Certainly you could have Ms. Important to note that Ms can mimic other illnesses. Make sure he does bloodwork to rule out 'Lymes Disease' for example, as that's one of the conditions that has Ms type symptoms associated with it. I was diagnosed in late July of last year via a brain MRI, C-spine MRI & Spinal Tap. My brain MRI showed lots of Ms type lesions & the spinal tap revealed high levels of protein 'o' bands normally associated with Ms. My neurologist who's great but not an Ms specialist, believes I've had Ms for sometime. He is very knowledgeable & was able to diagnose me quickly. I first saw him in June of last year. In my case my first Ms type symptom that gave me concern was awaking in mid May of last year with an obvious speech slurring issue & my right lower jaw felt stiffer then it should be, my smile was also downturned. This lasted at least a month.
Signs and symptoms of MS can include:
Muscle weakness, stiffness or cramps
Tingling, numbness or pain in your body
Tremor (shaking) in your arms or legs
Loss of balance
Problems walking or moving your arms or legs
Fatigue (feeling tired all the time)
Bladder or bowel problems
Thinking and memory problems
There are more symptoms then that are in this list but it gives you a good idea of them. In my case heat or stress can trigger worse symptoms. Generally I am always tired & always itchy (feel like bugs are crawling on my whether they are or aren't). Also I pee way too much & get IBS. Last but not least I get the heavy legs/ gait issues, brain fog/memory issues, depression/anxiety, OCD, insomnia, numbness & tingling in hands, feet & legs, issues gripping objects securely with hands, dry mouth, back & neck pain & stiffness, limb weakness & fatigue, language/ speech issues, ringing in my ears, the Ms hug & I get short fleeting dizzy spells & vision disturbances every so often. Of course those are far from all my symptoms. As for your symptoms they could be Ms & given the lesions they may very well be. Only your neurologist can say for sure. If I can be of any more help, feel free to connect with me on here & drop me an email.
Not all those who wander are lost - JRR Tolkien