Does Anyone Suffer With Numb/lop Sided Top Lip? | MyFibroTeam

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Does Anyone Suffer With Numb/lop Sided Top Lip?
A MyFibroTeam Member asked a question 💭

My sister is being checked for fibro also and asked do I suffer with a numb/lop sided lip. Until she mentioned it I never really thought it could be related as I do on occasions. She doesn't want to ask the Dr in case he thinks she mad. Her Dr has tried telling her on many occasions there is nothing wrong but as a sufferer myself I have urged her to keep going back.

posted September 17, 2018
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A MyFibroTeam Member

@A MyFibroTeam Member, I get burning tongue, mine seems to be related to eating fresh fruit, like pineapple, kiwi, and strawberries. The acid does it, as I think I am allergic to them however I love to eat fresh fruit. So I eat them and drink some decaf tea to dilute the burning tongue. Sometimes this works, sometimes I just suffer with it. I also get swollen sore on my lip or tongue from eating things I am allergic to. I am not sensitive to crappy food that isn't good for us but I prefer to eat healthy and take antihistamines to stop the allergic reactions! Weird that eating healthy food causes reactions in my mouth but eating junk food doesn't bother me, lol! Gentle hugs and hope your day turns out to be a good day today!

posted September 17, 2018
A MyFibroTeam Member

I have a burning mouth and sometimes my nose feels like I snorted cayenne pepper. MRI normal which looked at all the cranial nerves (that control the mouth/nose). I've been told the same thing over and over. Fibro. This disease brings on all sorts of HORRIFIC ailments. Some days I feel like I am going to make it through this and other days I just go to my car (if I am at work) and cry for an hour on my lunch break because of the sheer frustration. Until you've lived in the shoes of someone with fibro, you will never understand. It's not just muscle pain. It is all over weird shit (excuse my language). Numbness, sharp pains, shooting pains, aches, limbs that feel like they don't work at times, etc. I hate this disease and I literally get on my hands and knees at lest two times a week and pray to God to help me.

posted September 17, 2018
A MyFibroTeam Member

That's what I told her. We live in different countries and the medical profession is so different in the UK to Ireland Drs here do take time and are very sympathetic but hers has been a nightmare. I have told her to ask anyway.

posted September 17, 2018
A MyFibroTeam Member

Doctors have told me I was simply a hypochondriac. Well tests and years later!! I diagnosed myself with a few things and paid for the test myself. Looks like the doctor(s) were the asses and were wrong. I find that because I am thick, they tend to thing it all relates to obesity or the pain isn’t real. You should feel crazy telling your doctor your symptoms. The doctors job is to help you find solutions seeing as our research and knowledge isn’t to their extent.

posted September 17, 2018
A MyFibroTeam Member

Glad you found the broblem. Also sorry you found a problem. I hope that mskes sense.

posted September 17, 2018

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