Hi, I'm new on here.: I've had RA for about 25 years... - NRAS

NRAS

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Hi, I'm new on here.

Notabenenot profile image
26 Replies

I've had RA for about 25 years now, and it has been generally well controlled by drugs. At the moment though, I seem to have a "cold" which never goes away, and just now it's making me have catarrh, wheeze, cough, breathless, be very tired and really not able to do much. I do not seem to be able to shake it off - I've had it about 2 years now, so it's obviously not a real cold!

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Notabenenot profile image
Notabenenot
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26 Replies
keeta profile image
keeta

Hi love i think you should have a word with you Rhuemie doc .its been going on a long time and matbe your meds

Welcome to our family xx

Notabenenot profile image
Notabenenot in reply tokeeta

Thanks, Keeta,

Yes, I think I will after Christmas. Will get in touch with the Rheumatology nurse or my GP. Never know which is best!

keeta profile image
keeta in reply toNotabenenot

Most doctors don.t have a clue about RD and ill ask your nurse or Rhuemie doc for advice .so you might as well just ask them .but don.t leave it .hugs kathy xx

Notabenenot profile image
Notabenenot in reply tokeeta

Thanks, I'll take your advice!

keeta profile image
keeta in reply toNotabenenot

Xx

StormySeas profile image
StormySeas in reply tokeeta

I second that. RA nurses are the best route for advice as they're experts. General Practitioners often don't have the in-depth knowledge we need...

Notabenenot profile image
Notabenenot in reply toStormySeas

Thank you!

helixhelix profile image
helixhelix

Are you on a biologic? Ever since I started on them I've had a fake cold... costing a fortune in tissues!

Notabenenot profile image
Notabenenot in reply tohelixhelix

I don't know what a biologic is!

helixhelix profile image
helixhelix in reply toNotabenenot

Not methotrexate, hydroxychloroquine, leflunomide or sulphasalazine, but one of these newer drugs:

tocilizumab (Actemra)

certolizumab (Cimzia)

etanercept (Enbrel)

adalimumab (Humira)

anakinra (Kineret)

abatacept (Orencia)

infliximab (Remicade)

rituximab (Rituxan)

golimumab (Simponi)

Notabenenot profile image
Notabenenot in reply tohelixhelix

No, none of those

Stars27 profile image
Stars27 in reply toNotabenenot

I’m on a biologic and a lot of mornings wake with cold symptoms which are gone in an hour or two. It never seems to come to anything

Notabenenot profile image
Notabenenot in reply toStars27

Mine doesn't go - it varies from week to week - sometimes fairly negligible other times runny nose, sneezing, headache, aching joints and a wheezy throat - I sometimes think I'm hearing the cat but it's just me breathing!

helixhelix profile image
helixhelix in reply toNotabenenot

Maybe this....?

nhs.uk/conditions/non-aller...

Bubblyb profile image
Bubblyb in reply tohelixhelix

Thank you for this list, btw! 🌸

New50 profile image
New50 in reply tohelixhelix

After my visit to rheumatology. Finally someone listened and for the first time I am being given medication for my condition, which is prednisolone. I will be on this for 3 months till I see the consultant again. I have been given leaflets of drugs that are on offer are hydroxychloroquine methotrexate and sulfasalazine. You seem to understand the drugs on offer. I’m completely in the dark. Please could you give me some insight as to the difference. Thank you xxx

helixhelix profile image
helixhelix in reply toNew50

Have a look at these pages from NRAS. They're a good intro to the drugs.

nras.org.uk/dmards

Itis all a bit overwhelming to start with, so ask if you have more questions.

New50 profile image
New50 in reply tohelixhelix

Thank you. Xxx

New50 profile image
New50 in reply tohelixhelix

The site is dodgy it’s comes up as an unsafe site that if you click on it it steals info reads” unsecured site”

helixhelix profile image
helixhelix in reply toNew50

Bizarre! They are a very respectable national charity, and I use their site a lot.....

frechfield profile image
frechfield in reply tohelixhelix

Wow!! The list goes on.

Jillyanne profile image
Jillyanne

I would t bother with GP, go straight to your Rhuemy nurse .

Mine is far better than the specialist 👍👍

Good luck 😍

juliea793 profile image
juliea793

Hello..

After what I have just been through with similar symptoms I would get some professional to listen to your chest. I too had been on medication for RA for 30 years..

I ignored the symptoms and then had full blown heart problem..With that in mind whoever you can get an appointment with first to check your chest out..

I have learnt my lesson and now suffering with being off all medication and suffering with full blown flare up until I see Consultant early January for a review of medication.

Please do not ignore these symptoms and put your mind at rest...Good luck..

Notabenenot profile image
Notabenenot in reply tojuliea793

Thank you for that advice - it's been awhile since I had a chest xray. However, I dread being off the drugs, as the last time I had a methotrexate scare, and was off it for 7 weeks, I ended up in a wheelchair and unable to do anything with my arms and shoulders ( not able to eat properly, dress myself, do my hair among other things) and though going back on Metho has improved things, the damage has been permanent - still can't hold my arms up to do stuff, so I don't want that again!

juliea793 profile image
juliea793

I know where your coming from but no harm asking for a chest xray.

Notabenenot profile image
Notabenenot in reply tojuliea793

Yes, will definitely do that after Christmas - thank you

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