Jessica Nohren

#Iran #นักการเมืองหญิง #AsLaz #Als #endals #MND ##motorneuronedisease #lyme ##lymedisease #misdiagnosed #chronicillness #miraculous #Healing #saved #testimony #HappyEnding

@dralmiller Jared is from Texas diagnosed with ALS in 2023- he also discovered he had tickborne infection. Treatment has resulted in slowed/stopped progession, voice improvements along with Strength gains- Today he works a construction job- coaches baseball and continues to improve

@dralmiller Thank You. I am also going to have 3 other Reversals/ sustainable improvement from our Group reach out thru email...Faiths ALSFRS score was 27 in 2024. On April 22 2026 after treating TBI her ALSFRS score is 48. And the head of Neurology removed ALS from her medical records.

Just published! amazon.com/dp/B0GX3DDWPP/…

@dralmiller Bob is from NJ- He was diagnosed with ALS in Aug 2020. He was bedbound before treating tickborne infection and is now back to instructing Golf. He no longer had to treat tickborne infection. His only remaining issues are numbness in his fingertips.

@JessicaNohren Yes, have your mother's physician contact me.

@dralmiller @Caner132134q Thank You Dr Miller for all you do for the Lyme Community! I can't wait to read!!

@Caner132134q amazon.com/dp/B0GX3DDWPP/… just published!

@RWMaloneMD There is an entire community of people that have been diagnosed with ALS/MS and they actually have tickborne infection. My mother was diagnosed with ALS by Mayo clinic and others with EMGS that indicate ALS. Shealmost died. Before we got her into a Lyme literate practitioner

Declassified Documents Link U.S. Bioweapons Program to Lyme Disease Outbreak Exclusive: Military released 282,800 radioactive ticks, suppressed co-infection research for 40 years malone.news/p/declassified…

@patrickG731 Have you had accurate blood testing for tickborne infections?

@ThePOTSPostman Undiagnosed tickborn infection

I’m trying to learn more about MCAS. Not sure if I have it, I do have hEDS and POTS, so it would make sense with the devils trifecta. I know a lot of my followers suffer from it so can you please help educate me. My ENT ran a blood test on me and she said I didn’t have it through that but from what I have seen more extensive testing is needed.

#ALS #MS #Parkinsons #dementia #therootcause #borrelia #lyme #awarness #education #matters #openyoureyes #youdonthavetodie

@stella_chadwick Look into Borrelia and Bartonella

🔬 Back in 2018, research highlighted a potential link between gut bacteria, specifically Lactobacillus reuteri, and autism symptoms. Early studies in mice showed promising results, leading to small-scale human trials. While these trials have shown some improvements in social functioning, much more research is needed. ❓ We must ask: Why aren’t we pushing for more extensive research in this area? Many children are suffering from debilitating comorbidities alongside their autism, and we owe it to them to explore every potential treatment avenue. 🌟 If you're thriving as an autistic individual, we celebrate that—different experiences are valuable, and every perspective matters. But we must also recognise that not everyone’s journey is the same. For those facing significant challenges, we have a responsibility to continue researching and seeking solutions. 🚀 Let’s advocate for more studies and faster action. There’s potential here, and we can’t afford to wait. Citation:
📖 The Economist. "Gut instinct: Probiotic treatment shows promise for autism symptoms." Published 31 May 2018.

📰 TMC News, "Can autism be treated with a simple microbial-based therapy?" 2024.

As Lyme Disease Cases Spike In Illinois, Researchers Offer Sly Solution dlvr.it/Pc1xv0

Officials report an 'uptick' in Lyme Disease in Illinois.. Some tips to keep your family protected this weekend! wgem.com/story/35685945…

Lyme disease on rise in Illinois chicagotribune.com/news/local/ct-…

Illinois sees growing number of #Lyme disease cases. Girl bitten while walking to class on college campus. bit.ly/1BupDto

People don't like when I say it, but I call Lyme disease "covid of the woods". It's hyped up to be this big bad malady, and there's always a few nutballs who say that Lyme radically altered their lives (reminds me of "long covid"). Lots of people won't go in the woods anymore without basically wearing a HAZMAT suit. But I myself was diagnosed with long-term chronic untreated Lyme years ago. I was experiencing intense fatigue -- and then after a monthlong course of Doxycycline, I was good to go. Have since gotten many tick bites, including one with the "bullseye rash". No big deal. No doctors visits or problems of any kind to this day. I actually quite wonder if Appalachian folks worry about this disease as much as Northeastern Yankees do. They seem less prone to medical hysteria than us northerners. Hell, if Lyme was in the Deep South I can't see anyone down there letting it keep them from going hunting and riding out in the woods either. I don't let it keep me from camping or being in the woods. I'll wade in tall grass all day not even thinking about ticks and I'm always fine. Maybe I'm nuts but I'm not buying the whole "stay out of the woods because of a vague disease" thing.