Please help my body feels like I have been sunburnt all over with that tingling feeling I get this all the time but usually just in 1area have never had it all over before is this normal as I don't know what nomal is anymore x☹
It's normal for me Debbie 1966.
Starts mainly in my back, then travels anywhere.
X
Thank u Ripley started in my back yday then all over this morning x
Sorry to hear Debbie, I find by taking nettle extract it helps most times. X
Will try that thanksx
Oh bless ya Debbie1966 ... I feel for you.. I get the burning to. and it drives me nuts. I've been battling my extended Flare up and I'm getting the burning as per usual grrrrrr!! And sharp pains right down into even my fingers if I touch anything with slight pressure for the itsy bitsy to long!!!! arrrrrrhG... Even my butt and my hip have driven me mad this week from just sitting on it !! hah...
Take care Debbie1966, take is easy.... try relaxing as best you can and try to distract yourself from it. Myself, I think I'm going to relent and take half a sleeping tablet to 'get some sleep'...
Nite x
Thanks deb it is driving me crazy my back hips and butt r sore fed up of putting heat bags in microwave n going to be wrinkled by the amount of baths I have taken have to wait till hubby is home to help me into bath n make sure I ok as I also have vertigo at moment x
Gentle hugs xxxx☹
Hi debbie1966 I get tingling burning alot its been mainly in my legs especially my right leg. It drives me mad its a fibro symptom. symptoms vary to how long they last it could be a day can be longer. Ive had the burning tingling for 2 weeks now? fibro throws weird wonderful symptoms at us. try not to stress worry as it only makes our condition worse and causes us more pain. Symptoms affect different parts of our body and some sometimes just 1 part can be affected. fibro is just so variable Im afraid take care gentle hugs
Thank you Kaz it certainly keeps us wondering what next just when you think you have endured all the symptoms it gives you new ones to deal with just glad I have this site to ask questions as someone always knows about what new symptoms u have which always helps.This also stops you stressing too much thank you x
Gentle hugs xxxxxxxx 😞
your very welcome debbie fibro loves throwing weird wonderful symptoms at us. it keeps us quessing to what we are going to get next dont you love fibro NOT. take care gentle hugsxxxxxx
onwards upwards battle on x
Unfortunately is part of fibro. I usually get tingling feeling in my hands, and upper back and feet. Take care and sending you gentle hugs…
X
Hi Debbie, awful isn't it. Another hideous symptom on top of the painful joints etc. My tingling/feeling of sunburn has been diagnosed as Central Neuropathic Pain and is apparently sparked off by something external to your body, like a virus, chemical, insect bite etc etc etc. The condition is where the pain receptors in your body have been turned up to high volume so they detect pain where there probably isn't any.
I find if I have a bad sleep it is worse, if I am stressed it is worse or if I eat certain foods or come in contact with chemicals, such as bleach it is worse. Certain foods, like MSG, vinegar, preservatives, tomatoes, wine, salmon, bananas etc. I find the blander the food the less pain I get, isn't life grand/not. Each person is different and may be affected by different intolerances.
When I wake in the morning if my hands are sore I know I am in for a bad day. All you can do is rest, eat bland food, chicken, white cold water fish, rice, spring onions, oatmeal, certain fruits and vegetables and try and get a good sleep.
I take a low dose of Lyrica and it helps a little, especially with sleep. I can only take a low dose as I am very chemically sensitive and any more I would be overwhelmed by side effects.
I feel for you as I would not wish this condition on any one. I am just so grateful I have this forum and you wonderful people to share these 'trials and tribulations' with. My comfort is that if one can be careful there are days when life can be enjoyable. Look after yourself and keep on creating your beautiful paintings, when you can. My motto which should be tattooed on my forehead PACE YOURSELF. Cheers Meg
Thanks for your reply meg I try to pace myself not always easy did have a bad sleep so that probably not helped just put on new meds so will c how they go have tried so many that have been unable to take as I have a very high intolerance to meds x gentle hugs xx
Yes Debbie; me too..........I find this "burning pain" gets worse in the Hot weather, and Yes it is very painful............it is actually the first reason I started going to doctors, as I Couldn't understand where/why this was occurring, and it took at least 10 years before it was labelled Fibromyalgia Pain............lol hey??? this I treat with Amitriptylline, as it is the Only med that seems to help this particular pain..............let me know if you find something else that helps, as our Summer is coming and I am Dreading It.............Bron