trouble at night
Ive noticed that my symptoms (mostly the tingling) seems to be much worse in the evening than it is during the day. Also have a stronger sensation of needing to stretch put my arms and legs at night time. Is this muscle spasticity? And does anyone else notice an increase in their symptoms at night? Sorry but I'm relatively new to Ms and my neuro hasn't been the most helpful. Most of what I know I learner from others with MS so super grateful for this site!
*stretch out.* kindle auto corrected :)
You're less busy at night, so notice things more. Lying in bed, you'll be aware of so much more too.