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Vent away. It is now 2 weeks since I requested my SCR from my GP and I also have received nothing from them. If it weren’t for Dr Sunny and Medicann I would be venting too.

I do feel for you though; my GP here is paralysed due to being overloaded with over 20,000 patients for half a dozen doctors and the same again of “nurse practitioners”. There’s another surgery nearby that has a fantastic reputation which some of my neighbours are registered with but we are...

I did think that might be the case. Also as I was transferring I had a couple of prescriptions from my previous clinic that I imagine helped a lot.

Hi @mendit what they told me was to upload screenshots of the medications and consultations sections of the NHS app plus the main section with my name and NHS number which I did plus the transcripts of my consultations with my previous clinic and copies of my prescriptions. I also uploaded a...

The second month i was on MC I tired some different oil to the first month and my first reaction was that it didn’t work.Two weeks later I can tell you it definitely works, but I still prefer the first bottle I had.

I am still waiting for my GP to pull their finger out and send me my SCR but I emailed Medicann on Thursday and they told me what to do and by Saturday I had had my initial consultation and been accepted as a patient. I should add I was transferring from another clinic so it will be a bit...

Hi @Matt seems like we are the same age group and background. We’re all getting old and things don’t work like they used to. I have had sciatica so I know your pain. Legal MC is a godsend for me after 10 years of wandering in the wilderness of modern medical practice. All that’s left now is to...

My dermatologist back in 2018 would have prescribed CBMP if she could but her hands were tied. She just told me “if it works then go for it”. I didn’t go for it then because unless you grow it yourself you really don’t know what you’re getting.

Or even just hearing the original tune that they sampled :D

My condition is so rare when I was diagnosed my consultant showed me off to all his students (with my permission) and got to publish a paper on my diagnosis. He is long gone having moved to a different hospital but it would be nice if one of my consultants could publish a paper on how much CBMP...

Great times from what I can remember :D

Hi all, Ex-raver here who straightened himself out in the early noughties and then got diagnosed around 2015 with an extremely rare (1 in 100 million) hereditary auto-inflammatory condition. Since then I have seen the NHS crumble and have been round the houses many times while suffering...