Abnormally strong bladder
liayn85
Community member Posts: 31 Connected
It was recently brought to my attention by a friend during a vacation that I was rarely going to the bathroom, yet drinking a lot of liquids. I do not feel the need to go to the bathroom unless I really have to go and my bladder is very full. I easily get dehydrated, which I attribute to my spastic muscles, and so i drink maybe 70+ ounces of water throughout the day.
Is anyone else experiencing this? I am now a little concerned that maybe I am unknowingly harming my bladder due to any sensation or contraction that I may not be feeling. I have done some research online, and I only see the opposite, incontinence, as a condition associated with CP. I can spend the day out without using the bathroom, while all my female friends are going to the bathroom 2 or 3 times in that timeframe.
I have mild spastic hemiplegia. Also, I have always thought that because I learned to go to the toilet when I was one but didn't learn to walk until I was about 4, maybe because I had to wait for someone to take me for 3 years of my life I developed this strong bladder.
Is anyone else experiencing this? I am now a little concerned that maybe I am unknowingly harming my bladder due to any sensation or contraction that I may not be feeling. I have done some research online, and I only see the opposite, incontinence, as a condition associated with CP. I can spend the day out without using the bathroom, while all my female friends are going to the bathroom 2 or 3 times in that timeframe.
I have mild spastic hemiplegia. Also, I have always thought that because I learned to go to the toilet when I was one but didn't learn to walk until I was about 4, maybe because I had to wait for someone to take me for 3 years of my life I developed this strong bladder.
0
Comments
-
It sounds like you have quite the hypothesis of your own there! I have no experience in this area but I suggest, even if there are no negative health effects visible to you now, that you speak to a professional if possible. Just to be on the safe side and put your mind at ease?0
-
Yeah I'll see a doctor when I am able. I'm interested in getting feedback from other CP sufferers in case this is happening to anyone else.
After a lifetime of symptoms and conditions and syndromes and 21 years of PT and OT, plus a heightened need to know how my body is stressed etc., I'd say I'm pretty good at hypothesizing lol.0
Categories
- All Categories
- 13.7K Start here and say hello!
- 6.7K Coffee lounge
- 52 Games den
- 1.6K People power
- 34 Community noticeboard
- 21K Talk about life
- 4.8K Everyday life
- Current affairs
- 2.2K Families and carers
- 798 Education and skills
- 1.7K Work
- 387 Money and bills
- 3.2K Housing and independent living
- 811 Transport and travel
- 636 Relationships
- 56 Sex and intimacy
- 1.3K Mental health and wellbeing
- 2.3K Talk about your impairment
- 837 Rare, invisible, and undiagnosed conditions
- 886 Neurological impairments and pain
- 1.8K Cerebral Palsy Network
- 1.1K Autism and neurodiversity
- 33.7K Talk about your benefits
- 5.4K Employment and Support Allowance (ESA)
- 17.9K PIP, DLA, and AA
- 5.7K Universal Credit (UC)
- 4.7K Benefits and income