Thank you so much.
“We” don’t pay tariffs, the countries importing into US do. Will they raise prices/inflation? Sure, I guess, but that’s a shorter-term pain I’ll take to get to eliminating or decreasing income tax, etc. Not an economist, and my husband has the same concerns, but my two cents.
Thank you for this link!
That’s awesome - thank you for sharing!
Main paper links others. Here’s the chronic pain/muskuloskeletal link: https://www.midwesterndoctor.com/p/dmso-is-a-miraculous-therapy-for
Appreciate prayers for my mother. She has an appointment with a neurosurgeon about her Trigeminal Neuralgia today. I think, for her, it’s mostly to rule out the invasive MVD procedure and hopefully get clarity on other options she may pursue. I have posted before and know some of you have offered suggestions. I am hoping between this appointment and her next neurologist appointment in about a month some clarity comes and she will finally be willing to start making changes she can control to really help herself more (diet, vitamins, dmso, working through past trauma/conflict, etc.). 🙏
When the show was cancelled the writers worked on the comics. Season 3: Civil War. There’s also a Season 4.
Love that show. I’ve been meaning to rewatch it and read the comics.
I don’t think most here think these are unavailable. It’s about the lies perpetuated that normies still believe and widespread availability with clear dosing for humans without guesswork. IVM as horse paste and FDA telling us we aren’t farm animals (while simultaneously herding people like farm animals at fairgrounds for testing, ironically) was powerful to and damning to many people. I know people who believe in IVM that won’t take horse paste. GL with normies, even with pills. This is way bigger, imo.
I just found this, looking for info on holy basil as I’m a few days in using a tincture and it’s a game changer. Glad the mods left this up so I can see the brand you used because the tincture is a bit pricey. Have you continued it? How is it with longer term use?
Also: https://truthsocial.com/@DC_Draino/114144251555462661
Hadn’t seen this here, just know there’s been some confusion around what’s going on and thought this may be some good context on why DJT wants to primary Massie.
There was an anon who posted about trying Fenben with his dog just about a year ago (user 94f450d). He believes he started too late, but you can read his posts and comments, he kept us updated for about a month, here is the first day’s post: https://greatawakening.win/p/17sP6WsL8W/gonna-try-the-fenbendazole-cance/
This is the blog he was inspired by: https://www.prairiedoghall.com/curing-my-dogs-cancer/
You can buy panacur powder for dogs based on weight, but not sure on frequency and dosage for cancer. Liquid will be cheaper longer term. You can search through Truth/FloridaSharkman for more details. I’ll update if I can find it. Someone mentioned IVM, not sure that’s safe for (all) dogs.
Edit: Recent Q and A in dose for protocol B (cancer) for dogs:
https://truthsocial.com/group/floridasharkman-parasite-protocol/posts/114095350854333747
Protocol itself: https://www.floridasharkman.org/protocol/protocol/FloridaSharkman-Protocols.pdf#page14
I agree sun is best but not sure about supplements being toxic, I’ll have to look into that. I have recently heard that if you get enough sun in warmer months it can sustain you through winter, which I also had never heard.
Oh my goodness, thank you! I’ve run into the idea that the herpes simplex virus may be in the nerve. St. John’s Wort - are you able to take that with your gabapentin? I’ll have to look up interactions. It’s my mother, and I so would love her to try something more natural if she can get a reprieve and get off the other meds, but I do understand it has to be done safely. I also think she should be tested for vitamin levels, I suspect that is a factor too. Think she was diagnosed with fibromyalgia a decade or so ago, too, and has had migraines forever. It’s surely related and progressing, in my mind. God bless you, Fren, and good luck with your issues, too.
Family member has trigeminal neuralgia. They hit toxic on carbamazepine and have to scale back, leaving them in excruciating pain. I believe the neurologist wants to try this new Rx. I have researched supplements and other therapies, etc. but as they say you can lead a horse to water but can’t make them drink. Pharma has provided the only relief they’ve known and they are scared to take natural things due to potential interactions with the other Rxs. 🤦♀️ Hard to watch, so I support by encouragement and research and prayer. Thank you, moody, for sharing what has worked in your case.
A family member has trigeminal neuralgia and is facing anti-seizure meds not working anymore/toxic levels so must just live with the pain, or possible brain surgery. Not sure if this would be considered chronic, but I believe the neurologist has suggested it as last Rx option (never taken opioids) so maybe the attacks or episodes are considered acute? In any case, if/as I learn more I am happy to share here for anyone interested.
Yea, not enough long term studies. I read it hasn’t been so successful for sciatica.
Yep. I think someone I know may get to try this soon, not sure if it would be off-label or not, I just don’t know enough about pain. It concerns me while also holding some hope.
Yes, ty for the links! Seems you can get it soon, maybe depending on where you live and the condition.
Anyone have any experience or anecdotal info on the new pain med suzetrigine, brand name Journavx? Not sure if it’s even able to be prescribed yet…
Excellent point, too.
Hadn’t heard this. Sounds like spin on what happened during budget. Bold emphasis mine.
Originally, the spending package included the following:
-the Gabriella Miller Kids First Research Act 2.0., which would have extended the National Institutes of Health’s Gabriella Miller Kids First Research Program,
-the Accelerating Kids to Research Act, which would have made it easier for children from low-income families on Medicaid to receive specialized cancer treatment across state lines
-the Creating Hope Reauthorization Act, which would have extended a program incentivizing pediatric drug development that has already resulted in the development of 65 new medications
-the Give Kids a Chance Act, which would have allowed children with relapsed cancers to undergo treatments combining cancer drugs with other therapies
Despite members of Congress initially agreeing to include the above-described provisions, all mentions of pediatric cancer funding were removed from the final version of the spending package. Although the Gabriella Miller Kids First Research Act 2.0 was ultimately revised and passed as its own standalone bill, the other three provisions remain in limbo.
As another said, check FloridaSharkman (FSM) on Truth.
Here are his current protocols: https://www.floridasharkman.org/protocol/protocol/FloridaSharkman-Protocols.pdf#page14
Here are links to a few Truths from FSM related to esophagus cancer and Barrett’s esophagus. Short answer, sounds like he would recommend to start on the antiviral (AV) protocol, then B until resolved.
https://truthsocial.com/@FloridaSharkman/114100847532579183
https://truthsocial.com/@FloridaSharkman/114100860029591157
As an aside, if your friend insists on traditional chemo and radiation, IVM in particular will probably have studies showing it makes the chemo work better in a synergy. Similar with DMSO, which can also protect from radiation. That radiation will be super-rough. GL, Fren.