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THE CAST IS OFF ! Options
monty
#1 Posted : Wednesday, July 07, 2010 10:46:37 AM Quote
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Oh, you don't appreciate what bliss it is to scratch your leg until you haven't been able to do it for 4.5 months Blink

The cast (from toes to under knee) finally came off yesterday and I felt really wobbly at first. I have to learn a new way of walking now. The foot has been re-built (they have the technology) and it is very tender, but nothing like as painful as it was before the op. If I'm very careful and take my time, I should be pain free in that foot by the time the bones have sorted themselves out.

Ain't it grand the things they can do for us these days ThumpUp Years ago, we would be left at home, in pain, housebound and completely disabled.

I know some of you are going through a really rough time at the moment. But I have been there ... when the meds weren't working, or when I was waiting for them to work (and some of them take months before they have an effect). I even had to wait in pain for several months when the PCT were deciding whether I could have Retuximab. But now, the Rtx is working, my foot is mended and I can cope with the 'normal' pain I get from joints that have been damaged. So, my friends, don't despair - if your rheummy team are doing their job, you WILL get help and relief. But you have to communicate with them and build up a good relationship. I've been going to my rheummy team for 20 years now and (mostly) they care very much and always try to help when I tell them how much I am hurting.

Chin up and don't let 'Arthur' get you down.

Ann
"I cannot do everything. I accept that. Not being able to do everything is no excuse for doing nothing." ~ Helen Keller
Joanne C
#2 Posted : Wednesday, July 07, 2010 10:56:45 AM Quote
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Woohooo Ann!

That's wonderful news, so pleased you're finally free of the cast, rub loads of vitamin e cream in to help the skin recover from all that time in the cast.

Take things steady for a while, as I know from my foot surgery how easy it is to get caught out.

HUGS

Jo.
2012 Fundraising for the National Rheumatoid Arthritis Society (NRAS) http://uk.virginmoneygiving.com/RoboJo
Janet-G
#3 Posted : Wednesday, July 07, 2010 11:03:17 AM Quote
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Hi, i am newly diagnosed it was good to read your post as im feeling a bit down. Feel a bit better now, reading your posting means that i realise that i have to give the drugs time to work!
Janet
dorat
#4 Posted : Wednesday, July 07, 2010 11:09:58 AM Quote
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Hi Ann,

That's great news that the cast is removed at last! And it's lovely to hear things are going so well with you.
I too had a great relationship with my rheumy consultant who I had known for 9 years but unfortunately in January he left suddenly without notice so now I have to start again with someone new when they eventually appoint a new consultant, we have no rheumy team at all at the moment!

Hope your foot is painfree very soon.

Love, Doreen xx
Calmwater22
#5 Posted : Wednesday, July 07, 2010 1:31:25 PM Quote
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BigGrin Wonderful news Ann
not to much scratching mind! ThumpUp ThumpUp

lovely to hear,take care ohh yes wobbles u will be at first.
melly
cuddly cats make my world seem so much more fun
joeyvt
#6 Posted : Wednesday, July 07, 2010 2:12:52 PM Quote
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Hi Ann,

FABULOUS NEWS!!!

What you say is very true and very encouraging ... thank you!

Enjoy your new found freedom, scratching to your heart's content ThumpUp

Joanna
Julia17
#7 Posted : Wednesday, July 07, 2010 2:38:32 PM Quote
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Hi Anne

Good to hear from you, and that all is going so well ThumpUp now that the cast if off!

Wishing you all the best

Julia xx

lyn2
#8 Posted : Wednesday, July 07, 2010 3:28:26 PM Quote
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Hi Ann

I was only thinking of you last night, and wondering how things were! I was about to send you a text! Now I know that your leg is yours once again, I hope it gets stronger and stronger.

Don't do too much belly dancing just yet!

Love Lyn
annamaria
#9 Posted : Wednesday, July 07, 2010 3:51:57 PM Quote
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Hi Ann

I'm so pleased to hear this news from you, having been in the same position myself can really relate to it. Doesnt the leg look strange after all these months, very wasted and not a little in need of a wax!

You are so right about going gently on it especially at first. I definitely overdid it and then had a very painful swollen leg which they thought was a DVT, but turned out to be a fractured tibia 6 weeks later. They said it was because the osteoporosis I have took a knocking and I hadnt paced myself enough. So do be kind to youself, tempting though it is.

So glad you have a great rheumy team, it does make all the difference.

Pamper that leg and yourself, you deserve it!

Take care,
Love Liz
xx
Kathleen_C
#10 Posted : Wednesday, July 07, 2010 4:44:21 PM Quote
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That`s great nesw Ann - being able to scratch it yourself surely beats using a knitting needle!! I`m so glad you have such a good rheumy team too, and thanks for your positive words.

Take care, no running about after Trudy Scrumptious!

Kathleen x

Blue Star
#11 Posted : Wednesday, July 07, 2010 5:07:28 PM Quote
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Great news Ann ThumpUp , i too have a good relationship with my rheumy team, can i ask you how many goes have you had of Rituximab now ? i only ask because im on my second treatment now ( 2 x infusion for each treatment for people who dont know this) , and was told by my consultant i can only have 5 goes of it, have you been told this too ? and how long did you get between each infusion, i had 8 months but it only lasted 7 really,

Sophie x
Paula-C
#12 Posted : Wednesday, July 07, 2010 7:41:46 PM Quote
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So pleased to hear your Good News.

Be careful and don't go running around now that you can. Smile Smile

Nice and easy does it!!!

Take Care

Paula x x
Damned76
#13 Posted : Wednesday, July 07, 2010 8:36:11 PM Quote
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Great new Ann - take it steady!

Julie xx
lizziemouse
#14 Posted : Wednesday, July 07, 2010 10:00:36 PM Quote
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Lovely to hear your good news Ann ThumpUp ThumpUp
Lots of love from Liz (and Sophie) xxxxx
Maria_R
#15 Posted : Wednesday, July 07, 2010 10:36:32 PM Quote
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Brill news Ann- take it easy though!!

Maria x
monty
#16 Posted : Friday, July 09, 2010 12:52:47 AM Quote
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Thanks for all your encouragement. My leg is beginning to feel like my own now and there are less piles of dead skin about LOL Foot is still tender and does swell up by the end of the day but elevating the mattress at night does the trick. It is nice to walk about without sticks or crutches though ThumpUp

Kathleen - naughty naughty - you should never put a knitting needle down a cast - especially if you have such thin skin as me! I just put the fan on and put my foot in front of it in the hope that the cool air went up the cast BigGrin

Sophie - I have had 3 sessions of Rtx and no, I haven't been told of any restrictions on the amount I can have. My team just told me to ring up when I felt I needed another shot. The first was in January 08. This only lasted until August and I had my second in September 08. This one lasted well over a year and my third was in November 09. I am still feeling fine - just the odd flare up, but nothing major and not enough to ask for another dose yet. Several other people have found that the period between infusions increases the more you have. My crp is 'normal' - the only problem with my bloods is that I am anaemic, which often happens with people with RA - hence feeling so tired all the time. This is my third biologic - Enbrel and Infliximab didn't work for me and I am so relieved that there are now others we can have. Good luck with your treatment.

Thanks again everyone.

Warmest wishes, Ann
"I cannot do everything. I accept that. Not being able to do everything is no excuse for doing nothing." ~ Helen Keller
Blue Star
#17 Posted : Friday, July 09, 2010 12:37:48 PM Quote
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Thanks Ann, i too am anaemic, this is the first biologic ive tried as i can not have the others due to my lupus, just been the hospital this morning and they put me back on Sulfasazaline as i can not tolerate Methotrexate so hopefully this will help, dont know if its everyone or just some people who can only have 5 goes of the Rituximab , consultant told me and my mum it wipes something out of the immune system( can not remember what )and you have to have a rest from it.

Sophie x
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