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CHANGES AT MSWORLD - MSWORLD'S CLOSURE

We began with a mission and purpose to help others living with MS.

We were excited to get going!

And hit a few bumps along the way…

However, in all seriousness, we remain grateful for our amazing volunteers, members & all who have made MSWorld a valuable resource for all!

July 10, 2024, we celebrated the goodness of these past 28 years. With a heavy heart, we will be ending our services.

We need a financial miracle to keep going forward.

We thank all for your support.

MSWorld's website will close on October 16, 2024.

“I personally want to wish all of you the guidance to find this type of support, as so many do here. Also, my prayers and love extends beyond my understanding. It has been a pleasure to steward this journey.”

God Bless you, Kathleen

Kathleen Wilson
Founding President
❤️

we leave knowing that
we did our best and
stayed true to our mission and purpose.


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Wow. So this really wasn't an MS attack.

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    Wow. So this really wasn't an MS attack.

    OK, so I've had all kinds of posts on here the past month or so trying to figure out my new symptoms. Back story in my siggy and more recently, i had 3 new symptoms crop up in Aug/Sept, called the MS center, they had me come in for an appt, the NP was very concerned that i was getting c-spine lesions and ordered a brain and C-spine MRI. After seeing her 5 weeks ago, I had 4 new symptoms crop up.

    Had my follow-up appt yesterday and she went over my MRI ... no new lesions since last Nov! My MS specialist is on family emergency medical leave for a month so he wasn't there yesterday after all, and the NP will double-check this with the other MS specialist, but it really looks good.

    Based on my symptoms and the fact that a lot of them started to improve after DH randomly said a few weeks ago, "Maybe you have an electrolyte imbalance that's contributing to some of your muscle jerks and spasms and stuff. You should try drinking G2" ... and the fact that I had some symptoms pop up last month that seemed like hypoglycemia and BP dropping ... the NP really thinks I have an electrolyte imbalance and some related hypoglycemia and low BP issues, maybe a B12 deficiency, and should follow up with my PCP for blood work and further testing. (I see him Friday; new PCP so hopefully he's good!)

    I'm really amazed and thankful; here we were talking that I might need to move to Tysabri or Gilenya ... and all I really needed was some G2 and maybe a higher salt diet and more frequent snacks?? Incredible. We'll see what the PCP says for sure (I do have a STRONG family history of diabetes so we'll really need to figure out what's going on with the blood sugar issues) but I'm overjoyed that the MS is still stable for now after all. Thanks so much to all of you for your helpful responses to all my recent posts and questions. You guys are great!
    2001: 1st 2 relapses, "probable MS." 2007: 3rd relapse. Dx of RRMS confirmed by MS specialist. Started Cpx. (Off Cpx Feb 08-Mar 09 to start a family; twins!) Dec '09: Started Beta. Oct '13: Started Tecfidera. May '15: Considering Gilenya.

    #2
    Isn't it funny that we are happy when our medical problems turn out not to be what we expected ?!

    I am so happy for you that it seems like something simple for you to resolve your problems (well, simple compared to MS!).

    I had something similar happen with my IC bladder disorder. I was slowing getting worse and worse symptoms, and having more and more pain. I was depressed thinking about living that way for the rest of my life - especially after just getting my surprise MS diagnosis.

    Turns out I'd had kidney stones for 4 months and we didn't know it because the symptoms are so similar. I ended up with bilateral kidney stone blockages and had 5 procedures to take care of the problem. I was so happy to find out. I've been completely symptom-free since the last procedure !

    I was happy to have kidney stones because I knew it was temporary ! It's amazing how things can be put in a different perspective when you have major medical problems.

    Hope the news continues to get better for you and that everything will come under control easily and quickly.

    Comment


      #3
      Awesome news Hope!

      I think we all attribute weird going on's in our bodies to MS. "My head hurts, must be MS. My leg feels odd, must be MS. I forgot where I put the car keys, must be MS." We never give ourselves a break for just being human and having normal human problems

      Go drink your G2!
      dxd RRMS 7/2011 - Rebif 8/2011 - Tecfidera 7/2013

      Comment


        #4
        cosake - I have never heard anyone say they were happy to have kidney stones lol

        Those still take the cake for me on pain, but I agree, at least you knew it was temporary
        dxd RRMS 7/2011 - Rebif 8/2011 - Tecfidera 7/2013

        Comment


          #5
          So true; it does change your perspective.
          Thanks for the replies, you two!
          2001: 1st 2 relapses, "probable MS." 2007: 3rd relapse. Dx of RRMS confirmed by MS specialist. Started Cpx. (Off Cpx Feb 08-Mar 09 to start a family; twins!) Dec '09: Started Beta. Oct '13: Started Tecfidera. May '15: Considering Gilenya.

          Comment


            #6
            hope,

            Some medications can cause electrolyte imbalances. Steroids and Trileptal are a couple of them.
            Diagnosed 1984
            “Lightworkers aren’t here to avoid the darkness…they are here to transform the darkness through the illuminating power of love.” Muses from a mystic

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