My Medical Cannabis Journey in the UK – Ehlers Danlos Syndrome Treatment
Thanks for watching and learning about the benefits of medical cannabis. I can’t wait to share more as I hopefully continue to improve. My Instagram is …
I’m still wait for Gino testing they think I’ve got quite a few different types of EDS o wat fun only missed by 40 yrs now. I’ve asked my local authority about cannabis and they say they do not prescribe so I am still fighting that one with the NHS and nice. There is enough information research about people with EDS using cannabis it does work
Amazing! I'm so pleased for you hun. If only more Drs would see your video to see how much it helps. My GP is refusing to prescribe paracetamol suspension because there's 'no clinical evidence it works'. I have argued the evidence is that on tablets I was in extreme pain for 4 months ending up in Addenbrooke's wanting to die. To being at home 3 weeks not in much pain at all. We have to buy the paracetamol from the chemists. Can I ask which of the specialities you're under agreed to prescribe the sativex. No names just Rheumatology etc….xxx
You did a great job with this video Lucy! I’m so happy for you that you’ve had such amazing results and really glad you’re spreading the message to help other people too 😊
I've only today discovered you – and you are one AMAZING person Lucy. I'll now view your other vids chronologically.
Much love.
I’m still wait for Gino testing they think I’ve got quite a few different types of EDS o wat fun only missed by 40 yrs now. I’ve asked my local authority about cannabis and they say they do not prescribe so I am still fighting that one with the NHS and nice. There is enough information research about people with EDS using cannabis it does work
As a fellow Zebra I cant wait for the day this is available for all of us,thank you for spreading the word 💚🦓
Brilliant video. Thank you for sharing your story.
This isn't Warhammer
Amazing! I'm so pleased for you hun. If only more Drs would see your video to see how much it helps. My GP is refusing to prescribe paracetamol suspension because there's 'no clinical evidence it works'. I have argued the evidence is that on tablets I was in extreme pain for 4 months ending up in Addenbrooke's wanting to die. To being at home 3 weeks not in much pain at all. We have to buy the paracetamol from the chemists. Can I ask which of the specialities you're under agreed to prescribe the sativex. No names just Rheumatology etc….xxx
Yaaaassssss gal!!!! 😍😘
You did a great job with this video Lucy! I’m so happy for you that you’ve had such amazing results and really glad you’re spreading the message to help other people too 😊