ENDOMETRIOSIS - Support Group

Hello ladies!

I’m planning to start a support group for ladies ttc with endometriosis. Do pm if you guys are keen to join. Together we can make a difference.
 


Hi, im having endometriosis and hurts so badly. Im on painkillers and doctor is not recommending surgery. Any experience or advice?
 
Yup done ultrasound in KKH, SGH and Gleneagles. Im on Cerebrex now.
I really want to go for op because its affecting my daily living bu dr don't recommend due to the risk.
 
Yup done ultrasound in KKH, SGH and Gleneagles. Im on Cerebrex now.
I really want to go for op because its affecting my daily living bu dr don't recommend due to the risk.


Hi, im having endometriosis and hurts so badly. Im on painkillers and doctor is not recommending surgery. Any experience or advice?

What are the risk ? Are you ttc at this moment?

I had a surgery after I found out i had a pretty bad endometriosis of ovary after consulting two gynae in concurrence few years ago. Was advised to do a surgery with no delay as this issue can affect fertility.

You might want to find out more from your doctor(s) what are the alternatives beside painkillers.
 
Hi, how are things now?

Apologies for the late reply. I was swamped by work for the past few months. Zomg.

Let me know how I can help. I was diagnosed with severe endo since 6 years ago. Maybe I can be of some help. :)
 
suddenly had infection and went a&e. Warded a week to fight the infection then went back a month later for more scans. That’s when they confirmed.
 
Hi ladies, just want to share my experience. I was diagnosed with stage 4 endometriosis on 25 Mar 2020. I am currently see Dr Steven Teo, and his explanations are very clear with regards to the disease. He also explained the difference between a generalist and a specialist treatment.

I just had the endometriosis disease removed in both my ovaries and I feel so much better now. The pain right after the surgery was different. It used to be a throbbing pain or shooting pain down the legs. Now I'm just spotting because of Visanne, and the ache is like menses which I feel is because my ovaries are healing.
 
Hi May i join too, thou I’m Diagnose for mild endometriosis but ttc for a year.
I don’t think the support group exits because I haven’t got any reply from intelligent_babe. But I hope you’re doing well. Anyway you’re not alone even though the journey is lonely and painful.
 
Hello. If anyone is in this whatsapp/telegram endometriosis support group, can add me in? I tried to pm the thread starter but received no reply. Thanks.
 

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