So there are 3-4 people on twitter that I "follow" because of their LH symptoms and they are trying Tollovid. Some have been given Tollovid to be a case study.
There are others that are in support type groups that have tried apparently anything that someone else says works. Some have 2+ years of declining health. But when I see a person that says they have ordered and then show photos of Tollovid bottles in their hand --I try / follow their progress--symptoms--some of their dosing is "random"
B U T
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Here is woman that used "go fund page"?? she has been unable to work (chronic lyme for 12 years) then Covid: (I will clean the tweets for easier read)
Natalie Goodpaster, PhD
@NKGoodpaster
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16m
Day 11 of #Tollovid for #LongCovid. Very similar to yesterday. Today is probably the best I’ve felt since before Covid pneumonia. Not back to pre-Covid baseline yet, but getting there. Have a little PEM from going to the chiro yest but not much. /1
Cognition is now starting to improve. Still some memory issues and probs following speech (phone calls are tough) but it’s better. I can text a bit better. My voice is stronger. I can take steps without my walker. No immune symptoms, no POTS, no vertigo. Really amazing. /2
Full disclosure: I’ve purchased all my Tollovid up to this point from crowd sourcing funds in my GFM. However I have now agreed to be a case study for Todos and they are going to supply me with at least two bottles so I can do at least 25 days. BEYOND GRATEFUL. ????
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PRETTY DAMN INCREDIBLE for me to read about--hope it lasts for anyone and everyone that has gotten results from Tollovid
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