brone in your foot I’m fighting each time. I have to take a shower even using a handicap chair. It takes all the energy that I have in me right out of me. I don’t know if it has to do with the epilepsy condition along with the hydrocephalus condition or if it’s due to the break I had happened last month or a combination of both.
I give you a hug! Hydrocephalus can be a hazzle sometimes but controlled. Sz can be controlled but I fine harder to control! I am glad there is better medications out. I have a stool in shower to keep my balance! I wish you the best!
Question: How does epilepsy affect energy levels when performing daily activities like showering, especially while managing an injury?
Fatigue and exhaustion are common experiences for people with epilepsy, particularly when recovering from seizures or managing daily activities. Using safety equipment like a shower chair is Show Full Answer
Dont give up. I had to use a walker for two months after my wreck. I had shattered it and they had to find pieces to rebuild it again. It was very difficult at first, but its been over 6 months now, and although I still use a cane, I promise you...it'll get better!
Rhondaschnee, This whole entire thing has been a big challenge since I broke the bone last month. Tonight’s probably the worst with my ankle since I had the surgery done last month. I can’t put any weight on it whatsoever right now as restricted me to even do that so that tells me I’m gonna have to rely on my crutches only and that’s gonna restrict me from doing anything else like carrying things or fixing things like beverages and what not I wish there was an easier way when you’re non-weight-bearing but I don’t see any other easier way as of right now other than to keep staying on crutches
I had baths and washed my hair over the edge of the tub. I couldn’t put any weight on my foot so I found it easier that way. It’s not fully healed yet so when it’s really hurting I go back to the tub