Guest guest Posted August 29, 2008 Report Share Posted August 29, 2008 , Do you remember how long it took you to get in your " drug-induced " remission? I'm sure it varies with everyone as well but that is what the doctor is trying to do to me. THX, Paris [ ] Re: mtx question - for Steph Hi Steph I'm still on mtx (10 mg) and sulphasalazine: I've been on them 3 years now and am in a 'drug-induced' remission. That means, my joint swelling has disappeared, along with the other symptoms such as fatigue, joint pain, rosacea etc. (Everyone seems to have their own unique set of symptoms!) The only side-effects I've had from mtx are initial nausea (for the first few weeks while my body adjusted). That went away but I still often feel tired the day after I take it. I get mild mouth ulcers/sore mouth sometimes and take 'oracort' mouth ointment when required. Now and then my monthly blood tests show a decrease in white blood count so I am told to decrease my dosage until it returns to normal and then we increase it back again. I need 10 mg mtx (a low dose) to function well but others take up to 25mg (high dose). Dosage is a very individual thing, but they try and give you the lowest dose that is effective for you. You are closely monitored (monthly blood tests) and take folic acid to prevent nausea etc. The benefits of being able to function are well worth it!!! And yes, I have a glass of wine if I feel like it Having said all that, mtx won't suit everyone or work for everyone, but it is the 'gold standard' treatment - rheumatologists like to try it before resorting to the 'big gun' biologics, or will use mtx in conjunction with some of the biologics. Mtx has been used for over 50 years so they know everything about it - that gives me comfort Re. remission, I said I am in a 'drug-induced remission'. That means without my drugs my symptoms would flare up - they are just being suppressed at present. (In fact, they flare up if I reduce my mtx to 7.5mg!) I have had 2 proper remissions before though, where I was slowly weaned off the mtx and then stayed symptom-free for several years. I hope this will happen again of course, but for now I am grateful to be well enough to run for buses again (with my artificial hip)! Email me privately any time Steph, in NZ ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2008 Report Share Posted September 1, 2008 thanks you have made me feel better already. I and taking 20mg to start seems like alot, will I be weaned down later on?? how do can they tell how much you need and if your in remission my doctor never mentioned remission as a possiblity, I just want to have my life back but I don't like the sound of all the side effects, I would like to be around to see my daughter grow up. the idea of taking medication everyday for the rest of my life just seems so awful but so does not being able to walk or button my pants. I take my first dose wensday. Thanks for the info you've made me feel alot calmer about everything like there is hope. From: Paris Schake <sdfprs@...> Subject: Re: [ ] Re: mtx question - for Steph Date: Friday, August 29, 2008, 4:58 PM , Do you remember how long it took you to get in your " drug-induced " remission? I'm sure it varies with everyone as well but that is what the doctor is trying to do to me. THX, Paris [ ] Re: mtx question - for Steph Hi Steph I'm still on mtx (10 mg) and sulphasalazine: I've been on them 3 years now and am in a 'drug-induced' remission. That means, my joint swelling has disappeared, along with the other symptoms such as fatigue, joint pain, rosacea etc. (Everyone seems to have their own unique set of symptoms!) The only side-effects I've had from mtx are initial nausea (for the first few weeks while my body adjusted). That went away but I still often feel tired the day after I take it. I get mild mouth ulcers/sore mouth sometimes and take 'oracort' mouth ointment when required. Now and then my monthly blood tests show a decrease in white blood count so I am told to decrease my dosage until it returns to normal and then we increase it back again. I need 10 mg mtx (a low dose) to function well but others take up to 25mg (high dose). Dosage is a very individual thing, but they try and give you the lowest dose that is effective for you. You are closely monitored (monthly blood tests) and take folic acid to prevent nausea etc. The benefits of being able to function are well worth it!!! And yes, I have a glass of wine if I feel like it Having said all that, mtx won't suit everyone or work for everyone, but it is the 'gold standard' treatment - rheumatologists like to try it before resorting to the 'big gun' biologics, or will use mtx in conjunction with some of the biologics. Mtx has been used for over 50 years so they know everything about it - that gives me comfort Re. remission, I said I am in a 'drug-induced remission'. That means without my drugs my symptoms would flare up - they are just being suppressed at present. (In fact, they flare up if I reduce my mtx to 7.5mg!) I have had 2 proper remissions before though, where I was slowly weaned off the mtx and then stayed symptom-free for several years. I hope this will happen again of course, but for now I am grateful to be well enough to run for buses again (with my artificial hip)! Email me privately any time Steph, in NZ ------------ --------- --------- ------ Quote Link to comment Share on other sites More sharing options...
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