I had the worse flare yet this past week or two. I feel like I am still dealing with it. I started Methotrexate last Friday and am taking Prednisone. I have been in so much pain that I called work today after almost a week of staying home to let them know that I will be requesting short term disability to try and get over this and getting adjusted to my new meds.
I went ahead and saw my PCP today and asked for a referral to PT to get help regaining my strength because all I want to do is sleep and to learn what to do as far as splinting when I'm flaring. I will also request orthotics.
I have been fighting the short term disability route for the past month but I think I can be more productive in the long run at work and home if I just rest and take care of ME full time for a few weeks. My rheumy and I talked about this in my last appt and he said to let him know if I needed to go that route.
I think accepting that I need time to heal and regroup is a big step for me, I have already gone through the phase of not wanting to know about Drs for a bit and feeling upset about RA.
I say time to move on!!! It is ok, I am human and not superwoman. My husband says sometimes I am so stubborn and just go with: "I am woman hear me roar!" LOL He does know me.
I have been in so much pain lately and my hands and feet will swell all of a sudden and add to the discomfort I think rest will help me get better faster.
Any one have gone through this lately?



Hi, Martilla,
I am sorry you are in so much pain, but I am happy to hear that you are going to take short-term disability. I'm happy to hear your rheumy is listening to you now, and trying to help you. Please let us know how you are doing. I think rest will do you a lot of good and give your body time to get used to the meds.
Martilla, honestly, I feel as though I have been in a flare for months and months. I am hoping the humira I just started works. I think I have a good doctor now, and when she saw the MTX wasn't doing enough, she moved right on to a biologic. She gave me a choice of Humira or Simpoini, and I chose Humira. She knows I can't take much more of this pain and fatigue. I know it is hard, but hang in there, sweetie.
V