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Leg pain
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Severe Restless Leg
Hello all ! I have suffered from this horrible condition for 30 years. I have been on every medication known to help. It affects my life day and night! I even experience in my arms now. I currently am on anywhere from 5 to 8 mg daily of Ropinirole. And thats not helping. Long story short I accidently
Hello all ! I have suffered from this horrible condition for 30 years. I have been on every medication known to help. It affects my life day and night! I even experience in my arms now. I currently am on anywhere from 5 to 8 mg daily of Ropinirole. And thats not helping. Long story short I accidently
Gette1274
in
Restless Legs Syndrome
5 months ago
Duloxetine to Mirtazapine
I been on Gabapentin from 23.02.24 and was previously on Pramipexole but had compulsive eating so asked to change. I stopped Pramipexole straight away and moved to Gabapentin and went from 300mg three times a day to 900mg three times a day and not really helped me. Spoke to Dr today who’s decided I should
I been on Gabapentin from 23.02.24 and was previously on Pramipexole but had compulsive eating so asked to change. I stopped Pramipexole straight away and moved to Gabapentin and went from 300mg three times a day to 900mg three times a day and not really helped me. Spoke to Dr today who’s decided I should
Puggy1910
in
Restless Legs Syndrome
5 months ago
Hello after a forced absence.
I stopped getting email updates unexpectedly from PMRGCAuk and at the same time my husband started having health issues so most of my time was spent researching HIS symptoms and trying to make sense of it all. We are back in a waiting pattern till his 5 day EEG finally comes through so thought I would
I stopped getting email updates unexpectedly from PMRGCAuk and at the same time my husband started having health issues so most of my time was spent researching HIS symptoms and trying to make sense of it all. We are back in a waiting pattern till his 5 day EEG finally comes through so thought I would
Dydee
in
PMRGCAuk
8 months ago
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Gabapentin
I've suffered with rls for over 30 years which has gradually got worse and worse. I'm now 74. After taking dopamine agonists for years, then tramadol, codeine and trying Kratom nothing was working and my doctor and neurologist would and could not prescribe anything else. In the past I had tried Pregabalin
I've suffered with rls for over 30 years which has gradually got worse and worse. I'm now 74. After taking dopamine agonists for years, then tramadol, codeine and trying Kratom nothing was working and my doctor and neurologist would and could not prescribe anything else. In the past I had tried Pregabalin
Coeso
in
Restless Legs Syndrome
5 months ago
Cold Turkey Update
Some of you are familiar with my story so far so I will make this brief. Three years ago I was taking 6mg Pramepexole. It took me nearly three years to taper the dose down to 1.25. My idiotic Neurologist said he would no longer treat me unless I stoped taking Pramipexole. He writes my prescriptions
Some of you are familiar with my story so far so I will make this brief. Three years ago I was taking 6mg Pramepexole. It took me nearly three years to taper the dose down to 1.25. My idiotic Neurologist said he would no longer treat me unless I stoped taking Pramipexole. He writes my prescriptions
welschrispy
in
Restless Legs Syndrome
5 months ago
How much more can I take ?
Its a year now since I started the worst journey of my life getting off Ropinrole but I did it and Im proud . Yes daytime and evenings are much better but nights are still pure hell . I have had one nights sleep in a year and that was 1til 6am .Interestingly I was out that evening and only had 600 mgs
Its a year now since I started the worst journey of my life getting off Ropinrole but I did it and Im proud . Yes daytime and evenings are much better but nights are still pure hell . I have had one nights sleep in a year and that was 1til 6am .Interestingly I was out that evening and only had 600 mgs
Huntingleroy
in
Restless Legs Syndrome
5 months ago
Endo on the bladder
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Anyone else have the bladder and bowel endo? Willing to try anything, for any kind of relief. I have endo on and going into my bladder and now also effecting my bowel. It's triggered normally about day 3 of my period and last for a good 3 weeks. The first few days I just have to be near a toilet, when
Country-Girl100
in
Endometriosis UK
9 months ago
arthritis
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
having cervicogenic headaches from arthritis in neck. Any painkillers better than paracetamol that we can safely take? Thanks again.
Lindaj754
in
AF Association
9 months ago
not feeling good
The severity of the
leg
pain
has decreased in the last 4-6 weeks, but the frequency has increased. And did I mention the hot flashes are worse and more frequent. I know it’s like a lot of little things but I just don’t feel right. I walk every day.
The severity of the
leg
pain
has decreased in the last 4-6 weeks, but the frequency has increased. And did I mention the hot flashes are worse and more frequent. I know it’s like a lot of little things but I just don’t feel right. I walk every day.
JayJinxed8112
in
Advanced Prostate Cancer
1 year ago
taking trazodone with Gabapentin
First of all, I am so thankful for this community and the information I have found on here. I am finally getting relief from my RLS by taking gabapentin. My doctor has been way too conservative, starting me at 100mg and only increasing 100mg every week or two weeks. I am finally at a dosage of 1200mg
First of all, I am so thankful for this community and the information I have found on here. I am finally getting relief from my RLS by taking gabapentin. My doctor has been way too conservative, starting me at 100mg and only increasing 100mg every week or two weeks. I am finally at a dosage of 1200mg
Tbone87
in
Restless Legs Syndrome
5 months ago
How to deal with side effect of hot flashes and feeling hot all the time from pain meds?
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
How do you deal with the side effect of hot flashes and feeling hot all the time that is being caused from your pain medicine or antidepressants used for pain? I take Tramadol at the highest dosage everyday for my severe nerve pain from CRPS because it's the only thing that works for me. However it makes
Hidden
in
Neuro Support
9 months ago
How to deal with side effects of feeling hot from pain meds and antidepressants for pain?
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
How do you deal with the side effect of feeling hot all the time and having hot flashes that are caused from your pain medicine or your antidepressant used for pain? I take Tramadol at the highest dosage for my severe nerve pain from CRPS because it's the only thing that works for me however I find that
Hidden
in
Neuropathy Support
9 months ago
RSV and Flare
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
hi everyone, I seem to be in the wars a bit at the moment and need some advice: - diagnosed PMR and RA April 23 - dosage of 30mg pred and 20 mg methotrexate - gradually reduced pred to 10.5 as per Rhumetologist instructions - had a flare in calf muscles, increased pred to 12.5 - travelled to NYC
MegfromOz
in
PMRGCAuk
9 months ago
Lap appointment- scared and changed my mind on mirena coil??
I have terrible ovulation it lasts a week, severe pelvic pain, diarrhoea constipation, painful bowel/ bladder when using toilet, painful sex and rectal bleeding always mid cycle and on my period,
leg
pain
and pain before my period which lasts a week after my period so all in all rubbish!!
I have terrible ovulation it lasts a week, severe pelvic pain, diarrhoea constipation, painful bowel/ bladder when using toilet, painful sex and rectal bleeding always mid cycle and on my period,
leg
pain
and pain before my period which lasts a week after my period so all in all rubbish!!
SJ0514
in
Endometriosis UK
1 year ago
compressed vertebrae, i asked dr about stronger pain medication and they said no -- i wonder why?
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
Mum's got probably vertebral pain, is on an otc pain tablet, plus a step up from that, the prescription version. a dr friend of mine said she should be on something stronger like oxycodone. i asked specialist if Mum could have a stronger pain medication, and was told no. why's that? maybe cause elderly
MayGodBlessYou
in
Bone Health and Osteoporosis UK
9 months ago
PLMD and withdrawal
Three weeks ago I stopped (after tapering slowly) gabapentin. I have also been reducing morphine sulphate from 8mg by .01mL every 5 days for the last three weeks. PLMD off the charts. I take 2mg lunesta every 3 nights -- and not more -- in the hopes of not getting addicted. Those nights are better
Three weeks ago I stopped (after tapering slowly) gabapentin. I have also been reducing morphine sulphate from 8mg by .01mL every 5 days for the last three weeks. PLMD off the charts. I take 2mg lunesta every 3 nights -- and not more -- in the hopes of not getting addicted. Those nights are better
wantokporo
in
Restless Legs Syndrome
5 months ago
Adenomyosis/Endometriosis Pain Management
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
Hi All, Just looking for a bit of advice. I was diagnosed with Adenomyosis and Fibroids at 38. Its only been a year and a half but Im struggling hugely. I am very depressed and cant motivate myself day to day. I have constant pain in my lower abdomen, tailbone and Left bum. My pain has progressed
ABFr23
in
Endometriosis UK
9 months ago
Airing Pain 140: Out now!
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
[i]
Airing Pain
[/i] edition 140: Childhood Pain - Adverse Experiences and Parental Relationships is now available to listen to here: https://painconcern.org.uk/airing-pain-140-childhood-experiences/ Full transcript is available online and to download, as well as a captioned video on YouTube.
PainConcernHelpline
Pain Concern
in
Pain Concern
9 months ago
constipation from panadeine, or vertebra nerves, or both?
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
so docs have said constipation can be caused by pain medication and by the nerves of the vertebra, what's your experience, thanks any pain medication comments welcomed, i think. a dr friend of mine has used patches.
MayGodBlessYou
in
Bone Health and Osteoporosis UK
9 months ago
Pelvic Pain Worse at Night
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
Hi all. Currently undiagnosed/suspected endo. Trying to document when I get flare ups of pelvic pain/cramping and notice any links/triggers. I don’t have periods due to having the coil (used to have incredibly painful periods/heavy periods) but still suffering from pelvic pain. If I get any spotting
PBGV24
in
Endometriosis UK
9 months ago
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