Story time 🫶🏻
Anyone wants to share their story?
Here goes mine:
I started off with my left arm being completely numb since August last year, nothing made it better , my primary care didn’t do much about it other than muscle relaxers and an X ray that showed a muscle spasm ; i got a neurologist since I noticed that this wasnt gone after 2 months and had to wait until like January for the appointment, she ran some kind of neuropathy test, That didnt work then my feet started getting cold and numb, then that went up to my knees, my hip, that caused my lost control of my bladder, not feeling my hip, lost balance, she sent me for an mri test finding the lesions in my spine and my neck, which got me to win a 5 ⭐️ stay at the hospital for more testing and full brain and spine MRI with and without contrast fo findout more lesions in my brain aaaand BOOM! Diagnosis happened😌
Takes some time but least they found it lol how i look at mine atleast. 2022 had covid and is when things started going downhill. Was having trouble with my walking and then beginning of 2024 work put me into short term disability to try and find out what was wrong. Started thinking it was my legs and sent me to pediatrician who had me take a cat scan and sent me to pt. The pt felt the strength in my legs and thought my problems were something else and told my doc. Then got neurologist and an mri and then week later told by neurologist that I got ms and had me admitted to a bigger hospital with better equipment. Went through 4 days of treatment where they steal my blood run it through some machine thrn put it back with fake platelets. Spent a week in that hospital and 4 of the 5 days of treatment 4th day they stabbed the bell outta me and didn’t wanna put me through hell again and skipped last day. Was in June then august started ocrevus. Just had 3rd infusion 2nd dose in February next in august
Well for the past 3 years I've been having left side weakness with a lot of pain shooting down my neck brain fogging us not able to talk at times they did an MRI of my back and decided that my L4 and L5 was both and that was the reason I was having it to cut the story a little short Friday I lost total control of my left side and went to the hospital they thought I was having a stroke. So they did a whole bunch of testing and a head MRI to find out that I have the beginning stages of MS I'm not sure much more about it than that. But after I got the diagnosis I looked it up and it's like perfect for everything that's been going on with me. My primary care doctor acted like I was just crazy