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Finally got some information on the treatment for FND
I have requested physiotherapy, CBT (cognitive behavioral therapy), EEG (
electroencephalogram
), and fMRI (Functional Magnetic Resonance Imaging). I will keep everyone updated and let know how it goes. This is my last hope in the medical world before I go to a natural approach. Wish me good luck.
I have requested physiotherapy, CBT (cognitive behavioral therapy), EEG (
electroencephalogram
), and fMRI (Functional Magnetic Resonance Imaging). I will keep everyone updated and let know how it goes. This is my last hope in the medical world before I go to a natural approach. Wish me good luck.
BossStateofMind
in
Functional Neurological Disorder - FND Hope
4 months ago
Home video Ambulatory Electroencephalogram
Since my follow up with Neurologist with possible FND diagnosis, I have received an appointment to attend for a 24/48 hour HVA EEG. I’m interested to know who else may have had this procedure and what to expect. What are they investigating /eliminating ? Any positive and /or negatives to report are
Since my follow up with Neurologist with possible FND diagnosis, I have received an appointment to attend for a 24/48 hour HVA EEG. I’m interested to know who else may have had this procedure and what to expect. What are they investigating /eliminating ? Any positive and /or negatives to report are
Maynan17
in
FND Action
9 months ago
Research Demonstrates Massage Therapy’s Positive Role in Aiding Brain Health Jan 2024
Measures of EEG (
Electroencephalogram
) readings and results of five cognitive tests were examined. (1)
Balance and Stability:
• The International Journal of Therapeutic Massage and Bodywork published research showing short-term improvements in balance, neurological, and cardiovascular measures
Measures of EEG (
Electroencephalogram
) readings and results of five cognitive tests were examined. (1)
Balance and Stability:
• The International Journal of Therapeutic Massage and Bodywork published research showing short-term improvements in balance, neurological, and cardiovascular measures
Bolt_Upright
in
Cure Parkinson's
3 months ago
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Webinar: Charles Bonnet Syndrome
The second study has called for participants with frequent hallucinations to undergo an
electroencephalogram
(EEG) to see how brain activity changes before, during and after a hallucination.
The second study has called for participants with frequent hallucinations to undergo an
electroencephalogram
(EEG) to see how brain activity changes before, during and after a hallucination.
Carol_MacularSociety
Partner
in
Macular Society
9 months ago
Dad in ICU
My dad went on holiday from England to Alicante and two days in he had a cardiac arrest. He went to ICU after being in a private hospital where they said he’s heart had stopped between 15/20 mins but no records of this have been sent to the hosp. He was on sedation for around a week. They lifted
My dad went on holiday from England to Alicante and two days in he had a cardiac arrest. He went to ICU after being in a private hospital where they said he’s heart had stopped between 15/20 mins but no records of this have been sent to the hosp. He was on sedation for around a week. They lifted
Lolablu
in
ICUsteps
24 days ago
Antibiotic therapy. Now I have severe insomnia
On February 25th, 2024 I must have injured my gum and I got a tooth/gum infection which was treated first unsuccessfully with amoxicillin, then successfully with cephalexin for 7 days (Mar 3rd - Mar 10th, 2024). The night that I finished the cephalexin I had difficulty sleeping (5 hr 51min). Each night
On February 25th, 2024 I must have injured my gum and I got a tooth/gum infection which was treated first unsuccessfully with amoxicillin, then successfully with cephalexin for 7 days (Mar 3rd - Mar 10th, 2024). The night that I finished the cephalexin I had difficulty sleeping (5 hr 51min). Each night
kiefer
in
Thyroid UK
1 month ago
Any suggestions ?
Hi I've been diagnosed with fnd I have tremmers in my right leg and hand and my speech is affected also, the neurologist has put me for a EEG scan and that's not until April any one have any advice on how to help with my speech stutter slurred and repeating words I just don't know how to make it any
Hi I've been diagnosed with fnd I have tremmers in my right leg and hand and my speech is affected also, the neurologist has put me for a EEG scan and that's not until April any one have any advice on how to help with my speech stutter slurred and repeating words I just don't know how to make it any
Nicnacs1
in
Functional Neurological Disorder - FND Hope
2 months ago
Gelastic seizures advice
hi I’m a foster carer to a 2yr old boy who we have had since birth,who has a lot of underlying health issues . He suffers from a lot of issues with his gut which gives him lots of loose stools and vomiting ,he’s also had absence like episodes and a lot of unusual and inappropriate laughing with no apparent
hi I’m a foster carer to a 2yr old boy who we have had since birth,who has a lot of underlying health issues . He suffers from a lot of issues with his gut which gives him lots of loose stools and vomiting ,he’s also had absence like episodes and a lot of unusual and inappropriate laughing with no apparent
Heather2010
in
Epilepsy Action
2 months ago
FND diagnosis
So I have had a long battle with getting to the bottom of my problems and on Tuesday I finally got all confirmed.I have been having symptoms for around 6 years and a lot of GP appointments! I have been back and forth to the doctor where I probably had a full blood count once per year (all okay) a urine
So I have had a long battle with getting to the bottom of my problems and on Tuesday I finally got all confirmed.I have been having symptoms for around 6 years and a lot of GP appointments! I have been back and forth to the doctor where I probably had a full blood count once per year (all okay) a urine
Kee10
in
FND Action
3 months ago
FND diagnosis
So I have had a long battle with getting to the bottom of my problems and on Tuesday I finally got all confirmed.I have been having symptoms for around 6 years and a lot of GP appointments! I have been back and forth to the doctor where I probably had a full blood count once per year (all okay) a urine
So I have had a long battle with getting to the bottom of my problems and on Tuesday I finally got all confirmed.I have been having symptoms for around 6 years and a lot of GP appointments! I have been back and forth to the doctor where I probably had a full blood count once per year (all okay) a urine
Kee10
in
Functional Neurological Disorder - FND Hope
3 months ago
Another update on hubby
They took him off sedation, he was shaking after 20 minutes, not all the time. Dr says not fitting so not epilepsy, so no eeg at this stage. After another 30 mins he stopped shaking. Then the so and so went to sleep, lol. They've sedated him again now, but only on half amount so will be easier tomorrow
They took him off sedation, he was shaking after 20 minutes, not all the time. Dr says not fitting so not epilepsy, so no eeg at this stage. After another 30 mins he stopped shaking. Then the so and so went to sleep, lol. They've sedated him again now, but only on half amount so will be easier tomorrow
Castleview
in
British Heart Foundation
3 months ago
Brain imaging for FND?
So according to Neurosymptoms.org there is "Brain Imaging and other studies starting to show us how and why the nervous system goes wrong" (see image; screenshot from website). Has anyone experienced this as part of their diagnosis or ongoing investigation? I'm still flabbergasted after being told
So according to Neurosymptoms.org there is "Brain Imaging and other studies starting to show us how and why the nervous system goes wrong" (see image; screenshot from website). Has anyone experienced this as part of their diagnosis or ongoing investigation? I'm still flabbergasted after being told
daverussell
in
Functional Neurological Disorder - FND Hope
3 months ago
FND diagnosis - What now?
So CT, MRI and EEG all clear. I was told I have FND and given some leaflets. I now have a neurology appointment end of March. What's next? I don't know what I should do.My symptoms are linked to amnesia/memory and processing, and not physical (fortunately). I now have a complete feeling of disassociation
So CT, MRI and EEG all clear. I was told I have FND and given some leaflets. I now have a neurology appointment end of March. What's next? I don't know what I should do.My symptoms are linked to amnesia/memory and processing, and not physical (fortunately). I now have a complete feeling of disassociation
daverussell
in
Functional Neurological Disorder - FND Hope
3 months ago
Desperately need help pls
So since last writing my previous post my Son has been experiencing “cluster seizures” - whereby he goes into a trance like state, talks gibberish and he can’t remember events and has no memory of what has happened. He has had approximately 3 or 4 of these “events” between May and December. The December
So since last writing my previous post my Son has been experiencing “cluster seizures” - whereby he goes into a trance like state, talks gibberish and he can’t remember events and has no memory of what has happened. He has had approximately 3 or 4 of these “events” between May and December. The December
Lisamarsh
in
Headway
3 months ago
Anti-epileptic drug
Hi! I have epilepsy since 2002. I use anti-epileptic drugs. I have T too for 3 years. Sometimes it is better sometimes worse. The interesting thing is that it is far better when I take in the "Cosim" (lacosamide). Do anybody have experience like this? The bad thing is that it's effect is lower now..
Hi! I have epilepsy since 2002. I use anti-epileptic drugs. I have T too for 3 years. Sometimes it is better sometimes worse. The interesting thing is that it is far better when I take in the "Cosim" (lacosamide). Do anybody have experience like this? The bad thing is that it's effect is lower now..
kchrisX
in
Tinnitus UK
4 months ago
Question about the Symptoms - FND and/or Insomnia.
Do others experience symptoms like they are caused by lack-of-sleep but has been confirmed as a result of FND?I'm beginning to relate to the symptoms, but I'm still unsure whether they are simply down to insomnia and poor sleep due to Tinnitus 24/7. A lot of it could easily be related to Ménières, which
Do others experience symptoms like they are caused by lack-of-sleep but has been confirmed as a result of FND?I'm beginning to relate to the symptoms, but I'm still unsure whether they are simply down to insomnia and poor sleep due to Tinnitus 24/7. A lot of it could easily be related to Ménières, which
daverussell
in
Functional Neurological Disorder - FND Hope
4 months ago
Hello after a forced absence.
I stopped getting email updates unexpectedly from PMRGCAuk and at the same time my husband started having health issues so most of my time was spent researching HIS symptoms and trying to make sense of it all. We are back in a waiting pattern till his 5 day EEG finally comes through so thought I would
I stopped getting email updates unexpectedly from PMRGCAuk and at the same time my husband started having health issues so most of my time was spent researching HIS symptoms and trying to make sense of it all. We are back in a waiting pattern till his 5 day EEG finally comes through so thought I would
Dydee
in
PMRGCAuk
4 months ago
FND or effects from severe Tinnitus
I'm new to FND and awaiting a EEG. My question is could I have FND? I've read so much in a short space of time and in some respects it has severe physical effects and on the other hand iit seems a very broad diagnosis. Here is my story.., I've had tinnitus several years, though in the last two years
I'm new to FND and awaiting a EEG. My question is could I have FND? I've read so much in a short space of time and in some respects it has severe physical effects and on the other hand iit seems a very broad diagnosis. Here is my story.., I've had tinnitus several years, though in the last two years
daverussell
in
Functional Neurological Disorder - FND Hope
5 months ago
Tinnitus and Cognitive effects (a follow up from my previous post)
I'm posting the following excerpts as they make some interesting reading about Tinnitus and Cognitive effects including how we respond to tinnitus. So hopefully this is interesting all round and not only about me :). So... I posted a few weeks ago "Promethazine sleeping tablets following insomnia and
I'm posting the following excerpts as they make some interesting reading about Tinnitus and Cognitive effects including how we respond to tinnitus. So hopefully this is interesting all round and not only about me :). So... I posted a few weeks ago "Promethazine sleeping tablets following insomnia and
daverussell
in
Tinnitus UK
5 months ago
Not Alzheimer's, Maybe PTSD?
Hello! I just found this place. I've been searching for 6 years to find a solution to my short-term memory problems. They started the day my 47yo husband died unexpectedly. It's just my short-term memory. Apparently, this isn't uncommon and sometimes called 'widow brain' or 'grief brain.' I can
Hello! I just found this place. I've been searching for 6 years to find a solution to my short-term memory problems. They started the day my 47yo husband died unexpectedly. It's just my short-term memory. Apparently, this isn't uncommon and sometimes called 'widow brain' or 'grief brain.' I can
Hidden
in
Memory Health: Alzheimer's Support Group
5 months ago
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