Re: Dealing with my daughter's Covid induced MIS-C Quote:
Originally Posted by locusjag Was it selfish of us to think that we deserved a basic level comfortable hospital wait when our child was fighting for her life in there? |
Absolutely not. This is where our health care (or the lack of it) system fails us. You can choose to go to the hospital down the road or go into a flash 5 star joint and still end up being in the same situation. There is almost zero accountability and it almost feels like our Government does not care. Its as if human life is dispensable.
The example you shared about running to buy medicines, I found that frustrating, as a process. I had to do the same thing nine years ago, when our son was born. No issues during his birth, just general medicines that were needed from time and over the course of 5 days that my wife stayed in the hospital as she had a C section. It sounds like nothing has changed. I had to make several trips every day for something or the other. First, go pay for the medicines and get a receipt, run to another counter to get them and go back to the ward where my family was and hand over the medicines to the nurse. A process that took no less than half an hour each time (minimum) as there would almost always be a queue at the counters. For a country that prides itself to be the Software export hub of the world, it is a shame that we cannot streamline something as basic as this. To top it of, I had to pay a bribe to get my sons birth certificate! I dread walking into any hospital these days.
I speak from a different part of the world and would like to share an example of how things can be better. This is important for a patient and a parent as any hospital trip is stressful. A 5 year old child of a family we know well fell ill. Was around the lock down period, say ~June 2020. The child was diagnosed with Guillain Barre syndrome. This is a condition in which the immune system attacks the nerves. There is no cure for this. The family was devastated. That child is probably going to be breathing and eating through a tube for the rest of his life. He can barely walk. The child had to be relocated to Auckland, as Wellington, New Zealand did not have the means to look after him. They air lifted the child and family to Starship Children's hospital. This is the best Government hospital in all of New Zealand. He has been in hospital for the last 7 months and is likely to stay there for another 6 months, or longer. Fortunately for our friend, they let him work remotely. They have provided them with an apartment. Air lifting the child, hospital treatment which I am sure has amounted to several hundred thousand dollars by now, the apartment they have, is paid by the Government. If this backing was not there, the family would have gone broke a long time ago. Our friends have yet to tap into their medical insurance for anything. I know such things are not possible in India but our hospitals can do small things that can make life a little easier.
Our 9 year old went through a phase of anxiety and depression during the lock down. This triggered something called Tourette syndrome or Tic. Its nothing too serious (One must observe) and goes on its own. He has recovered for the most part today. We were concerned when he started shaking his head from side to side. Initially we thought it was his long hair falling on his forehead, eyes that was irritating him but there was a problem that we could not understand. We took an appointment at the Government hospital. I must admit that it was a long wait to meet the doctor. A country with a small population means there are just as few hospitals as well as doctors. Hospitals prioritize critically injured patients and there were quite a few walking in on that day. It was a wait for almost 5 hours to meet the doctor. I was sitting in the car as I felt it would be safer, even though we did not have a single case of covid reported in Wellington. During this long wait, a nurse kept coming to my wife from time to time asking if she needed anything, food and water was served. They finally met the doctor and walked out. No medicines or treatment was required. All we had to do was observe him. When they got back to the car, my wife was speechless. None of us had ever experienced such care and attention. There were no bills to be paid too.
I have never heard of MIS-C. I doubt if I would have survived what you did. I panic when my son gets a temperature. I can't stand the sight of seeing him weak. It makes me fragile. I am sure most parents can relate to this feeling. It still bothers me, the amount of drugs and steroids they have pumped into your daughter. The body isn't used to such high doses and can cause all sorts of problems. If you feel confident, meet someone at Kotakkal and talk to them about your daughters case. Not that they can give you anything that can further cure your daughter. She is anyway out of danger. Its more to get all those drugs flushed out of her body so things normalize and the body can start to look after itself.
Thank you. |