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Rank: Advanced Member  Groups: Registered
Joined: 9/27/2010 Posts: 136 Location: Stockton on Tees, Cleveland
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Hi its Louise again!!
I am due to start my enbrel on Monday morning. The enbrel has been delivered but I am really unsure as to whether or not to start it. I know it is a hard core drug and will strip my immune system. Is anyone taking enbrel or can anyone give me some advice?
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Rank: Advanced Member
Groups: Registered
Joined: 12/4/2009 Posts: 2,127 Location: Thornton Cleveleys
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Hi Louise I am not sure that I have introduced myself ... but I won't do it here and mess up the thread! I am on Enbrel and have been for about 7 years. Prior to that I was on Infliximab, another anti-tnf, which after 12 months started to lose it efficacy and I was moved onto Enbrel. For me it has been a fantastic drug! I have had RA for 22 years, and as a result have much joint damage and especially in my feet where surgery has been quite extensive. Enbrel gave me a new lease of life and has slowed down (although not stopped) the progress of the disease. My thoughts to you are that your practitioner must feel that this is the most appropriate drug for you. Anti-tnfs are not handed out lightly and you meet the criteria. You need this drug to continue to function, to have some quality of life which you perhaps won't otherwise have. Yes, this is a toxic drug, but you have a chronic long term disease with no cure. You will undoubtedly be more susceptible to infection (not ideal in your job), but if the RA remains uncontrolled you will suffer irreparable joint damage. You get one pair of feet, they can't be replaced! Your health is important, the job less so. Take the Enbrel ... you really do need it! All the best, Lyn x
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Rank: Advanced Member  Groups: Registered
Joined: 9/27/2010 Posts: 136 Location: Stockton on Tees, Cleveland
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Hi all
Took the plunge and did my first enbrel injection on Monday. Not as traumatic as I thought and so far I feel okay with no reaction at the injecton site. However still no real pain relief in my feet. How long does it take to have some effect?
Louise
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,157 Location: Huddersfield
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Hi Louise,
Well done with the injection! I don't know about Enbrel, but with Humira it took me 6 to 8 weeks and a flare before I felt any benefit. It is not a painkiller so you need to still take pain relief as you need it. Good luck with it, I hope it works well for you.
Love, Doreen xx
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Rank: Advanced Member  Groups: Registered
Joined: 9/27/2010 Posts: 136 Location: Stockton on Tees, Cleveland
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Thanks so much for your encouragement. I am still teaching and struggling to bear any pressure on my feet. Teaching sitting down is novel for the kids!!!Did you have any reaction to Humera? I was offered that but chose Enbrel.
Louise
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,157 Location: Huddersfield
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Hi Louise,
The only reaction I get is a red patch round the injection site for 48 hours, this only started occurring after I'd been on it about 8 months! I wasn't given a choice of drugs, my consultant just suggested Humira so I went with that. I can well understand you having to teach sitting down, no way could you be on your feet all day. Have you seen a podiatrist? I was given some insoles which have really helped my feet. Ask your GP or rheumy nurse to refer you.
Love, Doreen xx
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Rank: Advanced Member  Groups: Registered
Joined: 9/27/2010 Posts: 136 Location: Stockton on Tees, Cleveland
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Hi
Yeah I have seen the podiatrist and have insoles on my shoes but they make no difference what so ever apart from my shoes feeling really full. I use a stick to walk around just to help take the pressure off my feet. I am also struggling with tiredness and find that by the end of the school day I am shattered, but think it could be just the effects of the Amytriptiline that I take to combat pain.
Hopefully the Enbrel will kick in soon and I will get some relief.
Louise
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Rank: Advanced Member
Groups: Registered
Joined: 3/4/2010 Posts: 576
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Hi Louise - I'm with you on the 'full shoe' feeling that the insoles cause. My pod said he would refer me to get some 'hospital shoes' which I'm sure would cuase much amusement in classes but I have agreed. Don't know about you, but some classes I daren't sit down! I have a tall stool from Science which I perch on.
Hope you still feel ok and no side effects from the meds. Do you just take amitriptyline at night? I take 75mg about 2 hours before I need to be asleep and it usually works, but couldn't manage it in the day.
Let us know how you are getting on - good luck, Ailsa
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,157 Location: Huddersfield
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When I buy shoes now I get a wider fitting than I need and the insoles fit comfortably in them. Doreen xx
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Rank: Advanced Member  Groups: Registered
Joined: 9/27/2010 Posts: 136 Location: Stockton on Tees, Cleveland
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Hi Ailsa
i know what you mean about some classes and sitting down!!!!I find the kids just accept the walking stick and that I am slower moving about. I take 45mg of Amitriptyline at night, about an hour before I go to sleep. it means I sleep well which is good, especially at the moment because i cant bear the weight of the quilt on my left big toe.
On a morning I just take my anti inflamitory drug meloxicam and steroids which I am lowering each week now that I have started on Enbrel.
Where do you teach?
Louise
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Rank: Advanced Member  Groups: Registered
Joined: 12/7/2009 Posts: 89
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I bought a nice pair of extra wide shoes from a larger Clarks shop, slight heal, inner soles come out and a velcro strap,black and not ugly. My feet are very swollen, I've found these shoes very comfey. Also found if I don't let my quilt overhang on the bed it's not as heavy on my feet. Hope this helps, Kathleen xx
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