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Endometriosis and IBS
Hi I’m wondering if anyone else suffers from endometriosis & sever IBS. I had a terrible flare up over Christmas time & it’s settled but this week I have been in agony, the painkillers are so strong I just sleep, I have zero energy, have terrible hip & back pain. Just wondering how people cope? Pain
Hi I’m wondering if anyone else suffers from endometriosis & sever IBS. I had a terrible flare up over Christmas time & it’s settled but this week I have been in agony, the painkillers are so strong I just sleep, I have zero energy, have terrible hip & back pain. Just wondering how people cope? Pain
MrsMcdonald18
in
Endometriosis UK
4 years ago
Nothing to worry about
Hi I had this process in January and honestly didn’t feel a thing. Half hour afterwards I was sat up reading a gardening magazine and I never took a single painkiller. It’s fine, the few weeks after a bit of a trial as you have to take loads of drops and wear an eye shield at night.
Hi I had this process in January and honestly didn’t feel a thing. Half hour afterwards I was sat up reading a gardening magazine and I never took a single painkiller. It’s fine, the few weeks after a bit of a trial as you have to take loads of drops and wear an eye shield at night.
Lorraine-3
in
Glaucoma UK
4 years ago
Pain killers or not? Perplexed.
Hi, I have a dumb question. It's 3.5 weeks since my diagnostic laparoscopy, so I think the incision points are more or less healed. The consultant told me there was too much work to do in one day surgery session & needed an MRI and multi-discipline team to look at results. I was feeling virtuous, not
Hi, I have a dumb question. It's 3.5 weeks since my diagnostic laparoscopy, so I think the incision points are more or less healed. The consultant told me there was too much work to do in one day surgery session & needed an MRI and multi-discipline team to look at results. I was feeling virtuous, not
Hidden
in
Endometriosis UK
4 years ago
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Great advice from this site.
Having been in awful pain from osteoarthritis for several months treated with ever increasing pain killers two weeks ago in a phone consultation with my GP following a call to Support Line ' Do you think my PMR has relapsed?' She agreed to start me on 15mgs pred. practically instant relief but still
Having been in awful pain from osteoarthritis for several months treated with ever increasing pain killers two weeks ago in a phone consultation with my GP following a call to Support Line ' Do you think my PMR has relapsed?' She agreed to start me on 15mgs pred. practically instant relief but still
Heard
in
PMRGCAuk
4 years ago
Piriformis Syndrome
Hi everyone I was diagnosed with PMR in March 2020, started on 15 mg. Reduced by 1mg each month, had to return to 10 mg in January 2021. Decreasing slowly and now down to 8.5mg. Towards the end of January Piriformis pain came back, I’d experienced the same thing in October 2020. Have been doing
Hi everyone I was diagnosed with PMR in March 2020, started on 15 mg. Reduced by 1mg each month, had to return to 10 mg in January 2021. Decreasing slowly and now down to 8.5mg. Towards the end of January Piriformis pain came back, I’d experienced the same thing in October 2020. Have been doing
Tinasleepyhead
in
PMRGCAuk
4 years ago
Is this PSA drop good enough? from around 600 to 80 in 3 month on Zytiga for CRPC.
Father dx 2017, Gl 9, T4N1M1, PSA 944. ADT till summer 2020 when PSA got to 175 and scan showed SUPERSCAN. Then 4 rounds of Docetaxcel in aug- dec 2020. PSA droped from 202 to 42, then up again to 250. In 1 week it`s was already 305. So doctors decided to change therapy. But because of burrocracy more
Father dx 2017, Gl 9, T4N1M1, PSA 944. ADT till summer 2020 when PSA got to 175 and scan showed SUPERSCAN. Then 4 rounds of Docetaxcel in aug- dec 2020. PSA droped from 202 to 42, then up again to 250. In 1 week it`s was already 305. So doctors decided to change therapy. But because of burrocracy more
Zhyravlik
in
Advanced Prostate Cancer
4 years ago
Post Covid Vaccination
Good morning all, wondering if anyone is going through or had same/similar concerns after covid jab. I took vaccine on the 7/2, 5 days post vaccination my problems started. Was admitted on the 15/2 after my normal exchange transfusion which I have every 4 weeks. I suffered severe pain in my chest and
Good morning all, wondering if anyone is going through or had same/similar concerns after covid jab. I took vaccine on the 7/2, 5 days post vaccination my problems started. Was admitted on the 15/2 after my normal exchange transfusion which I have every 4 weeks. I suffered severe pain in my chest and
Della30
in
Living with Sickle Cell Disease
4 years ago
Please. Any advice appreciated
Hi ladies. I really need your help. I had my second laparoscopy in November and endo spread ☹️ . I need your opinions or advice because for the past two 3 weeks I have been in crippling pain again and painkillers yet again aren’t doing anything. I’m apprehensive about going to the docs about pain to
Hi ladies. I really need your help. I had my second laparoscopy in November and endo spread ☹️ . I need your opinions or advice because for the past two 3 weeks I have been in crippling pain again and painkillers yet again aren’t doing anything. I’m apprehensive about going to the docs about pain to
louisepercy2000
in
Endometriosis UK
4 years ago
It's back...
Hi, Its been ages since I posted on this site as I've had no real signs of my endo for years other than around my period. Then out of the blue a month ago I woke up with a severe pain in my right side that winded me to the point of taking pain killers and my hot water bottle. The pain disappeared and
Hi, Its been ages since I posted on this site as I've had no real signs of my endo for years other than around my period. Then out of the blue a month ago I woke up with a severe pain in my right side that winded me to the point of taking pain killers and my hot water bottle. The pain disappeared and
nsimpson
in
Endometriosis UK
4 years ago
Feeling a little lost... Any advice on what to do now?
Just had a phone call from rheumatology, I’ve been waiting on it for around 2 months with the promise that some sort of treatment or management plan would be started. It was a call from a completely different doctor who I’d never spoken to before, she spent around ten minutes on the phone and it wasn
Just had a phone call from rheumatology, I’ve been waiting on it for around 2 months with the promise that some sort of treatment or management plan would be started. It was a call from a completely different doctor who I’d never spoken to before, she spent around ten minutes on the phone and it wasn
Clokii
in
NRAS
4 years ago
Tingling, itchy numbness outer thigh
Hello all, Sending love and hugs to everyone. Just a question, does anyone else suffer with, tingling, itchy, numbness on their outer thigh but only one side? Mine is constantly on the left and it is driving me nuts! It doesn't matter if I am sitting, lying or walking it is always the same! I have been
Hello all, Sending love and hugs to everyone. Just a question, does anyone else suffer with, tingling, itchy, numbness on their outer thigh but only one side? Mine is constantly on the left and it is driving me nuts! It doesn't matter if I am sitting, lying or walking it is always the same! I have been
butterflygirl1
in
Fibromyalgia Action UK
4 years ago
Left foot in pain tingling sensation going up my leg
Hi my left foot has I've been in pain with for a week few days later I notice a little lump underneath it hurts to walk on stand on I get like tingling sensation going up my leg feel strange spoke to doctors over phone said inflammation arthritis in my left foot give me some strong pain killers takes
Hi my left foot has I've been in pain with for a week few days later I notice a little lump underneath it hurts to walk on stand on I get like tingling sensation going up my leg feel strange spoke to doctors over phone said inflammation arthritis in my left foot give me some strong pain killers takes
Jody00
in
MPN Voice
4 years ago
Bursitis type pain - Anyone else?
I have been experiencing severe pain in my right elbow, below my knees, and one big toe. It feels like my toe is broken and my elbow pain gets really severe at times. My doctor said it is just part of the fibro and it will go away when I lose weight and exercise more. Yes, I need to do that, but I also
I have been experiencing severe pain in my right elbow, below my knees, and one big toe. It feels like my toe is broken and my elbow pain gets really severe at times. My doctor said it is just part of the fibro and it will go away when I lose weight and exercise more. Yes, I need to do that, but I also
FibroJo79
in
Fibromyalgia Action UK
4 years ago
The Leukemia & Lymphoma Society (USA) Co-Pay Assistance Program provides up to $8,000 annually for CLL Patients' treatment expenses
http://view.e.lls.org/?qs=a2e7081f17eb653ddea40444656a1770bfdf0f4e301505d8af5f4f9cf3bf65ec8be0b13ac15508469314a0fe254f1b095390f32d492221fe510c3b354e19f49d&utm_source=sfmc&utm_medium=email&utm_campaign=CLL+Copay+Email&utm_term=Web+Version&utm_id=130124&sfmc_id=223991984 Financial Assistance with Chronic
http://view.e.lls.org/?qs=a2e7081f17eb653ddea40444656a1770bfdf0f4e301505d8af5f4f9cf3bf65ec8be0b13ac15508469314a0fe254f1b095390f32d492221fe510c3b354e19f49d&utm_source=sfmc&utm_medium=email&utm_campaign=CLL+Copay+Email&utm_term=Web+Version&utm_id=130124&sfmc_id=223991984 Financial Assistance with Chronic
lankisterguy
Volunteer
in
CLL Support
4 years ago
New member
On the 23rd of March 2020 I suddenly started with what I knew were the classic symptoms of PMR. My mother had the condition. We have recently retired to Mallorca and had not yet got our residency sorted and therefore our health cards so everything is on my E111 card. (We have just got residency status
On the 23rd of March 2020 I suddenly started with what I knew were the classic symptoms of PMR. My mother had the condition. We have recently retired to Mallorca and had not yet got our residency sorted and therefore our health cards so everything is on my E111 card. (We have just got residency status
Mahler2
in
PMRGCAuk
4 years ago
Update:Another period with rectal bleeding
So this is now the fifth period with rectal bleeding. Yesterday was my first period day.I saw a colorectal surgeon. She examined me and said there nothing she can see in term of lump in my rectum or bleeding from adheason.So my next stop will be the gynaecologist in two weeks. I have strong rectal pain
So this is now the fifth period with rectal bleeding. Yesterday was my first period day.I saw a colorectal surgeon. She examined me and said there nothing she can see in term of lump in my rectum or bleeding from adheason.So my next stop will be the gynaecologist in two weeks. I have strong rectal pain
Hana98
in
Endometriosis UK
4 years ago
W9✅........Graduation Day🏃♀️🥳🤩....Chuffed to bits!
Absolutely over the moon that I have actually completed this programme....yes me, who has always maintained that I haven’t got the stamina to run! It took me a bit longer than I had planned to compete W9 as I’ve had a rough couple of days due to chronic pain and have not been sleeping very well.....but
Absolutely over the moon that I have actually completed this programme....yes me, who has always maintained that I haven’t got the stamina to run! It took me a bit longer than I had planned to compete W9 as I’ve had a rough couple of days due to chronic pain and have not been sleeping very well.....but
Rwran18
in
Couch to 5K
4 years ago
Bust up with doctors!
I just had a phone call with a different doctor who is telling me now that nothing will ever help me with my fibromyalgia, I told him gabapentin isn’t helping me anymore he told me to stop them then made out I was just phoning for pain killers I told him I’m not able to sleep I’m in agony everything
I just had a phone call with a different doctor who is telling me now that nothing will ever help me with my fibromyalgia, I told him gabapentin isn’t helping me anymore he told me to stop them then made out I was just phoning for pain killers I told him I’m not able to sleep I’m in agony everything
Tiacoyle99
in
Fibromyalgia Action UK
4 years ago
im new here endometrios and endometrial cyst diagnosis sort of?
hi guys newbie 32 year old here found this great website and have been reading some forums and questions on here for the past couple of weeks to try and sort of see if others are going through what i am..some answers to questions are somewhat similar..my symptoms of weirdness i guess started when my
hi guys newbie 32 year old here found this great website and have been reading some forums and questions on here for the past couple of weeks to try and sort of see if others are going through what i am..some answers to questions are somewhat similar..my symptoms of weirdness i guess started when my
evilpunkypie
in
Endometriosis UK
4 years ago
Taking painkiller
Please can someone tell me if it’s safe taking painkillers when on stimulation injection, am taking Puregon and i have been getting unbearable headache 🤕 and backache,? I was thinking of take paracetamol but not even sure and
Please can someone tell me if it’s safe taking painkillers when on stimulation injection, am taking Puregon and i have been getting unbearable headache 🤕 and backache,? I was thinking of take paracetamol but not even sure and
angeln
in
Fertility Network UK
4 years ago
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