I agreed with the sentiment and suppossed ethos of a non profit org with real compassion for patients but i have yet to see it ,
CBD brothers, bud buddies/jeff ditchfield there might be alot more but not plugged in anymore but to me from what i see made a diff ,
The plan for i am billy clinic sounded nice for patients who feel they are getting ripped off by some serious capitalists that dont give a shit other than profits , charlotte even knew what she was doing with pricing and offering what these greedy bstards should be offering which is
COA fair pricing and
COA , imagine offering
COA as incentive to join clinic , thats sad what we accept with current clinics with no
COA n mould with only a few patients voicing concerns about it.
I have voiced concerns over kids not getting access to oils and i feel they are being left behind and i welcome any voice who supports that. For me i dont mind not getting access to cannabinoids on
NHS as long as kids can get them then i am happy , i would give up access to my meds for them , Thats me having epilepsy an a strong opinion on epilepsy and cannabis . I seen charlotte complain about the mould on flower etc but her clinic would be selling it so more than likely come to my clinic for better cheaper bud with
COA than stop access altogether
Look into own clinics see who owns what and rep they have in usa canada etc, some will be surprised and some not but some very very dodgy stuff that goes against OUR cannabis culture all for profits.
Sad if this is a capitalist venture as actions will speak louder than words.
In middle of it all is a young lad with a serious condition
Sad if releaf they have joined with but looks like it with same pricing