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Vagus nerve stimulation (VNS)
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Vagus nerve stimulation Possible future treatment.
Perhaps some good news for those who don't respond to drugs. https://read.qxmd.com/read/36400697/noninvasive-vagus-nerve-stimulation-a-new-therapeutic-approach-for-pharmacoresistant-restless-legs-syndrome Its early days but sounds like a worthwhile chance of improvement for severe cases. It might
Perhaps some good news for those who don't respond to drugs. https://read.qxmd.com/read/36400697/noninvasive-vagus-nerve-stimulation-a-new-therapeutic-approach-for-pharmacoresistant-restless-legs-syndrome Its early days but sounds like a worthwhile chance of improvement for severe cases. It might
Graham3196
in
Restless Legs Syndrome
1 year ago
Vagus Nerve Stimulation VNS for FND?
Has anyone had that Vagus Nerve Stimulation Treatment “
VNS
”?? If so I’d love to hear about it. Please share if it helped your symptoms or not.
Has anyone had that Vagus Nerve Stimulation Treatment “
VNS
”?? If so I’d love to hear about it. Please share if it helped your symptoms or not.
AjaStar
in
Functional Neurological Disorder - FND Hope
2 years ago
sudden onset of fibromyalgia. Is it possible ?
I would like to know if anyone experienced a sudden onset of fibromyalgia. In June 2021 I caught covid (delta variant) and the virus caused me afib (atrial fibrillation) but i was misdiagnosed for many months due to cardiologists' mistakes. At the end of December 2021 unfortunately i got covid again
I would like to know if anyone experienced a sudden onset of fibromyalgia. In June 2021 I caught covid (delta variant) and the virus caused me afib (atrial fibrillation) but i was misdiagnosed for many months due to cardiologists' mistakes. At the end of December 2021 unfortunately i got covid again
JoseT
in
Fibromyalgia Action UK
2 years ago
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Vagus nerve stimulation
I’ve read of electric stimulators implanted to stimulate the vagus nerve as a number of clinical trials are currently evaluating its effectiveness in the treatment of certain autoimmune dysfunctions. I am currently doing various vagus nerve impact exercises; Wimhoff breathing, ice showers/baths, standing
I’ve read of electric stimulators implanted to stimulate the vagus nerve as a number of clinical trials are currently evaluating its effectiveness in the treatment of certain autoimmune dysfunctions. I am currently doing various vagus nerve impact exercises; Wimhoff breathing, ice showers/baths, standing
Twadds
in
PMRGCAuk
2 years ago
Management of Parkinson's Disease?
He also provides comprehensive surgical options for epilepsy including resective surgery, laser thermal interstitial therapy (LITT), DBS, vagal nerve stimulation (
VNS
) and responsive neurostimulation (RNS). Dr.
He also provides comprehensive surgical options for epilepsy including resective surgery, laser thermal interstitial therapy (LITT), DBS, vagal nerve stimulation (
VNS
) and responsive neurostimulation (RNS). Dr.
Farooqji
in
Cure Parkinson's
2 years ago
Transcutaneous Vagus Nerve Stimulation - TENS type machine
Hello all - I have read good things about the above for lupus related fatigue. Does anyone have any recommendations for a machine ? I know about the exercises etc, but am more interested in treating the fatigue using a TENS type machine. I'm in the UK
Hello all - I have read good things about the above for lupus related fatigue. Does anyone have any recommendations for a machine ? I know about the exercises etc, but am more interested in treating the fatigue using a TENS type machine. I'm in the UK
Ophelia1
in
LUPUS UK
2 years ago
Vagus nerve stimulation improves gait
https://www.nature.com/articles/s41531-021-00190-x
https://www.nature.com/articles/s41531-021-00190-x
Hidden
in
Cure Parkinson's
2 years ago
What's people's experiences on Armour Dessicated thyroid tabs?
I recently changed to Armour Thyroid, although it's called Thyroid-S in Bali. 10 days in I'm suffering huge panic attacks and dissociation- had these before, but was hoping Armour would help calm these down a bit...panic attacks are lasting all day, shortness of breath, complete zoning out where my brain
I recently changed to Armour Thyroid, although it's called Thyroid-S in Bali. 10 days in I'm suffering huge panic attacks and dissociation- had these before, but was hoping Armour would help calm these down a bit...panic attacks are lasting all day, shortness of breath, complete zoning out where my brain
smilas
in
Thyroid UK
2 years ago
Vagus Nerve Stimulation for PD
We have posted about the Vagus Nerve and PD before. Here is one article on it: https://www.sciencedirect.com/science/article/pii/S1935861X20301960 So I was going through my Facebook groups to see what I can cut, and noticed my Vagus Nerve group. It made me put up or shut up and ask the simple question
We have posted about the Vagus Nerve and PD before. Here is one article on it: https://www.sciencedirect.com/science/article/pii/S1935861X20301960 So I was going through my Facebook groups to see what I can cut, and noticed my Vagus Nerve group. It made me put up or shut up and ask the simple question
Bolt_Upright
in
Cure Parkinson's
2 years ago
Vagal Nerve stimulation
Has anyone explored ways of stimulating the vagal nerve as a way of preventing AF as seems to be responsible for possibly the majority of Afib triggers? Wouldn't it be great if just like a pacemaker we could have a vagal nerve implant to give it a jolt when it's thinking of doing it's dirty work!!!
Has anyone explored ways of stimulating the vagal nerve as a way of preventing AF as seems to be responsible for possibly the majority of Afib triggers? Wouldn't it be great if just like a pacemaker we could have a vagal nerve implant to give it a jolt when it's thinking of doing it's dirty work!!!
Swimsyroke
in
AF Association
3 years ago
Vagus Nerve Stimulation on Ear with TENS Unit Improves HRV, Sleep, Depression, & More?
I can provide links to studies, but what I'm looking for are any experiences PWP have had with this. https://youtu.be/ZkC9RVFhlX8
I can provide links to studies, but what I'm looking for are any experiences PWP have had with this. https://youtu.be/ZkC9RVFhlX8
JAS9
in
Cure Parkinson's
3 years ago
Maybe I'll Buy A Vagus Nerve Stimulator To Use While Sitting With My Coronet Duo Red Light...
One month of non-invasive vagus nerve stimulation (nVNS), administered at home using a hand-held device by electroCore, improved walking and motor abilities, and eased freezing of gait in adults with Parkinson’s disease, according to data from a small clinical trial. ElectroCore’s nVNS device, called
One month of non-invasive vagus nerve stimulation (nVNS), administered at home using a hand-held device by electroCore, improved walking and motor abilities, and eased freezing of gait in adults with Parkinson’s disease, according to data from a small clinical trial. ElectroCore’s nVNS device, called
jimcaster
in
Cure Parkinson's
3 years ago
tVNS Vagal nerve stimulation
I know tVNS has been discussed in the past and I thought it would be worth while to let you know my husbands experience of this. As as a retired nurse I found the research on this really interesting. I suggested to my husband that this was worth trying in an attempt to reduce his horrible episodes of
I know tVNS has been discussed in the past and I thought it would be worth while to let you know my husbands experience of this. As as a retired nurse I found the research on this really interesting. I suggested to my husband that this was worth trying in an attempt to reduce his horrible episodes of
KathyN
in
AF Association
3 years ago
Still having seizures after brain surgery and VNS implanted.
They put in a
VNS
and still having small seizures.... any other ideas?
They put in a
VNS
and still having small seizures.... any other ideas?
abbygage
in
Encephalitis Society
3 years ago
Tens Machine Usage Guide
A lot of people have been asking me how to set up a Tens Machine for Vagus Nerve stimulation. Here is a useful video: https://www.youtube.com/watch?v=5ba5zyMo9VY&t=1s
A lot of people have been asking me how to set up a Tens Machine for Vagus Nerve stimulation. Here is a useful video: https://www.youtube.com/watch?v=5ba5zyMo9VY&t=1s
Philbs1980
in
IBS Network
3 years ago
VNS Surgery
Hey guys, has anyone had a
VNS
surgery before? I’m getting one in a few days and I’m starting to feel a tad bit nervous.
Hey guys, has anyone had a
VNS
surgery before? I’m getting one in a few days and I’m starting to feel a tad bit nervous.
odessbuh
in
Epilepsy Action
4 years ago
Stimulating Vagus nerve cuts AF by 85%
There's research showing an 85% reduction of AF through vagus nerve stimulation. This was done by passing a small current through the tragus (the little lump just in front of your earhole): https://www.ncbi.nlm.nih.gov/pubmed/32192678
There's research showing an 85% reduction of AF through vagus nerve stimulation. This was done by passing a small current through the tragus (the little lump just in front of your earhole): https://www.ncbi.nlm.nih.gov/pubmed/32192678
MarkS
in
AF Association
4 years ago
Help
Did the
VNS
cause this? They are not saying. Some reassurance from someone would help.
Did the
VNS
cause this? They are not saying. Some reassurance from someone would help.
Hummby
in
British Heart Foundation
4 years ago
Life with epilepsy
Hi I'm stephen 44 from leeds,13 years ago I was told I had epilepsy and it has just got worse to the point now I have 24 hour carers looking after me I have no freedom anymore,I know I need them because of this
vns
implant I was giving as I can die at any time having a fit,i need release
Hi I'm stephen 44 from leeds,13 years ago I was told I had epilepsy and it has just got worse to the point now I have 24 hour carers looking after me I have no freedom anymore,I know I need them because of this
vns
implant I was giving as I can die at any time having a fit,i need release
Kennos
in
Mental Health Support
4 years ago
"Sticky Blood" - Antiphospholipid Syndrome, POTS, Chronic Fatigue Syndrome and Fibromyalgia - The Dysautonomia Conference
by Cort Johnson | Aug 15, 2018 | This blog is part IV in a series of blogs covering the issues presented at the 2018 Dysautonomia International Conference in Nashville, Tennessee. APS and POTS and ME/CFS This is the fourth blog on issues presented in the 2018 Dysautonomia International Conference.
by Cort Johnson | Aug 15, 2018 | This blog is part IV in a series of blogs covering the issues presented at the 2018 Dysautonomia International Conference in Nashville, Tennessee. APS and POTS and ME/CFS This is the fourth blog on issues presented in the 2018 Dysautonomia International Conference.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
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