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Life After Caregiving

Sunday, July 31, 2011. Http:/ onepartwidow.blogspot.com/. Saturday, July 30, 2011. It has been a very long while since I have written. My therapist suggested that grief makes it very difficult to concentrate. I think she was right, but now that I find many of my everyday needs being met once again, I feel ready to write. I even painted a little a few weeks back. Thank you for being a part of my life. I hope that you choose to continue reading my musings. Sunday, March 20, 2011. I am angry today. The last...

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Life After Caregiving | nolongeracaregiver.blogspot.com Reviews
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Sunday, July 31, 2011. Http:/ onepartwidow.blogspot.com/. Saturday, July 30, 2011. It has been a very long while since I have written. My therapist suggested that grief makes it very difficult to concentrate. I think she was right, but now that I find many of my everyday needs being met once again, I feel ready to write. I even painted a little a few weeks back. Thank you for being a part of my life. I hope that you choose to continue reading my musings. Sunday, March 20, 2011. I am angry today. The last...
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Life After Caregiving | nolongeracaregiver.blogspot.com Reviews

https://nolongeracaregiver.blogspot.com

Sunday, July 31, 2011. Http:/ onepartwidow.blogspot.com/. Saturday, July 30, 2011. It has been a very long while since I have written. My therapist suggested that grief makes it very difficult to concentrate. I think she was right, but now that I find many of my everyday needs being met once again, I feel ready to write. I even painted a little a few weeks back. Thank you for being a part of my life. I hope that you choose to continue reading my musings. Sunday, March 20, 2011. I am angry today. The last...

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Life After Caregiving: MSA Awareness

http://nolongeracaregiver.blogspot.com/2011/02/msa-awareness.html

Wednesday, February 9, 2011. As many of you know, Dennis died of a rare neurological disorder called Multiple System Atrophy. This disease is considered an orphan disease, meaning it is so rare that it affects too few people to be given much thought by the medical community, politicians, and funding for research. Labels: Multiple System Atrophy Awareness. February 9, 2011 at 7:14 PM. I have signed the petition, Ann.wonderful idea. and quite a few people have seen it. Subscribe to: Post Comments (Atom).

2

Life After Caregiving: March 2011

http://nolongeracaregiver.blogspot.com/2011_03_01_archive.html

Sunday, March 20, 2011. I am angry today. The county wants every penny back that Dennis received for care. Yes, he had money left and I was afraid this would happen, but I am still angry that it has happened. I am angry at the social worker for not telling us that the help was simply a loan. I am angry that Dennis had to work to receive this loan. I am angry at Dennis for not gifting me the money like we discussed. I am angry at myself for being angry. Labels: Life after caregiving. This week I took care...

3

Life After Caregiving: Anger

http://nolongeracaregiver.blogspot.com/2011/03/anger.html

Sunday, March 20, 2011. I am angry today. The county wants every penny back that Dennis received for care. Yes, he had money left and I was afraid this would happen, but I am still angry that it has happened. I am angry at the social worker for not telling us that the help was simply a loan. I am angry that Dennis had to work to receive this loan. I am angry at Dennis for not gifting me the money like we discussed. I am angry at myself for being angry. Labels: Life after caregiving.

4

Life After Caregiving: July 2011

http://nolongeracaregiver.blogspot.com/2011_07_01_archive.html

Sunday, July 31, 2011. Http:/ onepartwidow.blogspot.com/. Saturday, July 30, 2011. It has been a very long while since I have written. My therapist suggested that grief makes it very difficult to concentrate. I think she was right, but now that I find many of my everyday needs being met once again, I feel ready to write. I even painted a little a few weeks back. Thank you for being a part of my life. I hope that you choose to continue reading my musings. Subscribe to: Posts (Atom).

5

Life After Caregiving: A Walk in the Graveyard

http://nolongeracaregiver.blogspot.com/2011/03/walk-in-graveyard.html

Sunday, March 13, 2011. A Walk in the Graveyard. I am back from a very helpful visit with my sister and brother-in-law in London. Jane and Ralph took great, nurturing care of me - feeding me, letting me be lazy, making plans for going places that I would enjoy, and taking long (for me, not for them) walks in various neighborhoods in London. For the first time in 2 or 3 years I let someone else take care of me. She was not able to remember much either, but did remember him both being aggravating by his ov...

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multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: Just the Two of Us

http://multiplesystematrophyandshy-drager.blogspot.com/2010/12/just-two-of-us.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Wednesday, December 29, 2010. Just the Two of Us. It isn't easy for Dennis to move, but every once in a while we manage to find a way to hold hands. Here we are in the champagne/martini bar before dinner while on the cruise. Labels: Dennis and Ann. December 29, 2010 at 10:56 AM.

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: October 2010

http://multiplesystematrophyandshy-drager.blogspot.com/2010_10_01_archive.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Sunday, October 31, 2010. It's late Sunday and we are covered in vomit and poop and a bit of blood. Dennis went out for one of his infamous walk for poo cruises around the hall with me. It was obvious he wasn't going a second round about half way through. But, ten minutes after ...

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: Dennis Died

http://multiplesystematrophyandshy-drager.blogspot.com/2011/01/dennis-died.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Saturday, January 8, 2011. I don't know what else to say right now. He died of complications due to his MSA. Thank you for following my blog. This comment has been removed by the author. January 8, 2011 at 10:03 AM. January 8, 2011 at 10:16 AM. January 8, 2011 at 11:10 AM. Im so...

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager

http://multiplesystematrophyandshy-drager.blogspot.com/2011/07/httponepartwidow.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Sunday, July 31, 2011. Http:/ onepartwidow.blogspot.com/. Looks like you have put a lot of effort in your blog, thank you for taking the time to write such useful information. January 15, 2012 at 8:47 AM. I love your blog, too bad you moved it.update it sometime! Yesterday was o...

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Multiple System Atrophy and Shy-Drager: January 2011

http://multiplesystematrophyandshy-drager.blogspot.com/2011_01_01_archive.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Wednesday, January 12, 2011. I hope you decide to join our journeys with us. Ann, after Dennnis. Labels: I will go on. Monday, January 10, 2011. About Saturday, 1/08/2011. But that was not to be the case. I was on the phone all evening with the on-call hospice nurse. We were...

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: Thank You

http://multiplesystematrophyandshy-drager.blogspot.com/2011/07/thank-you-to-each-of-you-for-following.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Saturday, July 30, 2011. Thank you to each of you for following my blog. It was written with love, pain and frustration. I started a new blog, Life After Care-giving, but it did not have the right feel for me. April 7, 2012 at 9:37 AM. April 11, 2012 at 1:17 PM. We transform ide...

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: My Parents

http://multiplesystematrophyandshy-drager.blogspot.com/2008/08/my-parents.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Tuesday, August 19, 2008. Now it is eight weeks later, her cast was off, she has completed some physical therapy, her teeth are fixed and there is only a tiny bruise remaining on her lip. She looked good and could eat her entire meal. I am fortunate to have both of my parents st...

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: Is it Parkinson's or MSA or SDS?

http://multiplesystematrophyandshy-drager.blogspot.com/2008/07/is-it-parkinsons-or-msa-or-sds.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Monday, July 7, 2008. Is it Parkinson's or MSA or SDS? Now, since this blog is not about the past, but the present, I will not bore you with stories of how fast his Parkinson's seemed to be progressing. I will tell you, however, that he did qualify for social security disabi...

multiplesystematrophyandshy-drager.blogspot.com multiplesystematrophyandshy-drager.blogspot.com

Multiple System Atrophy and Shy-Drager: Dennis' New Bed

http://multiplesystematrophyandshy-drager.blogspot.com/2011/01/dennis-new-bed.html

Multiple System Atrophy and Shy-Drager. A journal of living with Multiple System Atrophy. How we, a 58 year old woman and a 62 year old man, laugh, cry and love our way through Dennis' latest symptoms and newest diagnosis of MSA. Wednesday, January 5, 2011. Our new hospice organization already supplied Dennis with a new bed. It is a pressure guard mattress. Since I can't explain it well, I have put the link to the particular mattress that he has right here. December 30, 2012 at 10:50 AM. Subscribe to: Po...

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Life After Caregiving

Sunday, July 31, 2011. Http:/ onepartwidow.blogspot.com/. Saturday, July 30, 2011. It has been a very long while since I have written. My therapist suggested that grief makes it very difficult to concentrate. I think she was right, but now that I find many of my everyday needs being met once again, I feel ready to write. I even painted a little a few weeks back. Thank you for being a part of my life. I hope that you choose to continue reading my musings. Sunday, March 20, 2011. I am angry today. The last...

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