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levo&ndt
I got some Thyroid-s ndt and I would like to take with levo but I don't know exactly how to combine them. I know that I feel more human on ndt . The last time when I took it I had more energy and a good mood but I gained weight and my knees, ankles hurt and I had to take painkillers pills. I think there's
I got some Thyroid-s ndt and I would like to take with levo but I don't know exactly how to combine them. I know that I feel more human on ndt . The last time when I took it I had more energy and a good mood but I gained weight and my knees, ankles hurt and I had to take painkillers pills. I think there's
adin
in
Thyroid UK
2 years ago
Help.
So I’ve was in hospital on Monday and discharged Wednesday was told I have a block Fallopian tube and sent homr with pain killers even though I told them I can’t manage the pain on oral morph. I was then back in hospital Thursday morning to a different hospital where they blue lighted me in an ambulance
So I’ve was in hospital on Monday and discharged Wednesday was told I have a block Fallopian tube and sent homr with pain killers even though I told them I can’t manage the pain on oral morph. I was then back in hospital Thursday morning to a different hospital where they blue lighted me in an ambulance
Adeno2020
in
Endometriosis UK
2 years ago
Nerve damage and back pain - help or advice needed
I have had 5 spinal operations, and have a fusion from L3 - S1, my last operation was about 6 years ago.I have considerable nerve damage in my legs and feet, plus constant lower back pain. It’s been steadily getting worse and now I have upper back pain, neck pain, loss of sensation in my groin, shooting
I have had 5 spinal operations, and have a fusion from L3 - S1, my last operation was about 6 years ago.I have considerable nerve damage in my legs and feet, plus constant lower back pain. It’s been steadily getting worse and now I have upper back pain, neck pain, loss of sensation in my groin, shooting
Leiimarii
in
Pain Concern
2 years ago
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Tips for shoulder and back pain after endo laparoscopy?
Hello, just joined here. I had a laparoscopy yesterday and had inflamed areas in my pelvis removed. The pain in my stomach I can deal with but since waking up I’ve had the most horrendous cramping and pain in my shoulders and neck. I’ve tried all painkillers, heat and cold. Any advice?
Hello, just joined here. I had a laparoscopy yesterday and had inflamed areas in my pelvis removed. The pain in my stomach I can deal with but since waking up I’ve had the most horrendous cramping and pain in my shoulders and neck. I’ve tried all painkillers, heat and cold. Any advice?
Catrin57
in
Endometriosis UK
2 years ago
New approach to pain management
I was keen to investigate a drug-free approach to
pain
management
. Many of us are only too aware of the negative side effects of steroids, opioids etc and for me, any approach that does not depend on such is worth investigating.
I was keen to investigate a drug-free approach to
pain
management
. Many of us are only too aware of the negative side effects of steroids, opioids etc and for me, any approach that does not depend on such is worth investigating.
BiteyDelano
in
PMRGCAuk
3 years ago
Fistula
Hi ladies, has anyone had a similar experience to me. I started 3rd line chemo carbo/ gemcitabine in mid April. Within 36 hours or so I started to have horrible abdominal pain. I went to A&E as advised by oncology helpline and they gave me pain killers. A week later I was admitted to hospital. CT scan
Hi ladies, has anyone had a similar experience to me. I started 3rd line chemo carbo/ gemcitabine in mid April. Within 36 hours or so I started to have horrible abdominal pain. I went to A&E as advised by oncology helpline and they gave me pain killers. A week later I was admitted to hospital. CT scan
Duskygem
in
My Ovacome
2 years ago
Newly diagnosed with RA
I hope I'm writing on the correct page. 2013 was diagnosed with PMR and treated with Prednisolone. went into remission in 2019. All was fine. I had Jab 1 of Covid all ok. Had jab 2 of Covid and exactly a week later all my PMR symptoms returned, November 2021. I began prednisone again 7mgs and have been
I hope I'm writing on the correct page. 2013 was diagnosed with PMR and treated with Prednisolone. went into remission in 2019. All was fine. I had Jab 1 of Covid all ok. Had jab 2 of Covid and exactly a week later all my PMR symptoms returned, November 2021. I began prednisone again 7mgs and have been
tina-shelley
in
NRAS
2 years ago
Anyone elses bones absolutely ache??
One of my recurring pains at the moment has been aching bones. It feels like the centre of all my bones (mostly arms, fingers and legs) has this deep rooted numbing pain and I'm at such a loss with it. Someone with fibromyalgia has noticed a few things about how I am and thinks I have fibro as well
One of my recurring pains at the moment has been aching bones. It feels like the centre of all my bones (mostly arms, fingers and legs) has this deep rooted numbing pain and I'm at such a loss with it. Someone with fibromyalgia has noticed a few things about how I am and thinks I have fibro as well
ArtyPal
in
Endometriosis UK
2 years ago
What else is available?
I have done Carbo/Taxol, Avastin, Carbo/Caelyx, Rubrac a and now Anastrazole. I have a scan coming up, but lately can feel the cancer spreading and am resorting to pain killers. Can anyone who has had this many lines of chemo tell me what else was available for them to try, and also how successful it
I have done Carbo/Taxol, Avastin, Carbo/Caelyx, Rubrac a and now Anastrazole. I have a scan coming up, but lately can feel the cancer spreading and am resorting to pain killers. Can anyone who has had this many lines of chemo tell me what else was available for them to try, and also how successful it
27-359
in
My Ovacome
2 years ago
Latest visit to the Rhemy
Or we might even try
pain
management
. I asked why I should keep taking methotrexate if it was not working but she said it was helping me get off the steroids. Well, clearly not if I am already in pain at 8mg... The pains have changed over the years so maybe now I don't have PMR.
Or we might even try
pain
management
. I asked why I should keep taking methotrexate if it was not working but she said it was helping me get off the steroids. Well, clearly not if I am already in pain at 8mg... The pains have changed over the years so maybe now I don't have PMR.
Mamamia21
in
PMRGCAuk
2 years ago
Lip Biopsy - Is a lack of/missing saliva glands a ‘thing’?
Hello, I wonder if anyone can advise me. I’ve struggled with worsening sicca symptoms for years, the dry eyes from childhood. In the midst of a long and bad flare, I eventually got referred to a ‘lupus’ rheumatology clinic, following a weak pos ANA and speckled IgG, blood result. This was as Covid hit
Hello, I wonder if anyone can advise me. I’ve struggled with worsening sicca symptoms for years, the dry eyes from childhood. In the midst of a long and bad flare, I eventually got referred to a ‘lupus’ rheumatology clinic, following a weak pos ANA and speckled IgG, blood result. This was as Covid hit
UrsaP
in
Sjogren's Support
2 years ago
I'd like to hear people's experience with Linzess. I've been taking it for a week. 142mg. No pain relief.
I have constant ache in my lower right quadrant. All tests have come out negative.Have had this since July.
I have constant ache in my lower right quadrant. All tests have come out negative.Have had this since July.
Angelisse
in
IBS Network
2 years ago
Aches and Pains
I came off Rubraca in November, and since then have developed severe back ache. It hurts when I walk, sit and when I am in bed, but not continually! I am having a scan in a couple of weeks as the oncologist thinks it could be lymph node involvement behind my spine. I have been given Oramorph for pain
I came off Rubraca in November, and since then have developed severe back ache. It hurts when I walk, sit and when I am in bed, but not continually! I am having a scan in a couple of weeks as the oncologist thinks it could be lymph node involvement behind my spine. I have been given Oramorph for pain
27-359
in
My Ovacome
2 years ago
Spinal stenosis in the neck and pain
I have been referred to
pain
management
, physio and ENT. I have already tried these avenues in the past with no improvement. I am on sevredol fast acting morphine for the pain which is having minimal affect. I am not expecting any improvement by revisiting physio,
pain
management
or ENT.
I have been referred to
pain
management
, physio and ENT. I have already tried these avenues in the past with no improvement. I am on sevredol fast acting morphine for the pain which is having minimal affect. I am not expecting any improvement by revisiting physio,
pain
management
or ENT.
MalcolmCClark
in
Pain Concern
2 years ago
Pain medication recommendations for knee & ankle swelling & inflammation
I find that swelling in either of my knees or ankles triggers my RLS. Since I had a knee replacement 6 months ago, the swelling happens frequently as both legs readjust to the post-surgical healing. A new study revealed that ibuprofen and other NAISDS can cause fatal kidney disease, so my GP took me
I find that swelling in either of my knees or ankles triggers my RLS. Since I had a knee replacement 6 months ago, the swelling happens frequently as both legs readjust to the post-surgical healing. A new study revealed that ibuprofen and other NAISDS can cause fatal kidney disease, so my GP took me
Bganim1947
in
Restless Legs Syndrome
2 years ago
Coping with fibroids
Any suggestions with
pain
management
which doesn’t effect fertility? I use paracetamol (rarely, if
pain
makes moving impossible) and hot water bottles/heat pads ALL the time.
Any suggestions with
pain
management
which doesn’t effect fertility? I use paracetamol (rarely, if
pain
makes moving impossible) and hot water bottles/heat pads ALL the time.
troupe
in
Fertility Network UK
2 years ago
success
The head of their appeal process had never heard of opiod use for RLS and so were trying to pigeonhole me into their
pain
management
protocol for coverage. Hopefully this small victory will help others in a similar situation with this insurance company.
The head of their appeal process had never heard of opiod use for RLS and so were trying to pigeonhole me into their
pain
management
protocol for coverage. Hopefully this small victory will help others in a similar situation with this insurance company.
ziggypiggy
in
Restless Legs Syndrome
2 years ago
Help/advice about periods please!
I'm messaging here because I've been dismissed by male doctors before and I'm not sure whether to make an appointment or not. I've basically always had irregular periods but they've been getting worse and worse - heavier and more painful and I can never predict when I'll get it. Cycle length varies
I'm messaging here because I've been dismissed by male doctors before and I'm not sure whether to make an appointment or not. I've basically always had irregular periods but they've been getting worse and worse - heavier and more painful and I can never predict when I'll get it. Cycle length varies
Lizardelle
in
Women's Health
2 years ago
Updated
I have been on benepali for 5 weeks and I am feeling it working at last! I am not in as much pain as I was 5 weeks ago. I am only taking one lot of pain killers a day and sometimes 1 naproxen, so much improved. My fatigue has nearly gone. It only comes back when I do too much or on a Friday before my
I have been on benepali for 5 weeks and I am feeling it working at last! I am not in as much pain as I was 5 weeks ago. I am only taking one lot of pain killers a day and sometimes 1 naproxen, so much improved. My fatigue has nearly gone. It only comes back when I do too much or on a Friday before my
Carolsos
in
NRAS
2 years ago
Private GP to get NHS referral
Hi Ladies I hope you are doing as well as it can be A quick question and a few background notes. Suffering from pain for 10 years. The pain got stronger over time and now lasts longer. Last couple of years in particular were the worst. So far I couldn’t get even the right painkillers from my gp but
Hi Ladies I hope you are doing as well as it can be A quick question and a few background notes. Suffering from pain for 10 years. The pain got stronger over time and now lasts longer. Last couple of years in particular were the worst. So far I couldn’t get even the right painkillers from my gp but
Thisisme-
in
Endometriosis UK
2 years ago
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