Posts - Ehlers-Danlos Support UK | HealthUnlocked

Ehlers-Danlos Support UK

2,967 members • 937 posts

All posts for February 2020

Alternative to Lidocaine Patch?

Hi all, Wondering if anyone knows the name of or has any experience with any pain patch alternatives to Lidocaine please? I’ve tried these but it has no...

Hi all, Wondering if anyone knows the name of or has any experience with any pa...

OutOfStripes

•4 years ago

2 Replies

Never been unemployed

I have been self employed for most of my life. Always driven by myself. Finding it hard to not work now and trying to get something I can do . Just found...

I have been self employed for most of my life. Always driven by myself. Finding ...

Bobbassett

•4 years ago

1 Reply

I’m a newbie and looking for a bit of advice x

Hiya guys I’m 19 and have been through the mil a bit with my health since starting puberty and only recently me and my family have been wondering if there’s a...

Hiya guys I’m 19 and have been through the mil a bit with my health since starti...

Serena15

•4 years ago

8 Replies

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Snap, pop, pain... what is this? Is this how it starts? Or is it something else entirely?

Hi I am currently living with chronic joint pain in my shoulders, lower back and sporadically with other joints. My symptoms started a few years ago with...

Hi I am currently living with chronic joint pain in my shoulders, lower back a...

Daddy2aj

•4 years ago

5 Replies

Cambridge University survey for MCAS

Hi all, A group of Cambridge University students is doing a survey on MCAS. They reached out to me and asked me to circulate it. If you have a minute, please...

Hi all, A group of Cambridge University students is doing a survey on MCAS. They...

sq1111

•4 years ago

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Mast cell activation

Hi everyone. I'm sharing the first part of my interview with Dr. Tina Peers on her approach to treating mast cell activation syndrome, a common comorbidity of...

Hi everyone. I'm sharing the first part of my interview with Dr. Tina Peers on h...

sq1111

•4 years ago

6 Replies

Anyone have problems with feeling they are not disabled enough? What do you do about it?

Hey everyone, I have a bit of a worry and need to get it off my chest. I have EDS and like many of you guys here it was missed for ages, I got called a...

Hey everyone, I have a bit of a worry and need to get it off my chest. I have E...

emilyhedgehog

•4 years ago

3 Replies

Knee problems

Hi guys! I’ve always had major issues with my knees dislocating and subluxing but now even if I’m sitting in a chair too long they continuously dislocate!😖...

Hi guys! I’ve always had major issues with my knees dislocating and subluxing bu...

Littlenestofvipers

•4 years ago

2 Replies

Collagen supplements

Has anyone ever tried them? They are meant to be good for joint pain, skin and muscle mass. I was wondering if they help at all with hypermobility issues.

Has anyone ever tried them? They are meant to be good for joint pain, skin and m...

Taurea

•4 years ago

5 Replies

Physician with an undiagnosed condition--please help.

The ultimate irony: a physician who cannot figure out what is wrong with themselves. For my entire life, I have been hypermobile/flexible. During puberty, I...

The ultimate irony: a physician who cannot figure out what is wrong with themsel...

lmk22

•4 years ago

5 Replies

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Posts - Ehlers-Danlos Support UK | HealthUnlocked

Ehlers-Danlos Support UK

All posts for February 2020

Alternative to Lidocaine Patch?

Never been unemployed

I’m a newbie and looking for a bit of advice x

Snap, pop, pain... what is this? Is this how it starts? Or is it something else entirely?

Cambridge University survey for MCAS

Mast cell activation

Anyone have problems with feeling they are not disabled enough? What do you do about it?

Knee problems

Collagen supplements

Physician with an undiagnosed condition--please help.

Search posts

Latest poll

What other conditions have you been diagnosed with in addition to EDS?

Topics

Archive