No shortage
Apparently I'll have plenty talk about at my upcoming appointment with the neurologist. I've had one MRI that was consistent with CP but also indicated MS. It wasn't the news I wanted or even expected, but the puzzle pieces fit. I've been trying to be conscious of symptoms that also fit the diagnosis without spiraling into anxiety and hypochondria.
So I consulted google-- such a double edged sword. I read about the different types of MS and symptoms. I read about the MS hug which I haven't experienced exactly. I think I have a version of it in my neck. It gets strangely tight and I feel like I need to roll my neck and shoulders, but nothing really relieves it.
Then I realized my vision had been weird for the last year at least. Eye doctor said it could be the Pulfrich phenomenon--- MS.
Now for the last few days I've been feeling a sensation of an electrical shock going through my body. It's not especially painful-- it feels similar to touching a low voltage hot wire fence. I consulted the old frenemy google and the third result labeled it Dysesthesia. Ta-dah another MS symptom.
It's been hard for me because of my CP I just ignore almost everything unless it cannot be ignored. It's just been normal to have a quirky body. So to be more conscious of what is going on is pretty new for me. I don't want to show up with nothing to say at my appointment beside "idk something about an MRI and my doctor sent me to you."
I'm no doctor, but I am a researcher I even have a degree stored behind my dresser to prove it. I'm not using google in lieu of medical expertise, but I have questions and I don't have a doctor on speed dial. #MultipleSclerosis #CerebralPalsy #DoctorsAppointments #Google #Undiagnosed