Urgent: Need Advice on Type 1 Diabetes Mistake
Please be respectful and helpful if responding to posts. This is a place where people can come and learn about Type 1 and the challenges we face. A place to rant, show emotion, and ask insulin questions or pump questions. Additionally, if you are going to comment on posts please give it your all, don't leave out info or be short with anyone that could be misinterpreted. Surveys will be deleted unless they are paid or get prior approval and most inquires regarding surveys go ignored in our inbox.Anyone have vision problems because of EDS (Keratoconus)?
Ehlers Danlos Syndrome (EDS) is a underdiagnosed connective tissue disorder characterized by a genetic fault in collagen. It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! We welcome all EDS subtypes, hypermobility spectrum disorder, Loeys Dietz, unnamed genetic disorders that present like EDS, self-diagnosed & suspected zebras. || || || Crowdsourced medical care saves lives. We welcome medical advice!I just feel so low doing the same thing over and over and not sticking to promises I make to myself.
Welcome! This is a supportive recovery community and safe space for anyone experiencing or who has been affected by stimulant drug dependency, abuse and addiction - Any and all stimulants regardless of type or source at any level of use. StopSpeeding is not Anti-Psych or Anti-ADHD, we are Pro-Recovery. We are not professionals or experts - Just regular people who have been there that want to share experiences / resources, be supportive, help others and recover together.Questions to people with kc
r/Keratoconus is a safe and supportive community for people living with keratoconus and the people who care for them! Here you can share your keratoconus photos and videos, ask questions, talk about latest breakthroughs, post memes, and show everyone how you see the world by sharing KC vision simulations.Finally feel like the minoxdil side effects have gone
A subreddit to share experiences of suspected and verified side effects and adverse reactions from the popular hairloss drug Minoxidil. If you have suffered Minoxidil side effects or an adverse reaction, please join the subreddit and post your story. You can also report them to the FDA (via this link: https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=consumer.reporting1). For resources, please visit our chat https://t.me/minoxidilsideeffectsRecovered from Minoxidil Side effects
A subreddit to share experiences of suspected and verified side effects and adverse reactions from the popular hairloss drug Minoxidil. If you have suffered Minoxidil side effects or an adverse reaction, please join the subreddit and post your story. You can also report them to the FDA (via this link: https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=consumer.reporting1). For resources, please visit our chat https://t.me/minoxidilsideeffectsNew here. Any help would be appreciated.
r/Keratoconus is a safe and supportive community for people living with keratoconus and the people who care for them! Here you can share your keratoconus photos and videos, ask questions, talk about latest breakthroughs, post memes, and show everyone how you see the world by sharing KC vision simulations.This is what Minoxdil Side Effects has made me do..

A subreddit to share experiences of suspected and verified side effects and adverse reactions from the popular hairloss drug Minoxidil. If you have suffered Minoxidil side effects or an adverse reaction, please join the subreddit and post your story. You can also report them to the FDA (via this link: https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=consumer.reporting1). For resources, please visit our chat https://t.me/minoxidilsideeffects