[split] Dimethylfumarates and Psoriasis

[Caroline]

My apologies to Af, Caroline. As you point out, your alternative therapy has supporting evidence. That is what you want. I use an alternative therapy also. It has no evidence to support it other than my experience. My treatment has not gone to plan, if ever there was a plan. If my treatment were to become seamless I would wonder what I was missing or what was about to hit me. Yet I am very pleased with what I have been able to achieve. I caught a cold yesterday, so I hope my lymphocyte count has not crashed again. It presented with polyarthralgia as well, so I hope it isn't flu.

Regarding ASEA, I found a science based medicine article on it with the heading <ASEA is an expensive way to buy salt water, backed up by an enormous number of sciencey-sounding buzzwords and no meaningful evidence, all wrapped up in a multi-level marketing scheme designed to separate the credulous from their money. Don’t buy it. >. At least with raw kidney beans I know that there is a mechanism that will stimulate the production of T cells. A packet of raw kidney beans is much cheaper.

Cheers

Seen by the text on ASEA you found, it seems as I have read the same article, of course I have also scanned the Internet , but... to my opinion that was not science based, but instead more an opinion of the person that wrote it. There is no scientific base in his rejection. So... I also reject his opinion.
Could you perhaps dive a bit deeper in it? I have found the patent on which it is based and a bit been reading it. It appears to be based on much older patents that have expired again.
Added to that, the radicals in your body are so reactive because they carry an extra electron load.
I know it is possible to ionize water, as there are heating systems which are based on that principle, but in how far that also holds for ASEA is unclear to me.

Your treatment is backed by the 35 years of experience with DMF over here in the Netherlands and Germany. , so it certainly could last for a long time.
Hopefully your cold or flu did not kick down your lymphos too much.
Wish you quick recovery.

Cheers,
Caroline