The MS society launched this campaign on behalf of thousands of MS patients who are unable to get Sativex due to their location in the country. This campaign calls on people suffering from muscle spasms, regardless of where they find themselves in the UK. It also calls on every other person with friends and family members that are suffering from muscle spasms. The MS Society is begging for all to take action by contacting the local health service and also putting pressure on policymakers to enact a change in the health system.
Berner has a word for the guys who show up with a term sheet and…
So what are they doing instead of what we did? Standing in circles in public…
The state says flower, pre-rolls and vapes were already prohibited. Hemp retailers say years of…
Discover the strains that propelled Fast Buds to the winners circle at the 2026 Autoflower…
They smoke an absurd amount of weed, rap about everything from ketamine to pharmaceutical trials,…
A four-person Johns Hopkins pilot study found that 25 mg of oral THC could produce…