused this. I'm disappointed because, for whatever reason, it stops the head pressure and brain fog from occuring - which is by far the worst symptom I have. Maybe I should try Nasacort or Nasalcrom instead? Or perhaps these would cause the same reaction? Now that I'm thinking about, the one time I took Xyzal, I felt the same the next day. Maybe my body can't tolerate allergy medicine?
I felt so poorly yesterday that I started crying in front of my four-year old. The stress, fear, and sickness of the last eight weeks came pouring out. I felt guilty, but I couldn't stop it; this is becoming unbearable. I'm not sure how I'm going to work today. It's going to be one of those "take it a minute at a time" days.
have you tried checking your neck?
i found that my neck muscles are incredibly tense, along with my shoulders. when i put heat on my neck it relaxes my muscles and the pressure/tingling on my head eases. also when i massage my shoulder/neck it helps, along with my face muscles.
tight muscles in those areas can lead to headaches, tingling and pressure in the head.
just something to think about if you haven’t already. <3
what have people found helpful? and what are people doing to heal themselves?
i have found the MRI brain/spine and autoimmune tests helpful in ruling out other causes. i have been eating healthy and keeping active to heal. not taking any medications or supplements. not sure is time helping, or the healthier lifestyle
At the top of the page use the magnifying glass and search these.
- anti inflammatory
- youtube
- nerves
- b12
- vitamin
- vitamin d
- vitamin b12
- diet
- ivermectin
- presidone
- CT scan
- MRI
- dose
- medication
- supplements
Has anyone tried Flonase, Nasacort, or Nasalcrom for head pressure and brain fog?
I've seen all three suggested throughout this forum.
I tried Flonase on Saturday when I felt head pressure and brain fog coming on, and within 15 minutes, they were both gone. I was thrilled!
However, when I tried Flonase again on Sunday, I became extremely weak and fatigued 15 minutes afterwards. I didn't have the head pressure or brain fog, thankfully, but I felt severely physically sick - like one does with a nasty flu.
Now I'm wondering if it was just a coincidence or if the Flonase could have caused this. I'm disappointed because, for whatever reason, it stops the head pressure and brain fog from occuring - which is by far the worst symptom I have. Maybe I should try Nasacort or Nasalcrom instead? Or perhaps these would cause the same reaction? Now that I'm thinking about, the one time I took Xyzal, I felt the same the next day. Maybe my body can't tolerate allergy medicine?
I felt so poorly yesterday that I started crying in front of my four-year old. The stress, fear, and sickness of the last eight weeks came pouring out. I felt guilty, but I couldn't stop it; this is becoming unbearable. I'm not sure how I'm going to work today. It's going to be one of those "take it a minute at a time" days.
have you tried checking your neck?
i found that my neck muscles are incredibly tense, along with my shoulders. when i put heat on my neck it relaxes my muscles and the pressure/tingling on my head eases. also when i massage my shoulder/neck it helps, along with my face muscles.
tight muscles in those areas can lead to headaches, tingling and pressure in the head.
just something to think about if you haven’t already. <3
Since my vaccine 2+ months ago I have had constant neck aches, headaches, anxiety and a lot of other symptoms. Early on, I tried working on my neck muscles and even went to get a massage. Each time I tried working on these muscles the next several days all of my symptoms were significantly worse (especially the chest tightness/anxiety). I have no idea why it happened or if it was just a coincidence, but it happened every time. Its the weirdest thing because you would think it would have the opposite effect, or the benefits you listed.
Hello all,
Just a positive update. I'm now 3 months after my first and only Pfizer jab and I can report I am 95% better since more than a month with no major relapses. I already had days where I am 100% back to my old self. A positive update about my eye floaters, they are still there but they are getting smaller and more transparent with each day. My left eye is almost floaters free now. You can read about the symptoms I had in my past posts. I was more active on the forum about Tingling and Numbness cause those have been my most persistent symptoms (still have mild tingling sometimes in my limbs). 2 months ago I thought I was about to die, my symptoms were so awful, but there is hope. I didn't take any meds, just vitamins and lots of rest, meditation and walks even when my legs were hurting. I also had unexplained bruises in my legs hat I didn't link to the vaccine at first. Ater reading about other people experiencing this side effect I added it to my list. This symptom is also gone.
I was denied the exemption. I will never get the second shot. I am Germany based and it looks like it will become mandatory next year. I'm so sad about the lack of support and most of us being dismissed like we are crazy. All this suffering has to end.
Sending lots of energy and love your way.
Thank you for the positive report. I have the tingling and cramping, and I had a good weekend, but last night I had terrible tingling through my whole body. It gives me hope you are improving. I don't want to get another booster ever again. These symptoms are frightening.
Hi guys, my cardiologist just called me regarding my medical exemption for the second dose. He asked me how my side effects were, I said I still have lingering side effects but feeling a bit better. I told him I also have ocular issues. He said the vaccine doesn’t cause vision problems, he told me not to believe everything I see online LOL. Some of these doctors need to come on this forum.
The way these doctors are brushing us off is ridiculous. This cardiologist suggested me to take the second dose even though I had a laundry list of side effects including a pericarditis. ABSURD.
@milena90 I saw a video on YouTube that a man who was suffering from tinnitus after the vaccine said his symptom started to subside after a few months and by 6 months it was completely gone. I know that sounds like a long time but the healing process is also different for everybody. Just know it’s not likely that you will have it forever!
Thank you for this...I really needed to hear that!!
@jacquelynsauriol My faith in the medical community has dwindled significantly since this began. I'm not sure WHY providers aren't linking the vaccine to the myriad of side effects we've been reporting. Is it because they're afraid they'll lose their license? Is it because of pressure from colleagues - or pharmaceutical companies? Is it because they are truly that blind that they aren't able to make the connection that vaccines = side effects? I'm in disbelief.
Perhaps the FDA and CDC did believe the vaccines were safe with the limited data they had in the beginning. But it's been twelve months and I am positive they are now aware that they are not safe for everyone. Why not come forward with that information to the public - and especially the medical community?
The lack of transparency from the FDA and CDC is grounds enough to sue, in my opinion. If they are suggesting - even mandating - that the WORLD'S population receive these vaccines, but they are purposefully withholding vital information about adverse effects from the public, I would think they are opening themselves up to be sued out of their minds. But to do that, we're going to have to have hundreds of reputable scientists, virologists, etc. openly admit that these vaccines are harmful. And that's going to take a long time.
The mRNA seems to act the same as the COVID spike protein and my theory is that it's affecting our individual immune systems the same way COVID would. That's why we're seeing so many different reactions and timelines for healing - and why some people have no reaction at all. I think we're reacting to it the same way we would have reacted to COVID itself. Long story short, it's as if we're injecting ourselves with COVID.
Except it's worse, because we are injected with 60 - 200 micrograms of the mRNA (with Pfizer being 60 and Moderna being 200 after two doses) and our body has no way to stop it or lessen its severity (as it would if we were to acquire the virus naturally.) AND the vaccines come with additional toxins, such as polyethylene glycol, that our body must fight in addition to the spike protein.
The entire thing is a mess.
Exactly Put!!!
I have been doing some research on docs who treat floroquinoline toxicity. Dr ghalili in the US. One thing I have found is those patients have the same brain fog and other side effects from taking cipro or Levoquin. I have had a severe reaction to levoquin similar to the one I had with the shot but didn’t last this long…..just wondering if there is a connection. Those people also have all their tests come back fine