If you’d like to support Dianna during her recovery, you can do so here →
We just wanted to give you an update on Dianna’s health, since she’s been sick for a while and may not be returning for longer than we previously thought.
Her science videos are postponed until she can make a full recovery. We really appreciate everyone’s support here on her channel. We know Dianna wishes she could be here making videos and happily physicsing, but right now she needs to stay in bed and away from work until she makes a full recovery.
Special thank you to our X-Ray tier patrons: Steven Sorenson, Bill N, Michele Robichaux, David DiCamillo, Joe Pacheco, Anton Ragin, Lydia Fullard, zoddy, dheeraj mekala, David Johnston, Christopher Kemsley, Adrian Archuleta, Zoran Dekic, Austin Rose, Gnare, Bazinga_X, Mike Schneider, marcss, James Prokop, Carlos Patricio, Tommy Joseph, jeremy glowacki, Vishal Bedi, Matt Kaminski, Andrew Herstek, Vincent Argiro, Eddie Sabbah, Patrick Olson, Chris Wyma, Zalster, David Cichowski, Vikram Bhat, Margaux Lopez, Edi, Kenneth Hunter, Fabrice Eap
Music provided by APM
Host: Simone Giertz
Editor/Videographer: Levi Butner
Hi Everyone. Please ignore any comments or direct messages of users asking for donations that claim to either be, or work for Dianna. There are some spam/scammers posing as physics girl to ask for money. The Physics Girl team will never reach out directly through comments or messages to ask for donations of any kind. Thank you.
I have totally missed out on this lady and her videos!
A touching and very nice video by her friend, this! I wish and hope that Diana recovers and can get back to posting more videos, if that's something she'd like to do, but more importantly, that she recovers for her own sake.
Very well done by her friends and family, to help her out like this. ❤
Still here hoping she feels better. I'd hoped I would have heard good news before now. Still hoping things turn around. 😢❤
No I feel bad for her She never deserved to have COVID-19 I hope she'll get better soon.😢❤
I wish her she'll be fine. Accidentely got this channel in recommendations, very interesting. Respect from Russia.
You are a good friend. She will be proud of you ❤
Update:
Reset science suggests there is no such thing as long covid…
So she got soemthing else
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Chronic Fatigue can be caused by many different things but ME/CFS is caused by any of a group of viruses. I had the viral type and sought a cure for 16 years till I found out about microcurrent therapy which I tried and it totally got rid of the virus in 2 months. Slowly I regained my strength and 12 years later at 50 years old I was in the best shape of my life and was doing good at amateur motocross which is really a young mans sport. The 20 year olds which I was leaving behind in my dust were frustrated. Almost no one is aware of the battle amongst the different health recovery groups over a hundred years ago. The most successful therapy by doctors against microbes was this type. But then antibiotics were invented and Rockefeller wanted to make a killing and so he got the US government to conspire with him to silence all the other health groups other than the emerging pharmaceutical group. So the government went around to all the medical schools and threatened to remove their government approval if they didn't stop teaching all the other health modalities, especially the most successful one which was electromedicine. After 10 years electromedicine was completely forgotten.
Although I regained my health, the long term CFS infection left me with a weak immunity and so I was in the biggest risk group for Covid. But when I got Covid and started feeling my temperature higher I immediately did a 4 hour treatment and felt fine the next day. I continued with 2 hour daily treatments and other than a slight lung irritation by the virus felt no symptoms.
Long covid isnt real
hope you are well 😊
New here. All best to all from the UK.
Check out the FLCCC protocols – they are the real life life-savers.
At last! Answer this simple question! What percentage of patients with long COVID is vaccined?
It has been a year since this video how is she doing today hopefully she's well and out and about❤
I have been battling me/CFS as well since 2022. I was 21 and I’ve been bedridden pretty much daily since.
I miss Dianna. I hope she recovers soon. I can’t imagine what she is going through. We love you!
Wishing Dianna all the best for the future ,hurry back your missed .
My step-daughter has long covid and it seems to have triggered a latent thyroid problem which only made matters worse. Even then, she is nowhere in as bad a shape as Dianna. My heart goes out to her husband and wish him the strength he needs to get through this. He is one in a million.
I have ME/ CFS, and there is a lot of misinformation about it. ME/ CFS isn't getting tired, as in being sleepy like narcolepsy. It's crippling muscle weakness akin to MG/ MS etc., in which they baseline reduces. However, it's more than just muscle fatigue. I've had it for 9+ years. At my worst, I was bedridden for a whole year, unable to tolerate any stimuli; light, sound, touch, temperature, etc. I was left in a cold (constantly 16 degrees Celsius which resulted in frost nip, but I couldn't sweat due to anhidrosis, so I had no choice), dark room, and and earplugs constantly, which resulted in blind spots, and constant tinnitus/ muscle ear syndrome/ phantom sounds. I couldn't talk. I couldn't shower, as every water droplet felt more painful than a tattoo gun (coming from someone who is covered in tattoos). I developed allergies to everything, I did not have allergies to prior. I could not even use my phone, or watch tv to waste time, nor sleep as I had sever insomnia. I just laid, slowly losing my ability to think as my imagination disabled and would send electric shocks down my CNS, and brain cramps if I did. It's hard with ADHD to force yourself not to move. It's not like I didn't want to move, I was restless, and every time I tried, I'd get severe air hunger, and PEM which was a severely crippling electric shock that went down my CNS into my wings, disabling me for moving for hours.
However, I am mostly recovered (just cannot do extreme exercise everyday without rest), at least enough to live semi-normal due to a drug LDN (0.13mg is my sweet spot), which seemed to have neural anti-inflammatory effect to my HPA-Axis dysfunction (pseudo Cushing's, constant fight or flight).
Ivermectin zinc nattokinase, nicotine, pine needle tea, dandelion tinture.