RSDS: Question and Answers With A Reader

I received this question from someone through YouTube:

1happyhollie (8 hours ago) What is your supposed cure? Current medical opinion is that there is no cure, but a patient can sometimes go into periods of remission. If you have a way for those of us with crps/rsd to be cured, please share. It is a horrible disease to live with.

Here’s my response to her:

Well, I don’t know if I’ve found the cure, truthfully. I can only say that I have some of the most severe symptoms of RSDS and I am taking a vitamin and supplement regimen that is taking them away completely. The longer I’m on this and staying to a specific diet, the longer in-between doses I can go without having them come back. The supplements compliment the vitamins by giving my glands (hypothalamus, thyroid and adrenal) a break and a chance to heal. The healing is supported by the correct nutrient/vitamin regimen. It’s that simple and it’s saved my life because I felt like killing myself for quite some time as my symptoms intensified and became more frequent.
Honestly, I just may be one of the first, and could, for all I know be the first, to use Nutritional Response Testing (NRT) to help with this. And, since I’ve been studying online marketing at the same time I’m going through all this, I thought perhaps I should tell those who are suffering about my experience. That way if they want to try it to, they can see if it helps them the way it’s helping me. That’s all. The cost to find out if it works would be about $200-$300, based on my experience. But, after feeling like death would be the only way out, I tried this at my chiropractor’s recommendation and the first handful took all my RSDS pain away within an hour–100%!
I’m not making any money and I don’t have shares or stocks in Standard Process vitamins or affiliations that would lead to me making any money off of anyone trying this. I’m simply trying to help because of the miracles this has done to make it so I can work again, full time, and see hope for an RSDS pain free life.
The irony is that I am one of the only people whose injury just may never cure. Doctors usually/always say that if the injury that led to the RSDS isn’t healed then the RSDS cannot go into remission. My RSDS is definitely NOT in remission because the pain will return after a time (hours or a day or so, depending) if I don’t take the vits./supplmts. So, even with an ever-present catalyst that in itself leaves me with a 6-8 pain level in my lower back every day, I still manage to stop the burning skin and the nerve firings that are the RSDS pain “patches” all over my body. That, to me, is a testament to how the regimen manages to help my glands and therefore my parasympathetic.
Try it or don’t, but I would seriously consider it if I were you because I know that I wouldn’t have been alive (suicide) more than likely, had this not come into my life. And, I would’ve given ever single thing I own to anyone who could have done for me what this has. Doctors don’t know much and they just want to give pain medicine. What if this really will work? That’s a question I want everyone suffering like I have and do without this, to ask themselves. And, what would you have to lose?