• RokinRobn RokinRobn
    March 30, 2010
    Is there a healthier alternative to taking methotrexate???
    RokinRobn RokinRobn
    March 30, 2010

    I am looking for an alternative treatment besides methotrexate.... something healthier. Currently I am taking 7.5 mg a week.  I am concerned about the side effects-especially the liver . I realize it is a low dose- but has anyone had problems with that dosage??? any suggestions for something more naturopathic???

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  • Barb April 19, 2010
    Barb
    March 30, 2010

    Hi RokinRobin, I am only very new to all of this not even a year in yet. I have had a little bit of a problem with my liver but it was not due to the methotrexate but the arava. I have had really good readings with the methotrexate and i was on 20mg per week but now im on 10mg per week, since i started on the Humira. I am sorry i don't know of anything natural that you can substitute methorexate with. However I do know that you can have a few drinks whilst taking methotrexate. My Rhumy told me if i wanted to have a drink that was fine but i had to have 2 virgin days before and after having a drink. I am lucky because i would probably only have two or three drinks at a party perhaps 2 times a year. I hope this helps.

     

    Cheers godbless and best of luck xx Barb

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    • Barb
      April 19, 2010
      Barb
      April 19, 2010

      sorry i left out only 1 or 2 drinks is safe ... please don't think that its ok to drink anymore than that and only once or twice a year

      cheers again Barb xx

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    • Bluevelvet22
      December 18, 2013
      Bluevelvet22
      December 18, 2013

      I would like to know if there are any alternatives to DMARDS and Steroids. I was diagnosed with Rheumatoid Arthritis in October, with a high RH FACTOR and multiple joint involvement. So far a combination of the condition and the treatment (Prednisolone, Plaquenil, Sulphasalasine, and NSAIDS has left me seriously anaemic causing Hypertension and Cardiac Arrhythmia and I feel I've been to hell with the many and varioous side effects of these drugs with precious little improvement considering the 'price' I have paid in terms of serial blood tests and misdiagnosis of Iron deficiency anaemia. I would appreciate anyones' comments who have been where I am now as I feel very isolated.

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  • Vivian April 01, 2010
    Vivian
    March 30, 2010

    I do not know whether an alternative to methotrexate but I have been avoiding all nightshade vegetables (potatoes, tomatoes, peppers and eggplant) and I notice improvement.  Previously I was taking methotrexate and then I tried Plaquenil.  I am off everything and am not getting worse.......Hope this helps.

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    • sylvia
      March 08, 2014
      sylvia
      March 08, 2014

      HI Vivian - how are you doing now? I just started Methotrexate and I feel awful.

      Worse than before I started the medication.

      I went off all nightshades years ago and it did help with the osteo-arthritis.

      Sylvia

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    • njulja
      September 04, 2014
      njulja
      September 04, 2014

      Hi! I'm on Methotrexate from May 2013, now taking 6 x 2,5 mg once a week, I have no any problems (just some weekness in first weeks when the dosage was higher), also I take Deltacortene (prednisone, my medic gave me a plan, I started with higher dosage, now taking 5 mg every day), but I can say that if I forget to take deltacortene so the pain returns - I have one foot finger and one finger on my right arm promblem.

      I take the Vitalmix complex sometimes for 10-12 days with Royal Jelly or Ginseng - in the autumn and in the spring to help my immune system, and It is strange, but since I take the drugs, I have not the seasonal influence anymore...

      The other thing that helps me - fresh lemon juice every morning, it helps to purify the organism and to normalise some processes. Just squeese half of lemon (better from organic agriculture) in a glass and add some warm water (not hot!). I didn't believe that it will help, but on a fourth day I woke up and moved my arm without problems! Taking anyway Methotrexate and deltacortene according to my medic plan. But when I forget to buy the lemons, after 2 days the pain returned. So this is a proof of method is very valid!

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  • sunshinegal43oh March 30, 2010
    sunshinegal43oh
    March 30, 2010

    Hi RokinRobn,

     

     I'm on Methotrexate, too. I take 8 2.5mg pills per week (20mgs), and I've been on this dosage since April of 2009 without any liver problems thus far. I have bloodwork checked every two months, and have not had any problems for the year I've been taking this medication.

     I can't help with any other more healthy alternatives. I'm very happy with the Methotrexate.

    Sunshine

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    • RokinRobn
      March 30, 2010
      RokinRobn
      March 30, 2010

      hi Sunshine

      do you find that you are still able to have any alcohol?? or even several glasses of wine  a week.?  we keep actively socially so giving up wine may be tough.

      have you had any side effects at all? such as hair loss?

      I see my Rheumatologist in 2 weeks so I will find out how often he wants me to have Liver function tests.

      thanks for your response, robin

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    • Carole Wilk
      May 14, 2010
      Carole Wilk
      May 14, 2010

      I have an Auto Immune Disease RA..but there is something else going on in my body and I don't know what!  I am on  6  2.5 mg of methotrexate a week (15 mg)  and I can tell you my hair falls out all over the place.  I completely lost all of my eyebrows.  I have been on this since last summer June 2009.  I also take Synthroid for my hypo thyroid and I have plantar faciatis....I found it interesting that the foot problem is from the hypo thyroid.....I never heard of that.  I am going out to buy selenium...and hope it helps me.  Thanks  Carole

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    • Laugh often
      October 02, 2012
      Laugh often
      October 02, 2012

      Hi RokinRobin,I am on methotrexate 6 – 2.5mg for per week.  So far it is not working out for me.  Whenever I take it, I have headache and fever like flu symptoms. I need to go back to see if I can get other medication. Laughing

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  • Bonnie Tyner April 01, 2010
    Bonnie Tyner
    March 30, 2010

    Dear Robin,

     

    I too looked for alternatives to this medicine and found nothing.  I have been on it for a little over 10 yrs and so far so good, no problems.   I'm on 10 mg per wk.

    I did go off of it when I was  on 2.5 mg and had disasterous results that took me over 6 mos to find another suitable drug to start that would work for me.  I took myself off as I felt it was the only thing left that I was on and why did I need that one little pill?  Dumb! Dumb!  Dumb!  I even had a spell of Fibromyalgia that was excrutiatingly painful due to that as well.  May God bless you and all of us who are on these drugs.  I'm thankful they exist tho!   Bonnie

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  • gma2 April 24, 2010
    gma2
    March 30, 2010

    I've been concerned about taking MTX too.  I'm on .6 ml inject. once a week and stopped taking it once...that was bad, the pain was so bad so I started it up again.  I'm feeling better but still worry about the side effects.


    One rheumatologist told me that after a 30-year (if i remember that right) study it was found that those who take MTX live longer and have fewer heart attacks than those who don't.


    The good, the bad and the ugly...it's hard to just live with this problem and I still don't understand why my RH factor is negative, my rheumatologist says I have inflammatory arthritis and our expert here Lene says that is RA.  Doctors can be such a pain...Undecided 

     

    Lene is awesome and has answered so many questions for me...God bless you Lene and be well...

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    • maryam
      January 24, 2012
      maryam
      January 24, 2012

      i am taking 8 mg injections, it is hurting my stomach soo bad, i had to stop, i am going to see my doctor in a week.  The pain in my stomach i can not work with. i cannot stop working

       

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    • njulja
      September 04, 2014
      njulja
      September 04, 2014

      How are you now? I've had to take some gastric protection first week, but it was for deltacortene dosage fault (my fault, I forgot to take less according to the plan). Now I have no any problems, but I take the pills, not injections.

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