Experiences with

Klor-Con

Hey all, I'm concerned with using THC/CBD with my HWP. I read an article that stated that people with PD should avoid both forms and now I'm a bit worried. Of course, I cannot find that darn article now, but I have been giving my husband a 10mg gummy at night (Wana Stay Asleep) for a couple of months

I wrote previously about my goal to try CBN for sleep. Nothing helped me much with sleep. I had tried pretty much everything recommended including supplements and prescription meds. I bought some gummies with 10 mg each of THC CBD and CBN. I believe that these helped so I was motivated to make my own

hi all im gf df ( to help with the following ) and Ibs and diverticula disease( if that’s the right wording) I take a multi vitamin and mineral. Vitamin d (prescribed.) and a probiotic of the things I buy. I’m very bone hurty . Muscle aches etc . So feel Want to add some extra vits. Would glucosamine

Hi Everyone, I`m in the ongoing battle with PMR inflammation ,and Predisolone side effects . Is there a consensus about useful supplements to take . I`m already on Multi vits/minerals , vit c , vit b complex , cod liver oil . Omeprazole . I`m worried about bone density and have been suggested alendronic

I wanted to see if I was eligible for a free Covid test, just out of curiosity, not because I have it. It's quite a mission to find out the criteria but I finally tracked it down on the NICE website. It doesn't make for good reading, you'll have to be seriously ill before you don't have to pay for

Hi everyone, I’m just curious to know if any of you take cod liver oil and if so has it affected your gut/ibs in any way. I have just decided to try them because of my age (the menopause is causing me joint pain) but I’m always cautious with everything I take incase of a stomach upset.Thank you 😊

Hello, I'm currently on warfarin, omeprazole, amlodipine and valsartan. Besides trying to exercise and watch my diet, I'm thinking of consuming some heart supplements to strengthen my heart. Has anyone try anything good and can share? How about products from NatureFarm? Or any other supplements?

Hi everyone, My previous blood test results: 28th May TSH: 8.4 mu/L FT4: 12.1 pmol/L 9th July TSH: 10.9mu/L FT4: 11.6 pmol/L Thyroid Peroxidase ABS: 224 ku/L 20th August TSH: 0.13 mu/L FT4: 22.8 pmol/L I'm currently on 100mcg Levothyroxine. I was started on this dose straight away on 18th July.

Has anyone with RLS started taking Lexapro for anxiety? If yes, did it have any affects on your RLS? My RLS is pretty well controlled at this time with minimal drugs (100 mg Gabapentin) after finally getting off Pramipexole. I also use Melatonin, Valarian Root, and CBN. But most helpful, I think,

Hello I have only posted briefly before but read most of the posts. I am really in complete despair with regard to my 75 year old husband and the worsening of his RLS symptoms which are now intolerable. The situation is that he has had worsening RLS for about 5 years. Initially he found relief

The title is a bit dramatic but, following up on my last post I put my big girl pants on ( with difficulty because my hands and wrists are quite sore and not working right) and had an appointment with the mental health nurse. She was lovely but said if I'm in pain we need to address that rather than

Hello, I am not sure if I have posted here before. I have RA (diagnosed on the back of Polymyalgia Rheumatica) in 2022. I am still taking steroids (9mg per day) even though my inflammation levels have reduced, it takes a long time to come off them. I have been on Methotrexate for 5+ years and changed

I have recently started taking Co Codamol. I have since been told that I have high blood pressure, which is new to me & I have noticed my cheeks feel as if they are on fire. Could the Co Codamol cause this? Has anyone else had similar.

I am feeling at a bit confused, new to this adventure and feeling lost. Have been taking Hydroxychloroquine since early May. Not sure if it has helped or not. I know it can take a while, not been pain free but for a while during summer felt a bit more mobile, more active. GP px'd co-codamol

Thankyou for your answers I have mobility issues with my back RA drugs don't work but co codamol helps maybe it relaxes muscles I take sulfasalazine for my RA but my back is driving me mad

Can you take these two meds together,co codamol works for me but they say you can't use it with sulfasalazine anybody on here used it thankyou

Hi, I have been taking co-codamol for about a year, as needed, for the pain I get with gallstones. But I have found that it reallly helps my fibromyalgia pain, especially with sleeping, which I find very difficult due to pain. So far I have mostly resisted taking it unless I have bad gallstone pain

I am about to begin taking Buprenorphine prescribed by my doctor. I have another condition for which I take Co-codamol 30/500 at night for the pain. My GP didn't say not to continue taking this but I have read that they shouldn't be taken together. Does anybody have information about this? Is there anybody

I posted a few weeks ago about a new kind of pain, which went from groin to the top of my thigh and also from top of buttock downwards, but not to the knee so I knew it wasn't sciatica. It did ease for a bit and I managed to shoot a two day music festival - the organisers were fantastic, and provided

Hi everyone, I am due to travel long haul over the Xmas period celebrating big birthday. I am due my rutuximab infusion in December which is maintenance infusion. My thoughts are would I be best to wait until I return in January. I now only take cotrimoxazole on a daily basis. Has anyone experienced