Search
Search
About
Log in
Join
Experiences with
Cognitive impairment
Posts
Communities
743 public posts
Filter results
I have Periph Neuropathy, Cognitive Impairment, many side effects from Cancer surgery and Chemo. What other neurological tests can be done?
I have confirmed Peripheral Neuropathy,
Cognitive
Impairment
, many side effects from Cancer surgery and Chemotherapy (including cytopenia and spine damage).
I have confirmed Peripheral Neuropathy,
Cognitive
Impairment
, many side effects from Cancer surgery and Chemotherapy (including cytopenia and spine damage).
jfmITP
in
Functional Neurological Disorder - FND Hope
10 years ago
Muscle Function
The 2007 NICE guidelines http://www.nice.org.uk/guidance/cg53 suggest; Cognitive behavioural therapy and/or graded exercise therapy should be offered to people with mild or moderate CFS/ME and provided to those who choose these approaches, because currently these are the interventions for which there
The 2007 NICE guidelines http://www.nice.org.uk/guidance/cg53 suggest; Cognitive behavioural therapy and/or graded exercise therapy should be offered to people with mild or moderate CFS/ME and provided to those who choose these approaches, because currently these are the interventions for which there
Ian123
in
Myalgic Encephalomyelitis Community
10 years ago
Zoloft lobotomy and burning brain
(full description in my profile) CAT and MRI scans came out normal but despite the severe depression coming back, I was left with a paralysing sensation of early dementia (substantial
cognitive
and memory
impairment
), together with a permanent sensation that acid is being poured over my left frontal
(full description in my profile) CAT and MRI scans came out normal but despite the severe depression coming back, I was left with a paralysing sensation of early dementia (substantial
cognitive
and memory
impairment
), together with a permanent sensation that acid is being poured over my left frontal
opusensemble
in
Mental Health Support
10 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Any need of concern???
Mild Vascular
Cognitive
Impairment
Long term Memory Problems, Speech problem (mild early Small Vessel Disease & Partial empty sella Syndrome on MRI brain scan, Myeloproliferative Disorder ( controlled , I would be very grateful for any feed back ,before my mind runs away , much appreciated Pam
Mild Vascular
Cognitive
Impairment
Long term Memory Problems, Speech problem (mild early Small Vessel Disease & Partial empty sella Syndrome on MRI brain scan, Myeloproliferative Disorder ( controlled , I would be very grateful for any feed back ,before my mind runs away , much appreciated Pam
Phelpsy
in
MPN Voice
10 years ago
Reversible Cognitive, Motor and Driving Impairments in Severe Hypothyroidism
Cognitive
impairment
was characterized by declines on speeded executive tests. In contrast, episodic memory performance improved over time regardless of thyroid hormone status.
Cognitive
impairment
was characterized by declines on speeded executive tests. In contrast, episodic memory performance improved over time regardless of thyroid hormone status.
helvella
Thyroid UK
in
Thyroid UK
10 years ago
Thanks
For example my wife apart from the falls and vertical gaze palsy seems to be accelerating down the dementia path coupled with obsessive compulsive behaviour increased short term memory loss and some quite difficult to deal with personality traits along with
cognitive
impairment
- it all seems to
For example my wife apart from the falls and vertical gaze palsy seems to be accelerating down the dementia path coupled with obsessive compulsive behaviour increased short term memory loss and some quite difficult to deal with personality traits along with
cognitive
impairment
- it all seems to
Georgepa
in
PSP Association
10 years ago
slipped through the ne
general heading of
cognitive
impairment
, it is his one and only assessment in 35 years. my question is, is he entitled, as of right, to a neurologic assessment/ diagnosis?
general heading of
cognitive
impairment
, it is his one and only assessment in 35 years. my question is, is he entitled, as of right, to a neurologic assessment/ diagnosis?
KONIEV
in
Headway
10 years ago
Some of us with a long history of migraine have Hughes Syndrome/APS
Attempts at quantifying the prevalence of head-ache and migraine in Hughes syndrome (and in lupus) are limited by the well known diffculties in classification, 9 This is doubly important as the links with
cognitive
impairment
, in both lupus and in patients with antiphospholipid antibodies need Correspondence
Attempts at quantifying the prevalence of head-ache and migraine in Hughes syndrome (and in lupus) are limited by the well known diffculties in classification, 9 This is doubly important as the links with
cognitive
impairment
, in both lupus and in patients with antiphospholipid antibodies need Correspondence
MaryF
in
National Migraine Centre
10 years ago
CBT for IBS?
Hi all, has anyone ever tried cognitive behavioural therapy (CBT) for IBS? My Dr recommended it but I wondered if others had found it helpful? I tried Fodmap diet but it didn't work at all for me.
Hi all, has anyone ever tried cognitive behavioural therapy (CBT) for IBS? My Dr recommended it but I wondered if others had found it helpful? I tried Fodmap diet but it didn't work at all for me.
nbee29
in
IBS Network
10 years ago
Bullying Culture in NHS Mental Health Services Putting Vulnerable Patients at Risk
Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are increasingly at risk from a growing 'bullying' culture in the NHS that is ignoring Government-backed minimum guidelines for effective mental health
Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are increasingly at risk from a growing 'bullying' culture in the NHS that is ignoring Government-backed minimum guidelines for effective mental health
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
10 years ago
Bullying in the NHS, press release from BACP
Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are increasingly at risk from a growing 'bullying' culture in the NHS that is ignoring Government-backed minimum guidelines for effective mental health
Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are increasingly at risk from a growing 'bullying' culture in the NHS that is ignoring Government-backed minimum guidelines for effective mental health
MaryF
Administrator
in
Hughes Syndrome APS Forum
10 years ago
Bullying in the NHS
Press release via BACP Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are increasingly at risk from a growing 'bullying' culture in the NHS that is ignoring Government-backed minimum guidelines for
Press release via BACP Issued: 25th September 2014 by BABCP Board 'BULLYING CULTURE' IN NHS MENTAL HEALTH SERVICES PUTTING VULNERABLE PATIENTS AT RISK Vulnerable patients are increasingly at risk from a growing 'bullying' culture in the NHS that is ignoring Government-backed minimum guidelines for
MaryF
in
Thyroid UK
10 years ago
Blood Test for Depression and Efficacy of CBT?
So the science press brief from Northwestern University was widely reported earlier this week, including in the Daily Mail. Original press brief here: http://www.northwestern.edu/newscenter/stories/2014/09/first-blood-test-to-diagnose-depression-in-adults.html The same authors of this paper had published
So the science press brief from Northwestern University was widely reported earlier this week, including in the Daily Mail. Original press brief here: http://www.northwestern.edu/newscenter/stories/2014/09/first-blood-test-to-diagnose-depression-in-adults.html The same authors of this paper had published
Firestormm
in
Healthy Evidence
10 years ago
Hypothyroidism, B12 deff and a hole in my head...
Hello all, I have just signed up to ask for some advice, as I'm struggling with concentration, focus, memory and drive, among other things I suppose. I was diagnosed with Pernicious Anaemia in 2005, after being rushed into MAU with suspected leukaemia. I've been on injections every 3 months since
Hello all, I have just signed up to ask for some advice, as I'm struggling with concentration, focus, memory and drive, among other things I suppose. I was diagnosed with Pernicious Anaemia in 2005, after being rushed into MAU with suspected leukaemia. I've been on injections every 3 months since
VB_Aylesbury
in
Thyroid UK
10 years ago
What Happens if I Take Thyroxine with Adrenal Problems?
Symptoms may include: a sudden feeling of exhaustion, nausea, headache, inability to concentrate, trembling, muscle weakness, loss of peripheral circulation leading to numbness, lack of muscle control, giddiness, slurred speech, and
cognitive
impairment
.
Symptoms may include: a sudden feeling of exhaustion, nausea, headache, inability to concentrate, trembling, muscle weakness, loss of peripheral circulation leading to numbness, lack of muscle control, giddiness, slurred speech, and
cognitive
impairment
.
cc120
in
Thyroid UK
10 years ago
My GP says there is no physical cause for my PAF, is he right?
As some of you may remember I have had four ablations for my PAF which have improved it dramatically. But I still get occasional PAF and the EP has stated that I will have to live with it because my heart muscle is to thick for him to affect the area. I have accepted this
As some of you may remember I have had four ablations for my PAF which have improved it dramatically. But I still get occasional PAF and the EP has stated that I will have to live with it because my heart muscle is to thick for him to affect the area. I have accepted this
Timmo50
in
AF Association
10 years ago
Cognitive Behaviour Therapy
Hi all, just wondering if anyone has any experience of this in relation to Fibro, and what people's thoughts are on whether it's worth it or not. Ali
Hi all, just wondering if anyone has any experience of this in relation to Fibro, and what people's thoughts are on whether it's worth it or not. Ali
Ali_in_Somerset
in
Fibromyalgia Action UK
10 years ago
Pain management - hopes dashed!!
Hi all, Just to let you know my progress ( or not as it seems). I went to pain management clinic the other week, hoping for a miracle but sadly it wasn't ment to be :( I was told they couldnt help me other than to offer me cognitive therapy or counselling....whatever!! Has anyone else been to these
Hi all, Just to let you know my progress ( or not as it seems). I went to pain management clinic the other week, hoping for a miracle but sadly it wasn't ment to be :( I was told they couldnt help me other than to offer me cognitive therapy or counselling....whatever!! Has anyone else been to these
glassback
in
Fibromyalgia Action UK
10 years ago
Early Retirement due to ill health
Hello I was wondering if anyone has gone through the process of attending occupational health and several other agencies, physio, cognitive behaviour therapy, medical assessments. I have been attending all these groups and have yet to even see a form to request early retirement. I have another medical
Hello I was wondering if anyone has gone through the process of attending occupational health and several other agencies, physio, cognitive behaviour therapy, medical assessments. I have been attending all these groups and have yet to even see a form to request early retirement. I have another medical
ef59
in
Fibromyalgia Action UK
10 years ago
Getting to see a Consultant
Does anyone else have difficulty in getting their GP to refer them to a specialist? I'm sorry it is a long sage, but I just don't know where to go now. I had pain from sciatica, arthritis and tendonitis over many years along with episodes of bursitis and pain and tenderness that was undiagnosed. I
Does anyone else have difficulty in getting their GP to refer them to a specialist? I'm sorry it is a long sage, but I just don't know where to go now. I had pain from sciatica, arthritis and tendonitis over many years along with episodes of bursitis and pain and tenderness that was undiagnosed. I
Hidden
in
Fibromyalgia Action UK
10 years ago
1
...
31
32
33
...
38
Next page
10
20
30
Filter results
Clear filters
Posted in
All communities
Cure Parkinson's
93 results
Anxiety and Depression Support
83 results
Thyroid UK
53 results
View top 10 communities
Sort by
Most Relevant
Newest