Losing the will to live : I felt so pro... - Endometriosis UK

Endometriosis UK

73,857 members53,661 posts

Losing the will to live

xximilixx profile image
6 Replies

I felt so pro-active and as though things were progressing with a lot of doctors appointments but now I have to wait 12 weeks until I get to first see a gynaecologist.

Last night was bad, I ended up in a place I haven't been in since my teenage years, and I just can't imagine myself living another 3 months in this much pain just to talk to someone about where to go next.

I was just sat there googling the suicide rates of women with endometriosis and really wasn't surprised to find that at least 25% of people had considered It :(

I don't really know where I'm going with this but just thought i should write about it somewhere.

Written by
xximilixx profile image
xximilixx
To view profiles and participate in discussions please or .
6 Replies

What pain relief/meds are you using?

xximilixx profile image
xximilixx in reply to

mefenemic acid. It works for about an hour, but i can only take it twice a day at meal times, so the rest of the day im really hurting

in reply toxximilixx

The best thing to do is to go back to your GP and ask for more pain relief. You can take other things with the mefenamic acid, like paracetamol and co-codamol if you have it. I had been taking mefenamic acid since the age of 15, but once my disease progressed and my pain got worse I was taking it together with paracetamol, diclofenac and codeine in combination. I also had tramadol, and went to A&E for oramorph/IV morphine when those weren't enough. Diclofenac comes in tablets and suppositories and if you're not squeamish about using them, they are fantastic and quick acting.

Hope you can get to see your GP and get on a better combination of meds soon. x.

xximilixx profile image
xximilixx in reply to

Thanks for this! I wasn't sure whether I could take anything else with the mefenamic acid.

I've thought about going to A&E so often, theres been times where I've been awake for like 2 days crying from the pain and I just have to keep having hot baths to try and distract myself from how much it hurts.

I think im going to have to go back this week because I've got an ear / lymph node infection going on too so I may ask about different pain medications when i do x

in reply toxximilixx

If the pain is making you distressed, please go to A&E and get help. I know the first time you go is really hard, it feels stupid, but it's the right thing to do. It's what they are there for. x.

ThaliaThalia profile image
ThaliaThalia

Hang in there. I felt the same way. I'm proof that you can get your life back and live pain-free. Go to A&E if the pain's unmanageable and ask your G.P. to write to the consultant with a view to expediting the appointment. The pain is significantly reducing your quality of life. Your G.P needs to give you appropriate pain medication. Please also try quitting dairy, soy, alcohol, sugar and meat which all exacerbate the pain. Eat organic vegetables, especially greens. Take a good quality multivitamin with minerals, and supplement with fish oil to help reduce inflammation (I use Nordic Naturals). Hot water bottles and heat pads are useful, too. You WILL be okay. The pain is overwhelming and unbearable in the run up to surgery and the long waiting lists make us feel there's no end in sight. But there is. You WILL get the appointment you need and you can be pain-free again. Good luck and lots of love, x

Not what you're looking for?

You may also like...

Losing the will to live...

Hi everyone, sorry for this but don't know how much longer I can carry on feeling like this. I had...
jayneeb3 profile image

Confusion, depression and losing the will to live

Hey ladies. So, back on 4th June, I had my diagnostic laparoscopy to potentially diagnose...
Lofty1589 profile image

Losing the will to fight.

Hi guys, I'm new to all this, just joined today and wanted to ask people how long they waited...
Lunar97 profile image

Learning to live with endo

Heya. My names Charlie. I was diagnosed with Endo last Aug 2016 by lap and had some bits burnt...
Charlie877 profile image

Losing My Mind

Hi, I was diagnosed about 6 months ago and due to my age they wont do anything about it (i'm 37). I...
Sweety2015 profile image

Moderation team

See all
Msunited profile image
MsunitedModerator
LivWilliams27 profile image
LivWilliams27Moderator

Top community tags

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.