I have been finding it harder and harder to get time away from my children. With covid-19 it can be difficult to go outside my apartment. I have not had any significant time away since the start of the pandemic. My children are very attached to me. They want to always follow me and se what I am doing. They are able to take care of themselves, but they do not like to.
Today my uncle is going to be watching my boys so I can get some time with just my wife. We are just going to have a date in our apartment, but I am very excited about it. For the first time in a long time, I will be just responsible for myself.
Everyone needs a break sometimes even stay at home parents.
People think that being a stay-at-home parent is easy until they have to do it. I all the housework, cooking, cleaning, laundry, watch the children, teaching the children, shopping, and finances. I watch my brother’s children as well as my own when he needs me to.
We do not make much money so I make every meal from scratch to save money and make things healthier. I make my own spaghetti sauce, noodles, sausages, Alfaro sauces, bead and many other things. I often make meals that I can freeze for when we are not feeling very well. WE buy many of our ingrediencies in bulk so it is more cost effective.
My wife is able to work, but she has some health problems. Hemiplegic migraine they are not like regular migraines, the symptoms are closer to a stroke. She also has an auto immune disorder.
The only way they know see it not having a stroke is with an MRI. The hemiplegic migraines make it so see is unable to control her body at times. During those time she needs a lot of help. Some time she just has trouble speaking, but other time it is much worse. some of the time she is paralysis on one side of her body. Some time she completely loses control of her body and can on move at all
When she is having problems see needs help walking, bathing and eating. If she completely loses control, I cannot lift her I need to just make her comfort where ever she Is at.
We have tried to get help for her, but her condition it rare. Her neurologist will not even try to do anything and just sent us to a different neurologist about 3 hours drive from where we live.
The new neurologist wants her to he takes the medications that worsened her condition to prove she is having her condition to prove she is having her condition. They know she is having the condition but because they did not diagnose it. They also want her to medication not covered by our insurance that we cannot afford.
We can not afford to make her condition worse and drive over 3 hours for appoints that we don’t know will help.
Lately she has been having a Hemiplegic Migraine about twice a month. Stress can trigger them so I try to help her as much as I can.
