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Hydroxychloroquine Options
Audrey33
#1 Posted : Monday, December 26, 2011 3:27:36 PM Quote
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Hi everyone

has anyone ever been on Hydroxychloroquine ? i started them about 2 mths ago and some of the swelling has gone down on my hands and feet but the pain seams to be more as if the fluid was being a cussion for the bones. but when i rang the rummy help line before christmas she said it was just the fybromyalger that was causing the pain not the RA but i know the pain is getting worse but they keep saying that the RA is staying at the same level any body got or had this problem.

hope you are all OK and have not done two much.
Take Care

Audrey.
Julia17
#2 Posted : Monday, December 26, 2011 4:41:37 PM Quote
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Hi Audrey

Hope you have had a good Christmas.

I was on hydroxy at the beginning of my treatment, it didn t make any impression on me at all, but that was also the case with mtx and leflunomide. I hope others may be of more help to you on this matter.

Julia x
Rose-B
#3 Posted : Wednesday, December 28, 2011 9:46:45 PM Quote
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Location: Somerset


I was on this as beginning of my treatment as well but it did not work for me so it was stopped.

I know the helpline is shut at the moment but may be while ringing them as they may be
able to put you in touch with someone in the same position as you who could help you

Rose
sheila_G
#4 Posted : Thursday, December 29, 2011 12:04:02 AM Quote
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I was on hydroxychloroquine for a few years and along with mxt seemed to work well. Unfortunately I had to stop it because I started getting flashes in one eye. The doctors said they didn't think it was anything to do with hydroxy but according to the British Medical Journal if you have flashes or any other problem with your eyes whilst taking it it had to be stopped so I stopped it. Ask your Optician for the Amsler Eye Grid Test. A must if using hydroxy.

Sheila x
BarbieGirl
#5 Posted : Thursday, December 29, 2011 5:36:25 PM Quote
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Hi Audrey. I have been taking methotrexate and hydroxychloroquine together for around 2 years.
I know what you mean about the pain, and being told that the bloods are coming back ok, and it must be the fibromyalgia.
I have lots of hip pain, which they say isnt anything to do with my hip, but is my back and the fibro, my ankles are constantly painful, but as they dont count in the DAS My consultant keeps talking about an anti-TNF but so far it hasnt happened, I have an appointment on 9th January with the specialist nurse, so I am hoping they will get a move on!!! I have been awake most of the night again with pain, so even if the bloods are ok I'm not!!!
BARBARA
brendab
#6 Posted : Wednesday, January 25, 2012 12:04:32 PM Quote
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I have been on hydroxy for 4 years and it has worked well for me combined with a low dose of prednisolone. I also get hip pain as I have bursitis/tendonitis in both hips plus my arms and legs are tender to touch. I take amitriptyline as I had a piece of disc resting on a nerve and this changed my life. My rheumy suggested I increase this but I just take paracetamol. I was also recommended a gel called Pernaton which I slap on when my joints are particularly achy. I think it's very good. Hope this helps.
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