HOARSE VOICE: Hi, I seem to have an... - Vasculitis UK

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HOARSE VOICE

A_14 profile image
A_14
7 Replies

Hi, I seem to have an intermittent hoarse voice since I was diagnosed with WG. I don't have a sore throat apart from when I have to swallow constantly or try to clear what seems to be mucus out of my throat but there is nothing to cough up if I try to.

I am starting mycophenalate on Friday and currently on 10 mg of prednisolone.

Does anyone else with WG have these symptoms and if so, is there anything to minimise the problem?

Thanks

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bowler profile image
bowler

I am in the process of having/waiting for tests for WG, one of my symptoms is a hoarse voice.

hamble99b profile image
hamble99bVolunteer

one of my first W.G./G.P.A. symptoms was a hoarse voice.

have you had it investigated by an E.N.T. ?

A_14 profile image
A_14 in reply tohamble99b

I will mention it to my consultants next time I see them as it seems to be getting worse.#

Thanks

Katie18 profile image
Katie18

hi i have churg strauss and also struggle with similar symptoms. i use an inhaler for asthma and have already thought that aggravated it. im on 10mg prednisolone at the moment and as this reduces the ptoblem gets worse

Budapest profile image
Budapest

When I was first diagnosed with GPA, 5 years ago now, I had a very hoarse voice and dry, tickly throat so was referred for Speech & Language Therapy on the NHS. The SLT gave me exercises to strengthen my voice and also gave me advice on how to "save " my voice. I saw her infrequently for approx a year and again later, for 6 months, when I had a flare.

Referral for SLT was via the local ENT consultant.

I used to sip water frequently & had a prescribed saliva spray for a while. I also sucked Smintz ( a tiny sugar free "sweet" available in chemists & some supermarkets) when out and about & as necessary. They were recommended by my dentist. Chewing sugar free gum was also useful at times.

The symptoms gradually got better & I now have no difficulty at all with my voice.

If you are worried you should mention it to your doctor treating your condition. I have a hoarse voice too (and the same diagnosis) and most of my problems have been ENT related. I have been reassured that there is no live activity causing my hoarse voice but I do have scarring and some residual damage from when my WG was at it's worst. You will only get the reassurance you need from your doctor.

Cookyboy1 profile image
Cookyboy1

Yes I have the same as you, started on rituximab today then another 1000 mgs in 2 weeks and tnen reducing Prednisolone from 40 MG over a period of time to 5mg,,

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