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Questionn
Can a Patent Ductus Aerteriosus be diagnosed with a posterlateral thoracotomy then be monitor to make sure it closes?
Can a Patent Ductus Aerteriosus be diagnosed with a posterlateral thoracotomy then be monitor to make sure it closes?
LonerIQ
in
Lung Conditions Community Forum
11 months ago
Feeling a little disillusioned about TTFD and High Dose Thiamine (HDT):
My opinion: You can watch videos that say other B1’s are better; they are more powerful; they cross the BBB; etc. but you cannot find much (if any) info on long-term positive results [success stories]. Best to leave Benfothiamine, TTFD, Sulbutiamine, etc. alone and stay with what works for other people
My opinion: You can watch videos that say other B1’s are better; they are more powerful; they cross the BBB; etc. but you cannot find much (if any) info on long-term positive results [success stories]. Best to leave Benfothiamine, TTFD, Sulbutiamine, etc. alone and stay with what works for other people
Gcf51
in
Cure Parkinson's
11 months ago
v non-invasive treatment may offer significant relief to and restore gait function in patients with neurological disorders
To this end, the clinical researchers from Japan recruited twenty-three patients with PD or Parkinson’s syndrome. All study participants were randomly assigned to receive either the active treatment or a “sham” treatment that mimics the active treatment but does not offer any therapeutic benefit.
To this end, the clinical researchers from Japan recruited twenty-three patients with PD or Parkinson’s syndrome. All study participants were randomly assigned to receive either the active treatment or a “sham” treatment that mimics the active treatment but does not offer any therapeutic benefit.
Farooqji
in
Cure Parkinson's
11 months ago
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17 days post quad bypass surgery
i use medical marijuana for chronic pain from 5
spinal
fusion
surgeries. been using this alone for 3 years. i am suffering from a combination of chronic and acute pain with my heart surgery . i have found using opioids and MMJ is making the present pain much easier to deal with. yesterday i went to the
i use medical marijuana for chronic pain from 5
spinal
fusion
surgeries. been using this alone for 3 years. i am suffering from a combination of chronic and acute pain with my heart surgery . i have found using opioids and MMJ is making the present pain much easier to deal with. yesterday i went to the
coral2222
in
British Heart Foundation
2 years ago
Working with Fibromyalgia
Hi i was wondering how do everyone.cope with working i had a
spinal
fusion
and decompression 2 half years ago and now dignosed with Fibromyalgia in alot of pain lots of medication .i would love to go back to work but impossible feel so lost my life has really changed.x
Hi i was wondering how do everyone.cope with working i had a
spinal
fusion
and decompression 2 half years ago and now dignosed with Fibromyalgia in alot of pain lots of medication .i would love to go back to work but impossible feel so lost my life has really changed.x
Shartaylor0264
in
Fibromyalgia Action UK
2 years ago
spinal cord stimulator side effects
I wanted to know has anyone experienced itching skin ( mine is on my shoulder blades) following having a spinal cord stimulator fitted. I had mine fitted in 2018 and for some years now both my shoulder blades itch nearly all the time and drive me crazy, there is no rash or sign of anything on the skin
I wanted to know has anyone experienced itching skin ( mine is on my shoulder blades) following having a spinal cord stimulator fitted. I had mine fitted in 2018 and for some years now both my shoulder blades itch nearly all the time and drive me crazy, there is no rash or sign of anything on the skin
vihkins
in
Pain Concern
1 year ago
Advice
I am 65, recently diagnosed, no C/L medication so far. I just read this, An anticholinergic medication may be recommended to reduce symptoms of bothersome tremor in people with Parkinson disease under age 70 who do not have significant akinesia or difficulty walking. There are several anticholinergic
I am 65, recently diagnosed, no C/L medication so far. I just read this, An anticholinergic medication may be recommended to reduce symptoms of bothersome tremor in people with Parkinson disease under age 70 who do not have significant akinesia or difficulty walking. There are several anticholinergic
Patitou
in
Cure Parkinson's
1 year ago
The battle is over
Good morning, A week ago my brother aka Savkid passed away. He fought valiantly this cancer for just over 2 years since diagnosis. I am ever grateful that we had the time we did. I will miss him alot In the last month, he became increasingly weak after the second chemo (docetaxel) treatment, so treatments
Good morning, A week ago my brother aka Savkid passed away. He fought valiantly this cancer for just over 2 years since diagnosis. I am ever grateful that we had the time we did. I will miss him alot In the last month, he became increasingly weak after the second chemo (docetaxel) treatment, so treatments
Hidden
in
Advanced Prostate Cancer
1 year ago
sciatica
I’ve had sciatica for a few years. Was going to physical therapy and was helping. The day before Easter I fell and landed on my tail bone. Since then it’s back with a vengeance. My whole left leg gets numb. I had a left hip replacement in 2020. Drs say I have spinal stenosis and need spinal surgery.
I’ve had sciatica for a few years. Was going to physical therapy and was helping. The day before Easter I fell and landed on my tail bone. Since then it’s back with a vengeance. My whole left leg gets numb. I had a left hip replacement in 2020. Drs say I have spinal stenosis and need spinal surgery.
Nanny23
in
Pain Concern
1 year ago
remission then Rituxan again
I have had RA for 23 years. I actually went into remission 3 1/2 years ago and stopped Rituxan and methotrexate during that time. Then I get my second Covid and the Ra returned. I am back on Rituxan but it doesn’t seem to be slowing the Rituxan. Since I have not had the drugs in my body how long
I have had RA for 23 years. I actually went into remission 3 1/2 years ago and stopped Rituxan and methotrexate during that time. Then I get my second Covid and the Ra returned. I am back on Rituxan but it doesn’t seem to be slowing the Rituxan. Since I have not had the drugs in my body how long
Marycullen
in
NRAS
1 year ago
suprapubic catheter
Hi ,I’m looking to learn and get in touch with anyone who has experienced a suprapubic catheter.I’ve been doubly incontinent since I had spinal surgery with very little support this happened in 2007 .Since 2018 I have suffered with constant urine infections I am also disabled.I am now due to have a
Hi ,I’m looking to learn and get in touch with anyone who has experienced a suprapubic catheter.I’ve been doubly incontinent since I had spinal surgery with very little support this happened in 2007 .Since 2018 I have suffered with constant urine infections I am also disabled.I am now due to have a
J-68
in
Bladder Health UK
1 year ago
SI joint osteoarthritis
Anyone had successful si joint fusion?
Anyone had successful si joint fusion?
Jeaniem130
in
Cure Arthritis Community
1 year ago
Possible Outcome of Severe Spinal Stenosis
I had a Laminectomy for Severe Spinal Stenosis which initially worked but has now failed and is worse than before. I had a Triple Bypass and Mitral Valve Repair and have now been diagnosed with heart failure so I’m not able to take any of the normal pain relief medication. I was referred to the Pain
I had a Laminectomy for Severe Spinal Stenosis which initially worked but has now failed and is worse than before. I had a Triple Bypass and Mitral Valve Repair and have now been diagnosed with heart failure so I’m not able to take any of the normal pain relief medication. I was referred to the Pain
Davewm
in
Pain Concern
1 year ago
Jac68
Hi everyone this is my first post to you .I’ve had Incontinence since 2007 following spinal surgery and for the past 6 years have suffered from recurring uti infections and have been on antibiotics for 6 year s almost constantly .The uti infections started when I began the menopause I have just found
Hi everyone this is my first post to you .I’ve had Incontinence since 2007 following spinal surgery and for the past 6 years have suffered from recurring uti infections and have been on antibiotics for 6 year s almost constantly .The uti infections started when I began the menopause I have just found
J-68
in
Bladder Health UK
1 year ago
The Double Vision Issue with GCA
Hi all, I'm a GCA patient, having been diagnosed in AUG 2022. I started on 60 MG PRED, and after 9 months have titrated down to 12.5MG. I am under the care of a GP, ophthalmologist, and rheumatologist. PRIOR to being diagnosed with GCA, somewhere around MARCH 2022, I started noticing I had double
Hi all, I'm a GCA patient, having been diagnosed in AUG 2022. I started on 60 MG PRED, and after 9 months have titrated down to 12.5MG. I am under the care of a GP, ophthalmologist, and rheumatologist. PRIOR to being diagnosed with GCA, somewhere around MARCH 2022, I started noticing I had double
montebello
in
PMRGCAuk
1 year ago
Methylene Blue
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Trailing
in
Cure Parkinson's
1 year ago
Broken in all the right places?🧐🤔
This is me. I have permanent nerve damage on the majority of my left side from shoulder to hand to hip to shin. I have every excuse to wallow in self pity and take out my frustrations on the world and people around me...and I have, believe me. 2 Lower back fusion surgeries 5 days apart in '16 and a week
This is me. I have permanent nerve damage on the majority of my left side from shoulder to hand to hip to shin. I have every excuse to wallow in self pity and take out my frustrations on the world and people around me...and I have, believe me. 2 Lower back fusion surgeries 5 days apart in '16 and a week
LifeIsThePitts
in
Anxiety and Depression Support
1 year ago
Grateful survivor of Bacterial Spinal Meningitis, Spinal fusion, Stage IV kidney failure and COVID with natural immunity.
Greetings to any and all persons who may read my bio and be encouraged by the continuous love that God provides in a time of medical crisis. In no way do I intend to disparage the talented and dedicated members of the medical profession. I am into predictive and preventive medicine. As a patient
Greetings to any and all persons who may read my bio and be encouraged by the continuous love that God provides in a time of medical crisis. In no way do I intend to disparage the talented and dedicated members of the medical profession. I am into predictive and preventive medicine. As a patient
STA2017
in
Meningitis Now
2 years ago
Spinal cord stimulation for treatment of neuropathy
I came across the following article: Spinal Cord Stimulation May Help Diabetic Neuropathy A link to the article: https://www.medscape.com/viewarticle/990791?ecd=soc_fb_230419_mscpedt_news_mdscp_stimulation&faf=1 I wondered whether there has been research on spinal cord stimulation for treatment of
I came across the following article: Spinal Cord Stimulation May Help Diabetic Neuropathy A link to the article: https://www.medscape.com/viewarticle/990791?ecd=soc_fb_230419_mscpedt_news_mdscp_stimulation&faf=1 I wondered whether there has been research on spinal cord stimulation for treatment of
WiscGuy
in
Pernicious Anaemia Society
1 year ago
Microbiome in PD, RBD and 1st degree relatives
As much as I'd like to believe that one "bad" bacteria (desulfovibrio) is responsible for Parkinson's, I suspect the situation is more complicated than that, as this recently released study suggests; https://www.nature.com/articles/s41467-023-38248-4 Certainly the evidence is accumulating though, that
As much as I'd like to believe that one "bad" bacteria (desulfovibrio) is responsible for Parkinson's, I suspect the situation is more complicated than that, as this recently released study suggests; https://www.nature.com/articles/s41467-023-38248-4 Certainly the evidence is accumulating though, that
Rufous2
in
Cure Parkinson's
1 year ago
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