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Donna Steigleder
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Rising Tide by Lynn Steigleder
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How to contact Donna
Sometimes readers have a need to talk privately. If you want to send me an email about your MS or caregiver challenges or thriumps, I would love to hear from you. My email address is donnasteigleder@gmail.comPublic Service Warning: Do Not Purchase from Radical Mobility
If you are considering purchasing a 4-wheel drive wheelchair, please do not purchase from Radical Mobility. We bought one in 2009 from them. It never worked. We sent the parts to them to repair. They never returned them. We finally received the parts we sent them them this year (2015). Multiple customers of theirs have told us of similar issues. Please, do not make the same mistake we made. Look elsewhere. I'll share more if you contact me directly.
Tag Archives: Respite care
Reflections on Caregiving
New Year’s Day often brings a time of reflection, and for some, a time for establishing resolutions for change. My life tends not to be stable enough to attempt to create resolutions for change. However, I have been indulging in reflection quite … Continue reading
Posted in Ms Journey
Tagged Caregiving, family caregiving, Multiple Sclerosis, Respite care
3 Comments
Realities of Life
For the most part, our home life is fairly stable meaning we have the same things happening day in and day out. We have a routine – I get Lynn up for the morning and help him with his exercise, … Continue reading
Posted in Ms Journey
Tagged Caregiver, Caregiver Support, Disability, Financial planning, Multiple Sclerosis, Respite care, Support group
7 Comments
Something New to Deal With
Every time Lynn starts acting differently for several days in a row, I start to wonder if it means there’s some new problem we have to face. MS can affect so many different body parts and functions that I just never … Continue reading
Posted in Emotional Effects, Physical effects
Tagged Caregiver, Caregiver Support, Disability, Family caregiver, Health, Multiple Sclerosis, Respite care
3 Comments
Feeling Alone or Maybe Just Left Out
I always have guilt feelings when I write about any negative emotions I feel in being a caregiver but the fact is, I have them and I expect most other caregivers have them as well. It doesn’t mean we don’t love … Continue reading
Lack of Sleep. The Root of All Evil?
There are a lot of responsibilities and consequences in being a caregiver that I don’t like; things I would prefer not to do or which are difficult to manage, but the biggest challenge I have is lack of sleep. I think … Continue reading
Posted in Emotional Effects, Physical effects
Tagged Caregiver, Caregiver Support, Depression, Family caregiver, Health, Multiple Sclerosis, Respite care, sleep, stress
2 Comments
Confessions of a Stressed-Out Caregiver
Often when I meet someone who has just become a caregiver, they ask me how I do it; “How do you handle the daily stress of working and caregiving full time while still managing a home?” I always reply, “I … Continue reading
Posted in Ms Journey
Tagged Caregiver, Caregiver Support, Depression, family, Family caregiver, Multiple Sclerosis, Respite care, work/life balance
2 Comments
Blessings from Pain
I’m sure you have heard others reference the saying “turn lemons into lemonade.” It implies taking something bad and turning it into something good. Our pastor challenged us to think along those lines but with a different twist. When something … Continue reading
Posted in Ms Journey, Relationships
Tagged Blessings, Caregiver, Challenges, Disability, Family caregiver, life planning, Multiple Sclerosis, Respite care
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I Just Keep Going and Going and Going
In the past month, I have been taken to the emergency room twice with severe abdominal pain and vomiting. Each time they ruled out appendicitis (thank goodness) but obviously something is wrong. At this point, they believe I have two … Continue reading
What Resources are Available if I’m Not Around Anymore?
About this time last week, I was experiencing discomfort in my abdomen. As the hours progressed, the pain got worse until eventually it was so intense that I was vomiting. Unable to sit up, I was lying on the floor moaning … Continue reading
Posted in Ms Journey
Tagged Assisted living, Caregiver, Disability, family, Home health, In home care, Multiple Sclerosis, Respite care
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Waiting for the Next Shoe to Drop
I was talking to a fellow caregiver this week about an event that occurred to him and he made the comment, “Yeah, I’m just waiting for the next shoe to drop.” That comment really struck home. I confess; I’m like … Continue reading