Has anyone experienced changes io their b... - Cure Parkinson's

Cure Parkinson's

25,344 members26,643 posts

Has anyone experienced changes io their body odour?

Mark1 profile image
7 Replies

I have never had a strong natural scent (honestly!). However, even with a much reduced sense of smell, I noticed a change to my body odour in the year or so post diagnosis. Then, when I started sinemet, my body odour returned to normal! One of the more trivial changes with PD, but i should be interested to know if anyone has had a similar experience.

Written by
Mark1 profile image
Mark1
To view profiles and participate in discussions please or .
Read more about...
7 Replies
Mark1 profile image
Mark1

......and I wonder if dogs can smell PD in the way that they have been used, to amazing effect, to identify cancers?

Helshubby profile image
Helshubby

Hello again , YES but i didn't realise until my wife pointed it out .

ronn profile image
ronn

Another possibility is that there is a change in the way your olfactory system PERCEIVES odors, including your own. While my sense of smell was failing, many things smelled different, (worse), than before.

lmbanni profile image
lmbanni

Yes. My husband has this problem too. He is on Sinemet but it still happens now and then. I have to tell him because he has no sense of smell anymore. Wow we wondered if this was due to PD. Thank you for your question Mark1! We learn so much together here!!

I want to say something else too about this. He also perspires only on the left underarm like if a faucet was dripping!! This is so strange! Thankfully it does not always happen.

PatV profile image
PatV

I don't know because my sense of smell is diminished. I hope some kind person will tell me. It's getting harder to get in shower. I do know people in my pwp classes who complain of increased sweat. I rarely sweat but have water retention :(

Kristakj78 profile image
Kristakj78

I know this post is from a few months ago, but I ran across it surfing the web for Parkinsons and body odor. I hope this is an answer for me too. I have had very oily skin and an odor for a few years now. I recently have been given a PD diagnosis at 34 years old. I swear we through out a couch that wasn't even a year old due to it. As embarrassing as it's been, I finally gave in and went to a dermatologist (before the PD diagnosis) .......again, no answers (after a skin biopsy and MULTIPLE "trial" scripts. I'm hoping it is due to the PD. I'm hoping this is finally an answer.

_Eureka profile image
_Eureka

The woman who can smell PD: bbc.com/news/uk-scotland-34...

You may also like...

Has anyone with PD changed medication, when the initial one was not working?

his doctor and his response was to up the dose. However, by upping the dose it amplified his leg...

Has anyone experienced a skin rash from Ashwagandha?

me. https://healthunlocked.com/cure-parkinsons/posts/147423176/what-serum-levels-indicate-someone-is

Possible adverse reaction to a new generic brand of carbidopa/levodopa. Has anyone else experienced this?

The manufacturer changes often, but the pharmacy tells me that the pills \\"should\\" all be the...

travel- has anyone done a 12 hour time change?

Has anyone tried glutathione?

Clinical Glutathione as a treatment. Anyone had any experience with this? Thanks everyone. Biff