Unusual symptom: Hi all, has anybody lost... - My MSAA Community

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Unusual symptom

Sandydemop profile image
38 Replies

Hi all, has anybody lost their sense of taste? It's been a very strange week without being able to taste my food. I know you are going to say ask your doc. I will. But meanwhile has anybody else ever experienced this? Thanks!

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Sandydemop profile image
Sandydemop
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38 Replies
rjoneslaw profile image
rjoneslaw

What was the last thing that you ate or ingested before you lost your ability to taste?

I have never had that happen to me. I figured that question would at least give you a starting point to figuring out how it started.

greaterexp profile image
greaterexp

Yes. I can’t say I can’t taste at all, but my sense of taste is diminished and altered. I’ve always loved my cup of coffee in the morning, but it doesn’t taste good at all now. This has happened over the past two months or so. I was diagnosed in late 2016, and didn’t expect this symptom.

Sandydemop profile image
Sandydemop in reply to greaterexp

Hi there, thanks for writing back. I'm sorry about your coffee. This smell taste thing is really... bizarre. The other day I was trying to taste cauliflower but all I could get was the texture.. We never expect new symptoms do we? I want to ask G-d, Are there more challenges coming or should I say when? The good news is it's not my worst day since having MS. I hope you will tell your doctor about the symptom. (Here I am trying to take care of you.) :) Warm wishes and happy new year,

Sandy

greaterexp profile image
greaterexp in reply to Sandydemop

Thanks, Sandy. We do take care of one another here. We are like family that way.

Sandydemop profile image
Sandydemop in reply to greaterexp

Thanks. BTW, would you like to share your name? :)

greaterexp profile image
greaterexp in reply to Sandydemop

Erin

Sandydemop profile image
Sandydemop in reply to greaterexp

:) thank you very much Erin.

Jazzihorsecat profile image
Jazzihorsecat

I truly have Sandydemop, & welcome to our awesome MSer warrior family!😃👍💖 When I was in a relapse this past early year, everything tasted like H20 big time, even very hot & spicy foods, my neuro. Said its just the M.S. & not to worry about it, after getting the awesome book by Ann Boroch, "Healing Muliple Sclerosis", it subsided, especially starting the Candida Overgrowth cleanse. So, no worries. 💐💓Blessings---Jazmine🌹Rose💜

Sandydemop profile image
Sandydemop in reply to Jazzihorsecat

Dear Jazinco, Thanks for writing. Did it go away?

Jazzihorsecat profile image
Jazzihorsecat in reply to Sandydemop

👍😃Yes Sandy it did finally, my taste came back, which I am glad about cuz Man am I the chef of better than any Restaraunt here, so my C.G./Hub says!😛😃😉💓💛💙💘💞💖💐Love Ya! & Many Blessings to ya!💐---Jazzy🌹💜

jkdavid99 profile image
jkdavid99

Yes, i ended up in hospital in may for 3 days steroid and MRI. I had 30 more active lesions and lost my taste. NOTHING tasted even close to food. Even my favorite things were terrible. I tried everything but i basically lived on otter pops and lost 25 pounds. 6 months later i can taste again but food definitely tasts different now. Dr said it wasn't MS. I disagree

Good luck to you

jimeka profile image
jimeka in reply to jkdavid99

How are you doing? Blessings Jimeka 🦋

jkdavid99 profile image
jkdavid99 in reply to jimeka

Got results from latest mri. No new lesions and the others are slowly shrinking. That is great news but then a miserable cold decided to jump in. Colds for us isnot good. Still not able to drive or work but maybe soon, i hope.

jimeka profile image
jimeka in reply to jkdavid99

Maybe soon in the New Year. Take care of that cold, blessings Jimeka 🦋

Sandydemop profile image
Sandydemop in reply to jimeka

Hi Jimeka, thanks for writing. Wishing you the best New Year!

Sandydemop profile image
Sandydemop in reply to jkdavid99

Hi @jkdavid99, thanks for writing to me. I'm glad you can taste food again. I'll talk to my doc next week about it and see what she says. Usually, when I have a complaint, she says it wasn't the MS. :)

jkdavid99 profile image
jkdavid99 in reply to Sandydemop

In my experience it means they dont know

erash profile image
erash

Newer research theorizes that the loss of sense of smell is an early sign of MS as it is in Parkinson’s. It makes sense that taste could also b affected

Mssailor profile image
Mssailor in reply to erash

I lost my sense of smell later. I didn’t notice exactly when. It is one of my most annoying symptom. Do you know where you heard about this.

erash profile image
erash in reply to Mssailor

I think it was in an MS new daily feed. I will see if I can find and will post

Sandydemop profile image
Sandydemop in reply to erash

Hi erash, thanks for doing the research.

Sandydemop profile image
Sandydemop in reply to Mssailor

Hi @Mssailor, thanks for writing and really everybody who validated this bizarre thing.

ynggal profile image
ynggal in reply to erash

I agree with the research. The loss of my sense of smell was one of my first symptoms.

Mssailor profile image
Mssailor

Yes, it was the symptom that eventually led to my diagnosis. I lost my sense of taste in half my tongue.

Sandydemop profile image
Sandydemop in reply to Mssailor

strange-- half your tongue? Anyway, thanks for taking the time to follow up with me. Take care and Happy New Year

erash profile image
erash

google.com/search?q=MS%20an...

Here’s the article

Sandydemop profile image
Sandydemop in reply to erash

Thanks! very interesting. Not too hopeful but definitely educational. I was also interested in the linked articles about trans cranial stimulation which seem hopeful.

Brindisi1 profile image
Brindisi1

Thanks erase for link.

ynggal profile image
ynggal

My sense of smell is almost non existent and my sense of taste isn’t far behind. I guess it depends on where your brain lesions are. I know that I miss both senses terribly.

Sandydemop profile image
Sandydemop in reply to ynggal

Thanks for writing back. It's one of those things we take for granted until we don't have it, right?

sashaming1 profile image
sashaming1

I have, but due to a Brain Injury due to a fall and hitting my head.

kris1973 profile image
kris1973

Yes. Lost most of it 6 mos ago along with other senses. MRI showed new lesion in the area that affects the senses. Hasn’t gone away-probably still have 1/2 taste etc.

Sandydemop profile image
Sandydemop in reply to kris1973

Dear Kris, ugh. How are you adapting to that?

kris1973 profile image
kris1973 in reply to Sandydemop

Its ok-takes time to adjust. Getting there but food is not real appealing. Eating more healthy snack type meals. I normally don’t eat sweets but they taste the best now.l.🤣

Sandydemop profile image
Sandydemop in reply to kris1973

Thanks Kris, I find myself focusing more on the texture of the food. And yes, strong flavor like granny smith green apples taste great. Garlic too :)

quegh profile image
quegh

Yes I experienced it but I was kind of "out of it" so I never really noticed it at the time. It affected my sense of taste and smell at the same time. I could still taste and smell and I thought it was normal, but it was not.

The first time I ate after the sense of taste came back I spit out my food, I thought it had gone rotten, the sense of taste was overwhelming. When my sense of smell came back suddenly I realized why people were choking because the smell of garbage that I hadn't taken out of the house.

WCwaiting profile image
WCwaiting

I hope this is not the case but this is a common symptom of COVID-19. Loss of sense of smell and taste.

HensTooth profile image
HensTooth

WCwaiting I was going to write the same thing! Then I realized this post is from 1 year ago... 😂

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