I am not sure if this is a nationwide problem or a local one, but I do know that it is a present problem.
My seventh grader has 30 minutes for lunch, that is his only break during the school day besides the 3 minutes he has to get between classes and his locker if needed. More than half of the time he says he does not have enough time to make it through the line for food. There are so many children in his grade they split between two lunch times and yet, when there’s testing they are combined. Combining an entire grade into a situation where it is already difficult to buy lunch is bananas. Yes, I know I could pack lunch for him every day, he likes the options at the school.
My first grader has two recesses, one just for playing and then one during his lunch break. He has plenty of time to eat but not a ton of play time to be outside. I personally do not understand how they expect children to focus and get enough time outside to be kids when they are stuck in classrooms for 6-8 hours a day with tiny little breaks.
I do understand they are trying to put as much learning as possible into the day; would people really be up in arms if they add an hour to the school day to include more breaks and outdoor time? I would think that adding the hour for extra breaks and time to run around would be good, there are many working parents who either have to figure out child care for after school or arrange their schedules around it. For the families that don’t get home until dinner time because of jobs it’s usually not a great time to play outside during the fall and winter months.
Of course there’s the argument for after school activities and allowing time for that and if a person is set on having outdoor time than you can sign them up for those. Here’s the thing though, those things usually cost money, not all families have the ability to pay for all the things that go along with those. My children are hyper-mobile so they have crazy ligaments that move too much which makes injuries more likely and more severe. They have been told not to play contact sports, no soccer, no football, rugby, so that really limits the options in our house.
Do you have an opinion on the current amount of breaks for kids at school? I would like to hear them!
My first post on this page was about the stem cells I got for my MS. It’s a very expensive process and a personal choice because as of right now it still is not approved in the US so insurance does not cover it.
Ideally you have this procedure, you see improvement and you don’t have to do it again. Looking back I realize that the stem cells probably gave me a boost in energy during the first few months in addition to the other pleasant changes.
15 months later though I am seeing decline in the changes I originally saw. Whether this is due to my MS re-damaging the areas or what I am not sure. I am not a scientist, though I do love my research.
Originally, before my stem cells I hadn’t been able to feel my feet for nearly three years and then less than a week after the stem cells my feet magically reappeared, at least that’s how it felt. I also had moderate back pain in my spine since 1999 or 1998, honestly it was 20 years ago so I am not sure anymore, that was gone as well.
I thought this back pain was from the first car accident I was in but now that the pain is coming back after being gone for almost a year I am wondering if it is actually from the lesion on my spinal cord in the same area. I know I have an old lesion there because they told me that’s probably the reason I had severe MS “hugs” for several months in 2011.
That’s the kicker, so much money spent, so much hope put in because the pain was gone for the first time in 20 years and now, after a little more than a year it’s coming back. The feeling in my feet is slowly going away too. There is still enough there at the moment that I can sense them, but enough lost that I know what’s coming.
Would I do it all over again knowing? Probably, if I had to do it all over, it was a nice break from pain while I had it. Though I feel terrible that support I received to pay for the procedure ended up not being long term.
It’s been about 2 months since my piercing and it is still healing. They say 3-6 months but I heal slower because of MS and the meds I take for it. It got infected at the beginning because I touched it, slept on it and who knows what else but I got antibiotics for it and it’s been fine ever since. I’m still using the cleaning spray on it 2-4 times a day because I notice if it gets dry it starts to hurt.
As far as migraines go, I’ve gotten a few since the piercing but not nearly as many as before. I have had headaches every day this week that were strong but not migraine level. In short, I’d do it again because I have no clue if I had migraines caused by foods but I do know they’re no longer as strong or frequent.