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Interaction between supplements and selegiline
I'm on selegiline. Noticed worsening of symptoms when started taking 5-HTP. When checked from WebMD , it was confirmed that it is a result of interaction between the two. Wondering if there are supplements also that interact with PD medications. I guess that there may be some excel sheet or table available
I'm on selegiline. Noticed worsening of symptoms when started taking 5-HTP. When checked from WebMD , it was confirmed that it is a result of interaction between the two. Wondering if there are supplements also that interact with PD medications. I guess that there may be some excel sheet or table available
Farooqji
in
Cure Parkinson's
7 years ago
Joint replacement surgery & tremors
Has anyone out there had joint replacement surgery and did your tremors interfere with the healing process. It looks like I am headed for shoulder replacement surgery and it is on my Parkinson's side so I do have some tremors. I have severe degeneration of the shoulder structure, advanced arthritis
Has anyone out there had joint replacement surgery and did your tremors interfere with the healing process. It looks like I am headed for shoulder replacement surgery and it is on my Parkinson's side so I do have some tremors. I have severe degeneration of the shoulder structure, advanced arthritis
jahelg
in
Cure Parkinson's
7 years ago
Symphysis pubis fusion 2014
I had a pelvis
fusion
and now I am having Sacro Iliac
Joint
pain. Just wondering if anyone has experienced this and will I need another surgery down the road to fuse SI joints? Thank you for your input!
I had a pelvis
fusion
and now I am having Sacro Iliac
Joint
pain. Just wondering if anyone has experienced this and will I need another surgery down the road to fuse SI joints? Thank you for your input!
Belindaz
in
Pelvic Pain Support Network
7 years ago
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Another update on my Double vision suspected MG?
Well here I am back on after being referred on to neurologist who i saw this week.after spending 18months under hospital optomology where I feel I've wasted so much time my double vision is at its worst with the puffy lids and can't open eyelids only in the mornings after sleep. Neurologist thinks
Well here I am back on after being referred on to neurologist who i saw this week.after spending 18months under hospital optomology where I feel I've wasted so much time my double vision is at its worst with the puffy lids and can't open eyelids only in the mornings after sleep. Neurologist thinks
Hidden
in
Thyroid UK
7 years ago
Drugs to Avoid with CMT
Stumbled upon this and thought people might find it useful. It was in a published paper called Medication-induced exacerbation of neuropathy in Charcot Marie Tooth Disease link http://cmt.org.uk/wp-content/uploads/2015/04/NeuroMeds.pdf Proposed list of medications of concern to patients with CMT Definite
Stumbled upon this and thought people might find it useful. It was in a published paper called Medication-induced exacerbation of neuropathy in Charcot Marie Tooth Disease link http://cmt.org.uk/wp-content/uploads/2015/04/NeuroMeds.pdf Proposed list of medications of concern to patients with CMT Definite
Hidden
in
Charcot-Marie-Tooth UK
7 years ago
Rituxan
Hi all, I have a question for everyone. I have had RA for many years now and have tried almost every medicine known without any benefit. My Rhuemetologist thinks this may be B-cell related autoimmune problems and is wanting to start Rituxan infusions asap but my co-pay is $1739.03. I cant afford this
Hi all, I have a question for everyone. I have had RA for many years now and have tried almost every medicine known without any benefit. My Rhuemetologist thinks this may be B-cell related autoimmune problems and is wanting to start Rituxan infusions asap but my co-pay is $1739.03. I cant afford this
Maat2002
in
NRAS
7 years ago
Confused with all these benefits
Ok I had a call today from DWP to say that I had received no points from my medical assessment for ESA on 19/9 and that the benefit would be stopped from tomorrow!!! So as far as they are concerned after a l5-s1 spinal fusion in July , fibromyalgia and a history of depress I can work !! I now have
Ok I had a call today from DWP to say that I had received no points from my medical assessment for ESA on 19/9 and that the benefit would be stopped from tomorrow!!! So as far as they are concerned after a l5-s1 spinal fusion in July , fibromyalgia and a history of depress I can work !! I now have
Bellydot
in
Fibromyalgia Action UK
7 years ago
double vision
can anybody suggest any eye exercises to alleviate double vision brought on by .CA. thanks.
can anybody suggest any eye exercises to alleviate double vision brought on by .CA. thanks.
piglet3
in
Ataxia UK
7 years ago
Neurology referral
Finally, after having very weird symptoms for over 3 years, seeing hematology, rheumatology, immunology, infectious disease, oncology, radiology, nuclear medicine, sports medicine, joint replacement departments, dermatology and surgery. A pain doctor I saw last week asked if I had ever seen a neurologist
Finally, after having very weird symptoms for over 3 years, seeing hematology, rheumatology, immunology, infectious disease, oncology, radiology, nuclear medicine, sports medicine, joint replacement departments, dermatology and surgery. A pain doctor I saw last week asked if I had ever seen a neurologist
dwsurquhart
in
NRAS
7 years ago
Update on my MG test results
I wrote a few weeks back regarding swollen eyelids and not being able to open eyelids plus I have had double vision for 2 years been under optomology since May last year the blood test came back negative but they are now referring me to a Nuerologist as they said the test isn't 100 per cent. All
I wrote a few weeks back regarding swollen eyelids and not being able to open eyelids plus I have had double vision for 2 years been under optomology since May last year the blood test came back negative but they are now referring me to a Nuerologist as they said the test isn't 100 per cent. All
Hidden
in
Thyroid UK
7 years ago
Understanding Needed Please
Hi I've been diagnosed with being on the hypermobility joint spectrum, apparently all types of hypermobility come under this name now according to my UK geneticist. I was being assessed for EDS. I had a patella realignment when I was 7 so I knew back then what it was like to have easy dislocations etc
Hi I've been diagnosed with being on the hypermobility joint spectrum, apparently all types of hypermobility come under this name now according to my UK geneticist. I was being assessed for EDS. I had a patella realignment when I was 7 so I knew back then what it was like to have easy dislocations etc
Jk2833
in
Ehlers-Danlos Support UK
7 years ago
Stomping Your TOE & Hypermobility Syndrome
Like really HOW do hou know if done damage to toes if stomp your toe and suffering from Hypermobility Syndrome or as its also known Ehlers Danlos Syndrome. Guess thats why am asking others can you bend toe back like that when tense LIKE how are you apost to walk when just flips back. Currently am walking
Like really HOW do hou know if done damage to toes if stomp your toe and suffering from Hypermobility Syndrome or as its also known Ehlers Danlos Syndrome. Guess thats why am asking others can you bend toe back like that when tense LIKE how are you apost to walk when just flips back. Currently am walking
Hidden
in
Lung Conditions Community Forum
7 years ago
In pain 😭
My left side of my chest hurts, down my arm and in my neck. I know I have a messed up shoulder but idk what to do for it. I've just been rubbing muscle rub all over it since I can't take Tylenol or ibuprofen bc of my hiatal hernia and I have a inflamed bile duct In my liver.. My orthopedic doctor told
My left side of my chest hurts, down my arm and in my neck. I know I have a messed up shoulder but idk what to do for it. I've just been rubbing muscle rub all over it since I can't take Tylenol or ibuprofen bc of my hiatal hernia and I have a inflamed bile duct In my liver.. My orthopedic doctor told
Elizabeth04
in
Anxiety Support
7 years ago
AMAs in blood but nothing esle
I had AMAs in my blood but i have no symptoms, good cholesterol, normal ALP, ultra sound found no pathology for biliary. But I had to see a nurse practitioner at the GI dr. They want me to have follow- up bloodwork firvAMAs, ANAs and other test that I have not had. I have lost sleep for 8 weeks waiting
I had AMAs in my blood but i have no symptoms, good cholesterol, normal ALP, ultra sound found no pathology for biliary. But I had to see a nurse practitioner at the GI dr. They want me to have follow- up bloodwork firvAMAs, ANAs and other test that I have not had. I have lost sleep for 8 weeks waiting
SSMPCW123
in
PBC Foundation
7 years ago
May or May Not have PC
My PSA is 44. Has been gradually increasing for about 8 years. I know the PSA itself is of little value, but see it as a tool. My Naturopath has had a number between 60-100 for 20 years. I would only become concerned if it started leaping upward. One biopsy was enough. Won't do another. No surgery. No
My PSA is 44. Has been gradually increasing for about 8 years. I know the PSA itself is of little value, but see it as a tool. My Naturopath has had a number between 60-100 for 20 years. I would only become concerned if it started leaping upward. One biopsy was enough. Won't do another. No surgery. No
13thwarrior
in
Advanced Prostate Cancer
7 years ago
No concrete diagnosis yet
When I was 15 I had a major spinal
fusion
and shortly after my surgery I began having severe
joint
pain. My surgeon suggested I had arthritis in my hips and knees from my conformation.
When I was 15 I had a major spinal
fusion
and shortly after my surgery I began having severe
joint
pain. My surgeon suggested I had arthritis in my hips and knees from my conformation.
Dressagequeen
in
LUPUS UK
7 years ago
Handy again soon
Hi all...after 5 long years of being on a merry go round & being constantly fobbed off by my rheumatologist with non working copy procedures..appointments supposed to be every 3months..yet in oct this will be my appointment since Sept 16.will be 13months as hospital cancellations...I went & found a hero
Hi all...after 5 long years of being on a merry go round & being constantly fobbed off by my rheumatologist with non working copy procedures..appointments supposed to be every 3months..yet in oct this will be my appointment since Sept 16.will be 13months as hospital cancellations...I went & found a hero
Hidden
in
NRAS
7 years ago
Some Words of Encouragement. Severe RA and No Meds. right now. The Benefits of a Healthier Microbiome
Hi All those with RA. Many of you on this site have recently been diagnosed with Rheumatoid Arthritis and your Medics are yet to find something to control the disease activity levels. That stage is very painful and very scary. This post is not about recommending what is right for you, or to encourage
Hi All those with RA. Many of you on this site have recently been diagnosed with Rheumatoid Arthritis and your Medics are yet to find something to control the disease activity levels. That stage is very painful and very scary. This post is not about recommending what is right for you, or to encourage
AARA
in
NRAS
7 years ago
SI joint dysfunction
Has anybody had an SI
joint
fusion
done in the North of England and if so where please?
Has anybody had an SI
joint
fusion
done in the North of England and if so where please?
Emma2017
in
Action on Pain
7 years ago
Feel like screaming!
Coming up 4yrs ago I had a spinal fusion L5 S1 for degenerative spondylolsisthesis. I was told up to 2 yrs recovery, after this time I was by all means any better,but actually worse than before the op. After months of 2nd opinions, MRI scans,xrays etc I was sent to see a rheumatologist, where I was diagnosed
Coming up 4yrs ago I had a spinal fusion L5 S1 for degenerative spondylolsisthesis. I was told up to 2 yrs recovery, after this time I was by all means any better,but actually worse than before the op. After months of 2nd opinions, MRI scans,xrays etc I was sent to see a rheumatologist, where I was diagnosed
littledotty76
in
Pain Concern
7 years ago
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