For instance, I tasted the toothpaste as soon as I put the toothbrush in my mouth. When I was finishing up brushing my teeth, I could no longer the toothpaste. I've been dealing with this for years. Every year I used to think that it was my sinuses until I was dx and read up on the symptoms of MS. It's frustrating because when it comes to eating what's the purpose if it's like I'm chewing on site. Who's dealing with the same and how are you handling it?
I’ve completely lost all taste before. I’m glad its back makes eating that much better. 🤗 hang in there
I've been hanging in for 10 years but it's so frustrating especially when you're hungry. Why am I eating if it's like I'm chewing on air🤦🏾♀️ but we have to eat🤷🏾♀️. I haven't experienced any numbness and I pray I don't. I've already have numbness in my fingers the last 11 years.
Not sure it's my taste buds per se, but the front 1/3 of my tongue gets periods of numbness. Which is like 😒🤨🤦🤷.
Changes in taste are a common issue for people with multiple sclerosis (MS). About 25% of people with MS experience loss or changes in their sense of taste. This can be frustrating and impact the enjoyment of eating, leading to reduced appetite, low energy, and weight loss. Here are some key points to consider:
- MS Brain Show Full Answer