I came across a cool feature on my phone. It is a video creator that lets you choose photos or videos taken on your phone and creates a slideshow or video of memories. I just completed a review of 2013 using just the photos on my phone.
This process got me to thinking about the year that is coming to an end and what I've experienced, how I've grown and the pleasures I enjoyed. I tend to have a full life and this year was no different. Here are some of the memories that were stirred while making my year end video.
* A two year process with my disability claim ended. I received approval and an immense weight was lifted from my shoulders. With the absence of this stress, I was able to move forward with my healing process in my own way.
* I found an amazing doctor and am experiencing amazing healing through mind, body and spirit.
* I started this blog with the intent of recording my emotions, experiences and life challenge with fibromyalgia and to remind myself to keep an eye out for the gifts. I also shared it publicly on the off chance that others out there may be able to relate, be encouraged, inspired and motivated to take action in their own healing process. I've had surprising results, amazing feedback and followers from 39 countries.
* My family said 'goodbye' to a wonderful person who meant a great deal to us. Nancy, we love you and will always hold memories, of times together, close to our hearts.
* I'm taking a course through The Venus Project and loving it.
* I've opened to getting to know and spending time with like-minded peeps. I've made a couple of neat new friends.
* My children have impressed me, again. Their determination, dedication and focus to take a leap of faith and apply for private high schools shows me that they are willing to walk their own path in life. Many of their friends are not taking the same steps, some are discouraged by their parents and some don't feel they would get in. My three have shown that they are not afraid to try.
* My husband shows me how strong he is every day. He takes care of two senior parents. His father is 87, lives on his own and is a proud man. His mother has medical challenges and we moved her from her home of 20+ years to a nursing home. I know these changes and stresses of caring for parents has been hard on him and he has been a rock through it all.
I think I could go on and on although, I've probably posted most of it in my blog through the year. Strangely, I have to go back periodically and read my own posts because I don't remember them. Fibro brain, ya know.
I'm grateful for every moment of 2013! Stay tuned for a post on looking at what I'd like to do in 2014.
Thank you for reading, forwarding, and following!!!
Terri
Showing posts with label disability. Show all posts
Showing posts with label disability. Show all posts
Friday, December 27, 2013
Saturday, September 28, 2013
Perfect Example...Must See
This post is a follow-up to my post, Where you are is exactly where you're meant to be.
I know I just posted my blog for today, but I just had to share this amazing video. An amazing girl with a disability and her older loving brother...
Please Watch. Oh, and have a tissue close by :)
I know I just posted my blog for today, but I just had to share this amazing video. An amazing girl with a disability and her older loving brother...
Please Watch. Oh, and have a tissue close by :)
Monday, July 8, 2013
Being on Disability is a Full Time Job
If anyone out there has a life vest, I could sure use it about now. I spent six hours, today, reading health insurance information, prescription coverage options, trying to understand how disability payments and taxes work, dialing through the automated phone system at MassHealth, being transferred to yet another person who couldn't decipher my case.
My husband makes payments toward a family health plan, through his workplace, and due to my illness, the kids and I also receive MassHealth. Since I was approved for disability, I now receive Medicare and Health Safety Net. It took my fibro brain a few hours to understand the basics of it, so far. My husband is covered by one insurance, I'm covered by four and my children are covered by two. WHAT? Oh, and this will all change as of August 8th when our MassHealth is up for review. The review form is at least ten pages and asks the basic questions, that they already have the answers to, then progresses to a list of what you must provide as proof of everything you just filled out. I think I have to send a DNA sample, a dental imprint and a pap-smear test, but I'm not sure.
It's been two, long years of trying to prove that fibromyalgia is real and I live with it everyday. There are days when I'm unable to walk and days when sitting up is too painful, so I have no choice but to lay down. During the process of applying for disability, I worked with a great company. They did most of the paperwork, they kept track of what needed to happen next, they were available to answer any and all of my questions along the way, they were patient over the phone on those days when my communication and comprehension were poor. I'm so grateful that I didn't have to work my tail off to prove that I couldn't work.
I think there should be a sister company who manages the 'after approval' hoops and red tape. I'm exhausted from my work/non-work day, today. The first rule for someone with a chronic illness...don't over do it!
So, enough with my rant. I'm going to rest and relax and smile about what I accomplished today. Great things were completed, I'm contributing financially to my family again :) I had my family around, all day, and it was a beautiful, bright and sunny day. So much to celebrate!
Thanks for reading, forwarding and following my posts!!!
My husband makes payments toward a family health plan, through his workplace, and due to my illness, the kids and I also receive MassHealth. Since I was approved for disability, I now receive Medicare and Health Safety Net. It took my fibro brain a few hours to understand the basics of it, so far. My husband is covered by one insurance, I'm covered by four and my children are covered by two. WHAT? Oh, and this will all change as of August 8th when our MassHealth is up for review. The review form is at least ten pages and asks the basic questions, that they already have the answers to, then progresses to a list of what you must provide as proof of everything you just filled out. I think I have to send a DNA sample, a dental imprint and a pap-smear test, but I'm not sure.
It's been two, long years of trying to prove that fibromyalgia is real and I live with it everyday. There are days when I'm unable to walk and days when sitting up is too painful, so I have no choice but to lay down. During the process of applying for disability, I worked with a great company. They did most of the paperwork, they kept track of what needed to happen next, they were available to answer any and all of my questions along the way, they were patient over the phone on those days when my communication and comprehension were poor. I'm so grateful that I didn't have to work my tail off to prove that I couldn't work.I think there should be a sister company who manages the 'after approval' hoops and red tape. I'm exhausted from my work/non-work day, today. The first rule for someone with a chronic illness...don't over do it!
So, enough with my rant. I'm going to rest and relax and smile about what I accomplished today. Great things were completed, I'm contributing financially to my family again :) I had my family around, all day, and it was a beautiful, bright and sunny day. So much to celebrate!
Thanks for reading, forwarding and following my posts!!!
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