ACCEPTING INCONTINENC DIAPERS AND PULLUPS Community Group
HELPING EACH OTHER WITH INCONTINENCE ISSUES AND GETTING OVER THE SOCIAL STIGMA OF HAVING TO USE ,WEAR AND BUY ABSORBENT PRODUCT SUCH AS DIAPERS AND PULL-UPS
Accepting incontinence wear has not been a big problem for me. In 2013 I had an accident causing spinal injury, severe spasticity and double incontinence. This has left my anus and urethra permanently closed except when there is manual intervention such as nurses inserting their fingers during bowel evacuations or inserting a catheter up my urethra.
A consequence of this is that my incontinence wear does not normally have to absorb urine or faeces and so consists of a pad held in place by fixation pants. Is anyone else in a similar situation? Further information is on my journals page.
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I have toys. So the ones I have not used or need any more, are gone in the trash. One of my toys is just a regular hand held massager with an attachment. The other is a real insertable toy. This morning I ordered a new toy with attachments. It is small and has a brush like attachment and the other looks like a rose with a tiny tongue. I'll get it in about 2 weeks. Rechargable and...
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I can't believe this has gone on this long. So I don't have much hope of getting a tech job, but I saw an educational job that I thought might be really good. It would have been working at a university supporting high school students who are taking college classes. I did a mock interview with a friend and prepared extensively. It was at the university that I graduated from. I was very excited...


I myself am bladder incontinent and now having issues with IBC (CIC) to where I am just the opposite when it comes to my bladder. My bladder lets go full force when it wants to, even if I have been cathed like 5 mins before. As for bowels, I am stopped/blocked but there are times that I have leaks because of it when I pass gas. Because of all this, I have to have good diapers all the time.
I do hope that your care givers are very supportive and gentle when they work with you.
I have had minor pressure sores when something abnormal happened such as sleeping on a wet sheet when I had a catheter leak. Apart from that I have been free from pressure sores. The only protection I wear are inflatable plastic shoes overnight to prevent sores on my heels.
I find that 30mg Baclofen and 0.5mg Clarithromycin per day relieve spasms and seizures but I still have muscle tightness, mainly in the area that would be covered by a waistcoat.
I'm glad you are a little better. I have not changed much. I am thankful that my incontinence is not too much of a problem. It must be so depressing when an accident occurs - back or front - and also the uncertainty of whether it will happen again. My pad is changed as a matter of routine when getting up. It is also checked at the back each night by my carers when going to bed but has to be changed only about once every 3 or 4 weeks. I can't ever remember a leak at the front (but I have a nurse who likes to check it)
Good luck, Barry.
With best wishes, Barry