Below is the letter I wrote to AgeCare Corporate (headquarters to the company which runs AgeCare - Skypointe). With all the news about what is being seen our long term facilities , I thought to share my experiences, thoughts and observations as a resident in one of their residents. At the time of typing this (July 19, 2020), I have not received a response. July 12, 2020 Dear Drs. Hasmukh Patel and Kabir Jivraj. Hello. My name is Laura Jean Rutherford, I am 49 years old and I am currently a resident on 6W Martindale Long Term Care (LTC) wing at your AgeCare - Skypointe facility in Calgary, Alberta. During our global Covid-19 pandemic, the situation with Canada’s LTC facilities and senior residences have come under the microscope due to the high volume of deaths seen across Canada as well as in Calgary. I am writing this letter to express my observations and experiences at AgeCare - Skypointe from a resident point of view as well as someone who has worked in the healthcare field for ...
Pain. We endure pain in many forms. Depending on one’s tolerance, will determine if it needs to be treated. When I was abled-bodied, I basically took Tylenol for headaches or muscle pains. Even when I had gallbladder attacks, I just took Tums and a heating pad to relieve my pain. Guillian Barre Syndrome (GBS) is a rare autoimmune disease affecting the peripheral nerves. 1-2 people per 100,000 per year are diagnosed with GBS. Depending on your GBS sub variant, will determine how to treat you or the severity of the residual effects will be. Recovery can be quick or it can take up to 2 years to recover fully. Then there are GBS survivors who after 2-3 years where residual effects become permanent (that’s me!). There are some sub variants, such as AMSAN, which will fall in the 5%-10% range of those diagnosed where recovery impacts the autonomic system and could have a life-threatening or fatal outcome (that’s me too!). Recovery outcome is poor and will have residual effects ...
The one of the things that is taken from you when you are a quadriplegic, the ability to scratch an itch. It drives me crazy not being able to scratch my nose and head especially when it becomes itchy. For my nose, I wiggle it or make faces try to relieve it. If I don’t have success, I eventually have to call my HCAs to use Kleenex to scratch the sides of my nose. Such relief when they do. Now when my head itches, I hold off and hope the itchy feeling goes away. If it doesn’t, like the nose I have to call the HCAs for assistance to scratch my scalp. I must say I am lucky I have some talented HCAs - magic fingers who give great head massages. And this is when I feel like a cat. When you are petting or massaging your cat, they move into your hand and they start purring. Similar to me, either with their hands or with my wire device, when they start scratching, I move my head around to my relieve my itch. A big sigh of relief - it’s a little piece of heaven for me.
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