Experiences with

Naprosyn

5 months ago my GP mentioned Endometriosis to me. A few days later my period arrived and the agony continued. That sparked my first post in this forum. But I'm now at a stage with this illness where I'm feeling isolated. No one around me gets it. They ask 'What kind of pain?', 'How are you feeling?',

Im taking naproxen for the pain and zomig had migrains since 16 now 58 still here still trying to reduce them since menopause been worse now go blind for days unbearable pain does anyone else have this

... the other half shipped me off to hospital because I felt like someone was pushing a big stick into the top of my head. Combine this with a battering headache, neck ache, nausea and only just being able to walk from the car, and you'll be about there. In fairness, the doctor was very thorough. He

I was diagnosed with endo back in December. I didn't even think that I would be getting that diagnosis, I had always assumed all the pain I had was down to a cyst I had..lol..wish that it had been cause now that's been removed and then my pain would be ended.. but sadly no. I had a copper coil put in

Hi everyone have just joined this amazing site. I was diagnosed with RA exactly a year ago, and things have just gone from bad to worse. I am in constant pain and often can't bear to move. I suffer terrible fatigue and even the smallest tasks are often beyond me. Just when I think the pain couldn't possibly

Hello Everyone I've come to feeling stuck. I have had persistent back, joint pain and headaches over 15 years it has affected my quality of life as birthday and special occasions have been spent grinning-grimacing through the pain! I've had mixed experiences with doctors and have lost faith to a certain

Hi all , Moving on Saturday and my wrists/hands are so painful. Constantly tired and feel sick. My left wrist in particular is so stiff constantly and I cant bend it down at all. Its so hard to do anything especially carry my daughter whos 2. Hopefully at my 2nd rheumatologist apt in 2 weeks they'll

Hi all, I'm 25 years old and fed up. Where to start? Well, I was initially diagnosed in 2013, I had a huge cyst on my ovary, it burst the day before I was due an operation. I had a laparoscopy a few months later and they found deposits of endo on my ovaries and womb. After that I tried the depo, numerous

I have had 2 days off work this wk due to endo pain. It was excruciating bowel pain this morning that subsided to a dull bloats feeling. As you do not know when and how bad the flares are it's difficult to make an informed decision whether to phone in sick as it can just be a couple of hours of bad

Hello All, Please could anyone recommend any tablets chemical or herbal that you have taken that you have found help or at least ease the pain off a bit, my husband has just at long last been diagnosed with osteoarthritis in his big toe joint, he has been prescribed Naproxen which is all good and well

It's been a while since I've been on here as luckily for a year after my last laparoscopy in Feb 2015 showed that they couldn't find any endometriosis after finding some in a previous op. So I stopped my prostate injections and my HRT, had the coil fitted and strangely it all seem to disappear and I

Hi all, has anybody tried a product called Finitro, I get regular messages advertising it in facebook. I am seventy three and was diagnosed pmr seven years ago treated by 20mg preds reduced gradually to 5 mg but always had flares. after advice from rheumy stop completely in one month had tests scans

I was diagnosed in 2008, started with naproxen/paracetamol/sulphasalazine but the in 2009 with Humira that worked quickly and fantastically well.but I still take naproxen twice daily for on-going wrist and other pain. As I assume we all do, I have blood tests every few months to check liver and kidney

I am Tanya I have Rheumatoid Arthritis for 5 years I have weekly injections of methotrexate injections and etanercept injections along with folic acid and naproxen. These help keep my flare up under control most of the time. I am a complementary therapist so I am very interested in alternative methods

I am Tanya I have Rheumatoid Arthritis for 5 years I have weekly injections of methotrexate injections and etanercept injections along with folic acid and naproxen. These help keep my flare up under control most of the time. I am a complementary therapist so I am very interested in alternative methods

I am Tanya I have Rheumatoid Arthritis for 5 years I have weekly injections of methotrexate injections and etanercept injections along with folic acid and naproxen. These help keep my flare up under control most of the time. I am a complementary therapist so I am very interested in alternative methods

Hi everyone not been on here for a while but i have R/A plus low immune system was diagnosed about 5/6 years ago having joint pain in mainly my right thumb and feet i now believe its gone to my left hip as I'm in pain when walking /going upstairs shoppings agony now.Medication I'm on is 200 MG's hydroxychloroquine

Hello All I'm new here. I've suffered continuous headache and chronic migraine for 20 years. I've tried pretty much every treatment going. However, For up to 5 hours a day for the past 7 days now I've had a new type of headache that I've never had before ( in addition to normal headache.) The new pain

I am meant to be flying to Greece on Thursday and have developed a head cold my first in over a year! I am on Hydroxychloroquine, Sulphasalizine, Methotrexate plus Naproxen. Can I take decongestants etc. Should I even go?

Hi, I'm new here and signed up because I really need some help. A little background: I've had headaches continuously since I was about 14 years old and my various doctors have never investigated this. They've put me on several medications over the years, including amitryptilene, co-codamol, voltarol