California options?
Anyone in California know where to get good cannabis beverages? I see that home delivery is no longer permitted. And it seems like the cannabis shops don’t have good selections. Not sure what our options are at this point
Anyone in California know where to get good cannabis beverages? I see that home delivery is no longer permitted. And it seems like the cannabis shops don’t have good selections. Not sure what our options are at this point
I’m tapering up, started at 30mg twice daily (10 days in this far) and I’m supposed to go up to 60mg twice a day after 2 weeks. I think it’s making me feel a bit off, though it’s so hard to say with constant hormonal instability (perimenopause) and other things.
Sometimes I think it’s giving me more energy but then I seem to be getting really fatigued in the afternoon/early evening and that feels a bit different than the fatigue and PEM I’ve had more recently…. I don’t know….I feel like things are always changing between flares and crashes and periods of feeling better then more crashes or flare ups and I don’t know what is what.
Did anyone feel like this and then did better once going up to the higher dose?
lots of film crew trucks and vehicles not too far up from Monterey
Has anyone found pleasant ways to be alone when not at home? I have always enjoyed my alone time and now that I am in peri and my family is really stressing my nervous system beyond what I feel like I can handle, I am looking for ways to be alone (away from other people) when out of the house. Alone time at home is tough when anyone else is here and even when they‘re not home, it’s so hard to relax with the never ending to do list (and my velcro dog who I love so much but even she can feel smothering). The concept of peace and quiet has never meant more to me in my life than right now.
edit: thank you for lots of great ideas here! I probably should have clarified that solitude is the goal, even if kind of unrealistic, so maybe it’s about as few other human beings as possible 🤣
I’m about 3.5 years into ME/CFS and Long COVID. Got the Visible band/strap earlier this year and was constantly irritated with wearing it—couldn’t find a comfortable location anywhere on my wrist or arm. Tried a few different straps to no avail. And I never was able to make great use of the data in the app, like it didn’t have much of an impact. I got fed up with the strap bugging me a couple weeks ago and took it off. Haven‘t worn it since and there has been no discernible difference in my ability to pace or in my quality of life so I’m thinking this product is not really beneficial for me. Unfortunately, I paid the full year subscription up front so, that’s a loss.
If anyone has any recs to make it more comfortable, or useful, I’m open. I already have an Oura ring. Bought it 2 years ago before I was diagnosed and didn’t know what was wrong with me. Maybe because I was already getting some data through it and making habit changes, the visible experience was just meh?