I can’t believe what I’m doing. I really can’t. There’s a part of me that is completely and utterly freaking out. All I want to do is to get out of this situation. Right now. But I also know that I need to do this. “That’s right”, coos the nurse to me. We’re in a... Continue Reading →
Ah, that old friend of mine. It’s with me when I’m feeling great, and when I’m feeling low. It’s with me when I’m at home, and when I’m at work; when I’m with friends and when I’m alone. It’s my constant companion. THE PAIN. ENDO-PAIN. Let’s talk about endo-pain: the chronic pain associated with endometriosis.... Continue Reading →
“Oh no!” I’m bawling, “I sat by the fire for five minutes. I just didn’t think.” “You did what? I don’t understand. Calm down and tell me what happened.” “Bwaaaaaaaa, I sat bwa bwa bwa by the fire.” He’s looking at me puzzled. I’m now at a fully blown crying fit. You see, seven days... Continue Reading →
Do you have endometriosis? Do you have endo-fatigue? Let’s run a little test: Are you exhausted right now? Do you frequently wake up tired after a ‘good night’s sleep’? Do you frequently feel you have no ‘spare’ energy despite resting a lot? Did you say yes to at least one of the questions? Let me... Continue Reading →
“Yes, here it is. Yes, it does look like a dermoid cyst.” I emerge from behind the screen. I must be looking a bit worried, because she reassures me keenly that “they’re not that uncommon”, “it’s nothing to worry about really”, and I should “google it”. Back home, I’m on my iPad googling. “DERMOID” Wikipedia – because let’s be properly scientific about this – informs me that a dermoid cyst is a teratoma of a cystic nature that contains an array of developmentally mature, solid tissues. A solid cyst? Ok. Doesn’t sound that bad. It’s a what? A teratoma? I google that. “TERATOMA”
With Endometriosis, as with any serious illness, it's important to stay safe. To raise awareness of the disease and to encourage you, my fellow sufferers to take care of yourselves, I've collaborated (free of charge, this is not an advert) with the the ID Band Company on an article titled An endometriosis sufferer's fight to raise awareness. I'd love to learn if any of you already sports a medical band, necklace or some other form of medical alert identification. Personally, I'm loving the Hedlee Beaded Collection - who said that medical ID bands should be boring? - bring on the bling! This is serious stuff. As always, take care of yourselves.
My brain is frazzled. Regularly. And most of the time, there seems to be no solution. So I stew. I stew when I should be working. I stew when I’m out with friends. I stew when I should be sleeping. So I don’t sleep. I don’t do anything properly. I’m not mindful of anything. I... Continue Reading →
The business of making plans by an endometriosis sufferer is likely to be fraught with many potential pitfalls. The timing of your period, the need for frequent loo breaks, the likelihood of pain, tiredness, and inability to carry your own luggage, all need to be taken into account. But it is possible to plan and it is possible to find the window of opportunity. Here’s to life at it’s best, whatever that is.
Let me show you how project management techniques can help the chronically ill achieve more. Let me show you how by imitating professional project managers, you can and will successfully overcome the daily tests and trials that living with a debilitating chronic disease so often entails. What is your story? What have you achieved despite your crippling disease. How did you overcome the challenges of living with a long-term health condition? How did you interact with others to get them help you? What motivated you to keep going even though every fibre in your body was telling you to give up?