@Wayne - thanks for those links, but I can't see anything there that indicates DMSO can reduce brain inflammation.
@Hip -- Brain swelling is mentioned in this study: -- Dimethyl Sulfoxide Lowers ICP After Closed Head Trauma
Hello Stretched.Thanks for posting this article. His premise sure sounds and ‘feels right‘ to me. I’m ~30 years PWC and last year sprouted peripheral neuropathy, which is very painful in my feet. Further, I fell bad last Sept, 2019, and had a concussion. I’m now suffering post concussion syndrome. It’s symptoms are like a CFS crash with nausea and more brain fog. I think all this is interrelated; all symptoms are now compounded, ugh=&.
I sent the article to my neurologist: “If you buy into this, as I do, can you think of any medications that might treat my brain?” If he answers I’ll post his reply. (He’s a young type A, in high demand, who also believes MECFS is caused in the brain.) Fortunately, he’s been supportive with lots of blood work and image testing - unusual!
Hello joe.I can only look at it empirically, as there are dozens of potential explanations in theory for feeling the way I've felt for now 13 years and the way thousands of people feel. The chronic infection was a major and very convincing route to try out, took a ton of antibiotics for a while, never changed a thing. The adrenal fatigue was another, gave that a shot with treatments, nothing. Earlier there was the whole detox thing: 'my body is full of accumulated heavy metals', do a hair tissue mineral analysis and then treat with coffee enemas and regular physical exercise and supps. Nothing.
Beyond the GI symptoms with food intolerances, it seems the other area of the body that's really concerned would be...the brain. I mean "brainfog", cognitive impairment, memory or sleep problems. As said in the article the brain (hypothalamus etc) is responsible for lots of that. I do feel like... I guess my brain is ... loosely connected in the cranium, like it just won't function properly. The brain has to be one of the major concerned organs in this whole bizarre experience.
Is intranasal therapy common in the US or other places ? It seems extremely rare in France, if not nonexistent.
I’ll find it and take a look. Thanks.Hello Stretched.
Post concussion syndrome.
just FYI - in case you haven't already come across this info.
In book the Brain's Way of Healing, a neuroplasticity device called the PONs is great for treating post concussion syndrome. I used its cousin for a severe ME episode and all sorts of problems called the BrainPort. It was helpful. I found other neuroplasticity devices to be kinder to my brain though and highly recommend that book just for inspiration on what's out there.
Here’s a synopsis: Kirkus ReviewsI’ll find it and take a look. Thanks.
@StretchedI’ll find it and take a look. Thanks.
@Stretched
Hello .... are you by chance also hyper mobile? I'm just wondering since you have the username stretched?
what I learned since the book is that flexibility or tightness are meshed with "safety" and the brain knowing it's safe to move in certain ways.
Have you also done keto and Hyperbariac oxygen? There's a great neuroscientist whose early work has already inspired two human studies. It is surprising how helpful the two are together for many things.
@Stretched...
I've done many IV nutrients in order to bring healing to my brain. And in doing so, coupled what I learned in that book with what I learn from a myriad of schools of neuroplasticity training, also called neurostim by some of the schools. I myself prefer the term neuroplasticity ReTraining. Oh those stubborn memories and signals.
In any event, the BrainPort is not specifically mentioned in the book, mainly the PONS. But the BrainPort is available for purchase in Canada unlike the PONs which is more expensive and required to be return to the neuro clinic once a person's program with them is finished.
Have you also done keto and Hyperbariac oxygen? There's a great neuroscientist whose early work has already inspired two human studies. It is surprising how helpful the two are together for many things.
Hello joe.
I really like nasal spray NAD. Indeed it works better than sublingual forms. For the brain, I've done months of IV therapy. It was consecutive days of IV NAD that gave me the largest increase I've had in my many years of trying to get rid of this disease.
then when we added IV glutathione at the end, even better results.
I also enjoy getting Hyperbariac Oxygen but only do so when I'm in ketosis. The two together are researched and provide many benefits.
@Jo86 i sure hope nasal spray helps you. Do you have trouble digesting certain foods? Have you also tried simple things like B vitamin or glutathione shots? Not as easy to do, but they've been around for decades.Hi. Yeah I wanted to try the hyperbaric chamber thing but the doctor was super dismissive, in France docs are super conservative. The nasal stuff sounds pretty promising then, glad you're doing better.
@Stretched thx for those. What I could understand was interesting, the rest too technical.
I've read Doidge's book. Fascinating..” Doidge’s takeaway message is that mental activity correlates with neuronal activity, but we still do not know where thought takes place.
It's also about how new neural networks can be grown by physical activity. So for instance, if a stroke patient who has lost movement in a limb has it moved manually by someone else a new neural network can be formed in the brain.I’ve done some reading in neuroplasticity but haven’t really caught on as to how it works.
It seemed to be centered around eye movement and thought?
@andyguitar @StretchedI've read Doidge's book. Fascinating.
It's also about how new neural networks can be grown by physical activity. So for instance, if a stroke patient who has lost movement in a limb has it moved manually by someone else a new neural network can be formed in the brain.
Yes i'd agree that it could be of some help. But I'm not thinking it could help for brain inflammation which I suspect has it's origin outside of the brain. Put simply the body effecting the brain. But there are cases in which the persons symptoms began with a head injury. So if that caused brain damage neuroplastic training could be a way back to better health.A lot of ppl with severe ME are bedridden, unable to chew, digest, and are in considerable pain. Some of that **may** with lots of time and luck be able to be modestly overcome with neuroplasticity training... the form it might take will likely be different for all.
@andyguitar @Stretched
Neuroplasticity training is almost everything that you know when you are awake and likely things when you are asleep/in a coma too... .
Why I am a fan of it is because I had tremendous amounts of pain and many patterns of malfunctioning muscle and fascia patterns that were keeping me from having good function in the basics of eating, drinking, breathing, sleeping, walking, talking. .
@andyguitarYes i'd agree that it could be of some help. But I'm not thinking it could help for brain inflammation which I suspect has it's origin outside of the brain. Put simply the body effecting the brain. But there are cases in which the persons symptoms began with a head injury. So if that caused brain damage neuroplastic training could be a way back to better health.
Yeah I get your drift (probabably!) As we are getting a bit off the subject of the thread how about you start a new one on this subject?And maybe because I had my focus on fixing other things and knowing I needed new working patterns for swallowing and chewing and keeping all the things working in my skull and neck and throat and chest and stomach helped me achieve this grand side benefit