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Questions answered on the Live stream

Hey everyone! Here is a cut down of all the patreon questions Kyle answered on the Live stream. That way you guy's don't have to sift through 11 hours off footage to find them.

Again, thank you so much for the questions! We wanted to let you know that we're sorry not all questions could have been answered. Kyle got to as many as he could. He said honestly that the questions were so good, he could have filled the whole stream with them. Thank you so much for participating, Kyle said they really helped guide the stream. And we hope you got some useful answers here.

Thanks again everyone!

Comments

My heart skipped a few beats when I saw her looking better.

Robert DuPlaine

The interview with Dan Neuffer on the Health Rising YT channel is interesting.

LK

Read Ren’s comments at the bottom of the video. Sounds just like Diana.

Paul Ljucovic

I don’t know if you’ll see this. But just watched a video by Ren, a singer/artist. He was misdiagnosed for 10 years. Turns out he had Lyme disease. Symptoms eerily similar. Stem cell transplant saved his life. https://youtu.be/jaltehH_cNo?si=aIumIUg0I561FP9j

Paul Ljucovic

For you guys, I always keep an eye out for news of developments that bring hope of treatment for long COVID. Here's the latest article that I found: https://www.psychologytoday.com/us/blog/shouldstorm/202406/long-covid-looks-like-acute-infection-in-the-brain Researchers have narrowed their search, for an immune molecule to manipulate in order to improve long Covid, to interferon lambda.

Jean-Philippe Suter

Dear Diana and Kyle after a so long fight for life… please take your time to have a look on YouTube at @TheDiaryOfACEO Interview of Dr. Tim Spector and Dr. Wolf …. Or is it Wulf 🤔 The founders of Zoe.com ! It saved my life ! Hear them out it saved my life ! I have no affiliation with them . Love , Respect and hope from Sparta …. The old on…. In Greece .

Taleton

I am a paraplegic. I had a severe spinal chord injury when I was 29 and i am a complete paraplegic. I am now 65. Pressure sores have been something I have had to deal with, both from sitting in my chair and while in bed. It is one of the most covered topics while I was first injured and in rehab. I am wondering what kind of bed you are using. I have slept on everything from a regular spring mattress to advanced solutions wjile hospitalizef costing tens of thoudands of dollars. For the last decade I have been sleeping on a Sleep Number bed. They not only use air that distributes your weight more evenly, but they have incorporated what they call "responsive air" that changes the pressure on different parts of the bed effectively giving some pressure relief. These beds run from $2,000 to $5,000. But the extra money is for the extra "fancy" padding on top of the mattress. Mine is on the low end and I am a ridiculously enthusiadtic customer. I can not recommend these beds enough. I also have money and I would be willing to defray some or even most of the cost. If this sounds like something that interests you, you can either call Sleep Number or you can call me. I would be more than happy to help. Tim Kirwin Charlotte, NC tim@kirwin23.com 803-984-4581

Tim Kirwin

Thank you for making this video, as I couldn't follow the entire livestream. It does my heart good to hear the questions and answers but even more to see Dianna doing all she can, when she can. That determination and drive are still there and I can see that both she and Kyle are not just being smart about her recovery and needs, but being wise (which is kind of harder and more frustrating). I send you both love and support and my good thoughts for Dianna's system to be guided to recovery. Hugs!

Judith Montel

Levi, I would like to send a message to Dianna and Kyle. It may be a long shot and tough for them to believe as scientists but I am a mechanical engineer and disabled and have had some results from what I want to send to them. If they are interested you can contact me at this address john.shone920@passinbox.com

john

I've been wondering that, too. It wouldn't be surprising if it had an impact, but hoping so hard that it was minimal.

Carey Earthman

My wife and son suffered from long covid for almost 2 years after we all were infected in early 2020 well before the vaccine was available. We had recurring rounds of micoplasma pneumonia, my son stopped walking due to neuropathy and I lost sensation in my feet with poor blood circulation. My wife being an engineer and very in tune with her body and health quickly discovered a major link to histamines and her symptoms… her diet that allowed her to function consisted heavily on air fried broccoli which is the only food that she could tolerate. Eventually she was prescribed a solution that she ingested every meal to neutralize the histamines. This was one of the first turning points for her. Soon after we got involved with Dr Patterson’s long COVID research and discovered that most of the cytokines that were found to be associated with long COVID patients were 100s of times over threnormal levels of healthy adults. I was also tested and found to have cytokine levels that were significantly elevated and was prescibed an HIV medication off label to specifically target those cytokines and bring them back to normal levels. This was a breakthrough in my own recovery from long term fatigue after having contracted COVID. My wife was given multiple other medications targeting the specific cytokines that were elevated in her system and for a while she was getting better! Much better! It didn’t last forever though, based on more recent research she has been a part of, she has had persistent virus in her gut this entire time causing her to have flair ups of COVID out of the blue when we don’t go anywhere or into any public indoor spaces. We also were having regular flair ups of mono/EBV which has also been recently linked to COVID and long-COVID. After suffering liver damage and spline damage from the repeated EBV illnesses and having research data that showed the had persistent virus in her gut, she started on an antiviral regiment and probiotics to flush her gut and knock down the virus. Finally after a year of constant spline pain and limiting physical exertion to avoid further damage or hospitalization, she is regaining her ability to garden without crashing afterwards and being exhausted for days. There is a road to recovery, it may be a long one but from what I have seen from the videos including Dustin’s, you are doing everything right that you can do. I would encourage you to look into Dr Patterson’s research and protocol which aims to bring the immune system back under control and I would encourage you to have your gut tested for persistent virus as it is the perfect place for the virus to hang out while avoiding the immune system.

Benjamin Thompson

Hey Kyle! Thank you for being such a strong power and support in Diannas life. I don't think I know any person that would be as strong as you in such a situation. Hey Dianna! Thank you for being you, and for everything you have been giving us. My fingers are permanently crossed for you, and I hope at one point you will be able to stand up strong, and say "I did beat this!". Until then, our thoughts are with you. Always.

Robert Voje

I dont know if you've seen this yet but i saw this recently and thought of you guys... https://www.iflscience.com/signs-of-covid-virus-in-the-body-years-after-original-infection-75084?fbclid=IwZXh0bgNhZW0CMTAAAR370zHCEWop-x2ncI5V5O4Gx7x0ZZ7L9FCsu7JBLhoJVyJWWLuwteLKAgU_aem_ijQqdSEBGu919kCzVmLB5g

obie19

I don't suppose she can tolerate creatine? Maybe that can help maintain muscle and help with energy?

James

I am moved immensely by Kyle's courage, grace and determination in helping Dianna. My wife and I in Australia are thinking of you both during these difficult times.

Eng Lee

I only caught the last couple hours (David Putrino interview and on) but since then I have been continuously thinking about some of the things I learned, esp with regards to exercise vs. rehabilitation and what that means for someone with ME/CFS. Super clear informative stuff! Looking forward to digging into the rest of the 11 hours (!!) in the weeks ahead.

Aldona Dye

Wishing you the best! I hope you can listen to audio streaming. I enjoy Wayne Dyer and his inspiring information. I am looking forward to hearing more about your recovery and progress!

Kurt

Feel better

Martin Diderichsen

28:40 We're all rooting for the debut of Swole Girl.

SuperElectric

🥳❤️👍🏿

TwinSteel

I just bumped up my membership to support you two in this insanely difficult time. I would ask everyone here to go up one membership level, it's a coffee for us but it will make a huge difference to them.

Mike Brown

Thank you for compiling the questions for us

Suzanne Strickland

Thank you for all the work to plan and present the live stream. I hope, with time, we can move the needle.

Kevin Hayward

Also how is she doing after being on camera all day? I know there’s usually a delay with crashes—she’s fine right?

Tutor Tori

I was surprised to hear my question. Hoping we all combined are making a positive difference. Thanks so much for sharing what you know, sending positive vibes when ever we can. Best wishes, and please stay strong!

Carlin Comm

Great job Team Dianna!

Perry Berryhill

Christopher Belter of NIH provides lists pointing into the latest scientific literature on COVID. These are the original raw scientific findings. You can see them at: https://list.nih.gov/cgi-bin/wa.exe?A0=COVID19RESEARCH and you (probably) can sign up to get email alerts.

Thomas Schneider

Sending many ❤️❤️❤️❤️❤️❤️ I feel like I understand this disease so much more and I hope that the public awareness and understanding increases as a result of your effortz!

Mary Pittman

Thanks so much for answering my question on the live stream! I think about Dianna regularly, and I am so grateful to hear and see more about her everyday life that she had absolutely no obligation to show us. This is perhaps small comfort, but I have used Dianna's story to convince more than one person about the true danger and repercussions of COVID, even years after most consider the pandemic to be "over".

Claire B

they said theyll consult with Dianna but that theyd like to post the interviews separately :)

Sasha

I agree. I am planning to link to the interview with the doc for a class I teach and was just going to do it with timestamps but a cut out one would be awesome

Limberbutt McCubbins

Diana, I miss your videos and send you energy whenever I think of you! Lou

Lou Volpato

Diana u are a trooper and youll get thru this <3 I have nothing but faith and patience and love

zzzluvsk

I just finished watching the first 6 hours of the 11 hour one! 😂 But wanted to watch again, so this is great 🙏🏽 By the way I wanted to share one of Dianna's videos in an MCAS conversation on LinkedIn--will any informational parts of the livestream be available to the public on YouTube?

Tutor Tori

I study fibromyalgia and worked with folks with chronic pain for years. This sounds so similar to what they experience with ADLs! I am so happy to see y'all persisting despite the challenges and to see this posted because I missed the stream <3 ***edit I did want to share some hope and let you know that is does get better and community is so so important when dealing with stuff like this. You got this!!

Caitlin

Sending so so so much love <3

Xyla Foxlin


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