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Neurology (Expert Forum)
Increased sensitivity to odors
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Increased sensitivity to odors
by motheroftwo, Oct 29, 2004 12:00AM
Since begin dxed with als 3 yrs ago I have noticed an increased sense of smell which stops me from breathing for a few seconds.
I found out about Hyperosmia on the net, but cant find anything about what causes it and a treatment.
Do you have any idea what the cause is and a treatment?
"Hyperosmia is an abnormally increased sensitivity to odors or an abnormally increased sense of smell. Hyperosmia is also known as olfactory hyperesthesia and hyperesthesia olfactoria. Hyperosmia comes from the Greek word "hyper" meaning "above," and the Greek word "osme" meaning "sense of smell." Put the words together and you get "above sense of smell."
Thanks in advance for any replies.
I found out about Hyperosmia on the net, but cant find anything about what causes it and a treatment.
Do you have any idea what the cause is and a treatment?
"Hyperosmia is an abnormally increased sensitivity to odors or an abnormally increased sense of smell. Hyperosmia is also known as olfactory hyperesthesia and hyperesthesia olfactoria. Hyperosmia comes from the Greek word "hyper" meaning "above," and the Greek word "osme" meaning "sense of smell." Put the words together and you get "above sense of smell."
Thanks in advance for any replies.
Doctor's Answer
by CCF-Neuro-M.D.-CS, Nov 02, 2004 12:00AM
I am not aware of any relationship between ALS and increased sensitivity to odors. Intermittent changes in smell can occur with migraines or seizures. Loss of smell can occur with trauma or destructive mass lesions. You have not mentioned your medication, but that would be something to consider (possible side effect). Sorry I could not be more help. Good luck.
Also to add to this problem, when I touch certain materials such as fur, clothing, etc... it also takes my breath away just like the increased sense of smell does. Even when I wash my face and dry it, my face goes dry and again I cant breath until i put cream on.
I know it may sound stupid but it feels like my skin cant breath.
I know als is not meant to affect sensory signs but my als seems to do just that.