crazyH not "racist". That was over the top crazyH.
Some people are not accustomed to being surrounded by people who look different from themselves.
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Feeling paralysed with body pain on waking up
(69 Posts)Do any other GNs experience this...am used to having paralysis in hands and knee throbbings/stinging on a daily basis but this is something different which i haven't experienced before.
I awake and know immediately i cannot move as feel paralysed all down body and ache so much...I at least know am alive!!
Had right side THR in march and now my ?widespread OA seems to be affecting my whole body...is this normal?? Its soo scary...
Honestly, my whole body seems to be angry...am i Weird?
Takes so much longer to be able to get out of bed and function
the only white woman - how racist !
What was the colour of the Doctor you eventually saw ? Just asking……
MT61, Spitting on the floor may have been a sign the man was unfamiliar with our culture.
It is often regarded as more hygienic to spit on the floor than to swallow sputum or spit it into a hanky and them put hanky in pocket.
MT61, I know that these waiting rooms can be very uncomfortable. Please remember next time that foreign looking men can actually help you if you ask, and then you wont feel so isolated
Mt61 yes there’s always something to help us and potentially harm us re volterol suppositories…I’ve never been prescribed them and not sure I could do insertions now ..poor mobility🤔
Bea65
Afraid I live in a very built up town and not simple to change to different surgeries…the one I have is a joint practice and getting to either is close to my address..that’s probably why I am reluctant to change….
I have been put back on volterol suppositories which seem to help, but these can affect the heart & kidneys.
Afraid I live in a very built up town and not simple to change to different surgeries…the one I have is a joint practice and getting to either is close to my address..that’s probably why I am reluctant to change….
Bea65
[keepingquiet] there's a stampede on the phone lines @08:30 like most surgeries in my area... there is no same day service - where do you live...must move there!
[Liloldlady] ive thought this PMR.but need it confirmed..will update
[Mt61] its awful isn't it- mine is all over and cannot understand how intense the paralysis is...yes I do get my joints moving but I have to brain plan it....
[teabagwoman] hope you're feeling better .... the physio to my THR on right side has set me back with the long lasting groin pain which moves up into right abdominal wall...really need GP opinion but its an ongoing challenge to get appts...
I would honestly say change your gp....I live in a nw market town ....3 of our local gp practices ( mine included) only offer same day appointments ....routine, urgent, whatever .......as long as you phone in the first half hour you get an appointment....you don't have to hold, you are given the option to get a call back.
That's still over a week away.
Maybe you should change your GP, although I know this isn't always possible.
Ringing 111 is sometimes a way to get a quicker appointment.
Thank u all for responding .. have got face to face now on 22nd … not as soon as would have liked but at least it’s before the GPs are considering strike action on the 25th😳 heard this on news today
Maybe I’ll ring 111 but with heat am very lethargic
Might be worth calling 111 for advice OP. I'd also wonder if it's stations causing the stiffness, possibly try a different type. Hope you feel better soon x
Bea65
Do any other GNs experience this...am used to having paralysis in hands and knee throbbings/stinging on a daily basis but this is something different which i haven't experienced before.
I awake and know immediately i cannot move as feel paralysed all down body and ache so much...I at least know am alive!!
Had right side THR in march and now my ?widespread OA seems to be affecting my whole body...is this normal?? Its soo scary...
Honestly, my whole body seems to be angry...am i Weird?
Takes so much longer to be able to get out of bed and function
It is appalling follow up and by experience far to quick a reduction, some times you can only cut half a tablet down and then leave it months before you can cut another half. The slower you go the better you cope with the lower dosage. The hospital did it with me eventually rather than the GP, they were brilliant, saw them every months for a few years.
Rubyava
I was going to suggest the same.I have had PMR for the last 6 years....I think Im on top of it. Pain is usually bilateral in arms and pelvis especially in the mornings.
Worth mentioning to GP .Only way to diagnose is with a trial of steroid. I was suddenly pain free after 6 hours...after my first dose.
Then after a staring dose (25mgmfor me ) one has to wean off the steroids very slowly. Im down to 2.5 at the moment.
Good luck'
It is incorrect to say that is the way to diagnose it, it is the way to treat it, but diagnosis is done through a full blood test, where it shows a marker of the inflammation. Some show really well, others not so well, but no doctor will treat without the markers I am told. I had PMR for 8 years, so know about it well and had to be weaned off the Steroids by the hospital as the GP was doing it far too fast. I still suffer with the pain terribly and like BEA wake up in the morning terribly stiff and in severe pain but I would not describe my situation as feeling paralysed, I take my morning medication upon waking i.e. 2x 30/500 Sulphadeine and a slow release Morphine capsule, then roll on on to the floor on my yoga mat and warm my body up by doing various stretching exercised for 30 minutes. After that I can go in the bathroom. I am however in constant pain and just live on pain killers. I have been referred to the pain management clinic for the 3rd time, this time a more holistic one apparently. We will see I will try anything. In your case I would speak with 111, they will get a doctor's appointment for you without doubt. It is totally wrong to wait.
BlueBelle
So move away from the person offending you Mt61 or ask the person on the desk to speak to him and why the need to say it was full of non white people, horrid thing to say
And I don’t think much of your post either Colliemum it’s not wokery if there is such a word to not expect racist remarks
I told the security guy on my way out, who just shrugged his shoulders. As for moving, it was packed so no other seats to move to. I am not a racist.
If it had been a room full of white men I would have been off if any one of them had gobbed up phlegm. Obviously you aren’t that particular by sounds of it.
colliemum
Apologies, it wasn't the OP who posted about the demographic in A&E, I was actually supporting Mt61's comment.
Thank you Colliemum 🙏
So move away from the person offending you Mt61 or ask the person on the desk to speak to him and why the need to say it was full of non white people, horrid thing to say
And I don’t think much of your post either Colliemum it’s not wokery if there is such a word to not expect racist remarks
Mt61
I am the same, maybe not quite as bad as you. I feel like my bottom half doesn’t belong to the rest of my body!
I was put on a statins six months ago, so don’t know if that’s adding to the problem. It’s took me half hour of stretching, to get going. Now I am sat in a hot bath, soaking my joints.
Maybe you should see the doctor.
I have a scan book for next week to see what is going on with my legs.
I am also on statins and have stiff painful joints and back ache at night, as well as difficulty getting up stairs some days. I had an Xray, a bone scan and a check for arthritis markers, all clear except for some bone thinning. A hot bath helps during the day, but I find that the only thing that works to some extent at night is ibuprofen.
I do think statins have affected me, but I'd rather take my medication and be alive with aches and pains than be dead without them! I'd be interested to hear what they tell you after your scan.
My husband was diagnosed with Polymyalgia Rheumatica over 2 yrs ago and was put on 20mg of Steroids daily and then told to reduce them by 1mg every few weeks. The pains immediately reduced, but the trouble is every time he goes below 5mg all the pains come back. He has never had a follow up from our surgery. After contacting the surgery he was told to go back up to 10mg a day and he has now been given a follow up appointment at beginning of August. We are hoping he will then be given an appointment to see a Rheumatologist. Very poor service from our Drs surgery.
BlueBelle
So you left because A and E was full of non white people mostly men !!!!
Well bigger fool you
Yes probably but then I can’t do with people spitting.
Apologies, it wasn't the OP who posted about the demographic in A&E, I was actually supporting Mt61's comment.
I was more shocked at the guy gobbing up phlegm, then spitting out right near my foot, (I was wearing sandals) that was mostly to do with it why I left. Disgusting. I mean why spit on the floor when there was a toilet right across the waiting room? Probably worried he would loose his place, no doubt!
BlueBelle
So you left because A and E was full of non white people mostly men !!!!
Well bigger fool you
Is that what you take from the OP's posts? Good grief, is there no end to the bloody wokery.
I was going to suggest the same.I have had PMR for the last 6 years....I think Im on top of it. Pain is usually bilateral in arms and pelvis especially in the mornings.
Worth mentioning to GP .Only way to diagnose is with a trial of steroid. I was suddenly pain free after 6 hours...after my first dose.
Then after a staring dose (25mgmfor me ) one has to wean off the steroids very slowly. Im down to 2.5 at the moment.
Good luck'
Yes, me too.
Delila
Goodness me, ”the only white woman in the waiting room, and full of men”!!😱
I am shocked at that comment.
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