Month: January 2021

Posted on

Covid19 And My Mental Health

Will the ‘restrictions’ of Covid19 kill me before Covid19 does? Don’t get me wrong I know we have to abide by these restrictions and they are put in place for our good, for our protection. And I will follow these restrictions for myself and also for the safety of others.

But having said that, coming from someone who suffers from a mental illness; how am I going to survive? Because right now I have days where I feel I am loosing the battle. Every restriction that is in place are restrictions that trigger my depression and anxiety. I believe this pandemic is difficult even for someone who has good mental health. But those who suffer mental illness; this caged, confined, imprisoned pandemic, would make one worry and wonder if you can survive this hellish existence.

I have no problem in wearing a facemask, I believe it’s the selfless thing to do; if it makes us a little uncomfortable, I think we can tolerate that, especially if it meant protecting someone who is autoimmune comprised or vulnerable. Sometimes we just have to do the right thing and wear a mask, if not for ourselves, then do it for others. I know there are some who just cannot wear a mask because of medical reasons and therefore they have a medical exemption from their doctor. I do believe these people should really limit their outings around others. One for their own protection and two, for the protection of everyone else. To my disbelief there are still those who just blatantly refuse to wear it. Their reasoning; they just don’t want to live their life in ‘fear’. I think sometimes we need a little healthy fear and abide by the restrictions that the Health Care Professionals put in place for our protection. I believe that someone who refuses to wear a mask are just being selfish, careless and inconsiderate of others. I certainly don’t feel that all those who are wearing a mask are living in fear but they just have a lot of common sense. So I will ‘suck it up’ and wear my mask without complaint, it’s the least I can do.

I know right now the media, example ‘Bell Let’s Talk’, are encouraging those who are finding the stress and anxiety of the  pandemic is affecting their mental health and they are finding life very difficult. And I totally agree, talking is great therapy and is certainly a means to help each other through these tough days. But I guess there are sometimes, exceptions to every rule. Just yesterday, I was having a really tough day, how I was feeling was unexplainable but it was not good. I was desperately fighting to just cope, to just survive the day. And talking to someone was the last thing I wanted to do; I just wanted to close the door on everyone and just crawl inside myself. I know this was not right but talking wasn’t on the top of my list of coping. So, don’t do as I do but do as I say and talk to someone!

I believe the most trigger provoking restriction of this whole pandemic is, social distancing/living in a bubble.  Not being able to spend time with friends and not having a social life is just killing me. The things that once I took for granted, I now crave to do. Just being able to go to the grocery store and smile at the passing customers or stopping and having a chat to a friend we just bumped into. And then just not being able to hug those we meet. Those little things aren’t little anymore, they play havoc on our mental health, even when we don’t realize they are. But for me, getting out, socializing, interacting with others, sharing with others, were all therapy for my mental health. Those were things I desperately craved to help bring me through my dark days. But because of this pandemic I am very limited to what I can do.

We are so blessed here in Newfoundland and Labrador compared to others parts of Canada and the World. But we certainly can’t afford to let our guard down. It’s because of our abiding to the restrictions of Covid19, that I believe have helped to flatten the curve and keep our numbers down. So thanks to our Government and Health Care Professionals for doing such an amazing job. I believe our protection and well being were their top priority and they have to be commended.

One day, hopefully, we will be able to look back on this nightmare and thank God that it did not kill us but we survived. My heart goes out to the tens of thousands that have died because of this deadly virus; worldwide. To those we will never forget, to the families who are still grieving their loss, beyond sad! Even to this very day, we are far from being home free! Still this pandemic sweeps through the earth and taking thousands of lives with it. One day, just one day, maybe just CA one day, we will be free again. I believe we will never be the same again, in this generation, but we will learn once again to live a ‘New Normal’.

 

 

Posted on

2020; A Year We Would Not Soon Forget

January 20, 2017 was my first post to my blog; www.harrislisa72.com. Life & Times Of  “The Tuckers”. ‘Living with severe depression and anxiety. Raising a child with cerebral palsy. The ups and downs of life; the rain and the sunshine’. A form of therapy that brought me through many very dark days. And here I am, January 2, 2021; posting again. Never in my life did I think this blog would last for years and would eventually be published into a book. And may I go further and say, books (two at the least). I can always dream; dreams do come true. This, I feel, will be a cause to pause from writing about my illness. As therapeutic as blogging has been for me, it has also been exhausting and draining; I’ve been misunderstood, stigmatized, traumatized and ridiculed. But that came with no surprise to me; it’s what having a mental illness does to a person. But I still had to write the truth, no matter what. What was meant to start out as therapy for myself, also became a means to help others, through my own experiences with a mental illness. I learned that, much like everything in life, we cannot change the world; nor did I think I could. But I did think I could help one person at a time. And if that meant putting my heart and soul into my writing (raw & honest) then I was willing to do so.  If it meant helping someone else, to save one life, then I was successful in what I set out to do.

In 2012, I had my last relapse, and was told by my doctor that I would not be going back to work; if ever. And here I am in 2021, still fighting my disabling, crippling, tormenting illness; an illness that has left me fighting for that one ‘good day’. But inside this physical body a war is still raging against my mental health. Over the past few years, life has introduced many triggers, many uphill climbs, many times when I just had to crawl. But I fight with what I have and there are times when that may not be much. But I fight!

When I look back over the past year, and wonder how I survived, I really am in awe that I am doing as well as I am. The year was filled with much sadness, loss, sickness, discouragement and I could go on, but what amazes me the most, is that we are still fighting; fighting against all odds.

When Lauren was diagnosed with Spastic Quadriplegic Cerebral Palsy in 2014, we knew we were going to encounter many challenges and obstacles; but we had no idea just how many; it was one thing after another, there was no end. We were told, when she was around one year old, that her vision was affected, they just couldn’t tell us just how much she was seeing. Being the naïve parents we were, we just  thought,  when she gets a little older she’ll just need glasses and that’ll take care of her vision. We were so wrong again.  When she was referred to the CNIB (Canadian National Institute for the Blind), we were literary in shock. We realized then that Lauren’s vision was not going to be corrected with a pair of glasses. My God, how were we going to get through this? How were we going to accept this? Sometimes you just don’t have a choice. Then she was referred to APSEA (Atlantic Provinces Education Authority) in March 2020. Their findings were what led to her being diagnosed with CVI (Cortical Visual Impairment). This has more to do with how the brain is interpreting what the eye is seeing. There is no cure per se. With intervention, improvement is possible, but not a lot of hope, in my opinion.

The year, 2020, began with Lisa’s surgery on March 16. This surgery was supposedly a routine surgery that would only require an overnight stay in the hospital. However, due to complications resulting from the surgery, Lisa was rushed back into the OR for emergency , life-saving surgery on March 17. This surgery resulted in  her being put in ICU on a ventilator, fighting for her life.

And if that weren’t  bad enough, the hospital was now on lockdown due to the worldwide pandemic of the Covid19 virus. Lisa had to experience this all alone because there were no visitors allowed in the hospital;  not even her distraught husband. You talk about an hell on earth, and that was exactly what we were experiencing. Lisa stayed in the hospital for eight days. Once released, we thought we were on the road to recovery; so we thought. To make a long story short, within five months Lisa was back in the hospital from August 23- September 3, due to more complications from that first surgery back in March 16, 2020; a nightmare for us all, especially our two children, Logan & Lauren.

Then, once Lisa was back home and settled in again, she had to find the courage to tell me that my sweet niece, Tonya, had suddenly passed away. Shock, grief and bereavement totally shot me down! The feeling of disbelief consumed my mind. How could this be? She was so young! Our whole family was lost in a sea of grief. A part of all of us was missing; that piece of your heart that you hold close to you, had now gone to Heaven.

It seemed like the year could not get any worse, but the pandemic was sweeping the world! Schools were closed for the remainder of the school year. Lisa was pretty much out of commission; what was supposed to initially be a six week recovery period, ended up to be a full year for recovery. And, here we were with a child that had CP, requiring 24/7 care; care that we had to provide on our own.  All the while, we continued to try to give our nine year old little boy as normal a life as possible.  In spite of it all, he was a trooper and we are so proud of him.

I had to believe that God was in the midst of all this chaos, because this was something we could not handle in our human strength. I prayed for God’s strength, comfort and protection to make it through these most trying times. He was and is faithful!