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Cannot straighten knee Options
jenni_b
#1 Posted : Saturday, January 22, 2011 9:34:43 PM Quote
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Hi all

I havent been on for a while, such a lot is going wrong I dont know really where to start but my major issue really is the inability to straighten my left leg and that knee.

I have got some damage in there.

had an mri and there is fluid and a lot of other stuff going on with the muscles and ligaments. The rheummy did have a stab at it last appt and tried to drain some fluid off without success.

there is A LOT of what looks like fluid on the scan. He didnt want to dig around.

I am in the middle of trying to persue the hosp for anything that resembles an appt to see my rheummy. not heard from them in mths and just fed up with the whole bleeping lot of them.

Wondering when I do (ho ho) see the rheummy if i should ask to be assessed by a surgeon. The gp wont refer me, says this is the rheummys job.

Because I cant straighten it, I cannot walk. the other leg, my toes, ankles, lower back and hips and everything else is not stable to cope with a leg that I cannot stand on.

Sorry to be negative!

Its not the most exciting thing about me I promise!

Jenni xx

how to be a velvet bulldoser
BarbieGirl
#2 Posted : Saturday, January 22, 2011 9:47:44 PM Quote
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Hi Jenni, sorry to hear about the knee, have been keeping up on facebook, (great photos of Michael and Bernie by the way) How can it take so long to get an appointment? I know they say contact the GP, but mostly they dont like to do anything without the consultant's ok, so you're back to square one. Your mobility is a serious issue, and needs to be taken as such. Can only say I truly feel for you and will be thinking of you and sending lots of hugs and prayers your way x
BARBARA
dorat
#3 Posted : Saturday, January 22, 2011 9:54:55 PM Quote
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Hi Jenni,

So sorry to hear that your knee is so bad. You really need to be seen again soon by the rheumy.
Strange the GP won't refer you to a surgeon though. I've just been told my right knee is now bone on bone but the rheumys say they don't refer people to other consultants now, my GP will have to do it! Why do these things differ so much in different hospitals?
Hope you can get an appointment soon.

Love and hugs, Doreen xx
Ailsa-H
#4 Posted : Saturday, January 22, 2011 9:56:50 PM Quote
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Sorry to hear you are struggling Jenni - sounds really miserable and frustrating. Just wanted to say thinking of you and hope you get an appointment and some relief very soon XX Ailsa
suzanne_p
#5 Posted : Sunday, January 23, 2011 10:07:22 AM Quote
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Location: Buckinghamshire
hi Jenni,

so sorry to hear you're struggling with your knee.

i think the NHS is going through some big changes and they aren't benefiting the Patients !!

i'm like Doreen ... both my knee's are bone on bone but couldn't cope with having anything done at the mo.

hope you manage to get an appointment soon.

take care

Suzanne x
AnnieB
#6 Posted : Sunday, January 23, 2011 1:48:17 PM Quote
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Hi Jenni,

Its never ending with this disease and it would be lovely if people would make life easier for us instead of having to chase things up and wait.

So many of us don't like complaining but I think now and again we have to be a bit pushy, I would certainly ask your GP again.

Sorry you are in so much pain.

Anne x
LynW
#7 Posted : Sunday, January 23, 2011 3:32:07 PM Quote
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Location: Thornton Cleveleys
Hi Jenni

Sorry to hear about your knee problem. I had the same last year and was referred to Orthopaedics (by GP) who did the necessary tests, x-rays, MRI and then operated to repair torn cartilages and debride. He hoped by doing this he might be able to save the joint for a while longer. Also have similar problems with right knee, but this one locks up if I get it in the 'wrong' position. The left knee never really got much better and both knees have been aspirated and injected twice within seven weeks. Both have exremely thickened synovium which means the steroid is unlikely to reach the point where it does any good!

I've now been referred back to Orthopaedics (this time by Rheumatology) for the right knee and the Rheumatologist is looking into Synovectomy by injection. If this isn't available it looks like it will be a double knee replacement.

Jenni, I fully appreciate your problems and feel you need to perhaps push for an urgent appointment with Rheumatology and don't give up until you've got one (even using PALS). Unfortunately, I know how difficult this is having had my appointment pushed back to 15 months last year and already received three letters pushing me back for my next appointment in April, it's now June! I am told that this is due to the number of newly referred patients who have to be diagnosed and put on medication quickly. Consequently those of us with long term disease are shoved to the back of the queue Sad . I appreciate the limitations and lack of rheumatologists but it makes me very disgruntled when people such as us, with significant joint damage, are left without adequate support.

Please don't take no for an answer, hang in there. Hope you are able to sort something out soon.

Lyn x

My son, Ian, completed the BUPA Great North Run on 15th September running for the National Rheumatoid Arthritis Society (NRAS). You can read his story at http://www.justgiving.com/ianlukewilson

Damned76
#8 Posted : Sunday, January 23, 2011 8:04:54 PM Quote
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Thinking of you Jenni - I can't beleive they haven't got you an appointment after all you have been through. Can you still get the red boots on?

Juliexx
Audrey33
#9 Posted : Sunday, January 23, 2011 9:00:42 PM Quote
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Hi Jenni

sorry to hear you are so poorly and hope the pain easers soon for you, you are possibly suffering the new system they are bringing in it is call partial appoinments and this means that when you see you consulton they do not make you an appoinment from one visit to the next you have to ring up and make your own appoinments this is so there lists are low and they can say numbers are down.
I am under this as well but it is terabble as you have to keep remembering when you have to ring.

good luck with yours

Audrey.
Rose-B
#10 Posted : Sunday, January 23, 2011 10:33:49 PM Quote
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Hello Jenni

just wanted to let you know that thinking about you. Your have been so much. I certainly would
keep chasing them.

Good luck


Rose
Lorna-A
#11 Posted : Sunday, January 23, 2011 10:57:59 PM Quote
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Hi Jenni,

Do whatever it takes to get that appointment you so badly need. You have been through enough and you are as entitled as much as the next one to get a much needed appointment. I really feel for you at the moment, you are always always so cheerful and you are young with a young family, it is important to keep motivated.

I do really hope the appointment comes through soon for you.

Take care in the meantime Lorna x Smile
Paula-C
#12 Posted : Monday, January 24, 2011 4:04:06 PM Quote
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Hello Jenni

This really is unacceptable that you are being so let down by your hospital. You have severe RA and have been bady let down by them. You really should be on their priority list. You've got so may add on illness all due to this horrid illness and they just seem to be ignoring you.

It's such a pity you can't have the same care that I am receiving from my hospital, they really are so good.

Keep pushing for an appointment and don't give in. Do you think that the NRAS helpline can help by advising you of what to do?

If all else fails I would go and sit in the clinic and refuse to move until you get to see a consultant.

Hope something gets sorted soon.

Sending you a big hug.

Paula xx
jenni_b
#13 Posted : Wednesday, January 26, 2011 8:04:42 PM Quote
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thanks all

well, things have come to a bit of a head today.

I think I have a bit of a viral bug hanging about, my son has been unwell and off school and I think I have picked it up. Anyway- major flair and cannot move.

Neuro issues all very pronounced.

The joints are hot red and huge.

The gp has been and he is horrified at the state of things. He is ordering me a 3 wheeled walker to stop me furniture walking and took a load of bloods. He is going to keep ring rheumatology until he speaks to my consultant.

rather pleased he didnt just pack me off into the general!

Jenni xx
how to be a velvet bulldoser
SueB
#14 Posted : Wednesday, January 26, 2011 9:11:57 PM Quote
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Hi Jenni, I'm so sorry things are going so wrong at the moment. Lets hope your GP is really forceful. It is so wrong that you have to battle for treatment.
Hugs
SueThumpUp
AnnieB
#15 Posted : Thursday, January 27, 2011 10:18:47 AM Quote
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Hi Jenni,

At last someone is listening to you.

Really hope you now get some treatment.

Anne x
jeanb
#16 Posted : Thursday, January 27, 2011 5:58:51 PM Quote
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Any news from the GP yet Jen?
LynW
#17 Posted : Thursday, January 27, 2011 9:16:36 PM Quote
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Location: Thornton Cleveleys
Hi Jenni

Sorry to hear of your er ... decline! You could have done without this added nuisance. Hope your GP has been able to sort something. Keep us posted ThumpUp

Thinking of you,

Lyn x
My son, Ian, completed the BUPA Great North Run on 15th September running for the National Rheumatoid Arthritis Society (NRAS). You can read his story at http://www.justgiving.com/ianlukewilson

Rose-B
#18 Posted : Thursday, January 27, 2011 10:32:37 PM Quote
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Hello Jenni

Heres hoping you are feeling better today
jenni_b
#19 Posted : Friday, January 28, 2011 1:28:17 PM Quote
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right the sh*t has hit the fan.

CRP is 67

spoke to hospital
they asked me to write letters.

I am giving them both barrels.

Jenni
how to be a velvet bulldoser
LynW
#20 Posted : Friday, January 28, 2011 4:23:30 PM Quote
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Location: Thornton Cleveleys
Not good enough, I am fuming on your behalf! Mad How dare they treat sick people like this? Write letters? Is that some sort of inappropriate weird joke?

Please please don't take this sitting down (I'm sure you won't!); it is simply disgusting. I hope things improve on their own (as much as I doubt they will) and you find some relief from somewhere. If you need help to fire the "barrels" ... I'm sure lots of us will oblige. RollEyes

Take care Jenni,

Lyn x
My son, Ian, completed the BUPA Great North Run on 15th September running for the National Rheumatoid Arthritis Society (NRAS). You can read his story at http://www.justgiving.com/ianlukewilson

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