Skip to main content

Endometriosis: My Daily Challenges - Shower/Bath

Daily Challenge 2: Shower/Bath

A daily challenge when I have pain from Endometriosis burning up inside of me, is managing to get in and out of the shower/bath. Does anyone else need to sit down and have a rest once they come out of the shower?! Please say it's not just me! It can be exhausting! What some people take for granted can cause me so much pain! The energy it can take to carry out this simple task when you have Endo is unbelievable. The challenges I face can include:

  • Firstly, finding the energy/strength to go in!
  • Standing up in the shower, trying to wash your hair when you're in pain is no easy task!
  • If having a bath, (yes I know I get to lie down in between) but the energy it takes me to get in and don't mention getting back out of the bath is unreal. A few times I've panicked thinking I'm going to be stuck in there Either from pain and I've found myself not being able to move, or literally zero energy!  Let me assure you, it wouldn't be a pretty sight for whoever would have to come and help me!!
  • Drying afterwards. By this time I just want to sit down!
  • Now for my hair. To dry or not to dry?! By this point I would have had to have a rest. Given myself ten minutes to recompose. Do I go through the whole process of blow drying, brushing, straightening my hair or leave it au natural and end up with a frizzy mess. Any spoonie will tell you that you need to prioritise your spoons. Frizzy mess it is then... 
  • PJ's back on & rest!!

<< Click here for previous challenge <<      >> Click here for next challenge >>

#MyEndoDiary

Comments

  1. I can definitely relate to this. Sometimes I spend half my day building up the energy for a shower. Sadly we don't have a bath, and no room for a decent sized one. I have seriously considered putting a garden chair in the shower so I can rest halfway through.

    ReplyDelete
    Replies
    1. You're so right, I take all day to muster up some energy to go take a shower too! As for the garden chair... that is such a good idea! Lol

      Delete

Post a Comment

Popular posts from this blog

Endometriosis: Post op

Ok, so I thought I should update you all after my operation on Tuesday.  I have a lot of mixed emotions after the laparoscopy though and I promise to fill you all in soon. I'm sure many of you have felt the same way I'm feeling now so I will post in the near future about all the details. Sharing information is the best way to know we're not alone in this. But for the moment, I'm just getting my head around things and concentrating on recovery. UPDATED: Endometriosis was found in my ovaries as expected and removed. It was also found on my bowel, but it was left untreated. #MyEndoDiary ♡

A Day In The Life Of An Endo Girl - 16/04/13

Seeing as I've named my Blog 'My Endo Diary' I've decided to start this project, 'A Day In The Life Of An Endo Girl' to portray just a snippet of a day with Endometriosis. Women with Endo are not lazy. Some, such as myself suffer daily pain. Chronic pain. Sometimes mild, sometimes exhausting, sometimes severe. Small things hurt massively. What some people take for granted doing, can take all of my energy. Even down to doing the dishes or making food. Endo is unpredictable. Tomorrow may be a better day. It may be worse. If I look or sound OK one day it doesn't mean I'm better. I'm either hiding the pain from you (I've become quite good at this), having an 'up and down day' (explained below) or on the rare chance having a good day. Every day with Endo for me, is different. However at the moment, they all contain some sort of pain. So here's my first entry. 16/04/13                   5:45am Woken up by Endo pains, stabs in my hips

Endometriosis: 3rd Time Lucky?

August 25th. This will be the date of my next operation. My third. I have waited 12 months to get this date. Then, out of the blue, I receive a letter from the hospital. With only 12 days notice. In a way, that's good. Less time to stress. But for me, I'll stress no matter what. I'll just cram a year of waiting into 12 days of worry. I'm now down to 7 days. This time next week... Some people may think that knowing what will happen and how the day pans out etc, will be a benefit. A comfort perhaps. For me, it's the complete opposite. I know how emotional I will get. I know the feelings of panic, anxiousness and nervousness will build up. I know at certain points they'll peak and I'll break down. Just before I'm due to go down to theatre I'm guaranteed to start crying. The fear takes over and there's nothing I can do at that point but just trust the doctors and nurses. But that's normal I guess. Third time around, it will not be any