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From May 1, Australians living with a rare form of epilepsy will have access to a medicinal cannabis medicine, which is being listed on Australia’s Pharmaceutical Benefits Scheme (PBS) for the first time.https://www.dailytelegraph.com.au/news/nsw/cannabis-oil-subsidised-on-pbs-for-dravet-syndrome-severe-epilepsy/news-story/ad660de241da9c7d5d45cbbc63fd97d1 …
This listing will take a treatment costing $24,000 per year, to as little as $6.60 with a concession card. The Government’s commitment to ensuring that Australians can access affordable medicines, when they need them, remains rock solid.https://www.health.gov.au/ministers/the-hon-greg-hunt-mp/media/historic-pbs-listing-for-australians-with-a-rare-epilepsy-condition …
We don’t need your poison vaccines, we rather eat healthy, exercise, naturally people die daily, people who don’t eat healthy, people who have bad habits, (smoking, junk food, over drinking, obese) diabetes
these are the ones who could die earlier from pneumonia, naturally.
Wow you must really be fucking up to actually have to do good things and make good decisions. Well done. This is great news.
If patients were allowed to exercise their #humanrights
as they do in countries like Canada and the USA, and grow their own medical cannabis, there would be hundreds of thousands of patients helped instead of just 116. 
#HomeGrowAmnesty
#auspol
What about the rest of us that rely on Medicinal Cannabis for other illnesses? Why are the pharmaceuticals that caused me to get sicker covered & only cost $15/mth, but the Cannabis Oil that has allowed me to come off those meds & live a pain free life not & costs $300/mth
Good move.
Trouble is kids with other rare forms of epilepsy such as Rett & Lennox Gastrau Syndromes & many other forms of life threatening drug resistant epilepsy are left to suffer There are approximately 3000+ plus kids under 14yo just in Qld alone with drug resistant epilepsy left out
Well done 
....... keep going
Finally.
Legalise and decriminalise Cannabis.
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