Experiences with

Naprosyn

I have been dealing with urethral pain and bladder pressure for the past month and I have taken many tests and they have all come back clear. I’ve had blood tests, urine samples tested, CT scan and an ultrasound. At the moment the only thing that seems to help us Naproxen. I still feel pressure and without

For the last month I’ve had symptoms doctors can’t tell me what’s going on and it’s really frustrating I had period pain and took naprogesic pills to ease the pain (naprogesic pills contain naproxen and apparently naproxen triggers asthma) which I didn’t have at the time. Minutes later I started to

Hi I have been suffering with pericarditis for nearly 2 years. My initial attack was in January 2018. I was taken into hospital with a suspected heart attack - very scary! After being discharges with no diagnosis I went backwards and forwards to my GP with no luck. I then eventually went private -

Hi, I’ve been on all pills, combined pills, mini pills, implants, mirena coil and Zoladex injections for endometriosis pain relief alongside prescription medication such as mefenamic acid, naproxen etc. I’ve Had the laparoscopies but they couldn’t get to the endo. Now at the stage that my doctor is

I haven't felt this low in a while. There a few major factors in my life that don't feel quite right at the moment, but I don't know how/when to tackle them - my relationship and career being two of them, and I turn 30 in a week! I had some awful pain the other day, searing pain that takes your breath

Sorry to be writing again but RA nurse has just rung with blood results and frightened me re my hb 96 and platelets 481 . She was more concerned about this than my crp result. Any know why shes suggesting i get urgent gp app plz. Certainly not what i needed to here. Asked if taking naproxen . Thank u

I’m currently taking Millinette - 3 packs on 1 week off - this is my second break and I’m in absolute agony. I haven’t had a period since January I was diagnosed in March with Endometriosis. I have pain everyday even after the operation and I am currently on an 8 week pain management plan. The pain

Hi I’ve recently been diagnosed with endometriosis after having a laparoscopy about 2 months ago and Ive got my follow up app next week with my consultant I just wondered what other people’s treatments were , I’m in pain everyday and i was taking naproxen before they found out I had endometriosis but

I've just finished a 28 day course of 2 Naproxen daily (on 16th Sept) for Sciatica. Never had it before but I my heart goes out to anyone suffering from such pain. I've been passing black stools since then and I'm really scared that I have stomach bleeding. I see black stools are mentioned in the side

Is anyone taking Lansoprazole (I have been prescribed them as using Naproxen long term for arthritis pain)? If so, has anyone gained weight since taking it?

Hello... Although I am active on other HU forums it is my first time here. Arthritis runs through the female line of the family. My late mother had a replacement hip, and arthritis in theower spine and various joints. My sister now suffers similarly with arthritis in the hip and lower bank. Eleven years

Prior to my recent asthma deterioration my GP prescribed Naproxen for my migraines. I explained that I’ve never had any problems with Ibuprofen so I was happy with that. Now after this recent nasty flare I am reluctant to take it as I don’t know if it will trigger an attack. For those of you out there

Hi all I am so low at the moment feel like I just want to be able to make my children little again. My eldest boy is moving around 400 miles away to star a new job. My other son is going away to university in the same day next week. I am a mum of five and love my family dearly. It seems that with my

I was diagnosed with AIH in April and am gradually getting used to the various bodily changes brought about by the disease itself and the drugs. But one problem that won't go away is gout in my RH big thumb joint. it prevents me doing so many things like

Just need to vent my frustration somewhere, and here seems to be the safest place! I’m not really after advice, but if there is any, I’m all ears! I’m an Early Years Practitioner, working 3 days a week in a school based nursery. I am a week and a half back into work after a wonderful 5 week break

Rang for a doctor to call and check up on us as we can't get there. Stupid man just rang ask why we need a dr. He spoke to hubby and is sending him some stuff to help him go to the toilet. Then he asked why did I need a dr. explained to him I have Ra and all the other diseases He is sending me some naproxen

Was diognosed June 2017 have been tapering using dsm from 20mg since then got to 31/2mg then started to ache and Gp suggested that I go back up to 4mg which was fine. Gp also referred me to rummy and he want me off pred and prescribed me Naproxen 500mg x2 a day and they now want me to tapper 1mg pred

I'm so confused about my diagnosis and I cant stop thinking I've been diagnosed wrong , basically I was diagnosed with rheumatoid arthurites in april , started treatment about 7 weeks ago now on sulfasalazine 2 gram a day , I only have pain in my left index finger that's all no other joints are really

I have been suffering quite bad neck muscle pain for about 2 weeks, independent from PMR I think. Then on Friday night I experienced the worst pain ever, anywhere, in my right hand side chest muscles ( intercostal) and shoulder. So severe I could hardly breathe, or lie down. My H wanted to call 999,

Hi everyone I recently (july) had nerve root block injections around S1. I had these first around 3years ago and they worked amazing and I felt great with no pain aftetwards. However, in around March this year I started to feel the pain coming back again. It was managed with Tramadol and Pregablin, which