Search
Search
About
Log in
Join
Experiences with
Spinal Fusion
Posts
Communities
758 public posts
Filter results
Facet joints
Hi,I recently went to see a consultant. I have a.10 year history of l5/s1 disc protrusion. Pain has changed the last few years and has been more in the facet joints. I have had 2 lots of facet injections over the last 2 years however had a bad flare up about 5 months ago which I am still recovering
Hi,I recently went to see a consultant. I have a.10 year history of l5/s1 disc protrusion. Pain has changed the last few years and has been more in the facet joints. I have had 2 lots of facet injections over the last 2 years however had a bad flare up about 5 months ago which I am still recovering
AMS_1
in
Pain Concern
2 months ago
Spinal Stenosis
So, I propose that some tinnitus could be a warning bell for later things to come and that early intervention might prevent senility and tinnitus ………….has anyone had success relieving T via
spinal
fusion
?
So, I propose that some tinnitus could be a warning bell for later things to come and that early intervention might prevent senility and tinnitus ………….has anyone had success relieving T via
spinal
fusion
?
Wringing1212
in
Tinnitus UK
1 year ago
Surgery Today!
I’m having spinal surgery today in my neck. So glad it’s finally happening but rather nervous too. I have cervical stenosis and myelopathy so I’m hoping this operation will stop the progression of spinal cord damage 🤞🏻🤞🏻🤞🏻. Has anyone else had this happen. Not sure if it’s RA related or not.
I’m having spinal surgery today in my neck. So glad it’s finally happening but rather nervous too. I have cervical stenosis and myelopathy so I’m hoping this operation will stop the progression of spinal cord damage 🤞🏻🤞🏻🤞🏻. Has anyone else had this happen. Not sure if it’s RA related or not.
Kati66
in
NRAS
16 days ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Upper back pain
I just turned 61 and had
spinal
fusion
recently.
I just turned 61 and had
spinal
fusion
recently.
Jeaniem130
in
Pain Concern
1 year ago
UPDATE on my dad. A story of hope.❤️ #advancedPC
Hi my dad was diagnosed with advanced prostate cancer in Oct 2021. With Mets to spine, lungs, liver. He is 85. His PSA was 5000. (Today 28 months later his PSA is 0.031 and still dropping) He was told at the time he had 2 months to live. He had spinal surgery the morning after being diagnosed because
Hi my dad was diagnosed with advanced prostate cancer in Oct 2021. With Mets to spine, lungs, liver. He is 85. His PSA was 5000. (Today 28 months later his PSA is 0.031 and still dropping) He was told at the time he had 2 months to live. He had spinal surgery the morning after being diagnosed because
YC22
in
Advanced Prostate Cancer
2 months ago
Sacroiliac joint fusion
After many painful years I'm on the NHS list for sacroiliac joint fusion. Of course there is a 12 month waiting list. Has any one had this operation done privately? Struggling to find a private consultant in Yorkshire.
After many painful years I'm on the NHS list for sacroiliac joint fusion. Of course there is a 12 month waiting list. Has any one had this operation done privately? Struggling to find a private consultant in Yorkshire.
eeeee
in
Pelvic Pain Support Network
5 months ago
Foramintomy
Had decompression in addition to a
fusion
two year ago. . The
spinal
shocks have returned 😑
Had decompression in addition to a
fusion
two year ago. . The
spinal
shocks have returned 😑
Jeaniem130
in
Pain Concern
2 months ago
Goitre and Spinal Surgery
Hi. I am awaiting Cervical Spinal Surgery but also have a multinodular enlarged goitre. The spinals team says the goitre needs to come out first before they can get to the discs in my neck. It’s all a waiting game at the minute. I have a very high anaesthesia risk too. Intubation is difficult for
Hi. I am awaiting Cervical Spinal Surgery but also have a multinodular enlarged goitre. The spinals team says the goitre needs to come out first before they can get to the discs in my neck. It’s all a waiting game at the minute. I have a very high anaesthesia risk too. Intubation is difficult for
Tessann
in
Thyroid UK
6 months ago
SI joint fusion
Can anyone share what a typical recovery would entail?
Can anyone share what a typical recovery would entail?
Jeaniem130
in
Arthritis Action
8 months ago
Bring on more sh*t
Well as if the year hasn't been shit enough. I went into AF on Friday night and now on Digoxin and Eliquis blood thinners. This just tops my shitty year off.......I hope these 2 drugs don't make the RLS and nerve damage worse. The universe has really given me a kick in the teeth this year, with spinal
Well as if the year hasn't been shit enough. I went into AF on Friday night and now on Digoxin and Eliquis blood thinners. This just tops my shitty year off.......I hope these 2 drugs don't make the RLS and nerve damage worse. The universe has really given me a kick in the teeth this year, with spinal
Hidden
in
Neuropathy Support
7 months ago
More to add to my sh*tshow
Well as if the year hasn't been sh*t enough. I went into AF on Friday night and now on Digoxin and Eliquis blood thinners. This just tops my shitty year off.......I hope these 2 drugs don't make the RLS worse. The universe has really given me a kick in the teeth this year, with spinal surgery resulting
Well as if the year hasn't been sh*t enough. I went into AF on Friday night and now on Digoxin and Eliquis blood thinners. This just tops my shitty year off.......I hope these 2 drugs don't make the RLS worse. The universe has really given me a kick in the teeth this year, with spinal surgery resulting
Hidden
in
Restless Legs Syndrome
7 months ago
Mechanical mitral valve enquiries
Sorry for the long post but please share for me. I'm looking to speak to anyone that has had a Mitral metal heart valve replacement and required another operation specifically spinal surgery. Part of my new surgery requires me to have heperin injections instead of warfarin. I know some people have their
Sorry for the long post but please share for me. I'm looking to speak to anyone that has had a Mitral metal heart valve replacement and required another operation specifically spinal surgery. Part of my new surgery requires me to have heperin injections instead of warfarin. I know some people have their
Lynnsyd2
in
British Heart Foundation
8 months ago
Restless Leg Syndrome, neuromodulation..
Treatment was well tolerated, and no adverse events were reported. Our case series shows a potential role for self-administered taVNS in patients with severe pharmacoresistant RLS. Hartley S, Bao G, Russo A, Zagdoun M, Chevallier S, Lofaso F, Leotard A, Azabou E. Self-administered non-invasive vagus
Treatment was well tolerated, and no adverse events were reported. Our case series shows a potential role for self-administered taVNS in patients with severe pharmacoresistant RLS. Hartley S, Bao G, Russo A, Zagdoun M, Chevallier S, Lofaso F, Leotard A, Azabou E. Self-administered non-invasive vagus
House2
in
Restless Legs Syndrome
5 months ago
Suggestions on Supplements
Hello Friends, I need your opinion and advice on the supplements I am taking, and wish to add soon. Timings are +/- 45 mins. Currently taking: 8.30am R-Alpha Lipoic Acid 9.30am Omega 3 Super DHA, Curcumin Meriva, D3 2000iu 11am Vitamin C Complex, Ginkgo Biloba 12pm MCT oil 3.30pm GlyNAC 8pm Omega
Hello Friends, I need your opinion and advice on the supplements I am taking, and wish to add soon. Timings are +/- 45 mins. Currently taking: 8.30am R-Alpha Lipoic Acid 9.30am Omega 3 Super DHA, Curcumin Meriva, D3 2000iu 11am Vitamin C Complex, Ginkgo Biloba 12pm MCT oil 3.30pm GlyNAC 8pm Omega
JayPwP
in
Cure Parkinson's
26 days ago
Improvement of Blood Plasmalogens and Clinical Symptoms in Parkinson's Disease by Oral Administration of Ether Phospholipids:
You got plasmalogen? Any one likes scallops? It is a lengthy article, but our HU scientists will give us their opinion. I have to find the supplement now! https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049862/
You got plasmalogen? Any one likes scallops? It is a lengthy article, but our HU scientists will give us their opinion. I have to find the supplement now! https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049862/
Despe
in
Cure Parkinson's
30 days ago
Ginkgo Biloba And Drug Induced Parkinsonism
Dr. Mischley has Ginkgo Biloba on her list of PD supplements, but we have not talked much about Ginkgo Biloba (GB) on this forum in relation to PD. I was just looking at the following study which used GB in drug induced parkinsonism (DIP) at a dose of
240 mg/day of GB in three divided doses of 80
Dr. Mischley has Ginkgo Biloba on her list of PD supplements, but we have not talked much about Ginkgo Biloba (GB) on this forum in relation to PD. I was just looking at the following study which used GB in drug induced parkinsonism (DIP) at a dose of
240 mg/day of GB in three divided doses of 80
chartist
in
Cure Parkinson's
1 month ago
does anyone have experience of Benzatropine?
My doctor prescribed Benzatropine for dystonia, he didn’t have time to explain at my visiting. Also I know what he prescribed until I see it at CVS pharmacy. I googled it, seems I should stop taking other med include Amantadine and Rasagiline . Does anyone have knowledge and experience of Benzatropine
My doctor prescribed Benzatropine for dystonia, he didn’t have time to explain at my visiting. Also I know what he prescribed until I see it at CVS pharmacy. I googled it, seems I should stop taking other med include Amantadine and Rasagiline . Does anyone have knowledge and experience of Benzatropine
Grandsonlover
in
Cure Parkinson's
1 month ago
overdose
I was diagnosed Feb 1 2024. Is it possible to overdose on Co-Beneldopa 200 MG. I take three doses a day [3 x 200 mg]. I try to take them at 8-hour intervals but often screw up, as my memory is so bad. Any side effects of Co-Beneldopa?
I was diagnosed Feb 1 2024. Is it possible to overdose on Co-Beneldopa 200 MG. I take three doses a day [3 x 200 mg]. I try to take them at 8-hour intervals but often screw up, as my memory is so bad. Any side effects of Co-Beneldopa?
disilusioned
in
PSP Association
2 months ago
Pain Relief
Hi all Can “anyone” offer me some advice as I’m at the “end of my tether” with pain! I’ve had a Triple Bypass and Mitral Valve Repair. I’ve had a Shoulder Rotator Cuff Repair. I’ve had a Laminectomy for Severe Spinal Stenosis which unfortunately failed and is now worse than before the Surgery! I
Hi all Can “anyone” offer me some advice as I’m at the “end of my tether” with pain! I’ve had a Triple Bypass and Mitral Valve Repair. I’ve had a Shoulder Rotator Cuff Repair. I’ve had a Laminectomy for Severe Spinal Stenosis which unfortunately failed and is now worse than before the Surgery! I
Davewm
in
Pain Concern
5 months ago
Neuromodulation for PD “Glove ++” : Trials | Observations | Tips | # 2
Some notes on the 'gloves ' aspects and the challenges I've encountered from the ' pool' of Trial Participants. No doubt that in terms of ease of use , acceptance , ' benefits ' , detectable changes / differences - a PWP is first , MSA++ 2nd but PWP & LB ( even min severity ) is very challenging
Some notes on the 'gloves ' aspects and the challenges I've encountered from the ' pool' of Trial Participants. No doubt that in terms of ease of use , acceptance , ' benefits ' , detectable changes / differences - a PWP is first , MSA++ 2nd but PWP & LB ( even min severity ) is very challenging
NuroMod
in
Cure Parkinson's
3 months ago
1
2
3
...
38
Next page
10
20
30
Filter results
Clear filters
Posted in
All communities
Pain Concern
162 results
Cure Parkinson's
97 results
Couch to 5K
39 results
View top 10 communities
Sort by
Most Relevant
Newest