Any non-prescription meds for pain that anyone ca... - LUPUS UK

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Any non-prescription meds for pain that anyone can suggest?

0EmilyWanamaker0 profile image

With SLE, extreme pain is very common, and very irritating to not be able to focus on life with. I've tried Canabis oils and such but the pain relief only lasts about an hour. Ibuprofen does absolutely nothing for me...So does anyone have any pain med suggesting that don't require a prescription?

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0EmilyWanamaker0 profile image
0EmilyWanamaker0
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13 Replies
whisperit profile image
whisperit

What kind of pain, LupieGirl917? x

0EmilyWanamaker0 profile image
0EmilyWanamaker0 in reply towhisperit

Nerve pain is my main concern at the moment.

whisperit profile image
whisperit in reply to0EmilyWanamaker0

Thanks. That's a tough one. I have found that amitriptyline does help a bit, but of course that's a prescription med. Sometimes, gentle massage or distraction stimulation can help for some locations or types of pain or (for instance, a TENS machine ,which you can buy over the counter). If I get an intense but localised pain, or a headache, I do find ice/cold packs helpful.

I'm trying to get into meditation type techniques for chronic, generalised pain and discomfort but with limited success. Wish I had a good answer for you :( x

PasSukiClarke profile image
PasSukiClarke in reply to0EmilyWanamaker0

Hello there LupieGirl917. My name is Sukie and I wanted to say hello and add a comment about pain. Pain falls into different categories, once you have pinpointed the type of pain, i.e. Muscular or referred then you can tackle treating it. I have been in pain for 40 years, not all with Lupus but am an expert, because I have had to live with it and manage it. There is no magic cure or remedy. We have to juggle many different treatments and routines until we hit the right chord. If you specify the exact type of pain you are concerned with, when I check in later I will do my best to give you some good advice. Best Wishes. Sukie xx

You could try cutting out inflammatory foods to see if this does anything to tackle the root cause of the pain. Or upping your nutrient intake to see if any deficiencies might be contributory

0EmilyWanamaker0 profile image
0EmilyWanamaker0 in reply toovernighthearingloss

I've been cutting things out like numeric and sugary foods, but I also never consume dairy, due to me being lactose intolerant. It has helped some, but my pain is still present.

overnighthearingloss profile image
overnighthearingloss in reply to0EmilyWanamaker0

A lot of people react to wheat and wheat containing products. You could try reducing and see if it makes a difference. Wheat or flour is included in loads of foods, so if it is a factor you will have to start reading labels.

overnighthearingloss profile image
overnighthearingloss in reply to0EmilyWanamaker0

Mind you, I have just seen this so even pain meds may not be the answer and more reason to attempt to tackle the root cause whatever that is

shar.es/1LP4qj

overnighthearingloss profile image
overnighthearingloss in reply to0EmilyWanamaker0

You may also find something of use here

greenmedinfo.com/disease/pain

Cas70 profile image
Cas70

Hi - I have nerve pain and find that Olbas Oil rubbed in circular motion in the area really helps. There is a spray Biofreeze which does too. I found that all cannabis oils are different strengths so you might opt for a stronger one at night as I do. Good luck.

mo4eva profile image
mo4eva

You can also try not to eat artificial sweeteners! It does a number on your joints. I was drinking Mio at one point in my life trying to keep my weight down and wound up unable to walk from point A to point B without shuffling. As if I wasn't in enough pain.... couldn't figure it out.... my kidneys started revolting against me and everything..... come to find out artificial sweeteners are not your friendif you have connective tissue diseases.....between fibro and lupus I caused myself to have one of the worst flares ever

Paul_Howard profile image
Paul_HowardPartnerLUPUS UK

Hi 0EmilyWanamaker0 ,

As we are not medically qualified we cannot advise you about treatments or medications. We would suggest that you always discuss any complementary/alternative therapies with your consultant before starting them so that they can advise you of any potential adverse effects or interactions with other treatments.

We have an article on our website about pain management in lupus which has some information and tips you may find helpful - lupusuk.org.uk/pain-managem...

panda22 profile image
panda22

Not sure what you can take but do not take anything that has antii inflammatories in as these are really bad for your kidneys

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