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Myoovi - has anyone tried this and what do you think?
I've looking at getting the myoovi tens machine for my awful endo pain - has anyone tried it and can share whether it's been useful for them? X
I've looking at getting the myoovi tens machine for my awful endo pain - has anyone tried it and can share whether it's been useful for them? X
AFC007
in
Endometriosis UK
3 months ago
Tremor Assessment
Has anyone had a tremor assessment prior to deep brain stimulation?
Has anyone had a tremor assessment prior to deep brain stimulation?
Ostap
in
Ataxia UK
6 months ago
DBS: Medtronic question re. voice
Hi everyone. As many of you know I had DBS last August. Didn’t reverse my symptoms 5 years as was touted by my neuro but patched me up to fight another couple of rounds. When I was switched on, after a day or so I noticed that it was much harder to speak: volume and articulacy were much harder to produce
Hi everyone. As many of you know I had DBS last August. Didn’t reverse my symptoms 5 years as was touted by my neuro but patched me up to fight another couple of rounds. When I was switched on, after a day or so I noticed that it was much harder to speak: volume and articulacy were much harder to produce
jeeves19
in
Cure Parkinson's
6 months ago
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Seeking Advice: Non-Medication Methods for Managing Hand Joint Pain Flare-Ups
Hello everyone, I'm reaching out to this community for some advice and personal experiences. I have been living with lupus for six years now, and I've been dealing with joint pain in my hands for quite a while. I'm particularly interested in non-medication methods to manage flare-ups. I've heard
Hello everyone, I'm reaching out to this community for some advice and personal experiences. I have been living with lupus for six years now, and I've been dealing with joint pain in my hands for quite a while. I'm particularly interested in non-medication methods to manage flare-ups. I've heard
Sophieeeee
in
LUPUS UK
3 months ago
vagus nerve stimulation machines and Afib
Has anyone with AFib got any experience of using one of these machines, such as Nurosym, Amofit, Sensate?
Has anyone with AFib got any experience of using one of these machines, such as Nurosym, Amofit, Sensate?
MTBCyclist
in
Atrial Fibrillation Support
6 months ago
Insomnia
Hello, I was diagnosed PD when i was 37, now I'm 46 years old. 5 months ago i was DBS. After surgery, things did not go bad, but not as good I have expected. On March 7th i was reajusted the neurostimulator by my neourologist. On March 15th i started HDT Protocol, 50 mg sublingual on alternative days
Hello, I was diagnosed PD when i was 37, now I'm 46 years old. 5 months ago i was DBS. After surgery, things did not go bad, but not as good I have expected. On March 7th i was reajusted the neurostimulator by my neourologist. On March 15th i started HDT Protocol, 50 mg sublingual on alternative days
carlosgarcia2048
in
Cure Parkinson's
6 months ago
struggling to get diagnosed
Since I was 13 I have been dealing with significant pain in my lower abdomen and back, particularly during my menstrual cycle. The intensity of the pain has been increasing, to the point where it is impacting my ability to carry out normal daily activities some days. Additionally, I have been experiencing
Since I was 13 I have been dealing with significant pain in my lower abdomen and back, particularly during my menstrual cycle. The intensity of the pain has been increasing, to the point where it is impacting my ability to carry out normal daily activities some days. Additionally, I have been experiencing
Ca1t7yn
in
Endometriosis UK
4 months ago
Curious about using the tens unit
Has anyone tried this for RLS? If so, where did you place the pads and how much did it help?
Has anyone tried this for RLS? If so, where did you place the pads and how much did it help?
Fleur29
in
Restless Legs Syndrome
4 months ago
mannitol challenge test
has anyone had mannitol challenge test an didn't need to stop montelukast? Was your test positive (you had your asthma confirmed)?
has anyone had mannitol challenge test an didn't need to stop montelukast? Was your test positive (you had your asthma confirmed)?
sciencepotato
in
Lung Conditions Community Forum
11 months ago
AbbVie’s Produodopa approved by SMC to treat Parkinson’s disease patients in Scotland
AbbVie’s Produodopa (foslevodopa-foscarbidopa) has been accepted by the Scottish Medicines Consortium (SMC) for use within NHS Scotland to treat advanced levodopa-responsive Parkinson’s disease (PD). PD patients with severe motor fluctuations and hyperkinesia or dyskinesia when previous available combinations
AbbVie’s Produodopa (foslevodopa-foscarbidopa) has been accepted by the Scottish Medicines Consortium (SMC) for use within NHS Scotland to treat advanced levodopa-responsive Parkinson’s disease (PD). PD patients with severe motor fluctuations and hyperkinesia or dyskinesia when previous available combinations
Farooqji
in
Cure Parkinson's
7 months ago
First post.
Warning, long post. 2 am and I have cleaned the kitchen now I can move, even folded the t towels neatly in their box. I could do more but don’t want to wake hubby. I have always loved my fitness, I was a runner and training for an Ironman when things started to go wrong. First joint replacement at
Warning, long post. 2 am and I have cleaned the kitchen now I can move, even folded the t towels neatly in their box. I could do more but don’t want to wake hubby. I have always loved my fitness, I was a runner and training for an Ironman when things started to go wrong. First joint replacement at
TiaPasha
in
PMRGCAuk
4 months ago
Thanks for the replies to my previous post
Thanks for your replies to my first post everyone. Comforting to know I'm not alone in feeling overwhelmed by this, but I'm blown away by how many people are enduring this and find ectopics really debilitating. It's so sad that our feeling are dismissed as unimportant by people who have no idea what
Thanks for your replies to my first post everyone. Comforting to know I'm not alone in feeling overwhelmed by this, but I'm blown away by how many people are enduring this and find ectopics really debilitating. It's so sad that our feeling are dismissed as unimportant by people who have no idea what
dragonsinger
in
British Heart Foundation
7 months ago
Is this bladder endo
Hi all. I'm wondering if anyone with bladder endo has experienced anything like this, I have not had bladder endo mentioned however DIE rectosigmoid/ovarian cysts etc awaiting lap to get a full picture. Yesterday I was sat curled up no reason just comfort, when I moved I had the most intense pain from
Hi all. I'm wondering if anyone with bladder endo has experienced anything like this, I have not had bladder endo mentioned however DIE rectosigmoid/ovarian cysts etc awaiting lap to get a full picture. Yesterday I was sat curled up no reason just comfort, when I moved I had the most intense pain from
Lornalost89
in
Endometriosis UK
4 months ago
pain?
Anybody else have pain on waking, from hips and legs up to arms & shoulders--not explained by exercise or lack thereof? Can barely hobble about the house to get my meds and feed the cat. Sometimes it helps to tighten all the muscles to form an upright posture--but as soon as I loosen them to move, it
Anybody else have pain on waking, from hips and legs up to arms & shoulders--not explained by exercise or lack thereof? Can barely hobble about the house to get my meds and feed the cat. Sometimes it helps to tighten all the muscles to form an upright posture--but as soon as I loosen them to move, it
ottercat
in
Cure Parkinson's
7 months ago
The problematic 2nd dose of the day
Good evening. Wondering if anybody else experienced similar or if you’ve any idea why the following happens: my first CL of the day works reasonably well (although I only get two hours of relief from it). The second thought is really bad: after my first dose I go badly off (it’s been getting worse as
Good evening. Wondering if anybody else experienced similar or if you’ve any idea why the following happens: my first CL of the day works reasonably well (although I only get two hours of relief from it). The second thought is really bad: after my first dose I go badly off (it’s been getting worse as
jeeves19
in
Cure Parkinson's
7 months ago
DBS awake or under general anesthesia
I've been told that for my DBS operation I will be under general anesthesia. I'm just wondering what others have experienced. I like the idea of a good sleep and waking to find the operation over but I was under the impression that when done awake the patient can indicate when the probes are correctly
I've been told that for my DBS operation I will be under general anesthesia. I'm just wondering what others have experienced. I like the idea of a good sleep and waking to find the operation over but I was under the impression that when done awake the patient can indicate when the probes are correctly
gingerj
in
Cure Parkinson's
7 months ago
Turmeric ginger and black pepper
Anyone taken this as a capsule or the natural ingredients I've read quite a bit about these ingredients and they seem to possibly help with copd symptoms. Could anyone enlighten me whether its worth buying the manufactured capsules please ? X
Anyone taken this as a capsule or the natural ingredients I've read quite a bit about these ingredients and they seem to possibly help with copd symptoms. Could anyone enlighten me whether its worth buying the manufactured capsules please ? X
soulboy118
in
COPD Friends
11 months ago
Problem with EBV
Hi all I have active EBV, but I can't take Lysine because it reduces my sleep-5,6 hours and I sleep very poorly by waking up several times during the night. My question is, is there anything else that can successfully replace Lysine. I've tried taking Valtrex, but I'm even worse off it, because it's
Hi all I have active EBV, but I can't take Lysine because it reduces my sleep-5,6 hours and I sleep very poorly by waking up several times during the night. My question is, is there anything else that can successfully replace Lysine. I've tried taking Valtrex, but I'm even worse off it, because it's
Stongwave
in
Thyroid UK
1 year ago
The battle is over
Good morning, A week ago my brother aka Savkid passed away. He fought valiantly this cancer for just over 2 years since diagnosis. I am ever grateful that we had the time we did. I will miss him alot In the last month, he became increasingly weak after the second chemo (docetaxel) treatment, so treatments
Good morning, A week ago my brother aka Savkid passed away. He fought valiantly this cancer for just over 2 years since diagnosis. I am ever grateful that we had the time we did. I will miss him alot In the last month, he became increasingly weak after the second chemo (docetaxel) treatment, so treatments
Hidden
in
Advanced Prostate Cancer
1 year ago
Vagal a fib
I listened to a cardiologist on utube. He mentioned vagal a fib. Does any one what this is? It seems to be a younger cohort but I presume it comes with the usual meds. How can you find out if you have it? I seem to be able to stop a fib attacks with vagal manoeuvres and sometimes my a fib is brought
I listened to a cardiologist on utube. He mentioned vagal a fib. Does any one what this is? It seems to be a younger cohort but I presume it comes with the usual meds. How can you find out if you have it? I seem to be able to stop a fib attacks with vagal manoeuvres and sometimes my a fib is brought
TillyBoss
in
AF Association
7 months ago
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