Forum Replies Created

  • WonkyFace

    Member
    October 14, 2025 at 1:35 am in reply to: Burning smell and general update..

    Hi everyone – new to the site today.

    I am undiagnosed but over several months when I google my symptoms MG keeps coming up.
    I joined the site as only in the last week, I started noticing a burning smell and again my searches led me here!
    Specifically to this conversation.

    The smell started when I was lying in bed, and I said to my husband my daughter must be burning candles in her room & she is not allowed. He couldn’t smell anything and then I smelt it again the next night and decided it must be nextdoor’s open fire somehow wafting into our house (we can sometimes smell their food – old Victorian terrace).

    Next I smelt it in the pub, again husband couldnt smell it but assumed there was a wood fire I couldn’t see. Then later in the cinema.

    I’ve been Googling like mad because I have read links between Alzheimers and smell issues, although they tend to link to reduced smell.

    It is not unpleasant, like an autumn wood fire. And tends to happen from late afternoon.

    Only thing that thats changed recently is I’ve started to take statins – I wonder if any of you who have had the wood burning smell are also on statins?

    I am just hoping it is not a sign of something more sinister going on in that part of the brain!

  • WonkyFace

    Member
    October 18, 2025 at 7:49 am in reply to: Burning smell and general update..

    Sorry to be ignorant of this condition. Are any of those medications for lowering your lipids / cholesterol? It the only medication I have added recently, but of course it could be a coincidence.

    I have stopped taking the statins, and I haven’t had the smoke smell since.

    I joined here because Myasthenia Gravis had come up a few times before when I searched some off/on symptoms. I discounted it as a diagnosis when the symptoms went and I didn’t have the symptoms very bad.

    Main two I have noticed is one side of the face:
    – droopy eyelid and mouth
    – visual, hmm, ‘differences’ they are hard to describe because when I get my eyes checked they are the same & haven’t got much worse than would be expected for normal aging

    I find when I pull my hair back into a pony tail (maybe correcting the weakness) it helps with the vision.

    I also have dry-eyes, and ulcerative colitis (ie some autoimmune history) + occasional flares of knee arthritis and fatigue that can not be diagnosed.

    Does this sound like MG do you think?

    But yes the smells element is very interesting.