NRAS Logo
Logged in as: pedro-pmc Search | Moderate | Active Topics | My Profile | Members | Logout

New Topic Post Reply
hi again Options
heather1
#1 Posted : Monday, February 28, 2011 11:42:32 AM Quote
Rank: Advanced Member

Groups: Registered

Joined: 2/26/2010
Posts: 271
Location: hampshire
Hi everyone, havent been on for a while as Ive had a rotten flare in my back again and although Im back at work and the flare has subsided, still feeling very sore. Started last year when I had the swine flu/pneumonia jab and it sent my ast levels too high. So, I had to come off mx for 2 weeks and gradually work back up to 25mg per week which is what I was on. In the meantime I had a nasty cold/sinus infection and my gp put me on a weeks worth of steroids. Consequently when I went to see my consultant in December I was feeling ok and asked if I could stay on 15mg per week of mx. She agreed as long as I was feeling ok. Well, then the flare happened in eearly January! I went to see my rheummy nurse who suggested increasing the mx and I asked if I could increase the leflunomide instead as I had found this was a great help when I first started taking it last August. I told her how sick the mx makes me feel and she said that if this increase in lflu didnt work then I would have to increase mx and would I be interested in self injection. I said yes so, am going to see the consultant tomorrow for a check up and I know that mx is going to have to be increased as the leflo doesnt seem to have made a difference.

Has anyone out there had any experience of self injection please?

Hope you are all ok.

lots of love
Heather xxx

bpeal1
#2 Posted : Monday, February 28, 2011 12:51:44 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 12/13/2010
Posts: 118
Location: Shrivenham, Oxfordshire
Hello

I have just started injecting mxt. I did it for the first time at the hospital last Monday so this evening will be the first go on my own. So far so good I didn't feel sick at all last week (the tablets had made me feel very sick). I was very nervous about doing it (before RA I was needle phobic - amazing how quickly you get over that when you have needles stick in you all the time!) but actually I found it very easy and not at all worried about doing it this evening.

When I was first considering it I put a post in the drugs section of the forum 'methotrexate by injection' have a look in there as lots of people were very kind and shared their experiences with me and you will be able to see my posts as I went through the process of starting mxt injections.

It seems to have worked well for me so I hope it does for you too.

Becky
dvear
#3 Posted : Monday, February 28, 2011 1:05:12 PM Quote
Rank: Member

Groups: Registered

Joined: 9/29/2010
Posts: 27
I started injecting methotrexate in December and haven't felt sick since! It's definitely worth trying, I was told it is still possible to feel sick on the injections but nothing like as likely. I had reduced my mtx as it made me sick but like you the reduced dose didn't hold the RA at bay. I'm now injecting 20mg a week and I feel better than I have done in ages.

Good luck - let us know what you decide to do.

Dawn.
smith-j
#4 Posted : Monday, February 28, 2011 2:25:50 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 12/3/2009
Posts: 714
Heather

The Methotrexate injections are very easy to do. The needles are very fine and you don't feel them at all. I have done several different types of medications by injection and would say the Methotrexate are the most easy. I did have to come off them and go back onto the pills as I found the injections too toxic. A lot of people, however, have found them to be very beneficial in getting away from the side effects of the pills.

Jackie
x

heather1
#5 Posted : Monday, February 28, 2011 7:07:44 PM Quote
Rank: Advanced Member

Groups: Registered

Joined: 2/26/2010
Posts: 271
Location: hampshire
Hi, thanks for the replies, I'll let you know how I get on tomorrow.

Heather xxxxx
ceri44
#6 Posted : Monday, February 28, 2011 8:10:48 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 9/5/2010
Posts: 364
Location: mid glamorgan
Hi Heather
I used to inject methotrexate and its not too bad but 2 weeks ago I changed back to the tablets as the injections were making me very sleepy, like jackie I think they were too toxic.. Anyway the side effects ive had the last few days from the tablets (terrible headaches and sickness) make me wish id stayed on the injections so im going to ring rheumie nurse tomorrow. Never know what to do for the best! Good luck tomorrow and let us know how you get on xx
heather1
#7 Posted : Tuesday, March 01, 2011 2:06:59 PM Quote
Rank: Advanced Member

Groups: Registered

Joined: 2/26/2010
Posts: 271
Location: hampshire
Hi all, saw my consultant this morning. she is referring me for the injections, so shoul dhear in a couple of weeks. she did say that they are quite strong so will probably have toreduce the dose initially. she has also advised me to keep up with the extra leflunomide as they do take about 6 weeks or so to kick in.

I told her I had joined a gym (just for the swimming and aqua aerobics!!) and she said that was great as any low impact excercise to strengthen muscles is good. Ive always swum from a very early age and have done aquas in the past but due to the onset of this horrible condition hadnt been for a while.

thanks for all your replies. Will keep you posted re the injections!

Love Heather xxx
Users browsing this topic
New Topic Post Reply
Forum Jump  
You can post new topics in this forum.
You can reply to topics in this forum.
You cannot delete your posts in this forum.
You can edit your posts in this forum.
You cannot create polls in this forum.
You cannot vote in polls in this forum.

SoClean Theme By Jaben Cargman (Tiny Gecko)
Powered by YAF 1.9.3 | YAF © 2003-2009, Yet Another Forum.NET
This page was generated in 0.135 seconds.