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Problems with extended release Carbidopa Levodopa .
Extended release Carbidopa Levodopa in any form causes me problems. This includes Rytary, extended release Carbidopa Levodopa and entacapone. I get bradykinesia and Dystonia. Speech changes (i can not say any thing i want to say but i can read out loud anything i see if i write it i can say it or if
Extended release Carbidopa Levodopa in any form causes me problems. This includes Rytary, extended release Carbidopa Levodopa and entacapone. I get bradykinesia and Dystonia. Speech changes (i can not say any thing i want to say but i can read out loud anything i see if i write it i can say it or if
Bailey_Texas
in
Cure Parkinson's
7 years ago
Kallyfudging the great Manchester parkrun south Manchester
Got to parkrun today, managed to wakeup early enough to eat something, peanut butter on toast. Also ate well yesterday in preparation. Was hoping to knock about 30 seconds off my PB. Managed to pace myself better at the start, was also listening to very over-the-top music from a game I've just started
Got to parkrun today, managed to wakeup early enough to eat something, peanut butter on toast. Also ate well yesterday in preparation. Was hoping to knock about 30 seconds off my PB. Managed to pace myself better at the start, was also listening to very over-the-top music from a game I've just started
Kallyfudge
Graduate
in
Couch to 5K
7 years ago
S joint fusion surgery Jan 24 2017
I had a s
joint
fusion
Tuesday I can't put any weigh in my left foot pain is unbearable is that normal and how long till you don't use crutches.
I had a s
joint
fusion
Tuesday I can't put any weigh in my left foot pain is unbearable is that normal and how long till you don't use crutches.
Jmdc99
in
Pain Concern
7 years ago
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Spinal fusion L5 S1
Hi I am new here and wanted to see if I could get some more info. I have had severe continued pain in my lower pack for over 2 years now. I have tried steroid injections, nerve blocks, PT, pain meds, nerve meds, tens unit etc and no relief. I had my MRI and Dr thinks if the pain is this bad and nothing
Hi I am new here and wanted to see if I could get some more info. I have had severe continued pain in my lower pack for over 2 years now. I have tried steroid injections, nerve blocks, PT, pain meds, nerve meds, tens unit etc and no relief. I had my MRI and Dr thinks if the pain is this bad and nothing
jennwalton73
in
Pain Concern
7 years ago
Where To Go In London?
Hi all - I have Sjogren's and connective tissue disease, but over the past year I have been in excruciating pain and been to the GP and physio, and from what I've read here and what my physio indicates, I think I may have EDS (I know I am hypermobile). I have my annual appointment with my rheumatologist
Hi all - I have Sjogren's and connective tissue disease, but over the past year I have been in excruciating pain and been to the GP and physio, and from what I've read here and what my physio indicates, I think I may have EDS (I know I am hypermobile). I have my annual appointment with my rheumatologist
WpgGirl
in
Ehlers-Danlos Support UK
7 years ago
I'm scared
I havnt been diagnosed yet with AN, but my symptoms are what is given as AN. In 2004 I had an unexplained neurological event, following this I had Vertigo for 3 weeks straight and had to be hand led everywhere. This eventually passed and then in 2010 I developed tinnitus along with the begining of loosing
I havnt been diagnosed yet with AN, but my symptoms are what is given as AN. In 2004 I had an unexplained neurological event, following this I had Vertigo for 3 weeks straight and had to be hand led everywhere. This eventually passed and then in 2010 I developed tinnitus along with the begining of loosing
mutt1
in
Acoustic Neuroma Support
7 years ago
Not Yet Diagnosed
Hello everyone, I have had three knee surgeries in 20 months, the last with a second surgeon for a second opinion. He tells me I don't have typical osteoarthritis and is referring me to a rheumatologist. As a lot of us do, I have been on the internet trying to get information about how RA affects the
Hello everyone, I have had three knee surgeries in 20 months, the last with a second surgeon for a second opinion. He tells me I don't have typical osteoarthritis and is referring me to a rheumatologist. As a lot of us do, I have been on the internet trying to get information about how RA affects the
Vickicj1
in
NRAS
7 years ago
Is it Trigeminal Neuralgia
Hi I'm sorry to bother you guys but I'd like some insight to the symptoms of TN, since the 29th November 2016 I have had this horrendous pain on the left side of my forehead, just above my eyebrow. The pain is constant and in the last few days it has also started to add a stinging sensation. I also get
Hi I'm sorry to bother you guys but I'd like some insight to the symptoms of TN, since the 29th November 2016 I have had this horrendous pain on the left side of my forehead, just above my eyebrow. The pain is constant and in the last few days it has also started to add a stinging sensation. I also get
mutt1
in
Pain Concern
7 years ago
Soft tissue formation...or not in this case
Hi all. I have a question for you and would appreciate your thoughts... The thing is I have had three joint replacements in my CMC joint of my thumb (where thumb meets wrist). Two metal ball and socket joints - both failed when they dislocated. hen the surgeon tried a bio-absorbable spacer thing which
Hi all. I have a question for you and would appreciate your thoughts... The thing is I have had three joint replacements in my CMC joint of my thumb (where thumb meets wrist). Two metal ball and socket joints - both failed when they dislocated. hen the surgeon tried a bio-absorbable spacer thing which
Kaleidobrain
in
Ehlers-Danlos Support UK
7 years ago
MCP Joint replacement
Hi all, has anyone had an mcp joint replacement? Left hand index finger. How is movement etc afterwards? Particularly in relation to guitar playing.
Hi all, has anyone had an mcp joint replacement? Left hand index finger. How is movement etc afterwards? Particularly in relation to guitar playing.
cbrjet
in
NRAS
7 years ago
Hypermobility
Hi all, I have just discovered I also have Hypermobility on top of Fibromyalgia, Raynaud's phenomenon, Photosensitivity, Trigeminal neuralgia, Carpal tunnel syndrome and autonomic dysfunction.....seems like the list will just get bigger and bigger. Does anyone else on here have hypermobility? how does
Hi all, I have just discovered I also have Hypermobility on top of Fibromyalgia, Raynaud's phenomenon, Photosensitivity, Trigeminal neuralgia, Carpal tunnel syndrome and autonomic dysfunction.....seems like the list will just get bigger and bigger. Does anyone else on here have hypermobility? how does
Queencara78
in
Fibromyalgia Action UK
7 years ago
Leaky gut
Just wondering if anyone has been diagnosed with leaky gut , as I have been studying up on the gut and the amount of damage to other parts of the body due to this , can cause us to not absorb vitamins and which can also cause a bad bacteria growth which causes influmation that can cause neurological
Just wondering if anyone has been diagnosed with leaky gut , as I have been studying up on the gut and the amount of damage to other parts of the body due to this , can cause us to not absorb vitamins and which can also cause a bad bacteria growth which causes influmation that can cause neurological
Ronwyn
in
Functional Neurological Disorder - FND Hope
7 years ago
Chronic pain
Having had a spinal fusion have been left with chronic pain..was wondering if anyone has any new ideas for coping.. Thanks Diane
Having had a spinal fusion have been left with chronic pain..was wondering if anyone has any new ideas for coping.. Thanks Diane
dianef438
in
Pain Concern
7 years ago
Adrenal insufficency
As you all know by now....I have been on your forum for almost five years and have gained considerable information and insight in dealing with this awful disease. (I haveGSA and PMR. ) I have made it through shingles, spinal fusion and laminectomy surgery as well as two cataract operations. Just recently
As you all know by now....I have been on your forum for almost five years and have gained considerable information and insight in dealing with this awful disease. (I haveGSA and PMR. ) I have made it through shingles, spinal fusion and laminectomy surgery as well as two cataract operations. Just recently
30048
in
PMRGCAuk
7 years ago
Muscle Relaxer?
I have PD and am currently taking Azilect, Ropinerole, and Carbidopa/levidopa. I am very active, but lifted a heavy object yesterday and have painful muscle spasms in my lower back. Can I take a muscle relaxer - Carisoprodol - which is leftover from a spinal fusion I had before going on PD meds?
I have PD and am currently taking Azilect, Ropinerole, and Carbidopa/levidopa. I am very active, but lifted a heavy object yesterday and have painful muscle spasms in my lower back. Can I take a muscle relaxer - Carisoprodol - which is leftover from a spinal fusion I had before going on PD meds?
bjmettler
in
Cure Parkinson's
7 years ago
Vertical Double Vision anyone?
Was diagnosed with PA in 2013. A year before diagnosis was suffering bouts of what I now know as Vertical Double Vision. At first did not know how to describe it. I can see but can't make anything out and no balance. Took a couple of years to realize I just needed to close one eye. Just wondering if
Was diagnosed with PA in 2013. A year before diagnosis was suffering bouts of what I now know as Vertical Double Vision. At first did not know how to describe it. I can see but can't make anything out and no balance. Took a couple of years to realize I just needed to close one eye. Just wondering if
tflynnhk
in
Pernicious Anaemia Society
7 years ago
will be having l5-s1 spinal fusion surgery as well as laminectomy...need help!!
i am having l5-s1 spinal fusion surgery and a laminectomy. i want to know what the pain will be like after the surgery. please post answers. i will appreciate your input.....another question...what kind of care will i need after i am discharged from the hospital? thank you very much!!!
i am having l5-s1 spinal fusion surgery and a laminectomy. i want to know what the pain will be like after the surgery. please post answers. i will appreciate your input.....another question...what kind of care will i need after i am discharged from the hospital? thank you very much!!!
cathylackey8
in
Cloudy with a Chance of Pain
7 years ago
Elbow joint replacement....would you say yes?
I suffer from osteo arthritis in most joints ...had two partial knee replacements 6 years ago and they're great. I've had a thumb joint replacement - also great. However, following two arthroscopies in three years and injections, I'm suffering a great deal of pain and restricted movement in my right
I suffer from osteo arthritis in most joints ...had two partial knee replacements 6 years ago and they're great. I've had a thumb joint replacement - also great. However, following two arthroscopies in three years and injections, I'm suffering a great deal of pain and restricted movement in my right
Jillypops2
in
Arthritis Action
7 years ago
Intro- First time post
I feel foggy. Like I'm drunk, or hungover, or on cold medicine. Headaches, lightheadedness, fatigue. This is my 13th year of this, and I have been worked up for EVERYTHING!!! I've seen MD's and Naturopathic physicians. For a while I thought I had an autoimmune "sticky blood" issue, but top LA rheumy
I feel foggy. Like I'm drunk, or hungover, or on cold medicine. Headaches, lightheadedness, fatigue. This is my 13th year of this, and I have been worked up for EVERYTHING!!! I've seen MD's and Naturopathic physicians. For a while I thought I had an autoimmune "sticky blood" issue, but top LA rheumy
ehc918
in
Foggy's "Invisible Illness" Support
7 years ago
Joint replacement
I need my knee joint replaced. My surgeon says there are no differences to doing my knee from anyone else but I have had p.a for 25 years and I am sure there are differences. He says the two occasions whe ligaments snapped were common for people of my age. Where do I go for a surgeon who accepts it
I need my knee joint replaced. My surgeon says there are no differences to doing my knee from anyone else but I have had p.a for 25 years and I am sure there are differences. He says the two occasions whe ligaments snapped were common for people of my age. Where do I go for a surgeon who accepts it
Freebeer
in
Arthritis Action
8 years ago
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