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MS Caregiver Sharing | Sharing the struggles and triumphs of being a MS Caregiver

Sharing the struggles and triumphs of being a MS Caregiver

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MS Caregiver Sharing | Sharing the struggles and triumphs of being a MS Caregiver | mscaregiverdonna.wordpress.com Reviews

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Sharing the struggles and triumphs of being a MS Caregiver

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MS Caregiver Sharing | Sharing the struggles and triumphs of being a MS Caregiver | Page 2

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Sharing the struggles and triumphs of being a MS Caregiver. A Caregiver’s Bill of Rights. Newer posts →. Give Me a Hand. April 6, 2016. Someone asked me recently if I had ever written about how we adapted to Lynn’s loss of function in his hands. I haven’t but it’s a topic that might be helpful to some so here goes. And the diagnosis of MS. Continue reading at https:/ multiplesclerosis.net/caregiver/give-me-a-hand/. Adapting to a disability. I Just Keep Going and Going and Going. March 27, 2016. Continue ...

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Screaming on the Inside | MS Caregiver Sharing

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Sharing the struggles and triumphs of being a MS Caregiver. A Caregiver’s Bill of Rights. Stages of Grief: Anger. Finding the Will to Live →. Screaming on the Inside. July 26, 2015. This was written a few weeks ago. It’s not how I feel all the time but shows how difficult it can be. Please do not read this if you are not a caregiver. I do not want to cause anyone with MS to feel guilt or pain because you cannot help having this horrible, horrible condition if you have secondary. I put him to bed. Which i...

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Lynn’s Story | MS Caregiver Sharing

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Sharing the struggles and triumphs of being a MS Caregiver. A Caregiver’s Bill of Rights. FIRST SYMPTOMS OF MS. TESTING TO CONFIRM DIAGNOSIS. So one thing lead to another and he was diagnosed with MS in 2006. The head MRI. The neurosurgeon ordered (see “Our story”) showed lesions. The neurosurgeon sent him to a neurologist who did blood work and a lumbar puncture. A YEAR OF CHANGE. FINDING A NEW CAREER. His first novel was published and released in April 2009. August 25, 2015 at 4:34 pm. Your words are s...

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A Caregiver’s Bill of Rights | MS Caregiver Sharing

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Sharing the struggles and triumphs of being a MS Caregiver. A Caregiver’s Bill of Rights. A Caregiver’s Bill of Rights. Helping Lynn during family gathering. I have the right:. To take care of myself. This is not an act of selfishness. It will give me the capability of taking better care of my loved one. To seek help from others even though my loved one may object. I recognize the limits of my own endurance and strength. To get angry, be depressed, and express other difficult feelings occasionally. A Car...

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mscaregiverdonna | MS Caregiver Sharing

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Sharing the struggles and triumphs of being a MS Caregiver. A Caregiver’s Bill of Rights. I am a full-time caregiver for my spouse who has Multiple Sclerosis while I try to work full-time, take care of our home, and handle any number of other functions that used to be shared by the two of us. I'm learning that it's amazing what you can do when you have to and when you have God to send you the resources you need to manage moment by moment. Did You Miss Me? August 15, 2016. Something New to Deal With.

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Tips and Tools | We Rock... They Roll...

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We Rock… They Roll…. About those who rock…. Going to Rehab – Tips and Tools. From two SCI caregivers to other SCI caregivers…. Here you’ll start finding pages with helpful information and links. The web is HUGE and there is a lot of information out there for those caring for someone with a spinal cord injury. SO, I will find it for you and keep it somewhere here. I’ll do my best and if you have any suggestions, let me know! Share with the world! Click to email (Opens in new window). Follow Blog via Email.

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Growing old… | We Rock... They Roll...

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We Rock… They Roll…. About those who rock…. Going to Rehab – Tips and Tools. From two SCI caregivers to other SCI caregivers…. So, in staying a bit with the grandparent’s theme since I wanted to support Grandparent’s day which has already passed… BUT I thought I’d write about getting older. And no, not ME getting older. But the our grandparents, parents and society in general. Have you ever noticed that there seems to be an invisible age past which everyone becomes unable to think for themselves? Did she...

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Caregivingly Yours, MS Spouse Caregiver: December 2012

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Caregivingly Yours, MS Spouse Caregiver. Sharing the trial and error learned lessons of a MS spouse caregiver / carer about family, home care, and transition to the care facility era from 23 years of living with Multiple Sclerosis as a family . a ‘warts and all’ picture of living with MS. My Lung Cancer Odyssey. Sunday, December 30, 2012. Skiing with Multiple Sclerosis Dementia. Caregiving for a spouse with. Can take improvisation on my part. Caregivingly Yours, MS Caregiver @. My Lung Cancer Odyssey @.

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Musings of a Cranky Caregiver: Caregiver Aids #18: The Hydrant

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Musings of a Cranky Caregiver. A Blog About the Random Stuff that Floats Through My Brain. Sunday, May 25, 2014. Caregiver Aids #18: The Hydrant. In my opinion, they're expensive for what they're made of - about $25 on Allegro Medical and a bit more on Amazon - but they're the only product of their type I've found. Replacement hoses are available for about $7 or $8, which is good, because we rinse the hose every day but don't want to wash it with soap as we'll never get it completely rinsed out. As we we...

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Lyme resources | loving lyme caretaker

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For people who love people with Lyme Disease. Top Posts and Pages. Yet Another (But GREAT) List Of What Not To Say To The Chronically Ill. Follow loving lyme caretaker on WordPress.com. Follow Blog via Email. Enter your email address to follow this blog and receive notifications of new posts by email. Join 563 other followers. Yet Another (But GREAT) List Of What Not To Say To The Chronically Ill. Life loving people (they are us)…. For “outdoor-active-movers and shakers-life loving people”. When life giv...

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visual food… | loving lyme caretaker

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April 29, 2014. Top Posts and Pages. Yet Another (But GREAT) List Of What Not To Say To The Chronically Ill. Follow loving lyme caretaker on WordPress.com. Follow Blog via Email. Enter your email address to follow this blog and receive notifications of new posts by email. Join 563 other followers. Yet Another (But GREAT) List Of What Not To Say To The Chronically Ill. Life loving people (they are us)…. For “outdoor-active-movers and shakers-life loving people”. Ah, wellnesssss…. Leave a Reply Cancel reply.

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Wellness | loving lyme caretaker

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For people who love people with Lyme Disease. Top Posts and Pages. Yet Another (But GREAT) List Of What Not To Say To The Chronically Ill. Follow loving lyme caretaker on WordPress.com. Follow Blog via Email. Enter your email address to follow this blog and receive notifications of new posts by email. Join 563 other followers. Yet Another (But GREAT) List Of What Not To Say To The Chronically Ill. Life loving people (they are us)…. For “outdoor-active-movers and shakers-life loving people”. When life giv...

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MS Link List | Multiple Sclerosis Caregiving

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I’m an MS Caregiver. Doing Your Best Does Make it Better. Rick on July 28th, 2008. MS Means – Multiple Sclerosis, your Canadian source for practical MS information Rocky Mountain MS Center Multiple Sclerosis Clinical Trails on ClinicalTrials.gov – A service of the U.S. National Institutes of Health UCSF Multiple Sclerosis Center. Continue reading about Multiple Sclerosis Links. New Approach Could Treat MS and Other Autoimmune Diseases. The Value of Willful Denial. Do An Online MS Caregiver Survey. Great ...

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Caring for Yourself | Multiple Sclerosis Caregiving

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I’m an MS Caregiver. Doing Your Best Does Make it Better. Wishful Thinking: What If It Were Not Multiple Sclerosis? Rick on December 29th, 2010. It’s an odd thing I sometimes consider. (Trust me, I’m not crazy) – but once or twice a year I wonder, what if the neurologists are wrong? What if my wife doesn’t have Multiple Sclerosis? What if she has something that looks like MS but isn’t as bad? I know it’s wishful thinking. And I […]. Rick on December 21st, 2010. Thanks for Helping Each Other! When my daug...

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ALERT | Multiple Sclerosis Caregiving

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I’m an MS Caregiver. Doing Your Best Does Make it Better. ALERT: Voluntary Recall of Alcohol Prep Pads, Swabs and Swabsticks. Rick on January 16th, 2011. Continue reading about ALERT: Voluntary Recall of Alcohol Prep Pads, Swabs and Swabsticks. New Approach Could Treat MS and Other Autoimmune Diseases. The Value of Willful Denial. Do An Online MS Caregiver Survey. How Much Does Multiple Sclerosis Cost a Family? What’s the Name of My Memory Medicine? On How Much Does Multiple Sclerosis Cost a Family?

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I’m an MS Caregiver. Doing Your Best Does Make it Better. Rick on July 5th, 2014. Capital Public Radio offers a series of stories on family caregivers titled, “ Who Cares. 8220; In addition to the stories, CPR provides data on caregivers. The story, “ To Have and Have Not. 8220;, is especially poignant. Learn more at Who Cares. Rick on June 1st, 2014. I am excited for her and the potential for good which her future holds! Now that both daughters have reached the age of majority, I can look back and know ...

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MS Caregiver Sharing | Sharing the struggles and triumphs of being a MS Caregiver

Sharing the struggles and triumphs of being a MS Caregiver. A Caregiver’s Bill of Rights. Sorry I Haven’t Been Able to Write Lately. March 26, 2017. I guess most of you who have read my column. What Goes In Must Come Out. October 9, 2016. One of the joys of having a progressive disease. Is that everything changes. Just as you adjust to one change, something happens and the fix you had in place is no longer working. As Lynn’s caregiver. Now, my take on waste management. Bowel and bladder program. It took ...

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Thursday, April 28, 2011. Hello there MS caregivers of the world! It seems I've been gone so long that my blog background has been removed from the site where I got it! I'll get to fixing that eventually. The last time I posted, I was pretty low. Down in the dumps. Blah. But no more. Things have been happening, as things tend to do. And I've managed to crawl out of my own depths of despair. In fact, things are. And after many years of neglecting myself, I am finally learning that this is true. I challeng...

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