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Littlejoy
I had pelvic prolapse, cystocele and rectocele. Had pelvic prolapse repair 1 year ago, they took out uterus and tightened vagina to hold bladder & bowel. When I came too after op, they said I had a cyst one my left ovary so would need another op yo remove this. I have been in pain since op, it depends
I had pelvic prolapse, cystocele and rectocele. Had pelvic prolapse repair 1 year ago, they took out uterus and tightened vagina to hold bladder & bowel. When I came too after op, they said I had a cyst one my left ovary so would need another op yo remove this. I have been in pain since op, it depends
Operation
in
Pelvic Pain Support Network
6 days ago
Walking Speed
I know our bodies are different, but we all have something in common. Has anyone done or tried something besides ampyra that increased the speed that you walk? I've tried ampyra, dysport and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
I know our bodies are different, but we all have something in common. Has anyone done or tried something besides ampyra that increased the speed that you walk? I've tried ampyra, dysport and I'm still moving like a turtle. My legs still feel very heavy! I'm still hoping to be walking normal again!
Diva1976
in
My MSAA Community
1 month ago
I know Nitrous Oxide can cause b12 deficiency, but could Nitrogen Dioxide do it too?
I had low b12, took ppi and h2 before Mt body crashed. But I also realised that we did an experiment in the labs I was working in, when my body began to feel awful, around the time I started PPIs (before my body totally crashed months later) I know Nitrous Oxide messes with b12... Does anyone know
I had low b12, took ppi and h2 before Mt body crashed. But I also realised that we did an experiment in the labs I was working in, when my body began to feel awful, around the time I started PPIs (before my body totally crashed months later) I know Nitrous Oxide messes with b12... Does anyone know
Suffering_sunny
in
Pernicious Anaemia Society
2 months ago
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Cladribine
I have recently been diagnosed as having RRMS. I have only had 2 relapses in the past year, both of which involved temporary loss of eyesight. On both occasions, my vision returned to normal by itself, without any need or medication to be prescribed. However, my most recent MRI contrast scan shows that
I have recently been diagnosed as having RRMS. I have only had 2 relapses in the past year, both of which involved temporary loss of eyesight. On both occasions, my vision returned to normal by itself, without any need or medication to be prescribed. However, my most recent MRI contrast scan shows that
max011
in
My MSAA Community
2 months ago
Webinar: Increased dose of Eylea to extend treatment intervals
A renowned retinal specialist based in the US, Dr Kenneth Fan will join us this month to discuss the increased dose of licensed drug Eylea (aflibercept) to treat wet age-related macular degeneration and diabetic macular oedema. Dr Fan will talk more about the trials which have led to the increased 8mg
A renowned retinal specialist based in the US, Dr Kenneth Fan will join us this month to discuss the increased dose of licensed drug Eylea (aflibercept) to treat wet age-related macular degeneration and diabetic macular oedema. Dr Fan will talk more about the trials which have led to the increased 8mg
Carol_MacularSociety
Partner
in
Macular Society
2 months ago
Any practical tools to prevent computer vision syndrome?
Any practical tools to prevent computer vision syndrome (lower back and neck pain, eye dryness and strain)?
Any practical tools to prevent computer vision syndrome (lower back and neck pain, eye dryness and strain)?
bliinkai
in
Pain Concern
3 months ago
Do I have PMR?
I did some research on my own after having these pains in my shoulders, upper arms, hips and lower back. Getting out of bed, turning over in bed, getting up from a chair, or reaching for something was very painful. I’ve been having back issues with a slipped vertebrae for about 2 years. I’ve had 3 epidural
I did some research on my own after having these pains in my shoulders, upper arms, hips and lower back. Getting out of bed, turning over in bed, getting up from a chair, or reaching for something was very painful. I’ve been having back issues with a slipped vertebrae for about 2 years. I’ve had 3 epidural
Aqua47
in
PMRGCAuk
3 months ago
Prucalopride & Pelvic floor pain
Hi I have been suffering from rectal & pelvic floor pain for last 18 months. 2 months ago I was placed on Prucalopride as the magnesium citrate they I was taking stopped working. My pelvic floor pain & rectal spasm appears to be getting worse. I used to be able to sleep at night but now struggling
Hi I have been suffering from rectal & pelvic floor pain for last 18 months. 2 months ago I was placed on Prucalopride as the magnesium citrate they I was taking stopped working. My pelvic floor pain & rectal spasm appears to be getting worse. I used to be able to sleep at night but now struggling
Hopetobewell
in
Pelvic Pain Support Network
4 months ago
Alverine and/or Simalvia - (which is alverine citrate with simethicone.) Side effects.
I have recently been put on these. I have found that both the standard alverine citrate, which I had tried first, now the Simalvia, cause feelings of extreme anxiety about an hour after taking the tablet! Weird and not listed in the side effects. So far it seems ineffective on the pain anyway. Would
I have recently been put on these. I have found that both the standard alverine citrate, which I had tried first, now the Simalvia, cause feelings of extreme anxiety about an hour after taking the tablet! Weird and not listed in the side effects. So far it seems ineffective on the pain anyway. Would
emmjay77
in
IBS Network
4 months ago
MS Treatments
Hi. I was diagnosed with MS in 2011. I can get around but suffer with leg pain and have balance issues. I work full time but it is getting harder and harder to go so. Doctor started me on Rebif but had to switch to Copaxone due to liver enzymes escalating. I have been using Copaxone since 2012 with
Hi. I was diagnosed with MS in 2011. I can get around but suffer with leg pain and have balance issues. I work full time but it is getting harder and harder to go so. Doctor started me on Rebif but had to switch to Copaxone due to liver enzymes escalating. I have been using Copaxone since 2012 with
Caste19
in
My MSAA Community
8 months ago
Yellowish skin,
Hi,i have yellows.skin for 3 years.now but my liver test come back normal,i had a really high.consume alcohol,i look yellowish but with.normal bilirubin test,i have take.billirubin test seven times now,all normal,albumin normal,inr,normal,alt normal,what can it be?
Hi,i have yellows.skin for 3 years.now but my liver test come back normal,i had a really high.consume alcohol,i look yellowish but with.normal bilirubin test,i have take.billirubin test seven times now,all normal,albumin normal,inr,normal,alt normal,what can it be?
Okki49
in
British Liver Trust
5 months ago
Help with test results
Hi all. I've been having tests as my doctor believes I may have occupational asthma (I work with flour and other flour based ingredients). My blood results have come back as normal but my chest x-ray state the following which I don't understand... "Heart size and mediastinal contours are within normal
Hi all. I've been having tests as my doctor believes I may have occupational asthma (I work with flour and other flour based ingredients). My blood results have come back as normal but my chest x-ray state the following which I don't understand... "Heart size and mediastinal contours are within normal
EMJAY1401
in
Asthma Community Forum
5 months ago
Lanzaprozole and magnesium deficiency
Hi all, I was diagnosed with GCA in 2018. With the help and support of this group I came through some tough times, and will always be grateful for that. After a very gradual taper, I have now completed 13 months without prednisolone, and, fingers crossed, the GCA is still quiet. I am still having sub-cutaneous
Hi all, I was diagnosed with GCA in 2018. With the help and support of this group I came through some tough times, and will always be grateful for that. After a very gradual taper, I have now completed 13 months without prednisolone, and, fingers crossed, the GCA is still quiet. I am still having sub-cutaneous
Dontwannabesick
in
PMRGCAuk
6 months ago
What could be causing pain in the testicle?
Share you with my opinions. There are many reasons for testicular pain, the most common reason is chronic prostatitis, epididymitis and varicocele. Testicular pain is one of the main symptoms of chronic prostatitis. The main symptom of acute epididymitis is also testicular pain. If not treated for a
Share you with my opinions. There are many reasons for testicular pain, the most common reason is chronic prostatitis, epididymitis and varicocele. Testicular pain is one of the main symptoms of chronic prostatitis. The main symptom of acute epididymitis is also testicular pain. If not treated for a
Henry0831
in
Pain Concern
6 months ago
Respiratory Therapy Student
Hi All, I have been a member of the forum for 8ish years. I have bronchiectasis and had a LLL (left lower lobe) resection in 2019. I am 48 years old. The past 3 years I have been studying to become a Respiratory Therapist (RT). In the US, RTs work in hospitals managing critical care patients on ventilators
Hi All, I have been a member of the forum for 8ish years. I have bronchiectasis and had a LLL (left lower lobe) resection in 2019. I am 48 years old. The past 3 years I have been studying to become a Respiratory Therapist (RT). In the US, RTs work in hospitals managing critical care patients on ventilators
Schmu
in
Lung Conditions Community Forum
7 months ago
At last I know.
Spoke to the doctor today and at last I know I have ET .I have fibromyalgia and the symptoms got my brain thinking it was MF. My white blood cells have been raised for years, kept being given iron tablets. Infections all the time. But my husband died in 2019 and I moved in with my daughter. Her Dr. Took
Spoke to the doctor today and at last I know I have ET .I have fibromyalgia and the symptoms got my brain thinking it was MF. My white blood cells have been raised for years, kept being given iron tablets. Infections all the time. But my husband died in 2019 and I moved in with my daughter. Her Dr. Took
mag123ben
in
MPN Voice
4 hours ago
Sorry if this is depressing 😞
I feel trapped. I had my laparoscopy surgery in February and I was diagnosed with endometriosis. Since the surgery my pain has leveled up, it’s so much worse and it’s throughout the month, not just when I’m on my period anymore. I feel trapped by this illness, I have maybe one week out of the month where
I feel trapped. I had my laparoscopy surgery in February and I was diagnosed with endometriosis. Since the surgery my pain has leveled up, it’s so much worse and it’s throughout the month, not just when I’m on my period anymore. I feel trapped by this illness, I have maybe one week out of the month where
Law94
in
Endometriosis UK
6 hours ago
Updated Results on Armour
Hi everyone, Following up on my previous post, I eliminated T3 Liothyronine 25 mcg from my current Armour 150 mg dosage (1/2 tablet of 300 mg early morning). Here are my recent results: Tested 10 hrs after I took my half dosage of Armour: TSH (mIU/L)
0.01
Range: 0.40-4.50 T4 (THYROXINE
Hi everyone, Following up on my previous post, I eliminated T3 Liothyronine 25 mcg from my current Armour 150 mg dosage (1/2 tablet of 300 mg early morning). Here are my recent results: Tested 10 hrs after I took my half dosage of Armour: TSH (mIU/L)
0.01
Range: 0.40-4.50 T4 (THYROXINE
Moxyca
in
Thyroid UK
1 day ago
how do you deal with the bad days?
hi all, diagnosed with endo last November after a laparoscopy after about 14 years of symptoms and pain. Even though I’m glad to have the clarity about what the issue is as the uncertainty was awful, some days I just feel so sad and down that this is my future. I still have a lot of pain and especially
hi all, diagnosed with endo last November after a laparoscopy after about 14 years of symptoms and pain. Even though I’m glad to have the clarity about what the issue is as the uncertainty was awful, some days I just feel so sad and down that this is my future. I still have a lot of pain and especially
ar1497
in
Endometriosis UK
2 days ago
Want to tell Rheumy to Jog on Or not
waiting on phone appointment like 5 mins ago. just get letter says as loads of bollocks, basically as CCP and RF neg it's osteo with a bit of inflammation, letter says wants to try cortisone injections and if it helps she'll consider hydroxychloroquine, not what I remembered but I was quite angry.
waiting on phone appointment like 5 mins ago. just get letter says as loads of bollocks, basically as CCP and RF neg it's osteo with a bit of inflammation, letter says wants to try cortisone injections and if it helps she'll consider hydroxychloroquine, not what I remembered but I was quite angry.
Polo22
in
Thyroid UK
2 days ago
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