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Experiences with
Brain haemorrhage
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I need to change :(
I have a type of OCD that makes me worry about every single symptom i get. For example a head ache. My head goes into over drive and tells me I have a brain tumor or a pain in my leg is a blood clot. Im at the doctors probably once a week with something new. But no one listens. Ive been in the CBT waiting
I have a type of OCD that makes me worry about every single symptom i get. For example a head ache. My head goes into over drive and tells me I have a brain tumor or a pain in my leg is a blood clot. Im at the doctors probably once a week with something new. But no one listens. Ive been in the CBT waiting
sophieroxanne94
in
Anxiety Support
10 years ago
What procedure have you used to turn down your DBS stimulator?
I think my stimulator may be turned up too high because I started having some new type of dystonia after beginning lifting weights. What is the best way to make sure you have the right amount of stimulator amplitude or pulse width for therapeutic benefit?
I think my stimulator may be turned up too high because I started having some new type of dystonia after beginning lifting weights. What is the best way to make sure you have the right amount of stimulator amplitude or pulse width for therapeutic benefit?
AlabamaDoc
in
Cure Parkinson's
10 years ago
Neck & midline "tremors" developed after DBS for Parkinson's disease.
I had bilateral DBS for Parkinson's disease last year. For the first 3 months, I had absolutely no dystonia or dyskinesia. Then I started to develop a tremor in the back of neck and jaw associated with some dystonia of the back of my neck, middle back, and even abdominal muscles. Before DBS, I would
I had bilateral DBS for Parkinson's disease last year. For the first 3 months, I had absolutely no dystonia or dyskinesia. Then I started to develop a tremor in the back of neck and jaw associated with some dystonia of the back of my neck, middle back, and even abdominal muscles. Before DBS, I would
AlabamaDoc
in
Cure Parkinson's
10 years ago
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Is there anyone with DBS taking Madopar or Sinemet and then added Azilect?
This question is for a friend who is not 'online'. He has DBS and on Madopar several times a day. His DBS specialist prescribed him Azilect, several months ago, which he took for about one week, but stopped because he perceived no benefit. His specialist told him that he did not give it enough time
This question is for a friend who is not 'online'. He has DBS and on Madopar several times a day. His DBS specialist prescribed him Azilect, several months ago, which he took for about one week, but stopped because he perceived no benefit. His specialist told him that he did not give it enough time
Norton1
in
Cure Parkinson's
10 years ago
A change in diet?
Oh, and this is due to a
brain
haemorrhage
I had 2 years ago.
Oh, and this is due to a
brain
haemorrhage
I had 2 years ago.
B_S_A
in
Headway
10 years ago
What brain haemorrhage??
I just got 84/100 on a piece of coursework. Bragging over.
I just got 84/100 on a piece of coursework. Bragging over.
B_S_A
in
Headway
10 years ago
Hey there
Hey, my name's Ben and on 02/06/2012 I had a
brain
haemorrhage
. Turns out I have an arteriovenous malformation in my
brain
(AVM), which is basically a nest of poorly developed blood vessels that can bleed at any time causing a stroke.
Hey, my name's Ben and on 02/06/2012 I had a
brain
haemorrhage
. Turns out I have an arteriovenous malformation in my
brain
(AVM), which is basically a nest of poorly developed blood vessels that can bleed at any time causing a stroke.
B_S_A
in
Anxiety Support
10 years ago
Has anyone had shingles on their face ?
Hiya I had a really bad flare last week and the most horrendous headaches and pain in my eyes ....I thought that maybe my biologic Cimzia was not working but yesterday a rash appeared on the side of my face and after itching my head all night I went to to the Drs today and it's turned out I have shingles
Hiya I had a really bad flare last week and the most horrendous headaches and pain in my eyes ....I thought that maybe my biologic Cimzia was not working but yesterday a rash appeared on the side of my face and after itching my head all night I went to to the Drs today and it's turned out I have shingles
claireyj
in
NRAS
10 years ago
I was diagnosed with hypothyroidism when I was 39 I am now 53 and still feel unwell also started the menopause same time.
Have not had a period since, just lately I have been so low tearful, no energy, pain and now pain in my buttocks which I think is sciatica which is so painful. My recent TSH levels were 14,, I normal run between 2.3 - 2.4 they have upped my levothyroxine to 175mcg daily, this was I week ago and I still
Have not had a period since, just lately I have been so low tearful, no energy, pain and now pain in my buttocks which I think is sciatica which is so painful. My recent TSH levels were 14,, I normal run between 2.3 - 2.4 they have upped my levothyroxine to 175mcg daily, this was I week ago and I still
darb
in
Thyroid UK
10 years ago
Viral Meningitis Awareness Week
This week we have our 2nd viral meningitis awareness week. Each day of the week we’ll be being vocal about the true impact of the disease and letting people know that we are here to support everyone affected. Viral meningitis can affect anyone. There is a misconception that viral meningitis is a
This week we have our 2nd viral meningitis awareness week. Each day of the week we’ll be being vocal about the true impact of the disease and letting people know that we are here to support everyone affected. Viral meningitis can affect anyone. There is a misconception that viral meningitis is a
MNClaireD
Meningitis Now
in
Meningitis Now
10 years ago
Shingles vaccine--Has anyone had the shingles vaccine while taking methotrexate? Is it okay to do so?
shareasmile
in
NRAS
10 years ago
Why do I feel guilty for being sick and tired of feeling trapped?
I'm literally sick and tired of being trapped with what I can only call duty to care for my husband, who's been
brain
damaged for 13 years following a subarachnoid
haemorrhage
.
I'm literally sick and tired of being trapped with what I can only call duty to care for my husband, who's been
brain
damaged for 13 years following a subarachnoid
haemorrhage
.
Hidden
in
Headway
10 years ago
Many Doctors are using these under or over the counter Do not rush out and buy.
Lymediseaseguide.org/rife-machine-therapy-for-Lyme-disease I first came across these devices in the late 70's in the form of radionics they go by biofeedback quantum healing. Computer versions can get right under my skin: They are illegal as one of the comments says. Doctors and other practitioners
Lymediseaseguide.org/rife-machine-therapy-for-Lyme-disease I first came across these devices in the late 70's in the form of radionics they go by biofeedback quantum healing. Computer versions can get right under my skin: They are illegal as one of the comments says. Doctors and other practitioners
carolr
in
Thyroid UK
10 years ago
I've had LH facial palsy for a week the neurologist says to wait to see recovery but is there anything I should be doing in the meantime.
Does anybody have experience of palsy caused by
brain
haemorrhage
Does anybody have experience of palsy caused by
brain
haemorrhage
Kayarla
in
Facial Palsy UK
10 years ago
Anyone know what turning the impedance down on my DBS will do ? Its three weeks since, as each day comes so dose the pain .
Could or would the impedance being turn down ,take three weeks to kick in fully . I do not know if my PD has moved on or it the DBS. yours EXPORT.
Could or would the impedance being turn down ,take three weeks to kick in fully . I do not know if my PD has moved on or it the DBS. yours EXPORT.
export
in
Cure Parkinson's
10 years ago
SUPPORT & ACCEPTANCE
SORRY FOLKS I NEED A RANT. I KNOW WE'VE TALKED A LOT BOUT LACK OF SUPPORT & UNDERSTANDING POST BI. IT NEVER FAILS TO AMAZE HOW BAD THIS IS. TO CUT A LONG STORY SHORT MY SISTER & I HAVE GOT TO GET MY DAD'S HOUSE READY TO SELL. SO FAR HER ONLY COMMENT IS TO SAY "I DON'T CARE ABOUT THE HOUSE". FOR THE
SORRY FOLKS I NEED A RANT. I KNOW WE'VE TALKED A LOT BOUT LACK OF SUPPORT & UNDERSTANDING POST BI. IT NEVER FAILS TO AMAZE HOW BAD THIS IS. TO CUT A LONG STORY SHORT MY SISTER & I HAVE GOT TO GET MY DAD'S HOUSE READY TO SELL. SO FAR HER ONLY COMMENT IS TO SAY "I DON'T CARE ABOUT THE HOUSE". FOR THE
Hidden
in
Headway
10 years ago
Sah Help
Hi guys, its 17 months now since my subarachnoid
brain
haemorrhage
and Ive had a headache/eye pain for four days now. I hate going to the drs because they will just send me to a&e and I have two children to look after. Do any of you have occasions where you suffer bad headaches?
Hi guys, its 17 months now since my subarachnoid
brain
haemorrhage
and Ive had a headache/eye pain for four days now. I hate going to the drs because they will just send me to a&e and I have two children to look after. Do any of you have occasions where you suffer bad headaches?
jord38
in
Headway
10 years ago
Not sure whether this is a scleroderma rash or Lupus...any advice...it's extremely painful
Hi All, I have Mixed Connective Tissue Disease and I have woken up this morning with a really swollen wrist - nothing new there - but I have a strange, wheel rash on top of it. Not ring worm as I have had this before and I haven't had any tick bites etc so that rules out Lyme disease. It is flat,
Hi All, I have Mixed Connective Tissue Disease and I have woken up this morning with a really swollen wrist - nothing new there - but I have a strange, wheel rash on top of it. Not ring worm as I have had this before and I haven't had any tick bites etc so that rules out Lyme disease. It is flat,
cass1984
in
LUPUS UK
10 years ago
Blurry eyes.
Just wondered how many people suffer with blurry or distorted vision? Its something that freaks me out with anxiety but its another thing I'm starting to get more of, And me being me straight away thinks brain tumour in my anxiety mind, Then my sane mind kicks in.
Just wondered how many people suffer with blurry or distorted vision? Its something that freaks me out with anxiety but its another thing I'm starting to get more of, And me being me straight away thinks brain tumour in my anxiety mind, Then my sane mind kicks in.
miami
in
Anxiety Support
10 years ago
Micropsia
I wondered if I was the only person on the planet who suffers from permanent Micropsia after a hypoxia brain injury. There's not much information online and the only article I've found is here http://en.wikipedia.org/wiki/Micropsia Does anyone on here suffer from this condition ? It is very hard
I wondered if I was the only person on the planet who suffers from permanent Micropsia after a hypoxia brain injury. There's not much information online and the only article I've found is here http://en.wikipedia.org/wiki/Micropsia Does anyone on here suffer from this condition ? It is very hard
D0v3
in
Headway
10 years ago
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