My wife has eds type3 but it's wreck... - The Ehlers-Danlos...

The Ehlers-Danlos Support UK

3,046 members950 posts

My wife has eds type3 but it's wrecked both our lives

Christaylor4076 profile image
2 Replies

This evil horrible disease has finally played it's part on our marriage, in the way of causing, stress, upset dont know which way to turn when things get hard when you see your loved one in pain everyday of there lives, and there is nothing you can do as a husband when all you want to do is take it away from her.

Think there should be some help put in place for the sufferer for depression,stress,

Everything that comes with this evil condition it has caused our 21 year marriage to end up in divorce the wifes desision as I want to look after her till the day I take my last breath I love her so so much any body in this same ordeal

Written by
Christaylor4076 profile image
Christaylor4076
To view profiles and participate in discussions please or .
2 Replies

This is just a heartbreaking post. It sounds like you both haven’t found a way to function & maybe your wife is pushing you away to protect you or through guilt feeling like a burden on you. I really think you guys need counselling - I hope you both can agree to go - I actually think separately seeing the same counsellor would work well if it was possible.

I helped my mum recently with finding counselling and there’s a new Gov service where you can refer yourself online and they give you info on services near you - it’s a pay what you can afford scheme so if you can’t afford to pay you don’t have to. Me and my husband had trouble when I was diagnosed with scleroderma (also have EDS but mine is so mild) - it’s such a complex emotional situation as there is grief and stress and anxiety and all sorts going on.

happytulip profile image
happytulip

I'm so sorry to read this. It sounds like you are both having a very difficult time. Its so sad especially as you want to care for her.

I have limited experience, but hurtful nonetheless. I got diagnosed with EDS 3, Lupus, POTs and recurrent pericarditis. My fiance walked out on me three months later his parting words to me were, "have you seen what you look like now." I was in so much pain. I've not heard from him since. To say it destroyed my confidence is an understatement.

Not what you're looking for?

You may also like...

Is my only friendgiving me a hint?

I only have one friend left since i got diagnosed. She is my cousin and has numerous issues as...
Country4eva profile image

Where to get help on diagnosing EDs.

Hi, Where can I go to get genetic testing done for Ehlers Danlos. I live in East Sussex in the UK....
honeybea22 profile image

👋👋👋👋 from littleeffie

Hello all Many of you will have been missing our littleeffie...the other day I messaged her to...
EOLHPC profile image

Gastroparesis treatment (drugs or natural?)

Been suffering with stomach problems for months, posted a little while ago when it all began,...
AliPixie profile image

Paedeatric consultant needed

Hello all, My 11 year old daughter has been diagnosed with JHS and GORD (although I am now...
nicky1000 profile image

Moderation team

edsuknikki profile image
edsuknikkiPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.