Announcement

Collapse
No announcement yet.

Hello

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

    Hello

    Hello everyone, I ask currently 30 years old. Everything started when I was 25.

    My journey began five years ago the begining of this month. It started when I woke up one morning with a blurry left eye. I just thought my glasses were blurry. I kept wiping them, but nothing got better. I eventually closed my right eye three days later and notice I couldn't see!

    I went to my eye doctor, an ophthalmologist. Both he and his assistant kept going back and forth between eyes alarmed. He eventually said it was optic neuritis and told me what that is. He sent me to a neuron ophthalmologist the next day.

    The neuro ophthalmologist confirmed it was optic neuritis and sent me for an MRI.

    I eventually went to see a regular neurologist. I started to get dysesthesias on the right side of my face and right arm. My right arm had gone numb and tingly for two days. It is now weaker than my left. I also have muscles twitches. MRIs have picked up about ten legions, mostly on the right side. But this neurologist said I didn't have enough lesions to have MS (OK...). I know the MacDonald criteria has a legion count for people without enough syptoms, but it isnt more than ten.

    I started to see an MS specialist last year. He was angry I only ever had brain MRIs and no other tests. He ordered a c-spine MRI, blood tests, EVP, and OCT. They came back normal, but he said he's still monitoring me. He also said I might never had optic neuritis. He changed it to optical neuropathy. He is also in disagreement with the MRI reports by the radiologist.

    In late October early November, I had a headache that lasted six days that I had to go to the emergency room to get rid of. The same thing happened last week, but for four days, no ER visit. The ER couldn't figure out the cause. They were not migraines.

    I saw my neurologist on Monday, and he was very concerned about the headaches. He ordered more blood work and a brain and c-spine MRIs. I see him in May.

    I have been lurking on this site for two years, just now decided to make an account. Who knows. Maybe nothing is wrong with me. Or something no one is looking for.

    #2
    Hello and welcome! Sorry that you are having these symptoms. Your headache sounds awful. I am praying that you get answers and a resolution to your problems.

    Comment


      #3
      Hi Bldudas and welcome!

      I'm also sorry you have had these symptoms, but glad you have a specialist ordering all the necessary tests. What a run around ride you've been on. But hang on - something definitive will eventually come around. Just wish you didn't have to wait til May!!

      Take care of yourself!
      1st sx '89 Dx '99 w/RRMS - SP since 2010
      Administrator Message Boards/Moderator

      Comment


        #4
        Thank you
        These headaches have been nasty. But I get through them.
        Yes, I'm so flat I finally got someone who knrew more

        Comment


          #5
          WELCOME TO MS WORLD BIDUDAS!! we are very glad to have you here!
          If it were me, and it is not,, I would lean towards the MS specialist, they can make all the referrals to the specialists that you need to see. A regular doctor can also do this, but an MS specialist specializes in that area of expertise.
          I have both a "regular" ophthalmologist and a retinal eye surgeon ( who also handles MS patients) so I cannot complain of about eye doctors. And coincidentally,, I do not have them for my MS, I have them for my diabetes which I have had for 45 years, it was just pure coincidence and pure luck on my part.
          I wish you the best and I hope they figure everything out quickly for you.
          hunterd/HuntOP/Dave
          volunteer
          MS World
          hunterd@msworld.org
          PPMS DX 2001

          "ADAPT AND OVERCOME" - MY COUSIN

          Comment


            #6
            Hello and welcome to the message boards ! I have been posting here for about 4 years and I know that I have become somewhat of a broken record ! I want to repeat what I have learned from experiences and researching this MonSter !
            First, find and engage a 'bona fide' MS specialist neurologist ! A general neurologist doesn't have the MS knowlege . My MS specialist has 500 MS patients in his practice !
            Second, make sure your vitamin D level is above 30ng/ml. IMO that is critical ! I hope that you find a neurologist that understands that you are suffering and helps you. Good luck

            Comment


              #7
              Thank you everyone.

              I go for an MRI on Saturday, so I'll see how that goes.

              My vitamin D was around 42 my last blood test a few weeks ago. My B12 was 562. So I'm good there.

              This is all so frustrating at times.

              Comment


                #8
                Hi,
                Let us know what doc says about mri?
                All the best.

                Comment


                  #9
                  I shall. I don't go back until May.

                  Comment


                    #10
                    Originally posted by Bldudas View Post
                    I shall. I don't go back until May.
                    Hi Bldudas.

                    I can't offer any advise just wanted to let you know I'm in the same boat with you. I'm also 30 and have optic neuritis and brain lesions. My journey had only just started 3wks ago. My ophthalmologist thinks I have MS and my neuro thinks it could be anything. I'm glad to hear you went to a MS specialist as I'm considering doing the same. Anyway here if you need to vent. I'm feeling the frustration already... would have no idea what it would be like after 5yrs!

                    Comment

                    Working...
                    X