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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#1 | ||
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Hi, I was wondering if anyone else has this problem. When ever I eat something, I can't speak without slurring my words and sounding all mumbled. Also after I eat, I can't drink for at least 5 minutes after, I choke on my drink. Well this is when I can eat.
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#2 | ||
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Yes, I used to do that...and worse.
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#3 | ||
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Marble mouth.... quite familiar with it. It was one of my earliest symptoms. You've used a lot of muscles to go through the process of eating your food; they're tired.
Are you on any medication yet? or just going through the early stages of trying to find out what is going on? ... never mind these questions... I just saw your last post in the other thread. Try taking your mestinon ~30 minutes before eating; it will be at its peak efficiency around then. You should be able to eat a bit better then. Brian Last edited by Brennan068; 07-12-2012 at 06:30 PM. Reason: saw other post that answered questions I had... |
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#4 | |||
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Talking, eating and breathing all use the same muscles.
In myasthenia the problems is not so much muscle weakness, but muscle fatigue. You have to learn how to use muscles, let them rest and recover and then use them again. If I talk a bit more, I can't eat. If I eat a bit more, I can't breath. I can almost never eat and drink at the same time and many times I can't mix different textures of food. Also, certain tastes improve my swallowing and others do the opposite. It's a learning process of how to preserve your muscle strength, what makes your muscles stronger etc. By now I have learned to do it so well, that I don't even have to think about it. Also, missing a meal or two is less bad than choking on your food. Drinking in small sips gives you the same amount of fluids you would get drinking faster. |
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"Thanks for this!" says: | huntress (07-13-2012), pingpongman (07-13-2012) |
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Quote:
I have also learned to appreciate what I once took for granted. The advantage (and disadvantage) of MG is that you go from being unable to do things, to being able to do them and vice versa. It makes your life a roller-coaster, but it also repeatedly gives you abilities you were deprived of (it also repeatedly takes them away, but it depends on your point of view). Breathing difficulties no longer scare me (unless they are extreme), that has become part of my life. |
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#7 | ||
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Take note of the foods you are eating. For instance, I love hot peppers,but the MG symptoms worsen quicker when I have peppers in my food. Watch for the connection with foods and symptoms. Some have mentioned a quicker muscle fatique reaction to peanut butter. One friend of mine eats saurkraut everyday, his symptoms are much better with this food in his diet.
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#8 | ||
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Until recently, I couldn't make it through a burger without stopping half way through to let my jaw recover. It would just stop moving.
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#9 | ||
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![]() Quote:
So far it has been a miracle pill, I suppose you have tied that? FREDH |
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#10 | ||
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Junior Member
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I have the same problem; especially on very bad days. I realized that part of it was that I spent so much energy cutting my food that when it came time to chewing I was too tired and was just swallowing too big of bites. Having been on a puree diet and hating every moment of it I now avoid tough meats (i.e. chicken, steak and pork) and lean toward fish. If I am going to have them I ask my boyfriend to cut it up in small pieces for me- it's humiliating but I always think back to that puree. I also avoid stringy veggies such as cooked onions and melted cheeses.
Generally speaking if its a very very very bad night I eat mashed potatoes. I try to get my nutrients in the AM when I am stronger. |
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