How much SC do you save up before playing?
Do you guys place like 1 SC upon getting it, or do you try to save up a couple dollars until you play it? I’m interested in hearing strategies for highest RTP when it comes to grinding daily bonuses.
Do you guys place like 1 SC upon getting it, or do you try to save up a couple dollars until you play it? I’m interested in hearing strategies for highest RTP when it comes to grinding daily bonuses.
Won 100 SC on this site weeks ago, they will not verify my kyc no matter how many support tickets i open. i assumed they would be difficult because they ask for things like utility bills, but i’ve never had to wait this long. i would avoid this site
I go through phases honestly but it’s hard not to use my free bonuses on slots. I feel like you have the best chance to hit maybe a couple bucks, and go from there. I also like a lot of the multiplier roulette games but I feel like i don’t get as lucky with them. As for parlays, I have found good luck with 6-7 leg MLB moneyline parlays, something like 1$ > 50$
What’s you guys go to?
won 500 sc off a 30$ deposit. Tried to redeem. Was hit with this
For example, on Fliff you earn those purple experience points for placing picks with the gold coins. Once you get 200, you can exchange it for 2 SC. Are there any other sites like this?
World record? xD
My mom is nearing 15 days with no food or water. It’s almost impossible she has held on this long. Her body is so skinny and her skin has looked really bad for a while. But her heart just keeps pumping she doesn’t want to give in. She’s 65 with alzheimer’s related atrophy (i believe it to be a mix of basal / cortical atrophy.)
I was her main caregiver for about 5 years, and am about to be 24 myself. This whole thing has been a journey and a learning experience with her, and not easy, but i got to keep my promise of never having to put her anywhere. She got to sleep every single night of her diagnosis at her own house in her own bed, and I genuinely see that as an accomplishment what with all the UTI issues, etc…
Once she stopped walking, things went down hill pretty fast. It wasn’t long after that she stopped swallowing.
I have been keeping her on a cocktail of haldol, xanax, morphine, and ativan. I have been dosing these often just to err on the side of comfort. But last night I found myself hoping they would help her let go… It’s so hard going to bed every night thinking she won’t be there the next morning, and she just somehow is. Has anyone had experience with this? I really am ready for her to let go. I want her at peace and she has given me a lot of time to accept that.
Hi all - My mom is on end of life hospice care in my house, and I (23M) have been her primary carer for years. She is nearing her final few days, i can tell by her coloration, and she has also been about 11 days without food / water (she cannot swallow) and just liquid medicine. Currently she is taking: Morphine Sulfate, Hyoscine liquid, Lorazepam liquid, and Haldol liquid. I have also been dissolving normal xanax tablets in some water and delivering in the cheek. I was wondering, since I am giving so much liquid medicine in her gums & cheeks, would it be okay to maybe just deliver her a dose of each medicine every 30 mins instead of all the meds every 3-4 hours? I hate giving her so much liquid because she struggles with it….
then again I’m probably overthinking, I think this just mostly a big nerves post, I’m very scared of losing my mom and I just want her comfortable and with me but i also want her to let go and just be at peace. I like that her eyes are very low and I can tell she is not hurting… no cries or anything while she has been in bed, just surrounded by loving family. I loved her so much she was so an outgoing and shining light in the world, she never made enemies, she taught me how to AND to love life and i’m surrounded by a lot of loving family. My journey as a caregiver was very hard and not without struggles but I genuinely feel like it has changed how I see & value people, relationships, friends, family…. I’m lucky to have a lot of these things in abundance. And even though my mom was sick we got to spend alot of time together; I feel like I haven’t left anything unsaid, nothing she needs to know… because she knows how much i love her. When she got sick i promised her she would never be abandoned, and I got to keep that promise and keep her at home these 4 years.
So many big new scary feelings. Sorry for the ramble. This sub has been a serious help for me past couple days. I’ve also told the social and hospice workers I would like to pursue the grief counseling options they offer.
I’m 23(m) and i’ve been the primary caregiver for my mom for 3-4 years now. She has posterior cortical atrophy which is a rare disease but one of the most evil things i’ve had to watch. She stopped being able to communicate completely about a year and a half ago. one of her arms is completely paralyzed. She lost the ability to walk about a month ago, and in the last 3 days she has lost the ability to swallow. We have in-home hospice, so she is in a hospital bed, and i am regularly administering morphine + xanax (Haldol is the next medication i am going to try if she is still uncomfortable after pain + anxiety meds. I just don’t know how to make sense of anything. It all feels so backwards, knowing my mom is going to die in the next few days when she isn’t even 65 yet. It feels so unfair and overwhelming i just have so much death anxiety. I can’t sleep any of these past nights just constant cold sweats, i can’t eat… it is killing me. I have a lot of family support, hospice visits daily but being her primary caregiver for so long and knowing it’s about to end just doesn’t feel real. I don’t know. I just cannot stop ruminating in my thoughts, i can’t focus on anything and i’m crying all the time. I’ve never experienced this level of grief or sorrow in my life and it feels so unfair to my mom and makes me mad at the world. it’s so cruel