My tDCS Wish List

I have been reading studies, attending training, experimenting with, and writing about transcranial direct current stimulation (tDCS) for about two years now.  Needless to say, I am enthusiastic about what tDCS can do for many people who use it for depression, chronic pain, enhanced creativity, and memory. It may also may have positive effect for other important conditions such as stroke, Parkinson’s and Alzheimer’s – there are certainly studies that show that to be the case.


(Scientific American)

Given that it has positive effect on many who try it, it could improve the quality of life of millions of people around the world. All of this without drugs, without the cost of drugs, and with no significant side-effects.

With all the great things I’ve learned about tDCS, I thought I’d share a little of my tDCS Wish List for the next five years:

In The Next Five Years I Wish That:

  1. every appropriate medical practitioner (and counselor) would at least become aware of tDCS. A treatment this good, this simple, this safe, with so much positive effect should not be overlooked. It should be a tool in the kit of considered-treatments for every practitioner.
  2. that the popular press would at least make an attempt to write sensible and factual articles about tDCS. For example, it would be great to stop comparing tDCS to electro-shock treatment. Could they be any more different? Such mindless hype scares people who might be helped greatly by tDCS.
  3. that funding could be found to “get the word out” about tDCS. Because there are no drug company $ billions for magazine ads, TV commercials, and infomercials, it looks as though tDCS will always be a niche treatment, known by a lucky few – missed by millions it could help. I wonder how many lives could be vastly improved (or saved) if tDCS were as well-known as Viagra?
  4. that I could find one or more well-known, depressed, troubled Hollywood star(s), known for appearances in People Magazine and on TMZ – who would agree to a course of tDCS treatment. Once improved, those stars would have to be willing to speak about tDCS – the treatment that got them out of the pit. For better or worse, we live in a “star” powered society – such articles appearing in Hollywood rags and read and seen by millions could really help push tDCS towards a tipping point.
  5. that my second career be all about researching, writing, and speaking about the practical side of tDCS. There is a whole world full of people who need the help that this simple treatment can offer. A tDCS device can be as simple as a 9 volt battery, an inexpensive CRD diode, and a couple of sponges. Imagine the good that could be done!
  6. that I could find one or more philanthropists willing to join in the good work related to tDCS – and help a whole lot of people in the process! There are $ millions of research dollars flowing to universities and research centers all around the world looking at tDCS. But there is very little being done to get tDCS to the people who can benefit from it. If you are a philanthropist who really wants to make a difference in a very tangible way, feel free to contact me. Let’s get something started!


(One of the most important contributions of tDCS:
a simple treatment for the depression epidemic.)

Mark the date. At this point, for certain types of treatment, tDCS is well researched, simple, and considered safe. We all know that tDCS is barely known among the masses and the medical community. Ask any doctor you know  – I’d say the odds are about 1 in 100 that they know anything at all about tDCS.

What will things be like in 2018? By 2018, how many millions will have suffered for lack of access to a tDCS device and a tDCS trained professional? Can you help?

foc.us-mal-female-london-thumb
(A self-contained tDCS treatment headset. http://www.foc.us)

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9 comments on “My tDCS Wish List

  1. Pingback: Brent Williams' wish list » tDCS News

  2. I saw with interest your reference to using tdcs for Parkinsons – I search for info to alleviate symptoms of my wifes non-Parkinsons essential tremor – Google Scholar has helped but so many abstracts let you go no further without a fee – Do you know any resources for that area of focus that are free? Wouldn’t you know she won’t let me shave her head and slide the energized sponge around til the shaking stops – no sense of adventure there

    • Hi Fabe,

      I’m not aware of any site that would give you access to fee studies for free – with one possible exception. Do you live near a public library or college library? Often they have free access to all published studies. Worth checking out!

      Brent

  3. Hello,

    I’m a psychology student, and am set to graduate this December. My Cognitive Professor told me about the foc.us device earlier today during a meeting in his office. I was instantly intrigued, and since getting home I’ve been looking at some of your blogs on tDCS devices. You say in your wish list that you would like interested philanthropists to get involved. While I’m still only an Undergrad in Psychology I am more than willing to get involved in this new technology in any way I can. An email you can reach me at is wcs8296@uncw.edu. I really like your attitude and ideas on all this, so let me know if I can help you in any way.

    Thanks

  4. As I’m sure you are aware, not everyone reacts favourably to tDCS, so your point about a Hollywood Star undergoing a treatment and then discussing it in People Magazine is a double-edged sword. What happens if it has negative side-effects, or even worse, has a negative effect on their career (memory loss, speech changes, etc)?

    I’m currently buying a tDCS device myself, so don’t think I’m against it, but what you need before any of those items on your wishlist is: research and solid proof that tDCS can actually be of benefit to large numbers of people with very limited risk.

      • There is some evidence, for some people… there are currently ~ 7 billion people on earth… if a few thousand have had a positive experiences with this, it’s great, but that’s not enough for everyone to assume it’s safe and start tossing it out there for everyone.

        We are effectively in the very early stages of human trials, and most of us are doing it ourselves with no medical backup. There have been adverse reports of side effects, some of them quite serious.

        All I’m saying is, popularity and celebrity endorsements come *after* we’ve established that it’s safe for the vast majority of the population, *and* that it’s effective. We haven’t reached that stage yet.

      • What are the side effects you have read (or heard) about? From a reliable source? More serious that those caused by antidepressants (for example)?

        Just wondering.

        Brent

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