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Pelvic nerve damage
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Osteomat
Hi everyone. Has any of you used an osteomat and would like to share your experience with me. I am thinking to buy one. Besides suffering from RA which is manageable at present with MTX I suffer from deliberating pain of sciatica. I use the tens machine but is not easy at night and sometimes it gives
Hi everyone. Has any of you used an osteomat and would like to share your experience with me. I am thinking to buy one. Besides suffering from RA which is manageable at present with MTX I suffer from deliberating pain of sciatica. I use the tens machine but is not easy at night and sometimes it gives
mauritius21
in
NRAS
8 years ago
Harmony magazine is out - article about Lyme
The Thyroid UK member magazine, Harmony, has now gone out in the post! This issue includes a short article about Lyme disease which some of you may find interesting. It’s very difficult to find a doctor in the UK who treats Lyme disease and so we were very pleased to find out that Dr Jess P Armine
The Thyroid UK member magazine, Harmony, has now gone out in the post! This issue includes a short article about Lyme disease which some of you may find interesting. It’s very difficult to find a doctor in the UK who treats Lyme disease and so we were very pleased to find out that Dr Jess P Armine
lynmynott
Thyroid UK
in
Thyroid UK
8 years ago
Registrar's cock up!
Hi. About 18 months ago I had a spinal Neuro stimulater put in my back. (for those who don't know, it is basically a TENS machine but in your body. They then put a strip of electrodes in you spine). When I had my trial, the Dr found the optimal place for it. This was X-rayed and logged as the place to
Hi. About 18 months ago I had a spinal Neuro stimulater put in my back. (for those who don't know, it is basically a TENS machine but in your body. They then put a strip of electrodes in you spine). When I had my trial, the Dr found the optimal place for it. This was X-rayed and logged as the place to
badbackjonny
in
Pain Concern
8 years ago
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Where to go next?
Hi, firstly a slight intro - I'm 20 years old (nearly 21) and in my third year of uni studying Psychology and currently doing my dissertation. I have been suffering with Endo for around 6 years. I've been on multiple pills (from combined to progesterone only, last one was Cerezette), Depo injection for
Hi, firstly a slight intro - I'm 20 years old (nearly 21) and in my third year of uni studying Psychology and currently doing my dissertation. I have been suffering with Endo for around 6 years. I've been on multiple pills (from combined to progesterone only, last one was Cerezette), Depo injection for
Caitlin
in
Endometriosis UK
8 years ago
Functional Neurology
A while back I posted a question, “Does anybody else use functional neurology as a treatment program?” I did not hear from anybody that does, but many responses asking me what it’s about. So I will try to explain my experience with functional neurology in very layman’s terms. I was referred to a functional
A while back I posted a question, “Does anybody else use functional neurology as a treatment program?” I did not hear from anybody that does, but many responses asking me what it’s about. So I will try to explain my experience with functional neurology in very layman’s terms. I was referred to a functional
Don_oregon_duck
in
Cure Parkinson's
8 years ago
Lyme disease and stevia
I know that there are members who suffer from Lyme disease. This may be of interest:- http://www.greenmedinfo.com/blog/stevia-kills-lyme-disease-pathogen-better-antibiotics-preclinical-study?page=1
I know that there are members who suffer from Lyme disease. This may be of interest:- http://www.greenmedinfo.com/blog/stevia-kills-lyme-disease-pathogen-better-antibiotics-preclinical-study?page=1
Silver_Fairy
in
Thyroid UK
8 years ago
Dephead2
Hi. I was diagnosed with PMR in July. I started on 15 mg of predinisolone then and had 2 failed attempts at tapering as I went too fast. I then tapered much more slowly and am still on 12.5 mg. I have major issues with pain in my neck,shoulders and back being the worst. I have put on a lot of weight
Hi. I was diagnosed with PMR in July. I started on 15 mg of predinisolone then and had 2 failed attempts at tapering as I went too fast. I then tapered much more slowly and am still on 12.5 mg. I have major issues with pain in my neck,shoulders and back being the worst. I have put on a lot of weight
dephead2
in
PMRGCAuk
8 years ago
Co-Proxamol plea again
A HUGE THANK YOU to people who have signed the petition and to any friends or family of people who may feel like they could sign as well, also for comments. The gent who started the petition has also written a proto type letter to go to MPs should anybody feel they could do that, MPs can be emailed,
A HUGE THANK YOU to people who have signed the petition and to any friends or family of people who may feel like they could sign as well, also for comments. The gent who started the petition has also written a proto type letter to go to MPs should anybody feel they could do that, MPs can be emailed,
cheeriable
in
NRAS
8 years ago
TENS treatment
Have been trying TENS unit for nerve damage pain. Both my physical therapist and massage therapist say TENS may provide temporary symptom relief, but doesn't heal nerves any faster. It may also have some specific uses for knee replacement, etc. But I had so hoped that it would stimulate blood flow or
Have been trying TENS unit for nerve damage pain. Both my physical therapist and massage therapist say TENS may provide temporary symptom relief, but doesn't heal nerves any faster. It may also have some specific uses for knee replacement, etc. But I had so hoped that it would stimulate blood flow or
Hidden
in
Pelvic Pain Support Network
8 years ago
Stevia better for Lyme than antibiotics? How much more can nature give us without dreadful risks?
In the late 90's I got my first Stevia when visiting family in the US... used it for porridge and where needed in place of sugar. Once hypothyroidism diagnosed, decade+ later, I was so happy not to have been using sugar. I enjoyed stevia [particularly granulated], certainly good enough as a sweetener
In the late 90's I got my first Stevia when visiting family in the US... used it for porridge and where needed in place of sugar. Once hypothyroidism diagnosed, decade+ later, I was so happy not to have been using sugar. I enjoyed stevia [particularly granulated], certainly good enough as a sweetener
LindaC
in
Thyroid UK
8 years ago
Newbie , hello all...
I think it's
nerve
damage
, they said my
pelvic
area is spasm. Hope this is temporary, but my body telling something is wrong. Need to wait 4 months to see the consultant again. Only relief I get is lying on my side with a hot water bottle .
I think it's
nerve
damage
, they said my
pelvic
area is spasm. Hope this is temporary, but my body telling something is wrong. Need to wait 4 months to see the consultant again. Only relief I get is lying on my side with a hot water bottle .
Hidden
in
Pelvic Pain Support Network
8 years ago
Meningitis and Encephalitis
I had meningitis and encephalitis in November of 2011, and ever since then i have been left with daily headahces and regular "attacks". I've had a headache 24/7 all day every day for the last four years. it hasn't been easy and i have tried numerous medications and treatments. i'm only 17 and don't really
I had meningitis and encephalitis in November of 2011, and ever since then i have been left with daily headahces and regular "attacks". I've had a headache 24/7 all day every day for the last four years. it hasn't been easy and i have tried numerous medications and treatments. i'm only 17 and don't really
Hollie98
in
Meningitis Now
8 years ago
Frankincense Oil
Hi all, I am having a very tough time at the moment. I've had a constant migraine since around April 2015. I'm awaiting a lumbar puncture to check pressures and then a release of fluid for increased intracranial pressure. On MST & oramorph (and warfarin) but unfortunately the morphine is not helping
Hi all, I am having a very tough time at the moment. I've had a constant migraine since around April 2015. I'm awaiting a lumbar puncture to check pressures and then a release of fluid for increased intracranial pressure. On MST & oramorph (and warfarin) but unfortunately the morphine is not helping
Louise_Davies
in
Hughes Syndrome APS Forum
8 years ago
Frankincense Oil
Hi all, I am having a very tough time at the moment. I've had a constant migraine since around April 2015. I'm awaiting a lumbar puncture to check pressures and then a release of fluid for increased intracranial pressure. On MST & oramorph (and warfarin) but unfortunately the morphine is not helping
Hi all, I am having a very tough time at the moment. I've had a constant migraine since around April 2015. I'm awaiting a lumbar puncture to check pressures and then a release of fluid for increased intracranial pressure. On MST & oramorph (and warfarin) but unfortunately the morphine is not helping
Louise_Davies
in
National Migraine Centre
8 years ago
Spinal Fusion at L5-S1
Alright so I have reached my breaking point in back pain I have done everything in my power to avoid surgery but I can't take the pain anymore!!! I've done epidurals, pain meds, nerve block meds, chiropractic, physical therapy, and I've even tried my own strengthening routine (after lots of research)
Alright so I have reached my breaking point in back pain I have done everything in my power to avoid surgery but I can't take the pain anymore!!! I've done epidurals, pain meds, nerve block meds, chiropractic, physical therapy, and I've even tried my own strengthening routine (after lots of research)
AshMorgan77
in
Pain Concern
8 years ago
Secrets, lies & cheating
Why is everything so secretive with Parkinson's patients, why do they suddenly start telling lies and being deceitful in other ways, and, why do they suddenly think they can start cheating on their wives? My husband has now abandoned great, genuine friends for a group of old school boys - he hadn't
Why is everything so secretive with Parkinson's patients, why do they suddenly start telling lies and being deceitful in other ways, and, why do they suddenly think they can start cheating on their wives? My husband has now abandoned great, genuine friends for a group of old school boys - he hadn't
MrsJoyanna
in
Cure Parkinson's
8 years ago
What do you do to relieve your pain or take your mind off it ?
Thought it would be a good idea for anyone or everyone to share their method of pain relief and maybe some members would have good ideas to share, especially with new members. Is there anything that you helps, ease your pain in some way. Do you use pain killers, Do you use a tens Machine, Do you use
Thought it would be a good idea for anyone or everyone to share their method of pain relief and maybe some members would have good ideas to share, especially with new members. Is there anything that you helps, ease your pain in some way. Do you use pain killers, Do you use a tens Machine, Do you use
Janet28
in
Fibromyalgia Action UK
8 years ago
hypochondria- freaking out
hi everyone, I am currently freaking out. Let me tell you why. So I poked myself with this metal thing about 4 days ago. I went to the doctor and had to get a tetanus shot (just to be safe) even though I'm terrified of needles. I got the needle (2 days ago) and my arm has been sore since (i know its
hi everyone, I am currently freaking out. Let me tell you why. So I poked myself with this metal thing about 4 days ago. I went to the doctor and had to get a tetanus shot (just to be safe) even though I'm terrified of needles. I got the needle (2 days ago) and my arm has been sore since (i know its
toast122
in
Anxiety Support
8 years ago
Nerve block not working
Hi all, l am new to this site and wondered if any of you have had experience of pain down your legs and had a nerve root block injection I have a disc bulge at L5/S1 abutting both S1 nerve roots and have been in considerable pain for about 14 months. On 25th November l had a nerve block procedure carried
Hi all, l am new to this site and wondered if any of you have had experience of pain down your legs and had a nerve root block injection I have a disc bulge at L5/S1 abutting both S1 nerve roots and have been in considerable pain for about 14 months. On 25th November l had a nerve block procedure carried
Classicmike
in
Pain Concern
9 years ago
TENS Machine
Hi All Im really lucky that I only experience significant pain when im on my period, however takign painkillers leaves me feeling spaced out. Have any of you tried a TENS machine? if so what are they like and any recommendations?
Hi All Im really lucky that I only experience significant pain when im on my period, however takign painkillers leaves me feeling spaced out. Have any of you tried a TENS machine? if so what are they like and any recommendations?
Hidden
in
Endometriosis UK
8 years ago
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