Post by blackpebble on Feb 26, 2015 10:00:30 GMT -8
Do you perform intermittent self-catheterization? Do you like the way you carry and organize your supplies? Do you ever feel frustrated with the existing options for carrying and using your catheters and associated supplies?
I'm a medical student working with a team to design and produce a new carrying solution to assist everyone who performs intermittent self-catheterization. One of my teammates had a medical condition that required her to self-catheterize so we have both the right expertise and a deep personal connection.
We NEED your input!
Please email me at blackpebblemedical@gmail.com or post here if you could share your thoughts with us! Bonus points if you are in the Boston area or know of someone who is so that we can show you our prototypes in person.
I've never had to catheterize while away from home but I can see how a lot of people can benefit from something to organize their supplies. Good luck with your research!
Hi blackpebble and welcome to the forum. I just carry my catheters, lube and hand sanitizer in a backpack on the back of my wheelchair. I'm a low level paraplegic, L3, so it's easy for me. If I'm at home I just pee into a bottle and all my supplies are next to my bed if I'm out I use my backpack and attach a tube from a overnight bag attached to the end of my catheter so I can just pee into the toilet, easy as.
blackpebble, welcome to the forum. To be honest i think that most people use a backpack and keep catheters inside, especially if they are using their chair. Female catheters tend to be smaller and the ones that i have are also small and compact.
The thing is, most people will carry cleansing wipes this adds to the bulk. Females can use a large-ish handbag and guys, well, not all want to use a man bag lol.
If something specific was going to be supplied/developed then i would suggest maybe a collapsible and wipeable plastic container that isnt see through?
I think a piece of plastic that pops between the gap in the front of most public toilet seats would be the best invention ever! I have such a problem with my legs falling into that gap, and then my skin gets pinched between the seat and the toilet, and it's insanely difficult to spread my legs apart to gain access to my urethra to cath! That would make using public restrooms quite a bit more comfortable and easy.
Now that I have a spastic, rather than flaccid bladder--just discovered with urodynamics--I will be needing to cath. I cannot balance well on a toilet seat, so not sure if I will opt for IMC or SPC. Needing to cath while away from home seems a major dilemma, especially setting up a hygenic place to lay out what you need. kilg0retr0ut's idea of collapsible table appeals to me! blackpebble, I am interested to see your design, and have a pretty good sense for evaluating features.
Now that I have a spastic, rather than flaccid bladder--just discovered with urodynamics--I will be needing to cath. I cannot balance well on a toilet seat, so not sure if I will opt for IMC or SPC. Needing to cath while away from home seems a major dilemma, especially setting up a hygenic place to lay out what you need. kilg0retr0ut's idea of collapsible table appeals to me! blackpebble, I am interested to see your design, and have a pretty good sense for evaluating features.
wavewolf, this is the same as me, i cannot keep balance to catheter over a toilet either. It has been a huge issue when considering days out. The easiest way for me to catheter is on a medical bed. I have met some friends from my unit who can catheter in a chair, i cant imagine, shimmying down my chair to get some angle and then do it discreetly..It just wont happen. I tried to catheter once in the back of a travelling horsebox once!
I have so many self catheter nightmares, i could write a book but in all fairness if i wasnt stubborn about using an indwelling it would help but i really wont do that unless it is necessary.
Lαrα, that is why I am considering a SPC. Implantation is easily reversible, and it is so much easier to manage in public places. The idea of a tube coming out of my flesh seems so gross, but then wet clothes in a public place is also gross. Recently when I was in hospital, I looked at my IV and had a revelation: if you need it, you get used to seeing tubes coming out of places they "shouldn't". Kind of freed me to consider SPC with new perspective. I am waiting for another type of urodynamics to make final decision.
The risk part for me is that with my disease, allergies to antibiotics, and being on immune-suppressing meds, much greater chance of not healing, or sarcoid lesions forming at surgical site, or infections that are hard to treat. "Natural" is best, perhaps, even with all the B&B mishaps. However, if kidney relux is found, then catheterization of some sort will be a must.