Woke up this morning in terrible pain in my hips and legs so bad
I have had the same thing for weeks. Yesterday particularly down the left side. My leg was giving way.
O' no, poor you HOTpicks..really feeling for you right now., very gentle hugs from across the seas..be blessed...:-) xx
I've had it for weeks too, wakes me up through the night, this morning I was up at 2:30, took painkillers then slept, occasionally, on the sofa. I saw the Rheumatoligst last week, I said I thought I needed a new hip, she touched the sore bit exactly, it's one of the fibro hotspots. I'm glad I don't need a new hip but I'm stuck with the pain. She's referred me to the pain clinic and for nerve conduction tests as my spine is bad too. Have you seen anyone about your back? Sometimes we put everything down to Fibro when it might be something else.
take care
enjoy the sunshine
Shelagh xxx
Its getting worse i dont know what to do im taking a lot of tablets for it at mo
Thank you for your wishes im really down at mo being in so much pain wish i could just stay in bed its that bad hugs to youx
I havent seen anyone about my back cos its a fight to see anyone sooo tired and in pain really fed up with it all thanks for your reply really appreciate it hope they can sort you out hugsx
you just have to grit your teeth and wait for it to pass
thats what i do ,its just a bloody misery
i dont take any meds from gp
simply because i am very sensistive to meds
so theres no option but for me just to get oin with it
i use magneisum oil when i ache and it keeps me awake
iv brought a new gel to try for around the joints havnt tried it yet
called flexiseq i havent tried it yet.
because i am finishing up another one at the moment .
iv got a feeling that as several people on here have said the same at the same time about increased pain . it may be linked to the weather
my pain changes with the weather . if its biting cold i get a aching bone pain ,with contracting clawing muscles and tendons , when its humid like it has been the last few weeks ,i get tenderness pain i seem to feel swollen but with no signs of swelling and fatigue is also worse when the weather is warm .
Hi HOTpicks
Poor you, we all feel for you and hope you stay positive so the pains can be reduced. Think of a happy moment and build on that. If the sun is out go and sit in the sun. Gentle hugs for you and hope your day has been improving.
Take care x
Oh you poor thing, could you have a bath to help with pain. Gently hugs.Hope tomorrow is a better day.Mace223
Im going to thanks soo tired i appreciate your comment cheers all the best x
Sadly no sun today just laying down on settee sooo tired glad its a day off thanks for your reply its cheered me up a little sending hugs backx
Sending best wishes to youx
Thank you sending warmest thanks to ux
Warmest hugsto you all the bestx
if heat helps you , but you find hot water bottles a pain
try a electric over blanket that will keep you warm all night and keep your muscles relaxed
you can get them from argos and other places on line .
Cheersx
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thought you might find this interesting
Morning Hotpicks; I too have Fibro (plus the horrible CFS and Osteo); so can really feel your leg/hip pain.....as you prob know, it goes from one spot to another, and at times there are many SPOTS !!! at the same time. Besides all the meds that we have to take (and Endep/amitriptylline, being the best for this pain, that I find) I also use a gel called Dencorub with Aspirin-like pain-relief.(different to other Dencorubs etc), rub it into painful area, and then put hotpack onto area (for hips I also use 2 cushions to sit on). Although we feel as if it's the Hips, I've realized it's more in the Rump Muscles/side of hips areas. As for the legs, I also use the same gel, and then wear Tubi-grip over calves......I do know how you are feeling, for I at present am also actually having to put up with the same areas.....many people say it's "supposed to be only in arms/upper body etc", but I know that it goes ALL over many areas....even the muscles in my feet, if I do too much walking or wear shoes that do not have proper Arch support.....I have also learn't that it's important to "take those meds", for I JUST can't survive without them....not all the ones that the Information tells us work for each of us, but it is a case of "trial and error"...for example, my rhuemy and I both thought Cymbalta (which is highly recommended by the findings) would help me, but No, made my emotions a lot worse, so just stick to some Vitamin B Executive Stress....let me know how you get on with the above suggestions.......Bron
Hi tiswas; yes this is something that I have tried telling docs too....that the weather plays a Very big part in my symptoms....when Hot as we had here in Australia in November....a Heat Wave....my muscles were Screaming in pain...and in winter, my fingers (and other body parts), also play up....I find it even extremely difficult to type (have found special Osteo gloves/mittens...with fingertips removed, that help my hands).....I'm pleased I have read your piece, as you are the first that I have read who also feels the weather has a big part to play....Bron