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  • Is this still possible MS

    Hello! For the past really 7 years I have had on and off--more off than on--weird symptoms---days of headaches, tingling, numbness, joint pain, weakness-- most of this on the left side of my body. I have fainted to because of the pain...but its literally only like every 6 months...although really lately it has been more like every 3 months...if i workout I do feel it gets better...I have had 3 MRI's and each time they find nothin....When I saw a neurologist he was certain I had it and when my....
  • 3 days ago

    Leg Pain/ Arm Pain tingling and arms tired

    I'm a 14 year old male and a few days ago I started feeling like my arms are tired and I feel leg and arm pain. I am so scared that this is ALS. I've had a MRI for head pressure that I have had before and it was perfectly fine. I also have tingling in my feet and hands, but not too frequent. I have been stressing a lot over it. My arms can pick up things and move it just hurts and they are tired and want to stop moving. Could this be Als, MS, or the stress could cause these symptoms?
  • 12 days ago

    Depression and MS

    Depression is a major -- but highly treatable -- symptom associated with MS. What plan should be in place when flare-ups intensify sad thoughts? Learn more here: http://wb.md/2oRVhEL We want to hear from you. Have you experienced emotional changes such as depression since receiving your diagnosis?

  • 17 days ago

    How a Mom of 3 Manages Her MS

    Marleigh Brown, a busy mom of three, shares the daily routines that help her manage her MS symptoms and keep a positive outlook: http://wb.md/2o6LoPt What's your daily routine? We'd love to hear your tips.
  • 1 month ago

    unbearable itching

    I hate to wear clothing especially with seams or tags. I feel like i am being stung, eaten alive and I want to rip my skin off. Does anyone else get this symptom?
  • 1 month ago

    What to use to treat loss of energy?

    My aunt has had MS for about 20 years now. She has been treated here in the US and also in Europe. Unfortunately, her MS escalated rather quickly. She's been in a wheel chair for about 10+ years now. She asked me what kind of medicine she could use to help her energy level. She sits or lays down most of the time, so its difficult for her to gain energy. I would appreciate any advice or suggestions on this topic. Thank you for your help. JP
  • 1 month ago

    Week 4: Tips to Make a MS-Friendly Home

    Being at home with your MS means creating a space that's comfy, cozy, and works for you. This WebMD slideshow shows you how: http://wb.md/2neZrDF . Your occupational therapist or rehab specialist can help you know what changes to your home will help you the most. We want to hear from you: Have you made changes to your home?
  • 1 month ago

    Week 2: What Happens During a Relapse?

    With MS, you'll have good days and bad days. You might experience little to no symptoms for weeks or months, but then a flare-up or a relapse might occur out of the blue. During a flare-up you'll get new symptoms, or symptoms you already have will get worse. It's important to know that many people recover from their relapses without treatment, but there are several things your doctor can do to help you get through them. Here's what to know about the signs of a MS relapse and how to....
  • Is this possibly not MS-related?

    I was diagnosed with carpal tunnel syndrome in 2015. Then, I was diagnosed with RRMS the same year. I was told that I no longer have CTS anymore, and my orthopedic specialist thinks it's MS causing the issue. However, my neurologist isn't sure that It's MS-related. I have been on Tecfidera since June 2016. I received a steroid shot in my hand, and it only made it worse. Many medications have not helped either. This is what my hand feels like: As if I sat on my hand. Extreme numbness that....
  • 1 month ago

    Stem Cells

    How do you go about becoming part of the trials?