Chronically lost voice - any advice? - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,086 members651 posts

Chronically lost voice - any advice?

PugBex profile image
3 Replies

Hi, I'm fairly new here. I just wanted to know if anyone has advice for getting a chronically lost voice down to (probable) ME back? I've recovered pretty well and I'm no longer severe, but I still have no voice :/ It's really frustrating. I can whisper without pain, but anything above that hurts and feels like there's a pressure pushing down on my throat. I'm really unsure what to do because the Internet says that even for a voice lost due to a sore throat you shouldn't whisper because it can damage your vocal cords. But I was wondering that maybe if I start using it all the time to whisper that the pain will eventually stop? I just don't know. Any advice? Has anyone experienced this before?

Thank you so much for reading, and any replies or advice is appreciated :)

Written by
PugBex profile image
PugBex
To view profiles and participate in discussions please or .
3 Replies

Can't say I've experienced that myself, have you spoken with a Dr?

PugBex profile image
PugBex in reply to

Yes I have, but they've never been much help :/ They didn't do anything apart from a quick look at my throat with a tourch, but they couldn't find anything :/ I orginally lost it because of energy, but now I've got more energy and I'm getting better, my voice just isn't :/

in reply toPugBex

If you are in the UK or Ireland maybe you could contact Dr William Weir and see if he can come up with a solution. He is a leading light in the ME field and has helped me considerably.

Not what you're looking for?

You may also like...

Advice please

Hi, I was diagnosed in 2002 after having my daughter and than left to it. I was ill a lot but it...
Giz79 profile image

Dietary advice please

I'm new to this community, having joined the Fibro site earlier in the year. I have managed to...

Advice

Hi All I have a meeting with my manager and executive director tomorrow to discuss reducing my...
Natalie6289 profile image

Advice on pacing

I’m just waiting on formal diagnosis from the ME doctor but had phone call last week from the ME...
Lexilou70 profile image

How to shake off nasty comments from person at support group?

Hi everyone, I was able to go to a CFS support group meeting this Monday for the first time. The...

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.