Confused and scared.

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Nursekimmiexo
New Member


Date Joined Jul 2017
Total Posts : 1
   Posted 7/18/2017 7:53 AM (GMT -6)   
Hello, I am new here-- and have a question that I hope someone can answer. I apologize if this is lengthy:

Back in January, I woke up and couldn't see very well from my right eye. I thought it was eye strain and made an appointment with my eye doctor. He checked my eyes and gave me some stronger contacts and I thought that would be it. However, the next day, I could barely see with the new prescription and noticed my color vision was off in the right eye. I went back and he sent me to a retina specialist because he thought I had the beginnings of a detached retina. The specialist ran countless tests and couldn't find anything wrong, but suggested I have an MRI just to make sure I didn't have something going on with my optic nerve. My MRI showed: "Multiple foci of increased T2 and FLAIR signal in the periventricular and subcortical white matter bilaterally. The largest on the right measures 1.3 cm. The largest on the left measures 9.5mm. Several of the foci demonstrate a perpendicular orientation to the corpus callosum." I was sent to a neurologist and was asked a hundred questions- and things I thought were just weird things over the years (electricity feeling shooting down my neck/spine, tingling hands/feet, clumsiness, brain fog, forgetfulness, my legs just 'giving out' and me falling, a case of what I thought was Bell's Palsy but the neuro said no).... combined with my MRI made him suspect I had MS. I had another MRI of my neck and spine and one lesion was found on my cervical area. I was started on meds immediately with a brand new diagnosis of MS.

He also ordered lab work and my ANA kept coming back positive (three times) so I was sent to a rheumatologist. I just got a call saying all my tests were negative except the one for Sjrgren's, which was positive and he wanted to put me on some medication for it, no big deal.

The more I read though, the more confused I get. Can you have both of these diseases? Was I possibly misdiagnosed with MS? The rheumatologist didn't see too concerned and I haven't seen my neuro again since then. I do have the classic 'Dawson's finger lesions' on my scan... so I'm just freaking out wondering if I now have two things to deal with or if I was misdiagnosed all along.... any help is appreciated!

Gretchen1
Forum Moderator


Date Joined Jan 2007
Total Posts : 3531
   Posted 7/18/2017 8:39 AM (GMT -6)   
Dear Nursekimmiexo,

Welcome to HealingWell. I'm sorry you've found yourself looking for some answers. It does appear that you have two diseases to manage. Both MS and Sjogren's are considered auto-immune diseases. For some people, a malfunction in the immune system can result in a number of diseases.

I have 3 autoimmune diseases; MS, RA and Celiacs. It's tough, especially at first to deal with the loss of one's health. There is a grieving process. Be kind to yourself. Get professional help if you need it. Both diseases can be manageable.

If you suspect a misdiagnosis, seek a second opinion. You can contact your local branch of the MS Society. They can give you the names of local neurologists who are experienced with MS. The MS Society can also help with questions, counseling and many other services.

Ask as many questions as you may have. We are here to help. How are you doing managing new medications?
Diagnosed with MS July 2006

I have no lesions on my soul and so I live with no limits.
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