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Why have I got Lower Back Pain, Right Leg Pain and Left Leg Pins and Needles?
At this time I still only had aching in right
leg
, sometimes
pain
, which is mild pain so I don’t believe it to be sciatica(which was mentioned to me by GP), sometimes weakness.
At this time I still only had aching in right
leg
, sometimes
pain
, which is mild pain so I don’t believe it to be sciatica(which was mentioned to me by GP), sometimes weakness.
HappyThoughts95
in
Anxiety and Depression Support
1 year ago
NHS Attitudes on Worth of Life
My deep apologies to everyone for this post but I think it’s going to be a long one. Partly about PA and partly on NHS attitudes I am encountering about the worth of life. Warning for sensitive members, this post might be shocking. So you will know me through my posts regarding seizures and both neurological
My deep apologies to everyone for this post but I think it’s going to be a long one. Partly about PA and partly on NHS attitudes I am encountering about the worth of life. Warning for sensitive members, this post might be shocking. So you will know me through my posts regarding seizures and both neurological
RoseFlowerDew
in
Pernicious Anaemia Society
1 year ago
Muscle or arthritis pain right leg?
I've been on prednisolone since diagnosis of GCA in Oct 2022. Just reduced pred from 6mg to 5mg reducing by 1mg per month. All been fine but am now getting pain in my calf and right side of knee and middle/upper thigh. Sometimes get severe piercing pain (usually middle of night). No other symptoms
I've been on prednisolone since diagnosis of GCA in Oct 2022. Just reduced pred from 6mg to 5mg reducing by 1mg per month. All been fine but am now getting pain in my calf and right side of knee and middle/upper thigh. Sometimes get severe piercing pain (usually middle of night). No other symptoms
Galore
in
PMRGCAuk
1 year ago
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A wonderful GP
I started seeing a new GP who started work in my local GP practice just before covid and she has been Marvellous, she's from South Africa and really listens to me and I've told her about the advice I've been getting here and she said that she is going to look further into buprenorphine being used here
I started seeing a new GP who started work in my local GP practice just before covid and she has been Marvellous, she's from South Africa and really listens to me and I've told her about the advice I've been getting here and she said that she is going to look further into buprenorphine being used here
Loopylegs
in
Restless Legs Syndrome
1 year ago
HELP PLEASE
HELP PLEASE -Following your advice, Sue Johnson I have been reducing my Ropinirole and am now down to 1.5 mg. from the original 4 mg. per day. I was in hospital for 2 1/2 days on May2nd for successful bowel cancer surgery and this did not worsen my RLS. However I returned home yesterday after a further
HELP PLEASE -Following your advice, Sue Johnson I have been reducing my Ropinirole and am now down to 1.5 mg. from the original 4 mg. per day. I was in hospital for 2 1/2 days on May2nd for successful bowel cancer surgery and this did not worsen my RLS. However I returned home yesterday after a further
milly-22
in
Restless Legs Syndrome
1 year ago
Has this happened to you?
2 weeks post mechanical valve and aorta replacement, recovering ok even after contracting pneumonia in hospital day 2, home 1 week and taking my 5m warfarin as prescribed and some painkillers but less and less every day, going to anticoag clinic twice a week but the long weekend meant an extra day without
2 weeks post mechanical valve and aorta replacement, recovering ok even after contracting pneumonia in hospital day 2, home 1 week and taking my 5m warfarin as prescribed and some painkillers but less and less every day, going to anticoag clinic twice a week but the long weekend meant an extra day without
Pefki
in
British Heart Foundation
1 year ago
Mayb silly question
Have to ask all you lovely suffers of PMR, do you still reduce pred if you are in
pain
with other problems,for me it's my
leg
soft tissue damage, spoke to my dentist about it and said I've over stretched it, got a good laugh, on leaving I said thanks doc easer to see you than GP he then said thy were
Have to ask all you lovely suffers of PMR, do you still reduce pred if you are in
pain
with other problems,for me it's my
leg
soft tissue damage, spoke to my dentist about it and said I've over stretched it, got a good laugh, on leaving I said thanks doc easer to see you than GP he then said thy were
Harrywogan
in
PMRGCAuk
7 months ago
Methadone adjustment/Horizant
Just started methadone 1.5 mL. I have a lot of trouble with drug side effects. After years on pregabalin more or less successfully treating my PLMD, it started making me nervous/anxious so I tried Tylenol #2 which made me very nervous and now I am trying the methadone. Years ago I tried 5mg of methadone
Just started methadone 1.5 mL. I have a lot of trouble with drug side effects. After years on pregabalin more or less successfully treating my PLMD, it started making me nervous/anxious so I tried Tylenol #2 which made me very nervous and now I am trying the methadone. Years ago I tried 5mg of methadone
wantokporo
in
Restless Legs Syndrome
1 year ago
Back pain, still no answer
I received my results from some of the blood work I had done. I’m still trying to figure out why I have such excruciating back pain. So far, I have no answer. I usually don’t get relief from the pain pills better than a 6 on the scale of 1-10. I have to wait until I get a little relief to be able to
I received my results from some of the blood work I had done. I’m still trying to figure out why I have such excruciating back pain. So far, I have no answer. I usually don’t get relief from the pain pills better than a 6 on the scale of 1-10. I have to wait until I get a little relief to be able to
Amore55
in
My MSAA Community
1 year ago
Stable MRIs, worsening pain/spasticity and leg weakness.
I had to change neurologists a few years ago due to insurance, which has been really unfortunate since my MS seems to be getting worse and my neuro and his nurse/practitioner seem to be completely blown away by the fact that my MRIs are stable, but my MS is getting worse. Surely this is not unheard of
I had to change neurologists a few years ago due to insurance, which has been really unfortunate since my MS seems to be getting worse and my neuro and his nurse/practitioner seem to be completely blown away by the fact that my MRIs are stable, but my MS is getting worse. Surely this is not unheard of
CatsandCars
in
My MSAA Community
11 months ago
Levodopa vs Other Parkinson medicines against Fatigue
He did a complete change over of medications as follows: Ropinirole (0.5 mg) 1-1-0-1 Amantadine(100mg)1-1-0-1 Safinamide (50mg) - 1-0-0-1 Sinemet (110mg)- 0.25-0-0.25-0 (only if needed) The problem now is: No drug induced dystonia Deliberating fatigue Lower back
pain
Leg
feeling uneasy
He did a complete change over of medications as follows: Ropinirole (0.5 mg) 1-1-0-1 Amantadine(100mg)1-1-0-1 Safinamide (50mg) - 1-0-0-1 Sinemet (110mg)- 0.25-0-0.25-0 (only if needed) The problem now is: No drug induced dystonia Deliberating fatigue Lower back
pain
Leg
feeling uneasy
gdineshnathan
in
Cure Parkinson's
11 months ago
OsteoArthritis v RA
The physio did an ultrasound and showed that along side meniscal wear and tear - that the medial meniscus “extrudes” on extending the
leg
which probably accounts for the
pain
that puts me on my back. It’s most likely been like this for nearly a year.
The physio did an ultrasound and showed that along side meniscal wear and tear - that the medial meniscus “extrudes” on extending the
leg
which probably accounts for the
pain
that puts me on my back. It’s most likely been like this for nearly a year.
TheBoys
in
NRAS
1 year ago
Knee injury - sigh.
Started my running journey around five years ago and I've been going through a real purple patch recently as have clocked up two personal bests for the 5k and have generally been running faster and at a consistent pace (always conversational - I checked that by muttering to myself every so often!).
Started my running journey around five years ago and I've been going through a real purple patch recently as have clocked up two personal bests for the 5k and have generally been running faster and at a consistent pace (always conversational - I checked that by muttering to myself every so often!).
Crolla
in
Couch to 5K
1 year ago
Follow on re groin and hip pains
I do struggle with this a bit mostly in my feet and that absolutely crucifying
pain
I get in the groin and the top of the
leg
so maybe just upping the pred a bit might see it improve.
I do struggle with this a bit mostly in my feet and that absolutely crucifying
pain
I get in the groin and the top of the
leg
so maybe just upping the pred a bit might see it improve.
LozzaSandstrom
in
PMRGCAuk
1 year ago
electric tug down leg
Hi, I have just had another back surgery, fusing L5 to S1 and pelvis for nerve
pain
that is going down the back of my
leg
, front of knee and top of foot. It feels like someone has an electric cattle prod and running it up and down the back of my leg, it is horrendous.
Hi, I have just had another back surgery, fusing L5 to S1 and pelvis for nerve
pain
that is going down the back of my
leg
, front of knee and top of foot. It feels like someone has an electric cattle prod and running it up and down the back of my leg, it is horrendous.
Heretolearn65
in
Neuropathy Support
2 months ago
hand hold needed - post lap ovulation pain
and pressure, left pelvic
pain
,
pain
down left
leg
and in my lower back. just feeling really deflated I’ve put myself through the surgery (and expense) to feel worse not better.
and pressure, left pelvic
pain
,
pain
down left
leg
and in my lower back. just feeling really deflated I’ve put myself through the surgery (and expense) to feel worse not better.
Endofitall
in
Endometriosis UK
8 months ago
Repeated episodes of unconsciousness due to potential Thyroid Storm?
I am currently taking 125mcg T4, and 18.75mcg T3 split into two daily doses (overall, 2/3 of a 25mcg tablet of T3). I’ve been taking T3 for around 5 years now. In terms of feeling better, it’s been a *huge* success. However, I’ve also been having episodes of unconsciousness over the past 5 years
I am currently taking 125mcg T4, and 18.75mcg T3 split into two daily doses (overall, 2/3 of a 25mcg tablet of T3). I’ve been taking T3 for around 5 years now. In terms of feeling better, it’s been a *huge* success. However, I’ve also been having episodes of unconsciousness over the past 5 years
Abi-Abster
in
Thyroid UK
1 year ago
bowel issue
hello, I posted before and should of mentioned this also that every time I open my bowels I have to take a painkiller and lie down until it takes affect, as I mentioned before my treatment ended twelve weeks ago, how long will this carry on as I am going to have to become employed again and I don’t know
hello, I posted before and should of mentioned this also that every time I open my bowels I have to take a painkiller and lie down until it takes affect, as I mentioned before my treatment ended twelve weeks ago, how long will this carry on as I am going to have to become employed again and I don’t know
Emiliejo
in
Pelvic Radiation Disease Association
1 year ago
Buprenorphine and nausea
I will be switching from methadone to buprenorphine. How common is nausea as a side effect? Does it go away over time? My doctor gave me 60 anti-nausea pills, but insurance hasn't approved my switch to buprenorphine yet. Just wondering what to anticipate. I asked to change because of some cognitive
I will be switching from methadone to buprenorphine. How common is nausea as a side effect? Does it go away over time? My doctor gave me 60 anti-nausea pills, but insurance hasn't approved my switch to buprenorphine yet. Just wondering what to anticipate. I asked to change because of some cognitive
ratfancy
in
Restless Legs Syndrome
1 year ago
Common Symptoms.
I find it helpful when someone posts or replies with a symptom not included in the medical field's list that I do experience. Often with the comment I used to have this symptom prior to treatment. When Trigeminal neuralgia was mentioned a light went on for me and it was helpful to have a name for what
I find it helpful when someone posts or replies with a symptom not included in the medical field's list that I do experience. Often with the comment I used to have this symptom prior to treatment. When Trigeminal neuralgia was mentioned a light went on for me and it was helpful to have a name for what
WIZARD6787
in
Pernicious Anaemia Society
1 year ago
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