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nferia

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  1. "We had a couple "warm days" and my whole body panicked, because, it's dreading the Summer "event"... meaning, months of hell. Pain. Discomfort.... "

    1. , oh, goodness. I'm sorry. I hope the temps drop back down to more seasonal numbers and you can enjoy the Spring with minimal discomfort. And I am so sorry you are looking at some upcoming months of serious pain and unpleasantness.

      Best, Erin, Team Member.

  2. "Random question. Have you ever been told you likely have RA on top of your MS diagnosis?"

    1. ,
      That's a great question.
      It is quite common to have more than one auto-immune disease.
      Many in this community have been diagnosed with both RA and MS.
      This article may provide some helpful insight:
      https://multiplesclerosis.net/living-with-ms/multiple-autoimmune-syndrome
      ~Doreen (Team Member)

    2. thank you. I was told by my dr that my mild arthritis has developed into RA in my hands, hips, lumbar, and right shoulder and elbow... so, basically, all over. I am already in pain all the time but, it's scary knowing it is going to get much worse. Does that make sense? Thank you for the article.

  3. "I just suffered a flare in my ankle joints. I thought the pain in my hands was bad. NOPE!"

    1. , ouch! I'm so sorry you were dealing with a flare! How are you recovering? Are you still in the midst of the flare or is it starting to dissipate?

      Best, Erin, Team Member.

    2. Still dealing. My hubby won't let me try to walk anywhere but the loo. Or my pc. Forcing me to use either my crutches or cane.

    3. , awww. I'm glad he's trying to take care of you, even if you might find it a little intense at times. Are you feeling steadier on your feet or are you pretty glad to have the crutches/cane?

      Best, Erin, Team Member.

    4. honestly, i am happier just staying off my feet. they really hurt. it's like my hands. they are numb but, the joints are screaming.

    5. Hope today is much better for you! -Latoya (Team Member)

  4. "I have been so "lucky" this summer. MS symptoms are not enough... no, we had to add PMDD to the mix. Yay me. Sarcasm in play."

    1. ,
      You threw me off for a second...I guess I was hopeful.
      How are things going today? Are you currently being treated for PMDD?
      ~Doreen (Team Member)