Experiences with

Klor-Con

For some reason, my title typed in backward. In case it's still backward when I post it, this concerns DMSO and RLS. I learned about DMSO this past year as a possible treatment for pain relief and healing for another person in my home. If you do some research, DMSO almost sounds too good to be true,

Still exploring sleep options for sleep deprived tired hubby. Am exploring CBN/CBD oil Head and Heal and also exploring as back up if these don't work Camino THC/ CBD gummies. Any other suggestions appreciated. Also unsure of drug interaction as he is on Orgovyx, Zytega, Cylais, Flomax, prednisone.

I have had good results from THC in gummies. However, you must try several kinds to find one that works as I have noticed a great deal of variation on the effects, even in the same batch. Sometimes I don't feel it at all and other times it seems that I need only a little bit. In general, I think that

Good morning. I am hoping some kind person will have a look at my recent blood results and help me interpret them before I see my GP. Serum TSH - 0.286 (abnormal) Normal range 0.35-4.94 Serum Free T4 - 14.0 pmol/l (normal range 9-19 pmol/l) Serum Free T3 - 4.0 pmol/l (Normal.range 2.4 - 6 pmol/l)

Before you all groan thinking this has been covered , as I well know slightly different. More just feedback from ones on Adalimumab which I started last week, do any of you take supplements while on this? In particular Biotin, Cod liver oil, and Glucosamine Chondroitin? I will enquire via RA advice

I've only just found this site and already learning. May I outline my journey so far and hope helpful as opposed to waffle. Early April 2024 I slipped on a slimy wet paving stone and fell very heavily on my left thigh. After a couple of weeks then top of opposite arm started to be painful and achy.

Hi Everyone, Had my appointment today at the doctors, I wasn’t even booked in to see a Dr in the end but actually a nurse. She told me she was checking my bloods for my yearly diabetic review which was news to me as I thought I was there to talk about my iron levels etc. She informed me that everything

Hello you lovely well informed people. Does anyone have any experience of Co-trimoxazole? I've been prescribed it to treat a mycobacterium called nocardia. I have Brochiectasis and this blighter has taken lodgings in my lungs. I'm due a conversation with my consultant soon as he wants / needs to discus

I live I. The UK and have suffered RLS for at least 40 years. I was recently sent sor by a GP at my surgery who I have never met before. She wanted to discuss my medication. I was previously on Pramipexole (not sure of dose) , but approximately 3 years ago my prescription was changed to 50gms of Pregabalin

I am trying to come off Ropinirole. I have gradually reduced my dosage from 2.5mg to a half mg. I’m not getting much sleep and am unable to sit from midday onwards without the rls being a problem. My GP is not very helpful and is unlikely to prescribe an opioid to help this final stage. She has prescribed

Six days I hurt my back. I took co codamol and ibrufen every 4 hours and then amitriptyline 20mg for two nights. From Wednesday night to Thursday night. I then stopped. I have been reading about ototoxicity in meds and the potential damage to the ear. Apparently al these meds are ototoxicite. I already

I’ve been bobbing around between 10 mg and 8 mg for the past six months. I manage to get the dosage down and then my hips/legs start playing up and feel very uncomfortable, so I'd up the dosage. On the advice of my rheumatologist I’m slowly reducing my dosage and am now down to 8.5 mg and I’ve now

Hi I’ve managed to get down to 3 pramipexole in the evenings(I was taking 6-7). I’m ok in the day as I’m working as a heating and plumbing engineer so constantly on the move, but as soon as I get home and relax, within 30mins my legs are going crazy!! I started taking gabapentin about 5 weeks ago but

I have moderate RLS treated by co codamol and PanadolI take a good multivit,magnesium and turmeric.A pro and prebiotic and avoid processed food. Yet my Ferratin levels remain very low not near 100 advised How can I increase them and any other advise please?

My GP referred me to rheumatology in December for an 'official' fibromyalgia diagnosis and POTS investigation. I was on Patient Access yesterday to check the date of the referral and chase it up, when I spotted a document I hadn't seen before and clicked on it to see what it was. It was a letter from

Following a heart attack & stent (Jan 2024) I was mostly fine for almost a year but since last December I am getting chest pains with nausea on a regular basis. I have been given a spray & told it is stable angina (I was sent to A&E twice when it started). I think it is unstable angina as it usually

Does anyone have summer and winter settings on combination dosage ? What level of change do you make ? I am only 2 years in but I seem to be hitting the same "slump" in November, More tired, less tolerant, several brain fog starts to the day . I am awaiting blood test results but looking to increase

I have had to pick out this very hard stone like pebbles for at least 8/9 months if not longer I had colonoscopy 19th Oct 2024 ( polyp history) none that time thanks it is March and still doing it now up to 2/4 times a day that leaves me shredded to bits up my bum I feel I have "NO CHOICE" but to carry

Last year was awful. Pneumonia 4 times and respiratory infections every 6 ish weeks. My daily antibiotic was stopped,Doxycycline, because of ? Arthralgia. So much joint pain some days I just cried. Had a routine call from the ILD nurses a fortnight ago. Come in for a repeat blood test they suggested

Last Saturday night (it’s Thursday now) I turned over in bed and felt excruciating pain in my lower back. I was very uncomfortable all Sunday and went to GP on Monday am. She asked all the relevant questions and like me thought I may have had my first fracture. She arranged for me to have an X-ray which