A visit to the TMS lab, and some questions answered
I’ve started getting quite a few questions about the TMS work I’m participating in at Alvaro Pascual-Leone’s lab in Boston http://www.tmslab.org/ I’m going to answer a few of them here. Feel free to ask your own questions in the comments. I’ll try to answer, and I’ll run any technical or medical questions past Alvaro, Shirley, and the other doctors to make sure I have the facts straight.
What is TMS?
As we think, our brains generate small electrical signals. These signals pass through our nerves to work our muscles, and the pass within our brains to create our thoughts and memories. All our nerves work on electricity – nerves in our eyes, ears, and even our nose generate electrical signals that our brain interprets and processes.
TMS uses the principle of electromagnetic induction to add its own signal to the signals running along our neural pathways. TMS is very precise, so we can aim it at fairly specific paths. For example, we can use TMS to stimulate one finger in the hand. By applying TMS pulses to the part of the brain that controls it, we can make the finger twitch.
These pulses can augment the function of a brain area, or they can inhibit it. So you might say they allow us to “speed up” or “slow down” small parts of the brain. The TMS equipment we’re using in this work focuses on a bit less than 1% of the brain mass.
So how could it help people with autism?
Shirley and Alvaro developed a theory that some parts of the autistic mind are over-active, and those overactive parts sort of overwhelm the other parts. By “slowing down” the over-active areas they hoped to bring about an improvement in overall function.
In this first study, several areas were targeted over four sessions.
So far, my results look very, very promising. Really exciting stuff. We also have positive initial results from a few others in the study. But it’s too soon to say more – we need to analyze the data and run more experiments.
Now, if I may, I’d like to show you what it looks like. Meet Shirley Fecteau, PhD, the leader of this particular study. She’s an instructor at Harvard Medical School and a part of Dr. Pascual-Leone’s team at Beth Israel Deaconess Medical Center.
Shirley is French-Canadian. One of the things I've noticed is that people have come from all over the world to work in these Harvard programs. They really do get the best and the brightest from all over.
In this image you can see me getting TMS to the right front of my brain.
She's holding the coil against the side of my head. The black headband has some targets on it that allow two computer cameras on the wall to track my head so she can keep the coil in the right spot. You’ll notice I have a blank expression. That’s because the TMS induces an almost meditative state in me. The picture you see is not a setup, it’s real TMS.
This next shot shows a bit more of the setup. You can see the cameras on the wall, looking down at the chair. Those cameras feed the computer below, which tells Shirley where to hold the TMS coil. Fellow Aspergian Michael Wilcox is in the chair, and he's going to write about his TMS experience on his own site, which is http://www.mfw.us/ The fellow with the camera is filming is for a Canadian Television documentary based upon Dr. Norman Doidge's book The Brain That Changes Itself. Dr. Doidge and the crew came to see us 2 weeks ago and I took the chance to shoot a bunch of photos.
In this photo, you can see the brain map and the targets for stimulation.
The upper right view has some small colored dots . . . those are the target areas. The pair of cameras on the wall match points on my face with the MRI images to show them where to place the TMS coil.
The crosshairs on the left show the coil (the black) dot with the target area being the X
This shot shows the actual TMS machine:
Here's a better view of the TMS coil, on my son Cubby's head:
The hose coming out of the coil is an air line, to pass air through the coil to cool it. The coil is a figure 8 of wire in the blue plastic casing.
And a few more questions before I go . . .
Does TMS damage or kill brain cells?
In my previous post, I described some pretty dramatic effects from TMS. Someone on the http://www.ageofautism.com/ site asked if those vivid images were produced by "millions of neurons dying off."
TMS does not injure or kill brain cells. In this study, we are using what's called functional MRI imagery to watch brain activity before, after, and even during TMS. We can see areas become less active, or more active, and we see them return to their pre-TMS states. We can say with certainty that TMS is not killing brain cells.
We are able to watch the areas of the brain that we stimulate change and evolve.
In addition, Alvaro and other neuroscientists have observed the effects of TMS during open-brain surgical procedures in patients. TMS alters the signals passed through the neurons. It does not burn them out.
Is TMS like ECT, electro convulsive or shock treatment?
Not really. It's only similar in that they are both electrical processes. To use an analogy, TMS is like touching your fingers across the terminals of a AA battery. ECT is like throwing a cable over a high-tension electric powerline. Needless to say, both are electrical experiences but their effect on the person is drastically differrent.
TMS is a low-energy and highly focused procedure that's aimed at less than 1% of the brain mass. It's painless and in fact induces something of a tranquil state while it's being done. For me, TMS has produced a lasting elevation of mood and made me somewhat calmer overall.
ECT, on the other hand, is a very violent, high energy jolt to the whole brain. It induces seizures and it's so painful that people must be under general anesthesia. As you can see, none of that happens with TMS.
I'm aware that any tool that reaches into the brain and alters the way we think is scary. I guess it's not as scary for me because I have a good understanding of the electronic principles, and I'm seeing it unfold firsthand. And it's also exciting. The results I am seeing are truly like science fiction come to life.
What is TMS?
As we think, our brains generate small electrical signals. These signals pass through our nerves to work our muscles, and the pass within our brains to create our thoughts and memories. All our nerves work on electricity – nerves in our eyes, ears, and even our nose generate electrical signals that our brain interprets and processes.
TMS uses the principle of electromagnetic induction to add its own signal to the signals running along our neural pathways. TMS is very precise, so we can aim it at fairly specific paths. For example, we can use TMS to stimulate one finger in the hand. By applying TMS pulses to the part of the brain that controls it, we can make the finger twitch.
These pulses can augment the function of a brain area, or they can inhibit it. So you might say they allow us to “speed up” or “slow down” small parts of the brain. The TMS equipment we’re using in this work focuses on a bit less than 1% of the brain mass.
So how could it help people with autism?
Shirley and Alvaro developed a theory that some parts of the autistic mind are over-active, and those overactive parts sort of overwhelm the other parts. By “slowing down” the over-active areas they hoped to bring about an improvement in overall function.
In this first study, several areas were targeted over four sessions.
So far, my results look very, very promising. Really exciting stuff. We also have positive initial results from a few others in the study. But it’s too soon to say more – we need to analyze the data and run more experiments.
Now, if I may, I’d like to show you what it looks like. Meet Shirley Fecteau, PhD, the leader of this particular study. She’s an instructor at Harvard Medical School and a part of Dr. Pascual-Leone’s team at Beth Israel Deaconess Medical Center.
Shirley is French-Canadian. One of the things I've noticed is that people have come from all over the world to work in these Harvard programs. They really do get the best and the brightest from all over.
In this image you can see me getting TMS to the right front of my brain.
She's holding the coil against the side of my head. The black headband has some targets on it that allow two computer cameras on the wall to track my head so she can keep the coil in the right spot. You’ll notice I have a blank expression. That’s because the TMS induces an almost meditative state in me. The picture you see is not a setup, it’s real TMS.
This next shot shows a bit more of the setup. You can see the cameras on the wall, looking down at the chair. Those cameras feed the computer below, which tells Shirley where to hold the TMS coil. Fellow Aspergian Michael Wilcox is in the chair, and he's going to write about his TMS experience on his own site, which is http://www.mfw.us/ The fellow with the camera is filming is for a Canadian Television documentary based upon Dr. Norman Doidge's book The Brain That Changes Itself. Dr. Doidge and the crew came to see us 2 weeks ago and I took the chance to shoot a bunch of photos.
In this photo, you can see the brain map and the targets for stimulation.
The upper right view has some small colored dots . . . those are the target areas. The pair of cameras on the wall match points on my face with the MRI images to show them where to place the TMS coil.
The crosshairs on the left show the coil (the black) dot with the target area being the X
This shot shows the actual TMS machine:
Here's a better view of the TMS coil, on my son Cubby's head:
The hose coming out of the coil is an air line, to pass air through the coil to cool it. The coil is a figure 8 of wire in the blue plastic casing.
And a few more questions before I go . . .
Does TMS damage or kill brain cells?
In my previous post, I described some pretty dramatic effects from TMS. Someone on the http://www.ageofautism.com/ site asked if those vivid images were produced by "millions of neurons dying off."
TMS does not injure or kill brain cells. In this study, we are using what's called functional MRI imagery to watch brain activity before, after, and even during TMS. We can see areas become less active, or more active, and we see them return to their pre-TMS states. We can say with certainty that TMS is not killing brain cells.
We are able to watch the areas of the brain that we stimulate change and evolve.
In addition, Alvaro and other neuroscientists have observed the effects of TMS during open-brain surgical procedures in patients. TMS alters the signals passed through the neurons. It does not burn them out.
Is TMS like ECT, electro convulsive or shock treatment?
Not really. It's only similar in that they are both electrical processes. To use an analogy, TMS is like touching your fingers across the terminals of a AA battery. ECT is like throwing a cable over a high-tension electric powerline. Needless to say, both are electrical experiences but their effect on the person is drastically differrent.
TMS is a low-energy and highly focused procedure that's aimed at less than 1% of the brain mass. It's painless and in fact induces something of a tranquil state while it's being done. For me, TMS has produced a lasting elevation of mood and made me somewhat calmer overall.
ECT, on the other hand, is a very violent, high energy jolt to the whole brain. It induces seizures and it's so painful that people must be under general anesthesia. As you can see, none of that happens with TMS.
I'm aware that any tool that reaches into the brain and alters the way we think is scary. I guess it's not as scary for me because I have a good understanding of the electronic principles, and I'm seeing it unfold firsthand. And it's also exciting. The results I am seeing are truly like science fiction come to life.
Comments
Thanks for visiting my blog. Always makes me feel good!
Must. Learn. More! Love this. THanks for sharing it with us.
Check out what Dr. Healy (Former head of NIH) said on Imus today. I managed to live transcribe some of it on Age of Autism. Should have gone to Katie Gibbs school instead of BC! I don't type fast enough.
K
You can get TMS right now at BIDMC in Boston, but it's not covered by insurance yet.
TMS is also used to aid stroke recovery. Applications in epileptic s and others are being explored right now.
Look, I've not forgotten about the interview I did with you. I'm waiting to have it coincide with the paperback release in June.
Wasn't that right? A new release? Was it here? Or maybe I'm confusing you with Patricia?
xx
Kanani
And if you think TMS is an effective beauty treatment . . . you got me mixed up with someone else in those photos!
Regarding your previous post, it seems to me you have a rare condition called "synesthesia" (i.e., the ability to "see" music). This is considered by many to be an extraordinary gift, almost like ESP. Congrats on getting it back.
I am going to meet your brother this Thursday when he makes an appearance in Chicago's north suburbs. I'm really looking forward to it.
Thanks for your kind words. ECT is such a risky crapshoot. I tried to stop the treatments and begged my father to stop them; but the doctor convinced my father that she needed at least 12 of them to receive any benefit. At one point my Mom could not remember how to spell her own name! She has aged 15 years in the last five and is very, very frail now.
I am so thankful for this TMS research that John is participating in because I sincerely believe that the most obvious benefit has been his elevation of mood. I am so hopeful about this study. I suspect that TMS will someday routinely be used to treat people that have OCD, phobias, anxiety, and depression.
Hey, btw... I liked your financial recap about your advance. Very clear. I'm sure there are other expenses as well, and I think we'd love you to write about this for The Writerly Pause or I could just phone you.
xx
Yer crazy beauty fanatic, Kanani
John, this is fascinating beyond words. I feel like you're sharing with us the start of a major breakthrough in medicine. I'm so glad you feel it's a positive experience, and that you're reaping benefit from it. TMS has the potential for so many more applications.
Thank you for sharing your journey with us!!!!
I remember a few years ago I was doing as much reading as possible about people who stutter (both of my children stutter). And a doctor in Israel hypothesized about the role of dopamine in the brain. The way he explained it, I felt totally convinced. Now others are catching up to his research. People who stutter seem to have too much dopamine; people with Parkinsons disease don't have enough dopamine. This is a tangent, I know. But studies about the brain are so interesting to me.
Can TMS help my son NOT throw away his schoolwork he didn't finish on time or doesn't want or know how to do??? :)
I do not know the specific answer with respect TMS's ability to affect your son's behavior.
The larger issue is that TMS is still in the research labs. We've got to verify results on grownups, then extend the study into kids, and then begin the longer process of government approval.
I can say from experience that it's science fiction made real, but we've got a lot to learn before deploying it as a tested and validated therapy for the public.
(Yes, the doctor is cute, but so are you and Cubby).
Woof!
I wonder--if there's any validity to that theory--if TMS is in some way improving communication between the two hemisheres of your brain?
Fascinating stuff. I"m so glad that you're enjoying.
I want a coil!
your book and the CD of the book.
Our son Sam, 38,learned he had
Aspberger's about five years ago.
He is learning, just as you have,
about himself and how to negociate
this world, it's messy and hopeful
as at the same time. We were talking the other day about your
book and he said, " I want to know
how JEB met his second wife and what happened to his first one." I
said he should go on your blog. He
said you didn't really tell about
that in your book. He is thinking
about this as he is the recently
divorced father of three young
children, one with Aspberger's and
he is wanting to be in another relationship and doesn't really
know how to do it. And so it goes... Your recent experience with
TMS is very exciting and hopeful.
Do you have any dates to be in The
Twin Cities of Minneapolis/St. Paul?
We would love to see you here. How
would I go about making that happen?
Thanks for connecting so well with
us out here. Susan Hardman
has done something like this for
his Parkinsonism. This is hopeful
for our son Sam, 38, who is in the
Aspberger's club. Sam wants to know more about what caused the
breakup of your first marriage and
how you met your second wife. He
says you didn't explain much in the
book. As recently divorced Aspie
with three children he is trying to
figure out how to be in a new relationship and struggling alot.
I've encouraged him to get on line
and ask you himself. Thanks for
being so out there with your story
It helps us all. Susan Hardman
The mom
has done something like this for
his Parkinsonism. This is hopeful
for our son Sam, 38, who is in the
Aspberger's club. Sam wants to know more about what caused the
breakup of your first marriage and
how you met your second wife. He
says you didn't explain much in the
book. As recently divorced Aspie
with three children he is trying to
figure out how to be in a new relationship and struggling alot.
I've encouraged him to get on line
and ask you himself. Thanks for
being so out there with your story
It helps us all. Susan Hardman
The mom
TMS coming. We are learning much
from you and our son Sam, 38, is
walking through this Aspberger's
journey with you. He wants to know
more about your marriages as he
says your book didn't go into much
detail. He is trying to connect
with someone after a divorce and
finding it hard. Thus the question. Thanks so much for your
being out there and helping all of
us Aspies and families. Susan Hardman
TMS coming. We are learning much
from you and our son Sam, 38, is
walking through this Aspberger's
journey with you. He wants to know
more about your marriages as he
says your book didn't go into much
detail. He is trying to connect
with someone after a divorce and
finding it hard. Thus the question. Thanks so much for your
being out there and helping all of
us Aspies and families. Susan Hardman