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RSD LIVE EVENT is happening in 18 days
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… my Rejection Sensitive Dysphoria (RSD)… Less than 24 hours to use your Skool Tribe ONLY early bird discount for the very first LIIIIIIVE course on Sat 18th July at 3:30pm You’ll learn more about RSD, tell tale signs, triggers, neurology, endocrinology, my own reflections from personal experience, and applying RAISE to help you manage it forever!! Watch the video, just because I’m an idiot and then the link will be in the comments… Quick her my amygdala wakes up…
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Live RSD Course: Understanding Rejection Sensitive Dysphoria & Practical Tools
What day of the week works best for you? (nb: Weekday training will be in the evening and weekend training will be during the day I’m hosting an exclusive live RSD (Rejection Sensitive Dysphoria) course designed specifically for ADHD brains. I'll explain what RSD actually is, why it affects ADHD individuals more intensely, and teach you two practical tools - one for immediate moments and one for long-term management. You'll receive workbooks to keep and have the opportunity to work through your own real situation in an interactive, small-group setting. The course is limited to just 20 people. The course runs for an hour the week of Sunday, July 12th, and you get to vote on which day and time works best for you.
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Live RSD Course: Understanding Rejection Sensitive Dysphoria & Practical Tools
Jaw clenching
Hey all, just wondering if anyone is suffering with jaw clenching(bruxism) when on meds? And have you found anything that helps with it please? I’ve got a gum shield(Amazon one) as I’ve not been able to get to the dentist yet,I’ve had Botox. Still trying to figure out what might make it worse, but in the meantime I’m back to blowing bubbles off my tongue, which stops me from clenching.
Hello from America
Hi all, I'm from the US (Virginia's Appalachian Mountains) and saw this community and @Richard Forbes-Ritte video sounded like something I need to look into, as I was diagnosed mid 40s a few years ago. Hoping to learn a bit and always happy to spend time with people who get it.
Intro and Info!
Hi to anyone UK based! 👋 I'm Steve, based in Nottingham, England, and I was officially diagnosed with combined ADHD in April this year. This might help someone out there in the UK, so going to quickly share the process I went through recently to get my diagnosis and medication. (Disclaimer: I ‘think’ this is 100% the right order and accurate, obviously for a stupid adhd brain and we all know what that means for memory. Also please note, this is just my own experience to provide context on what the process looked like for me, Happy to answer any questions but I’m not a clinician and the meds can affect people in different ways.) Firstly, Call your GP and request to start an ADHD evaluation via the ‘Right To Choose’ process 💡➡️ This is important because it means that your GP will take over your care once you finish your tritation (more on that in a second), so you’re not restricted to just one private company providing meds. You then will be provided a link which will provide you a list of local providers available to take on the initial assessment. Mine showed me a waiting time for the assessment, and a waiting time for the medication. I went with Harrow Health. Check reviews online, but don’t read too much into all of them just check for any repeating patterns. With HH some reviews were varied but nearly all said the clinicians were excellent. HH had a 0 week waiting time for both appointments and medication waiting time, so was a no brainer really. Once you choose your provider, they’ll give you a letter to download to fill In Your details and provide to your GP, then once the GP surgery (this was the longest delay in the whole thing for me) Upon receipt of this, you then are sent a link for your provided (Harrow Health in my case) and you’ll have a few things to fill in, and there’s also a couple of forms for people close to you to fill in. I can’t remember exactly but they’re looking for evidence from your childhood (parent to full for example) and present day evidence. If you can’t get a parent to fill in the childhood part don’t worry, I couldn’t (it gives an option to N/A it) and just explained to my clinician in my appointment, and she said we’d just have to cover childhood aspects on the call.Once the call got booked, it all moved pretty quickly. I was on the phone with the clinician for a couple of hours before she confirmed my combined diagnosis, and gave me a code to take to a local pharmacy to pick up my medication.The tritiation phase is the process of slowly increasing the dosage over a few weeks to see your reaction. I was started on 18mg Methylphenidate, and was booked on a second call for roughly two weeks time. At that call they then upped my meds after another 10-14 days (18mg-36mg-54mg) and after a third call when they were happy with my reaction to the meds, my details got passed to the gp to then take over my care.Things to note:
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