Awesome. Made my day to hear this news. :flag2:

I’m sorry —- I didn’t see this post!!

I have switched my CBD to CannaKids version — and the CannaKids THC.....


Now — having said that — since my second diagnosis of cancer - this time in the Lymph Nodes and Lungs..... I did the 60 grams in 90 days thing — then just went with CBD only for maintenance (it has a small amount of THC) — so was doing 4/10ths of the syringe - it’s 800 mg of CBD — with 41 mg of THC (so 320mg of CBD and 16 mg or so of THC) — so was maintaining this intake - nighttime only.... for months now....

LATELY — Because of complaining to my NEW canna coach — I switched to “micro dosing” — taking small amount in the morning - noon - afternoon - and a bit more at bedtime - so taking in MORE THC — less CBD — and not having that “hung over til noon” feeling every day. I’ve added a PAX 3 vape thing and keeping the heat low - so vaping “flower” for getting some directly in to my lungs. Turns out — if you keep the heat down low - the flower doesn’t “smoke” - when it doesn’t burn the THC - you get the good stuff but without the “high”..... Learning all this as I go - but as of this May — I’ve managed to make it 3 years — not the 6 months they gave me in 2016!! Funny —- I also - at the advice of my coach - switched to Sativa flower (Maui Wowie) - and away from the heavy Indica..... and I have to tell you she has me feeling 400% better. Wake up feeling good — doing some stuff during the day — and NO napping — or rarely napping..... where I was sleeping during the day a lot... and just not feeling well. I’m very thankful for her help.

https://www.azmmjcoach.com/

Great to hear your feeling more energy and still taking care of business. Keep on fighting and love life like you've been doing. Happy Easter to you and the family.

Thanks Wayne!!

It’s been a long strange 3 years I can tell ya!!

Best news I've heard in a long time! Rock on!

I like it better when you are napping.

Fixed it for ya....


I like it better when you are lapping.....

Awesome news buddy! Hope to see you again soon, maybe Columbus.

So this update won’t be fun for anyone to read....

I had a PET Scan Friday — and the docs called and their words were “it’s spread everywhere”. Bones - glute (weird huh) - galbladder - soft tissue in my back (the stab wound I described on Facebook)... many more lymph nodes - lungs.... and a cyst on the brain. Yep - that’s pretty much “everywhere”.

I know in my heart that THC and CBD is what got me the extra 3 years I’ve had since the first “you’ve got 6 months to live”.... and I probably should have taken more and done it for longer with the second diagnosis... but I wanted to experiment and see if I could just hold it at bay with CBD and less THC so that quality of life would be “balanced” — less high — thus more “doing”. The things I like to do are not conducive to being stoned. So I went with an attitude of “if I can just stretch this out a bit” versus going for a complete cure.

I did the 60 grams in 90 days the second time around — and when my next CT scan showed the cancer spot had only grown 1cm — I was good with that “pace”. The difference was it didn’t knock it clear out like it had with my liver cancer. I knew this was going to be a tougher battle because of the location. The lymph nodes vs the liver. The liver is going to filter 100% of your blood so it’s going to get a full on hit of the THC/CBD - whereas the lymph nodes live in a different environment.... they use lymph fluid.... As I sit here today - I’d have made the same choice.

What I did wrong was to stop taking anything when the Mayo guys said I had cured the liver cancer (9 months after the initial diagnosis). I should have probably kept up with a maintenance dose. But chose to keep my ammo dry and stopped taking anything. My thinking at the time was - I don’t want my body to get used to this - I’d rather keep this in reserve for a full shock and awe should I need it again. Who the Fk knows. It’s just guessing. I’m still happy I stayed away from the whole chemo bit.

So I’ve traded in the “pot” for morphine..... now it’s just managing end of life. What a long strange trip it’s been!

Never met you Weld but your courage and take life by the horns attitude is very inspiring.
Best wishes