Humira?
CJHunter
Member Posts: 1,038
Hi All, hope things are ticking over ok for you all, if not big hugs n best wishes.
OK I have just returned from dermatology. I know its not arthur related but it is in a roundabout way bare with me.
For those who dont know i had a diagnosis of PsA for 12 ish years and treated for, then rheummy left and newbie changed diagnosis to :its in ya head. My gp sent me to a new consultant in london and i was diagnosed with Fibro and possibly PsA but he wasnt sure as I was on meds for the Psoriasis.
Anyhow the appointment today dermatology say I now qualify to go on bilogics meds and Humira has been the one suggested.
Well my questions to you lovely people are this: whats it like to inject?, what are the things to look out for and anything else u can think of.
Cheers :?
OK I have just returned from dermatology. I know its not arthur related but it is in a roundabout way bare with me.
For those who dont know i had a diagnosis of PsA for 12 ish years and treated for, then rheummy left and newbie changed diagnosis to :its in ya head. My gp sent me to a new consultant in london and i was diagnosed with Fibro and possibly PsA but he wasnt sure as I was on meds for the Psoriasis.
Anyhow the appointment today dermatology say I now qualify to go on bilogics meds and Humira has been the one suggested.
Well my questions to you lovely people are this: whats it like to inject?, what are the things to look out for and anything else u can think of.
Cheers :?
Clare xx

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Comments
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Hi Clare
lovely to see you
Now I know nothing!!
But I do know that it is good that you now qualify for biologics and that humira helps a fair few folks here. If they are still posting l am sure they will be along soon.
As for injecting.....well......I am certain they will train you and give you a chance to practise first.
Love and luck
Toni xxx0 -
I'm another who can't help, Clare, but I do hope it all goes well.If at first you don't succeed, then skydiving definitely isn't for you.
Steven Wright0 -
Me to Clare as it is OA I have hope all goes well for you............Marie xxSmile a while and while you smile
smile another smile and soon there
will be miles and miles of smiles
just because you smiled I wish your
day is full of Smiles0 -
I have been taking humira for 4 months and has worked wonders for me.i only had a little psoriasis but that has all gone now.my arthritics is so much better to .it never bothered me about injecting myself.i take injection out of fridge 1/2 hour before I inject it .by leaving it out it takes some of the sting out of the injection sometimes it does not sting at all and if it does only lasts about 10 secs.nurse will come and show you how to do your first injection .hope all go's well for you
Bye for now
Milly0 -
I've been on humira since October for RA,I too like Milly have had extremely good results swellings have gone down and joint pains have lessened a great deal.I take my injection out of the fridge 15 to 20 mins before hand,I have not had problems with injecting myself and only needed the one visit by a nurse.I hope if you go on humira you get good results too. Mig0
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Thank you all, I hope it works for skin and bones as well :roll:Clare xx0
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Hi!
Funnily enough I a just about to do my Humira jab - the pen is sitting next to me 'warming up' as I browse the forums...
I have definite RA possibly PsA too as I have mild psoriasis but my father has bad skin problems (thankfully no joint issues!) so the diagnosis is blurry.
Humira does seem to be doing something positive for me - I have my review next Tuesday to see how bloods are. The jab is pretty easy to do and so far I've had no side effects. I'm pretty squeamish but just get it done and out of the way so I can get on with my day.
It has had a noticeable effect on fatigue levels but I do find I *peak* and then tail off as next jab is due.
Good luck and hope it works for you!
Nx0
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