Posts - Ehlers-Danlos Support UK | HealthUnlocked

Ehlers-Danlos Support UK

2,952 members935 posts

All posts for December 2018

Vascular EDS gene testing in UK

Hello, I have a diagnosis of hypermobile EDS made clinically with no genetic te...
bombsh3ll profile image

Reply to are we the first in the family

I'm the first and my daughter also has it. We have type 3. So we use lots of ace...
KittenMam profile image

Any advice please

Hi there I’ve been diagnosed with hyper mobility EDS for the past 10 years rough...
Trd29 profile image
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Talking to others with similar problems does nothing to improve services and access.

After several miserable years of harassment by Social Services to "go out in the...
budgiefriend profile image

Post Your Top 5 Relief Managing Hacks for EDS/HSD

I was thinking whilst at work today that it might be a good idea for all of us w...
MontgomeryJ profile image

Do family members have the same condition or are you the first in your family?

Hi does anyone with HEDS diagnosis have another family member with the same thin...
Danlos166 profile image

Blue badge & bus pass

My son has hEDS and POTS, since going to OT he was recommended to apply for blue...
Anne2018 profile image

Thumb pain after accident

On Tuesday I hurt my thumb. Partner threw a cushion at me play fighting and it c...
Gracey86 profile image

EDS and cold weather

Hello! I’m new and wanted to ask about your experiences with EDS and cold weathe...
carleton profile image

EDS Dentist Recommendations (London..Herts..)

Hello, I have been having gum problems which could be EDS related or something e...
MontgomeryJ profile image

Seeking a Diagnosis (Cont...)

Hello, I have recently become aware that I might have EDS after seeing several c...
MontgomeryJ profile image

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