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Not new to MS but new to me having MS

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    Not new to MS but new to me having MS

    Hi all!
    in September2015, after getting my daughter to College and other stressors,I started having blurred vision in my left eye. The Ophthalmologist found an inflamed optic nerv. That's how it all started. Within five month I have seen a Neuroophthalmologist who ordered MRI's of Brain and Spine w/wo contrast. Long story short, first they thought I had a brain tumor because the lesion was a tumorfactive one which means large looking like a tumor and I also had word finding difficulty and major brain fog. They decided it was inflammatory,follow up MRI showed big lesion resolved almost completely but a new lesion was found. Then referral to Neurologist specialist in MS on February 4th. After all other exclusion through blood work, he diagnosed me with MS and wants me to start DMD.
    it is a complete shock to me!! The reason why? Because I'm the Caregiver of my Husband who has MS for over 20 years! How is this possible?. Thanks for listening, would love the support of other people.

    #2
    Hi ClaudiaK,

    Welcome to MSWorld! Sorry to hear of your diagnosis. Wow. What a shock that must've been to be diagnosed with MS as well! Good luck choosing a DMD. There are certainly more choices than 20 years ago! Does your husband take one? How is doing? Please know everyone has their own unique course of MS as well.

    Hope you find this site to be as informative and supportive as I have. Also hope you take some time to check out all we have to offer, and check out Chat Rooms, too.

    Best of luck.
    Kimba

    “When you change the way you look at things, the things you look at change.” ― Max Planck

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      #3
      WELCOME TO MS WORLD! WOW! what are the chances of that happening, as was already stated, every case of MS is different. But you probably already know some of these things. You came to the right place for support, if anything is on your mind just say whatever it is. I wish you nothing but the best!
      hunterd/HuntOP/Dave
      volunteer
      MS World
      hunterd@msworld.org
      PPMS DX 2001

      "ADAPT AND OVERCOME" - MY COUSIN

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        #4
        Hi kimba22
        my husband is taking Rebif which I also chose to take. He is in the wheelchair but still working. It's more physical with him, with me it's more fatigue and cognitive problems. My family kinda brushes my condition under the table because it's not visible like my husband's symptoms. I continue to be what I was before my diagnosis, supportive and hopeful that we can get through this together. Next week, the MS Liveline Nurse will come and teach me how to do the injections, will be wired to do it myself having seen my husband do it for so long.

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          #5
          Thanks Hunterd for the kind words. It means so much to me to have a ms family who understands me. Will keep you posted. Hope you're doing alright. Looking forward to Spring. I'm not a Winter person, don't have heat sensitivity jet like so many people with MS.

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