Forum Replies Created

  • Carla Epps

    Member
    January 20, 2020 at 3:03 pm in reply to: It was hard to breath. Was it my MS?

    Hello Ed.  I read your experience and it sounded all too familiar to something I experienced a few years ago. I  was having labored breathing and not able to take deep breaths in and out. It was a time when I was having increased neurological symptoms. Both my primary care physician and my neurologist at the time were concerned it was a function of my MS. I was referred to a pulmonologist who ran a series of tests and concluded that it was asthma. I was put on an inhaler for 1-2 months and was able to fade it out once the season changed…thankfully. To think that my MS was considered a possible culprit was terrifying.   The journey continues…

  • Carla Epps

    Member
    March 2, 2019 at 6:06 am in reply to: Are you on Ocrevus? How is it going?

    Hello there! I’ve had 4 full doses of Ocrevus so far and I have to say it has helped significantly with my fatigue and strength, particularly in my upper body. As far as my lower extremities, it has allowed me to start conditioning them. I’m hoping that Ocrevus coupled with Physical Therapy will allow for further improvements in hips, legs and feet. Time will tell. I’m viewing Ocrevus as an “In the meantime” therapy as I watch and wait for Stem Cell Research to continue progressing.

    Back to Ocrevus, its effectiveness becomes clear to me the month before I’m due for an infusion because the weakness & fatigue resurface.  My MS team has moved my infusion up a month earlier for the next one so I’ll see how that goes. I’ll continue to keep you all posted.

  • Carla Epps

    Member
    February 26, 2019 at 3:38 am in reply to: What activity do you do that challenges your mind?

    Bananagrams is my favorite!!!! I also like headbandz which I play frequently with my children.

  • Carla Epps

    Member
    December 7, 2018 at 7:13 pm in reply to: What is the first thing you would do if you were free from MS?

    I’d go hiking with my kids!

  • Yes Debi, I most certainly will.

    Thank you for sharing Ed! That is encouraging to hear.

    1. I’ve had 3 infusions of Ocrevus and find this news congruent with my experience. In fact, I’ve found that it not only preserves but strengthens my upper extremities. My lower extremities, not so much. I will continue to monitor. I would welcome other’s experience on Ocrevus
  • Carla Epps

    Member
    October 9, 2018 at 11:20 am in reply to: Which MS symptom impacts your life the most?

    Pardon me as I learn to navigate through these forums. I would have to say spasticity coupled with lower extremity weakness have the most significant impact on my life. To address these, Intense PT has been helpful but not an overnight solution.