It's a beautiful summer's day today. We are going to have another hot day. So I need to make sure that I drink enough as I haven't been so dehydrated that my brain scrambles completely, and as my husband says, I become like a 2-year-old - for three years now. I'm not able to tell when I begin to get dehydrated, as I just become extremely sleepy, and I used to drink so much water that my ileostomy would kick it out as fast as it could, also taking my proper sodium/potassium ratio with it.
Fortunately, after 30 years of marriage, my full-time caregiver husband can tell by my speech if I need to start drinking my electrolytes - which I will do straight away. Having no IV access is a pain in the neck, and having IV fluid put in through a sub-cut line in my abdomen is slow and it takes a long time for me to become "me" again....
I am having a lot of pain. I'm on palliative pain medication, and since I'm a Dutch Kiwi, I'm stubborn, as I want to keep my pain meds as low as I can possibly get it without having to deal with breakthrough pain. But hubby talks sense into me and tells me that I need to take extra pain relief when my pain gets out of control. (Don't worry - I do not have a bowel obstruction ;-) ).
I am going to take it easy. Read for a while.
I hope you are all doing relatively well!
MeetAnOstoMate is a remarkable community of 41,406 members.
“I found real people, real humor, and answers I couldn’t get anywhere else.”
“The support here impressed my husband’s medical team - they plan to recommend it.”
“This community saved me when I thought I was a freak. Now I’m thriving.”
“Thank god for this site - I finally knew what to ask my surgeon.”
This site is a godsend. As a newbie (colostomy on Nov 8, '21), I look at it every day for a number of reasons. Reading what people are going through makes me grateful that my elective surgery because of a severe case of IBS-C is nothing compared to what they have been through and are still living with.
I don't have to go to the hospital for anything related to my ostomy. I feel sorry for those who do and am in awe of those who can use humor to describe their ordeal. I identify with those who express their fears. I especially identify with those who are depressed because I am clinically depressed and have general anxiety disorder. How ironic that having a colostomy eliminated some of the depression and anxiety that the IBS created. I've been widowed twice and I'm on match.com.
I immediately included my operation in my profile and am pleased to say it doesn't seem to make a difference.
And there is much humor on this site and it's one of the reasons I enjoy it so much.
I could name numerous things I've learned from reading people's comments/questions/answers.
After months following on a daily basis, my only negative comment is I don't like listing the most popular members.
It's not that I don't like these people; I do. It's that I think it elicits some "Facebook"-like banter or comments that are gratuitous.
I don't do any social media and think that its merits are overshadowed by too much negativity.
Meetanostomate is in no way negative. I just think the gallery of "popularity" detracts from what is an excellent website that deals with a serious issue that causes a myriad of emotions.
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