5mg woes
Welcome to the Mounjaro UK Support Group, a community dedicated to individuals across the United Kingdom who are using or interested in Mounjaro (tirzepatide) for diabetes management and weight loss. This forum is designed as a space for sharing experiences, advice, and support related to the use of Mounjaro. #weightloss #mounjaro
One month update
Welcome to the Mounjaro UK Support Group, a community dedicated to individuals across the United Kingdom who are using or interested in Mounjaro (tirzepatide) for diabetes management and weight loss. This forum is designed as a space for sharing experiences, advice, and support related to the use of Mounjaro. #weightloss #mounjaro
Painting over scratches?
A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.
Hip difficulties but nothing on scans?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Isn’t it tiring to be rare?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Pinky finger MCP instability? What do?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Why is sitting so uncomfortable?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Can beta blockers help with heat intolerance?
Postural orthostatic tachycardia syndrome (POTS) is a form of dysautonomia that is estimated to impact between 1,000,000 and 3,000,000 Americans, and millions more around the world. POTS is a form of orthostatic intolerance that is associated with the presence of excessive tachycardia and many other symptoms upon standing. Learn more at [Dysautonomia International](http://www.dysautonomiainternational.org/page.php?ID=30)
“Stressed” feeling after standing for too long?
Postural orthostatic tachycardia syndrome (POTS) is a form of dysautonomia that is estimated to impact between 1,000,000 and 3,000,000 Americans, and millions more around the world. POTS is a form of orthostatic intolerance that is associated with the presence of excessive tachycardia and many other symptoms upon standing. Learn more at [Dysautonomia International](http://www.dysautonomiainternational.org/page.php?ID=30)
Fun with depression
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
No, Aran jumpers were not used to identify drowned sailors.
This is a place to vent, complain, and bitch about crafts and the crafting communities. Get those frustrations off your chest, no matter how petty they may be. Name comes from Bitch Eating Crackers. "Everything this person does annoys you, even something as simple as eating crackers."
Why is this thing not the size it should be?
This is a place to vent, complain, and bitch about crafts and the crafting communities. Get those frustrations off your chest, no matter how petty they may be. Name comes from Bitch Eating Crackers. "Everything this person does annoys you, even something as simple as eating crackers."
What are you saving your fabric scraps for, the quilt you’re never going to make?
This is a place to vent, complain, and bitch about crafts and the crafting communities. Get those frustrations off your chest, no matter how petty they may be. Name comes from Bitch Eating Crackers. "Everything this person does annoys you, even something as simple as eating crackers."
When you ask for decaf coffee and get caffeine.
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
I’ve got Covid, in the middle of a heatwave, with dysautonomia.
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
Teeth/ jaw shifting?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Just put a deposit down on my first active chair!
A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.
You know you have dysautonomia when you own 5 water bottles and they’re all for different things.
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
Public transport dysautonomia induced panic attacks are not the one
Dysautonomia is an umbrella term for conditions in which the autonomic nervous system malfunctions.
Invacare Action opinions?
A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.
Shark week has ruined me
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Feel like I’ve hit all the milestones today.
A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.
First trip out in wheelchair, and I feel amazing!
A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.
Brain fog is terrifying
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
Malabsorption?
This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n
