newbie

peterpie
peterpie Member Posts: 4
edited 29. Aug 2011, 17:39 in Say Hello Archive
Hi all,

I am a newbie to this site, but have had arthritis for 25+ years (reactive / inflammatory). During this time I have been given several different diagnosis / prognosis of my condition, resulting in lots of different types of medication and surgery......!!!!!!

I had and still have a lot of faith in the Anti TNF medication that I have been taking (Humira for 6 months / and now Enbrel), but I am getting a lot of 'naughty' side effects from them (fatigue / nausea / reflux), and the tablets the doctor gives me to counter them all seem to have the same 'side effects' i.e. need to sleep loads........

Am l alone in this? or is it common as l am still trying to keep down a job, but feel l may lose it soon........

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Comments

  • weejean
    weejean Member Posts: 346
    edited 30. Nov -0001, 00:00
    Hi Peterpie

    Welcome to the forum :grin:

    I cant give you any advice as I have OA but I am sure someone will be along shortly who can help you. I have had loads of great advice and support from the people here, they are a wonderful bunch. Hope to see you around. Take care xx
    Big Hugs
    Jean xx
  • peterpie
    peterpie Member Posts: 4
    edited 30. Nov -0001, 00:00
    Thanks Jean,

    means a lot....

    :grin:
  • dreamdaisy
    dreamdaisy Member Posts: 31,520
    edited 30. Nov -0001, 00:00
    Hi peterpie, it's nice to meet you. I have had the chance to try three anti TNFs and I am not that impressed by them: some on here have had wonderful results (which is good) and they are now being given much earlier than they used, which may have some bearing on matters or not: we are all very different in how we react to these things.

    I do not suffer badly with side-effects from the humira which I began in July 2009. That has done a wonderful job in bringing down my inflammatory markers and keeping them low but I have still had to have my knees drained etc. I think this has 'worked' for so long as it is supported by injected meth and I am also taking sulphasalazine. I was eventually diagnosed with PA (psoriatic athritis), a sero-negative version of this dross and I now have moderate to severe OA in my knees (probably thanks to the PA damage.) I am fifiteen years into the PA, as for the other I have no idea how long that has been lurking but I found out about it in April.

    I was told I would be able to ditch the crutches when I began the humira - the pain dullers too. I haven't been able to do either. I run my own small business which is now shrinking at the same rate as the arthritis is biting, so ending that is something I keep considering, but I like the fact that it gives me something to do and people to see, otherwise life would be very, very quiet. As I am sure you are aware an arthritic's life is one of compromises: I am all for carrying on with work etc for as long as I can but once it comes to the point of causing more harm than good I shall stop. Fighting the tiredness is part of the constant battle, it is as much a factor of arthritis as the pain etc.

    What other meds are you taking with the anti TNF? DD
    Have you got the despatches? No, I always walk like this. Eddie Braben
  • frogmorton
    frogmorton Member Posts: 30,267
    edited 30. Nov -0001, 00:00
    Hi Peter

    Good to meet you. I am glad you ahve found this forum bacuse it is so supportive and helpful - you can feel very alone with it all can't you?

    I have inflamatory arththritis as well as a bit of OA for goos measure.

    I agree withh you that the mediactions all seem to have their own side effects :roll: Honestly one of them even has joint pain listed!!!

    It iS good to meet you....hope you decide to stay.

    Love

    Toni xx
  • Ankyspond
    Ankyspond Member Posts: 626
    edited 30. Nov -0001, 00:00
    peterpie wrote:
    Hi all,

    I am a newbie to this site, but have had arthritis for 25+ years (reactive / inflammatory). During this time I have been given several different diagnosis / prognosis of my condition, resulting in lots of different types of medication and surgery......!!!!!!

    I had and still have a lot of faith in the Anti TNF medication that I have been taking (Humira for 6 months / and now Enbrel), but I am getting a lot of 'naughty' side effects from them (fatigue / nausea / reflux), and the tablets the doctor gives me to counter them all seem to have the same 'side effects' i.e. need to sleep loads........

    Am l alone in this? or is it common as l am still trying to keep down a job, but feel l may lose it soon........

    Hi,

    I am on Anti TNF Enbrel and been on it since last November, I feel tired but put it down to busy lifestyle and AS but mayble the meds. I have had no other side effects and the difference is amazing. xx
    AS Sufferer
    Live, love and enjoy life, live each day as though it's your last!

Hi, Welcome!

The community is a safe space for people living with and connected to arthritis to ask questions and share experiences. Get started by registering here and posting your first comment or question!

Hi, Welcome!

The community is a safe space for people living with and connected to arthritis to ask questions and share experiences. Get started by registering here and posting your first comment or question!