Experiences with

Intercourse pain

The surgery was ineffective at relieving my symptoms (agonizing intercourse and period pain) which have recently worsened considerably.

Last november, after 5 years of constant issues (pain & bleeding during intercourse, pressure and pain, bad periods and cramping, slightly odd bowel movements around periods etc *also worth noting all of this was happening while on different forms of contraception) i was referred for a laparoscopy which

My symptoms for the past 3 years have been heavy bleeding, pelvic pain and painful intercourse/pain on going to the toilet. In the past 6 months, the pain on my bowel has been horrendous. I had a Colonoscopy in January, but nothing was found inside the bowel.

I have been taking shot of Prolia and shot of methotrexate every Tuesday.i have no pain but have tender spots on my head and if does not hurt to touch. I only seem to have it in my temple are and top and back of head.. I had a mri of my head a few years ago. I have had a couple of bad concussions 2

Has anyone in our group tried the antispasmodic Spasfon? Generic name is Phloroglucinol. It is approved and is an over the counter medication in France, Spain and I believe in a few other countries but not in the U.S. The research studies that I reviewed shows promise for IBS-D related pain and

Source: https://www.youtube.com/watch?v=L6CtKeOAzGE BUT the likelihood of patients to respond to these treatments is lower if treated for 5+ years with dopaminergics. The reason being the upregulation of D1 receptor responsible for sensitivity to pain and abnormal sensations.

I’m from Ireland so very little knowledge of RLS by doctors here!! I weaned off premipexole as I mentioned here in my last post. I cannot take gabapentin as it really upsets my stomach. I am now taking 1 codipar tablet before bed. I find it helps quite a bit but am worried that I will become dependent

Acetyl-DL-leucine in two individuals with REM sleep behavior disorder improves symptoms, reverses loss of striatal dopamine-transporter binding and stabilizes pathological metabolic brain pattern—case reports: https://www.nature.com/articles/s41467-024-51502-7#:~:text=In%202020%2C%20we%20treated%20a

hello all My question is about the Pneumovax-23 and Prevnar 13. I got the Prevnar 13 in 2015 The Pneumovax-23 in 2015 as well. Is it time to get these again? I live in the US. On W/W for over 20 years. Having immune globulin infusions for the last 5 years or so. Thank you for any insight.

the Vimpat stopped working to completely resolve my RLS. Recent MRIs showed multiple Tarlov cysts on my spine, which is possibly causing the left leg pain and movement. It is positional and separate from the RLS in both legs in my arms and body. I see a new neurosurgeon next week. I’ve had multiple

I have suffered from a range of issues from 15 with periods; bleeding and pain with intercourse, severe leg pain, always bleeding/spotting outside of periods, bad period pains, UTI like symptoms and odd bowel movements around the time of my period.

I took one dulcolax last night at about 10pm. I had 3 bowel movements in the space of an hour, 11am-12pm today. No pain or discomfort. I felt amazing after but it’s now 3:30pm and i feel like i’m constipated again and that there is still more to be released. Shall I take another one tonight to clear

I am in chronic pain in spine painkillers not helping. What I need help with is the way it all makes me feel I have no ffamily or friends . Isolated. I get panicky when pain is out of control, I feel freaked out and alone and am devoid of positive feelings everything everyday feels bleak no respite

Im starting to get a strong pain in my left leg every winter especially in mid night, ten years ago I did a surgery in that leg but now the pain is a so far from the surgery area the surgery area is in the top of leg under the Patella bone but the pain is in middle of the leg especially in the right

I am not using the medical industries term. I am using the term inflammation to describe my symptoms of stuffy head and theeth ache. It feels like my body is attacking itself. I can cause my inflammation with physical stress which is not acceptable to me. I chose not to accept I have to live life in

hey guys , I don’t really know where to start and have never posted before but always read on here for help and advice ! But I’m unsure where to turn now since I was 11, I have dealt with awful periods & typical endo symptoms and been fighting since then for some kind of help but never got far. I’m

what’s the best painkiller to take that does not irritate atrophic gastritis? Thanks 🙏

I am 23 Female, was diagnosed with IBS around 3 years ago after all the tests ruled out Chrons and IBD. Since then I have been left to figure it out on my own. 2 years on codeine phosphate for the pain, with no gut lining tablets. Any pain medication starts a flare up, flare ups can go on for days- weeks

On Nov 7, 2024 I had a one hour reclast infusion. Because my body often responds negatively to medications, the Dr. decided it would be best for me to do a very slow infusion. Generally they are 15-20 min. infusions. There weren't any problems with the actual infusion. Within 24 hours I felt like I

Hi. I fractured my spine (L2) in May this year. It's severely increased my lower back pain that I've had for years. Now I can do little, such as housework, walking for long, standing for more than a few minutes before legs go weak etc. I'm unable to take any painkillers apart from Paracetamol