Forum Replies Created
-
AuthorPosts
-
The VA pays Gilead $50,000 per treatment (even though Dr Schinazi, who invented Sof, did it while working for the VA and the VA and NIH funded him). But even with the discount they’re saying they can’t afford to treat all veterans and there are still thousands of undiagnosed Veterans under their care.
In June 2015, the VA said they had a total of 233,000 Veterans under their care but only 180,000 were eligible for treatment (and that meant that they’ve had a viral load and genotype done. Can you imagine that? The assholes can deny treatment by not doing the tests they’re supposed to do. So they have treated a total of only 39,000 Veterans (that includes treatment with interferon). Since interferon came out on the market in 1991, that means that in 24 years the VA has only treated 39,000 (8,000 with the new treatments). At that pace, most of them will die.
The VA is so corrupt we are actually attempting the impossible but we keep trying. I visit this forum because when I see what Australians have done and how supportive they are of one another, it renews my faith in mankind.
PP
PP
It won’t happen.
The only time the NIH has “March in” rights to break the patent or grant other companies a license to produce generics, is if the company that holds the patent has not made efforts to commercialize it within an agreed upon time frame or if the “action is necessary to alleviate health or safety needs that are not being met by the company holding the patent.So they have no grounds for using Bayh-Dole….and why would you want to anyway. If the patent is broken and other companies are given permission to develop generics, it would take years to get approval from the FDA. We can’t wait years.
Let me put it this way, the NIH has always refused to get involved when requests were made for them to interfere because of pricing issues. For example, in 2004, the HIV group complained to them and asked them to interfere when the drug company increased the price of a med 400%.
“The NIH denied the petition finding no grounds to exercise its march-in rights. The NIH cited:
The availability of Norvir to patients with AIDS.
That there was no evidence that health and safety needs were not adequately met by Abbott, and
That the NIH should not address the issue of drug pricing, only Congress.”So If you want to break patent Congress would have to do it.
PP
Tell her she’s not allowed to visit Australia
P
Just adding sources for Vit B
Relationship between B12 concentration and HCV replication and viral load
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC33138/
P
I believe that insulin resistance promotes anemia.
Ribavirin is taken into the red blood cells where it is converted to ribavirin triphosphate. Since red cells lack the enzymes needed to hydrolyze ribavirin triphosphate, it is “trapped” in the red cells, where it depletes the cells’ ATP. The resulting ATP deficiency impairs antioxidant defense mechanisms and induces oxidative membrane damage on the red cells, causing hemolysis….end result…anemia
Normal mitochondria react to insulin by boosting production of ATP by 90 %. But the mitochondria from insulin-resistant people only boost ATP production by 5%.
So that would mean that insulin resistance promotes anemia, right? Or maybe it means I have too much time on my hands to come up with wild theories, :unsure
PP
During interferon treatment you would want to avoid anything that’s anti inflammatory (like Milk Thistle) because interferon is
PRO inflammatory. That’s how it elicits a response from the immune system.PP
But what if you have a patient who’s insulin resistant? Then you have mitochondrial degeneration and declining ATP status
Normal mitochondria react to insulin by boosting production of ATP, by 90 %. But the mitochondria from insulin-resistant people only boosts ATP production by 5 % and you need ATP to make SAMe (plus Ribavirin also depletes ATP).Selenium, Co-Q10 and Vit C are mitochondrial antioxidants. Plus, Vit C reduces the risk of gallstones (which is sometimes a problem during treatment).
.
PPYou’re right. It was overkill. The patient had failed treatment twice so this was our last chance and we had to make it count.
We thought SAMe dosing would be critical because if you give huge doses of something that oxidises, during a situation of high oxidative stress, it could become pro-oxidant and under normal circumstances it would be recycled.. So I contacted Dr Paul Steir who I’d worked with in the past. He did some of the first SAMe studies at UCLA. He said….“I had the idea of doing a pilot study with HCV and SAMe to see if shifting the transmethylation pathway towards producing glutethion would have a positive impact on liver repair and the ability to limit tissue damage from the virus, but I never really got it off the ground.”
We chose 1600mg because that’s the dose used in one small study we found. Next we asked George who I had just discovered at a forum that had given him his own section to keep him out of the way because nobody understood him and he said…..
“SAMe is just the active form of methionine. But methionine cannot convert to cysteine (hence glutathione) without going through SAMe. Roughly 50% of methionine goes into SAMe (the rest into protein). folic acid and B12 or betaine recycle methionine/SAMe, while B6 converts to cysteine. NAC is the best way to elevate cysteine directly. Now, glycine is a byproduct of the methylation of folic acid/folate (same thing); so a healthy methylation cycle using folate-B12 (rather than betaine) should supply all the glycine you need. But glycine is a common amino acid in any case, as is glutamate/glutamic acid (same thing); cysteine is the rate-limiting one because it is rare.
The other way to elevate glutathione is to recycle it directly, either enzymatically (B2, selenium, niacinamide) or with some special antioxidants – ALA, OPCs, astaxanthin, melatonin. Another way is to spare it by quenching free radicals before they oxidise PUFAs – vitamin E and OPCs will do this; vitamin E at doses of at least 800iu, Grape Seed Extract at 200-600mg daily in 2-3 doses. But don’t take GSE with riibavirin as it can theoretically interfere with absorption in gut (leave a 2-3 hour gap). The beauty of OPCs/GSE is that it definitely recycles vitamin C, very noticably reducing the requirement. All antioxidants help methylation, because B12 is easily oxidized and oxidative stress is a major interference with the methylation cycle.
One additional vitamin I would consider using is niacinamide (not niacin). Firstly, recycling glutathione depends on NADH and supplementing niacinamide is one way of elevating glutathione. It is hepatoprotective for this reason (but because B3 is a methyl acceptor, it is not safe for people with very poor methylation- it may then compete with choline synthesis, elevating AST/ALT. But this only happens to 1.8% of people supplementing high-dose B3 without other supplements or dietary changes. In thousands of patients supplementing high-dose B3 as part of a multi-supplement regime including methylation factors there has never ben a case of elevated enzymes.
But the main reason to supplement niacinamide with interferon has to do with the way that interferon degrades tryptophan to try to make extra NAD(H). This pathway is wasteful of tryptophan (it takes 60mg tryptophan to make 1mg b3) and results in the depression caused by interferon, as well as diarrhea and skin problems. Supplementing 1.5g niacinamide daily elevated tryptophan by 40% in HIV patients, one of many groups suffering the same tryptophan catabolism that interferon causes. If B6 is deficient the tryptophan-B3 pathway becomes a black hole. I have supplemented 2g niacinamide daily for 3 months now without problems, I sleep well, feel “healthy” and my moods are more stable than ever. SAMe makes me anxious and methionine can make me hypomanic, there is a fine balance between methyl donors and methyl acceptors – methyl donors synthesis adrenaline and dopamine, if there are inadequate methyl acceptors (mainly B3 but also B1) the synthesis of stimulant neurotransmitters can be excessive – especially if tryptophan is being catabolised, because serotonin should be in balance with dopamine.
Look up zinc and interferon – zinc definitely increases SVR.
I will get back to you later with more on this. You seem to be on the right track.”George is a musician. He has no medical background. So we became a team. I mean who needs a medical background when you have wild theories, right?
PPhaha….yeah, for a long time. I arrived there by mistake. Someone invited me to a forum and then her mother got ill and she had to leave for a while. So I arrived thinking I was in the right forum. By the time I found out I had already started a “Treatment Train” of 12 people. (I was the original creator of the treatment train, you know). I wanted to prove that if you teach people you can maximize treatment success. One of them decided that they would all be ships from Star Trek and put a USS before their name. I was Dr Bonebreaker and I was supposed to cuss all the time….
I don’t like Science fiction so I knew nothing about Star Trek and had to learn so I could talk like them. When eJoy banned me they all left with me. Only one didn’t clear. eJoy has tried to imitate the treatment train but has never been able to replicate it.
Thank you for reminding me. USSCbert hasn’t cleared yet…and I never leave my ships behind.
“I have faith of the heart
I’m going where my heart will take me”PP
Many of the groups are pharma sponsored.
PP
-
AuthorPosts