I managed to get some things done, but just feel exhausted and not very focused. When I say I'm not very focused, I don't actually mean the lack of focus caused by severe fatigue and brain fog (which we all know happens with people with Fibromyalgia).
I actually have gotten multiple hours of sleep in a row, without waking up thinking people were walking into my house or worrying about my children or whatever else. It's been a really nice change. Hopefully, my sleeping patterns will continue to improve. So, my lack of focus doesn't have anything that I can tell to do with fatigue and I'm not feeling particularly foggy.
Today, my not feeling focused has more to do with not feeling very connected to the universe or myself today or feeling terribly confident in MY hopes and goals. As a result, my motivation levels are on the low side at the moment. With only so much I can do each day before my body stops, I find myself spending my time and energy on everyone but me.
Currently, my efforts are focused on cleaning and reorganizing the house, fundraising for one daughter, maintaining an equilibrium with my other daughter so she feels valued also, trying to stay afloat, taking care of pets, and losing myself a little in the process.
Truthfully, as a mother, I lost myself a long time ago and really starting finding ME again through this blog and developing a purpose that drives me to keep moving and going forward. A purpose that is greater than myself, greater than trying to do as much as possible for everyone else, greater than a clean house or anything else.
My purpose is to help raise Fibromyalgia Awareness and make this world better for people who like myself have Fibromyalgia and realize we have a lot to learn about coping with and living with this syndrome.
Most of all, I want to get through to people who have loved ones with Fibromyalgia that Fibromyalgia is REAL and it changes everything in your life. Sometimes those changes may be inconvenient or difficult, not just for the person with Fibromyalgia, but for you as well. Comparing the way of life before Fibromyalgia is not productive or helpful, life will never be the same way it once was, but given time and effort and genuine caring, it can become something positive and beautiful in a different way.
Anyway, due to feeling this lack of connectedness and focus at the moment, I started looking for something that made me feel just a little more connected and as usual I found it. The search took longer than usual and required some effort, but I found an inspiration that has me heading towards the right direction again.
The inspiration I found was this video of Paulo Cohelo Quotes. I actually LOVE his quotes, stories, books, blog. You name it, I'm inspired by it (at least when it's in English and I can understand it). So this video found me at the right time and place, I hope you enjoy it also.
Some people go through life without realizing what their purpose is. Others never walk in their purpose. I hear you about the focus,but you have not lost your way, you are staying on your purpose path, despite the obstacles that need to be overcome. In my eyes you are an overcomer and victorious!
ReplyDeleteHi,
ReplyDeleteWill you please post a link to your Blog at The Fibromyalgia Community? Our members will appreciate it.
Members include: Those living Fibro, Family and Friends, Experts, Support Groups.
It's easy to do, just cut and paste the link and it automatically links back to your website. You can also add Articles, News, Photos and Videos if you like.
Email me if you need any help or would like me to do it for you.
Please feel free to share as often and as much as you like.
The Fibromyalgia Community: http://www.vorts.com/fibromyalgia/
I hope you consider sharing with us.
Thank you,
James Kaufman, Editor
My wife Julie lives with Fibro
Retha, Thanks for your words of encouragement. You are right, I need to simply view it as an obstacle to overcome, not that I've lost my way. Thank you!
ReplyDeleteJames, I just tried to set that up on the Fibromyalgia community for you. I hope that helps!
ReplyDeleteI have CFS and today had not been my best day, so I totally relate to what you are saying!! I'm with you on just doing what you can when you can.
ReplyDeleteJeanine, I always enjoy connecting with someone who can truly relate like you! We really do need to simply do the best that we can when we can!
ReplyDelete