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Duloxetine
My consultant has mentioned this SNRI to me as a possibility to help with chronic pain from neck bone spurs. Has anyone taken this long term and found it to be beneficial? Thanks
My consultant has mentioned this SNRI to me as a possibility to help with chronic pain from neck bone spurs. Has anyone taken this long term and found it to be beneficial? Thanks
yorkshirelad1
in
Pain Concern
6 months ago
Newly diagnosed
Hi all... Well at long last ive finally found a doctor who doesnt make me feel like im going insane or the pains all in my mind... im a 55 year old store manager and over the last 6 months my pain and fatigue has got worse and both myself and friends and family could see my deterioration. I finally got
Hi all... Well at long last ive finally found a doctor who doesnt make me feel like im going insane or the pains all in my mind... im a 55 year old store manager and over the last 6 months my pain and fatigue has got worse and both myself and friends and family could see my deterioration. I finally got
Crazyangel40
in
Fibromyalgia Action UK
6 months ago
Dizziness from Zytiga/prednisone?
my MO tried something out of the ordinary - let me have a 'vacation' from ADT for a short while, even though i am Castrate -resistant. he was hoping we coudl keep PSA down while my Testosterone recovered, to see if that woudl make me feel better. to use his words, i have 'complained bitterly of the
my MO tried something out of the ordinary - let me have a 'vacation' from ADT for a short while, even though i am Castrate -resistant. he was hoping we coudl keep PSA down while my Testosterone recovered, to see if that woudl make me feel better. to use his words, i have 'complained bitterly of the
Tonwantonga
in
Advanced Prostate Cancer
6 months ago
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Diagnosis of Pudendal Neuralgia - 43, Female, Asia
Hello all, First of all, I am so glad to have found this group where people understand the debility that an illness like Pudendal Neuralgia [PN] causes. I had a very bad UTI that went on for 3 months, took 8 rounds of antibiotics before it was out of my system. In its wake, I have been left with PN.
Hello all, First of all, I am so glad to have found this group where people understand the debility that an illness like Pudendal Neuralgia [PN] causes. I had a very bad UTI that went on for 3 months, took 8 rounds of antibiotics before it was out of my system. In its wake, I have been left with PN.
Moonsorrow
in
Pelvic Pain Support Network
6 months ago
SSRI'S
I was taking Paroxetine with good success for many years unfortunately it stopped working last November after being diagnosed with ptsd. Doctor suggested i tried another ssri started sertraline at beginning of year and it didn't suit me so started escitalopram in March and by June i settled well on 20mg
I was taking Paroxetine with good success for many years unfortunately it stopped working last November after being diagnosed with ptsd. Doctor suggested i tried another ssri started sertraline at beginning of year and it didn't suit me so started escitalopram in March and by June i settled well on 20mg
Lynzlou
in
Anxiety and Depression Support
6 months ago
Advice
Hi, I wondered if anyone could help.I've tried duloxetine & even though it helped massively with the pain I had awful side effects. Any suggestions on other meds please
Hi, I wondered if anyone could help.I've tried duloxetine & even though it helped massively with the pain I had awful side effects. Any suggestions on other meds please
Roxanne-40
in
Fibromyalgia Action UK
6 months ago
Ibs bam
I have ibs and bile acid malabsorption seen gastroenterologist on monday shes ruling out ibd and cronhs but i am still not convinced dont know of wat she said as still get loads of stomach pain specially before and after bowel movements she did say it could b scar tissue nerve damage or fibromalgyia
I have ibs and bile acid malabsorption seen gastroenterologist on monday shes ruling out ibd and cronhs but i am still not convinced dont know of wat she said as still get loads of stomach pain specially before and after bowel movements she did say it could b scar tissue nerve damage or fibromalgyia
Netbet22
in
IBS Network
6 months ago
Bnp level
Hi,I had wolff Parkinson white, suffered years of bad palpitations until I got offered an ablation, unfortunately the ablation wasnt straight forward due to my extra pathway being so close to my AV node, high risk of heart block, anyhow decided it takes the risk as I was told I'd be 5 x more likely to
Hi,I had wolff Parkinson white, suffered years of bad palpitations until I got offered an ablation, unfortunately the ablation wasnt straight forward due to my extra pathway being so close to my AV node, high risk of heart block, anyhow decided it takes the risk as I was told I'd be 5 x more likely to
Nomis21
in
British Heart Foundation
7 months ago
Test results
Hi - I had my blood test results back CPR 5 CK 203 they wouldn’t do the ERS test at my doctors surgery .unknowingly My rheumatologist looked at the results and sent me an email yesterday saying no inflammation and has referred me to another consultant prof Emma Clarke bristol for 2nd opinion to look
Hi - I had my blood test results back CPR 5 CK 203 they wouldn’t do the ERS test at my doctors surgery .unknowingly My rheumatologist looked at the results and sent me an email yesterday saying no inflammation and has referred me to another consultant prof Emma Clarke bristol for 2nd opinion to look
Glutusmaximus
in
PMRGCAuk
7 months ago
Sharing wonder effects of Duloxetine/ Cymbalta
had chemo/radiation 2013 for anal cancer; 6 years later, struck with incontinence and not feeling my toes, ataxia, weak hands. Nothing worked. Just had neurologist, last week, confirm that I had progressive chemotherapy induced peripheral neuropathy (CIPN). He prescribed Cymbalta 30mg....and it has
had chemo/radiation 2013 for anal cancer; 6 years later, struck with incontinence and not feeling my toes, ataxia, weak hands. Nothing worked. Just had neurologist, last week, confirm that I had progressive chemotherapy induced peripheral neuropathy (CIPN). He prescribed Cymbalta 30mg....and it has
USAPRDA
in
Pelvic Radiation Disease Association
7 months ago
Gabapentin and Oxycodone
Hi I'm back, looking for more advice from the wise ones on HealthUnlocked. I recently came off Pramipexole and persuaded my (UK NHS) neurologist to prescribed Oxycodone/Nalazone. I take 10mgs in the morning and 20 about 7.00pm (any later and it doesn't work). This led to an improvement, but my sleep
Hi I'm back, looking for more advice from the wise ones on HealthUnlocked. I recently came off Pramipexole and persuaded my (UK NHS) neurologist to prescribed Oxycodone/Nalazone. I take 10mgs in the morning and 20 about 7.00pm (any later and it doesn't work). This led to an improvement, but my sleep
RLSHell
in
Restless Legs Syndrome
7 months ago
Pramipexole RLS symptoms worse
Just started taking Pramipexole for RLS for the first night. Wow, didn’t know the symptoms would become totally overwhelming all over body too.is this normal, does it settle down? I have Fibromyalgia, which means I also take Duloxetine for the pain and am medication sensitive, but never thought it would
Just started taking Pramipexole for RLS for the first night. Wow, didn’t know the symptoms would become totally overwhelming all over body too.is this normal, does it settle down? I have Fibromyalgia, which means I also take Duloxetine for the pain and am medication sensitive, but never thought it would
Fra3021
in
Restless Legs Syndrome
7 months ago
duloxetine
Hi - has anyone been put on duloxetine My consultant put me on it last week not sure what it is for I know it’s an antidepressant which I suppose I need to cope with the not knowing why I’ve been hurting so much. has anyone noticed it helped with anything else. after a couple of days I noticed my knees
Hi - has anyone been put on duloxetine My consultant put me on it last week not sure what it is for I know it’s an antidepressant which I suppose I need to cope with the not knowing why I’ve been hurting so much. has anyone noticed it helped with anything else. after a couple of days I noticed my knees
Glutusmaximus
in
PMRGCAuk
7 months ago
Duloxetine and insomnia
Hi all I reached out to the group recently about switching to duloxetine from amitriptyline and got lots of helpful advice. I’m now on 30mg of duloxetine and will be increasing further soon but I’m struggling with the side effect of not sleeping. I know it’s common but hoped this would have passed after
Hi all I reached out to the group recently about switching to duloxetine from amitriptyline and got lots of helpful advice. I’m now on 30mg of duloxetine and will be increasing further soon but I’m struggling with the side effect of not sleeping. I know it’s common but hoped this would have passed after
Winter_night
in
Fibromyalgia Action UK
7 months ago
RLS returned after taking Duloxetine
Had RLS for many years, associated with Fibromyalgia. Having taken Amitriptylene, Nortriptyline , Pregabalin for my Fibro, my RLS has been under control. Recently started taking Duloxetine to help my Fibro and my RLS has returned with a vengeance. I get very little sleep, as soon as my head hits pillow
Had RLS for many years, associated with Fibromyalgia. Having taken Amitriptylene, Nortriptyline , Pregabalin for my Fibro, my RLS has been under control. Recently started taking Duloxetine to help my Fibro and my RLS has returned with a vengeance. I get very little sleep, as soon as my head hits pillow
Fra3021
in
Restless Legs Syndrome
7 months ago
Antidepressants 👎
Hi this is my first post here. Was just wondering if anyone can’t tolerate the side effects from antidepressants? I’ve had bouts of depression for 28 years. In my 20s I tried lots but couldn’t get on with any. The longest I stayed on one was Prozac for maybe 6 months but they made me emotionless and
Hi this is my first post here. Was just wondering if anyone can’t tolerate the side effects from antidepressants? I’ve had bouts of depression for 28 years. In my 20s I tried lots but couldn’t get on with any. The longest I stayed on one was Prozac for maybe 6 months but they made me emotionless and
Hidden
in
Anxiety and Depression Support
8 months ago
Urgent CT scan & Duloxetine
In the past couple of weeks; my migraines have been so severe, I have been unable to attend work. Last week my manager sent me home, as she is very concerned about me and didn't think I was ready to return in my "return to work interview". I visited the doctors on Friday, and I have been signed off work
In the past couple of weeks; my migraines have been so severe, I have been unable to attend work. Last week my manager sent me home, as she is very concerned about me and didn't think I was ready to return in my "return to work interview". I visited the doctors on Friday, and I have been signed off work
AMG26
in
Migraine Support
8 months ago
Duloxetine
I have 'moderate' CFSME/Fibromyalgia. I was diagnosed around ten years ago. I am also predisposed to familial clinical depression and have had that on and off since I was a teenager. I've tried many SSRIs over the years but whilst they were okay, I never felt like myself. I'm usually a glass
I have 'moderate' CFSME/Fibromyalgia. I was diagnosed around ten years ago. I am also predisposed to familial clinical depression and have had that on and off since I was a teenager. I've tried many SSRIs over the years but whilst they were okay, I never felt like myself. I'm usually a glass
Hoffgrad
in
Fibromyalgia Action UK
8 months ago
I am so tired, what do I do
I was diagnosed with fybro in 2018 after many years of suffering. I have done 39 years in full time employment, having to travel on buses, trams, underground/overground trains. It was a struggle at times but i needed to have my sanity, i could not sit at home all day as movement does ease the pain. I
I was diagnosed with fybro in 2018 after many years of suffering. I have done 39 years in full time employment, having to travel on buses, trams, underground/overground trains. It was a struggle at times but i needed to have my sanity, i could not sit at home all day as movement does ease the pain. I
Itgoesonandon
in
Fibromyalgia Action UK
8 months ago
Head zaps and migraine
Good morning all, Just wondering if anyone has experienced head zaps as part of a migraine.I'm still taking Sertraline and Mirtazapine and I haven't missed a dose. I got head zaps when I came off Paroxetine but they eased up as soon as I started the Sertraline. Yesterday, for the first time in years
Good morning all, Just wondering if anyone has experienced head zaps as part of a migraine.I'm still taking Sertraline and Mirtazapine and I haven't missed a dose. I got head zaps when I came off Paroxetine but they eased up as soon as I started the Sertraline. Yesterday, for the first time in years
Jackiez
in
Heal My PTSD
8 months ago
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