Living With Meningocele And Its Challenges

Manukwi

Dec 06, 2011 7:08 pm

Dear Friends,

I was born with Meningocele and was operated on at the age of 1 year. The result was that I had no control of urine and bowel. Then in Jan. 1975, I underwent another operation for urinary diversion (Cap. Chloromycetin post-op.), which I think is called ileostomy.

Now I have a stoma outside, on the right side of my stomach, through which urine comes out and fills the urine bag that is fitted on my stoma. For bowel control, I maintain a food diet so that I am not in trouble, for others and myself. There are lots of ups and downs, but the fact is a fact and I have to accept it. I am unmarried and manage everything myself.

This is my small introduction.

Take care of your health.

Regards.

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mild_mannered_super_hero

Dec 07, 2011 3:08 pm

Hello and welcome to the forum. You might get more views if you post this under the "Lets Talk" section of this same forum. I will add the link...

https://www.meetanostomate.org/discussion-forum/viewforum.php?f=9

This portion of the forum doesn't get much traffic, and I'm sure there are others who would like to welcome you. Regards, mmsh.........
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Why Join MeetAnOstoMate?

First off, this is a pretty cool site with 37,000 members who truly understand you.

It's not all about ostomy. We talk about everything.

Many come here for advice or to give advice, others have found good friends, and some have even found love. Most importantly, people here are honest and genuinely care.

🛑 Privacy is very important - we have many features that are only visible to members, ensuring a safe and secure environment for you to share and connect.

Create an account and you will be amazed by the warmth of this community.

Manukwi

Dec 07, 2011 8:08 pm

Hi Dear,

Thanks for your mail. I will post in the Let's Talk section.

Take care,

Bye.

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