Search
Search
About
Log in
Join
Experiences with
Brain haemorrhage
Posts
Communities
2,123 public posts
Filter results
Study examines the potential of spinal cord stimulation
A new study lays a new way of treating PD out " A new study finds that spinal cord stimulation could represent an alternate therapy for people with Parkinson’s disease that is resistant to conventional treatments. The researchers claim that this emerging technology may help decrease pain and improve
A new study lays a new way of treating PD out " A new study finds that spinal cord stimulation could represent an alternate therapy for people with Parkinson’s disease that is resistant to conventional treatments. The researchers claim that this emerging technology may help decrease pain and improve
Abdiqani
in
Cure Parkinson's
4 years ago
Spinal Cord Stimulation Alleviates Parkinson’s Pain in Small Study
Spinal cord stimulation can effectively decrease pain, and also may help alleviate motor symptoms, in people with Parkinson’s disease (PD), regardless of whether patients have previously undergone deep brain stimulation, a small study suggests. https://parkinsonsnewstoday.com/2020/10/02/spinal-cord-stimulation-alleviates-parkinsons-pain-small-study-suggests
Spinal cord stimulation can effectively decrease pain, and also may help alleviate motor symptoms, in people with Parkinson’s disease (PD), regardless of whether patients have previously undergone deep brain stimulation, a small study suggests. https://parkinsonsnewstoday.com/2020/10/02/spinal-cord-stimulation-alleviates-parkinsons-pain-small-study-suggests
JayPwP
in
Cure Parkinson's
4 years ago
Life insurance
Can anyone suggest a UK firm they’ve personally used, that doesn’t refuse people who’ve had a
brain
haemorrhage
? Thanks.
Can anyone suggest a UK firm they’ve personally used, that doesn’t refuse people who’ve had a
brain
haemorrhage
? Thanks.
HereHareHere
in
Brain Aneurysm Support
4 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Confused!
Originally one neurologist diagnosed my condition as Mayasthenia Gravis. Later others attributed it to Cerebellar Ataxia having seen MRI, CT etc. Recently discovered an enlarged Thymus which is often associated with Mayasthenia G. Wonder if I have both!! Any information?
Originally one neurologist diagnosed my condition as Mayasthenia Gravis. Later others attributed it to Cerebellar Ataxia having seen MRI, CT etc. Recently discovered an enlarged Thymus which is often associated with Mayasthenia G. Wonder if I have both!! Any information?
dennisataxia
in
Ataxia UK
4 years ago
Has anyone had meningitis more than once? How do you cope?
Hi, I was wondering if anyone has had meningitis more than once? I had meningococcal disease when I was 4 years old and lost most of my hearing in my left ear . I also had it when I was 9 years old due to having the vaccine, this form was viral meningitis but I was still hospitalised. I also lost my
Hi, I was wondering if anyone has had meningitis more than once? I had meningococcal disease when I was 4 years old and lost most of my hearing in my left ear . I also had it when I was 9 years old due to having the vaccine, this form was viral meningitis but I was still hospitalised. I also lost my
ahsatan89
in
Meningitis Now
4 years ago
Brain Haemorrhage recovery
Hi 5 weeks ago my 39 year old boyfriend suffered a massive intracerebral
haemorrhage
on the front right side of his
brain
. He was given a craniotomy to remove the bleed. He was in icu for 3 weeks and in an induced coma for 2 of those. He was given a less than 50% chance of survival.
Hi 5 weeks ago my 39 year old boyfriend suffered a massive intracerebral
haemorrhage
on the front right side of his
brain
. He was given a craniotomy to remove the bleed. He was in icu for 3 weeks and in an induced coma for 2 of those. He was given a less than 50% chance of survival.
GABMX
in
Headway
4 years ago
Shingles Shot
Is it safe to get the shingles shot if I have CLL? If yes, which one ?
Is it safe to get the shingles shot if I have CLL? If yes, which one ?
CouldBworse
in
CLL Support
4 years ago
Melatonin For Parkinson's Disease (Pt. 2)
In case you missed part 1, here is a link to it : https://healthunlocked.com/parkinsonsmovement/posts/143507411/melatonin-for-parkinsons-disease....finally Melatonin is the only naturally occurring substance in the body that I have found that can help return the body toward homeostasis through multiple
In case you missed part 1, here is a link to it : https://healthunlocked.com/parkinsonsmovement/posts/143507411/melatonin-for-parkinsons-disease....finally Melatonin is the only naturally occurring substance in the body that I have found that can help return the body toward homeostasis through multiple
chartist
in
Cure Parkinson's
4 years ago
Our virtual pub took place today. I believe everybody enjoyed it. Next Sunday, 9/27, 2nd HU virtual gathering @ 5 PM London time.
50+ people gave me their email addresses. 25 people plugged in. We got to introduce ourselves and put a face to the name. Zoom has 4 breakout rooms. In order to allow more substantive conversation, next week, I thought I would send the 1st ten who plug-in to one breakout room and the 2nd 10
50+ people gave me their email addresses. 25 people plugged in. We got to introduce ourselves and put a face to the name. Zoom has 4 breakout rooms. In order to allow more substantive conversation, next week, I thought I would send the 1st ten who plug-in to one breakout room and the 2nd 10
MBAnderson
in
Cure Parkinson's
4 years ago
acoustic neuroma ?
Hi . I am having tinnitus in one ear only and my doc has referred me for a MRI scan to rule out acoustic neuroma. As you can probably understand my HA has now gone through the roof ,i cant eat i cant sleep and i am scared to death of having the MRI ,i have a wait of around 6 weeks before i even get the
Hi . I am having tinnitus in one ear only and my doc has referred me for a MRI scan to rule out acoustic neuroma. As you can probably understand my HA has now gone through the roof ,i cant eat i cant sleep and i am scared to death of having the MRI ,i have a wait of around 6 weeks before i even get the
lynstone60
in
Anxiety Support
4 years ago
Lonely
I had a
brain
haemorrhage
2 years ago my life as totally changed lost my job lost friends and suffer with terrible anxiety I'm not the same person I was full of life independent now I have mixing with people talking and going out everyone I'm close to life is moving on and I feel stuck can't see anything
I had a
brain
haemorrhage
2 years ago my life as totally changed lost my job lost friends and suffer with terrible anxiety I'm not the same person I was full of life independent now I have mixing with people talking and going out everyone I'm close to life is moving on and I feel stuck can't see anything
Gym1bunny
in
Living with Anxiety
4 years ago
Seeking Information
I have joined here today. I have Power of Atorney for my 41 year old son. He suffered a severe Brain bleed caused by a benign tumour He is now left with severe short term memory, plus other related Aquired Brain Injury problems. At 41 he is a very frustrated young man desperate to lead a happier life
I have joined here today. I have Power of Atorney for my 41 year old son. He suffered a severe Brain bleed caused by a benign tumour He is now left with severe short term memory, plus other related Aquired Brain Injury problems. At 41 he is a very frustrated young man desperate to lead a happier life
Saltness
in
Headway
4 years ago
DBS doesn't seem to work?
I had DBS surgery 2 month ago and had 2 programming sessions, but still far from feeling any better. I can say, My tremors and distonia on presurgery status, taking much more medication than before and still having bad days (mostly of them). Does it mean failure of DBS? I don't know what to do. I feel
I had DBS surgery 2 month ago and had 2 programming sessions, but still far from feeling any better. I can say, My tremors and distonia on presurgery status, taking much more medication than before and still having bad days (mostly of them). Does it mean failure of DBS? I don't know what to do. I feel
koshca
in
Cure Parkinson's
4 years ago
Any studies on longterm effects of live shingles vaccine and PMR
I was wondering if anyone knows of any studies that have been done about those of us that contracted PMR after taking the live shingles vaccine. I wonder if PMR will last as long in our system as the shingles vaccine antibodies are active in our system? The pharmacist says the antibodies last 5+years
I was wondering if anyone knows of any studies that have been done about those of us that contracted PMR after taking the live shingles vaccine. I wonder if PMR will last as long in our system as the shingles vaccine antibodies are active in our system? The pharmacist says the antibodies last 5+years
Linny3
in
PMRGCAuk
4 years ago
Medication and DBS
Hi all. My husband diagnosed with PD two years ago (almost). He refused to take any medication. It seems PD had some progress. I have a feeling he is now thinking about treatment or medication. He asked me how long usually takes to be on medication before going for DBS. (He is 44years old) Do you
Hi all. My husband diagnosed with PD two years ago (almost). He refused to take any medication. It seems PD had some progress. I have a feeling he is now thinking about treatment or medication. He asked me how long usually takes to be on medication before going for DBS. (He is 44years old) Do you
Parsa
in
Cure Parkinson's
4 years ago
Focused Ultrasound Therapy, FDA-approved for Essential Tremors
Focused ultrasound is a completely non-invasive method of thalamotomy - a procedure in which a predefined small volume of brain tissue containing nerve cells causing the tremor is destroyed - that could be an effective option for certain patients. It is performed while the patient is awake and involves
Focused ultrasound is a completely non-invasive method of thalamotomy - a procedure in which a predefined small volume of brain tissue containing nerve cells causing the tremor is destroyed - that could be an effective option for certain patients. It is performed while the patient is awake and involves
Pa-zzi69
in
Cure Parkinson's
4 years ago
Shingles vaccine
Shingles vaccine. Hi am am ETJak2+, I am unable to have the live shingles vaccine with nhs, but I have read that there is an inert vaccine available. Has anyone had this on the nhs and if so how did you achieve it. Thank you in advance.
Shingles vaccine. Hi am am ETJak2+, I am unable to have the live shingles vaccine with nhs, but I have read that there is an inert vaccine available. Has anyone had this on the nhs and if so how did you achieve it. Thank you in advance.
Hydrox
in
MPN Voice
4 years ago
Viral meningitis last month
Last month, July 2020, I was diagnosed with viral meningitis after being misdiagnosed with covid (by two different md). So it went on for about 11 days before being diagnosed at the tail end of it. Now, a month later I am still having grogginess and eye spots, major fatigue. Several other lingering symptoms
Last month, July 2020, I was diagnosed with viral meningitis after being misdiagnosed with covid (by two different md). So it went on for about 11 days before being diagnosed at the tail end of it. Now, a month later I am still having grogginess and eye spots, major fatigue. Several other lingering symptoms
MrsMagu
in
Meningitis Now
4 years ago
Chemo side effects
Hello, I'm currently on cycle no. 7 (chemo and immunatherapy) for terminal stage 4 lung cancer with 5 more cycles to go and am finding the side effects following treatment are getting worse and it takes me longer to recover. I seem to spend more time feeling rough than anything and somedays I feel like
Hello, I'm currently on cycle no. 7 (chemo and immunatherapy) for terminal stage 4 lung cancer with 5 more cycles to go and am finding the side effects following treatment are getting worse and it takes me longer to recover. I seem to spend more time feeling rough than anything and somedays I feel like
Bailey19260
in
The Roy Castle Lung Cancer Foundation
4 years ago
Seeking some help for my Surgery
I unfortunately suffered a traumatic brain injury in February this year. I had to have a craniotomy to basically save my life with my brain swelling. I was wondering if anybody could help regarding my upcoming surgery and how my life will be afterwards? I have a Cranioplasty 3rd August and was just
I unfortunately suffered a traumatic brain injury in February this year. I had to have a craniotomy to basically save my life with my brain swelling. I was wondering if anybody could help regarding my upcoming surgery and how my life will be afterwards? I have a Cranioplasty 3rd August and was just
PCranston95
in
Headway
4 years ago
1
...
24
25
26
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Cure Parkinson's
786 results
Headway
266 results
Meningitis Now
231 results
View top 10 communities
Sort by
Most Relevant
Newest