I did know about the carrot leaves, I got a handful of carrots and they were sooo good! I got a couple tomatoes, a bunch of cherry tomatoes, one cucumber, about 6 zucchini. I even got a couple watermelons but they didn’t grow fast enough before it froze. I tried pumpkins but again started too late. This year I’m ready! I have heat mats, grow lights, I’m going to try the milk jug greenhouses, and I even got a hydroponic to grow lettuce. No mRNA veggies for this family 😂 husband teases me about my expensive tomatoes and carrots but next year hopefully it will balance out and be cost effective 🙏
Can someone add a “Karen” haircut on this guys pic 😆wow, I can just see him with his hands on his hips demanding to see the manager.
That’s fantastic! I started my garden first time in spring but it wasn’t super successful as I didn’t know what I was doing. I have a whole Arsenal of seeds from baker creek I’m excited to try and my 16 yo has become obsessed with peppers. I save my very weak lilac potatoes that I did get and I’m going to try to get slips so I won’t have to purchase them again,
Ok I’m bummed I didn’t know most of this before now especially because I grew lilac sweet potatoes. The vines and leaves were beautiful and my potatoes were not successful 🤨 I could have at least used the leaves! Thanks so much for sharing
Wow! Yup definitely changing. Crazy about her ears, that must be miserable! Prayers she doesn’t have any other problems from here out.
I have to laugh because you know the deep state is in constant panic every time he does something like this. When they get complacent then he drops the bomb 😆
A few years ago I had to have back surgery, well before covid, for the first time I had to wear the compression socks to prevent blood clots. My mom had knee surgery when I was a teen and she got a blood clot after surgery. Compression socks during surgery is not new, I think it depends on age or type of surgery. In my early 20’s had mouth surgery in the army…no compression socks. Had to have a broken piece of bone removed from wrist mid 20’s no compression socks. No doubts though they will move the compression socks to younger and younger patients as blood clots become “normal” for them. They aren’t normal for young people….middle age yes. So compression socks aren’t new, I used them in 2016 for back surgery.
I think some people do but most on here don’t because we have friends/family who have taken the jab. Most of my 10 yo daughters friends have had it. A girl had a seizure at the field trip I chaperoned- it was “out of the blue” and girl was absolutely jabbed. You’ll get people with very little compassion everywhere and some people are angry and say mean things in anger. Half my nieces/nephews are jabbed (out of 17). My neighbors who I like, parents of my kids friends, people I go to church with. No I don’t want them to die, it makes me sad when people say that. Seeing kids die is the worse.
There is something going around (probably released as Gates just did another event 201 that targets kids). Went through my house and others I know. Fevers lasting many days, my oldest got a cough, we normally (oldest is 18) don’t have kids sick for more than 24-48 hours. My youngest (9) ran a high fever in and off for 3-4 days. Same for 16, and 10yo. It just each differently, 12 yo didn’t get it. Five of the six kids did. Nephew got it, his mom runs a homeschool and it went through all the kids- none (except one) being jabbed. We used zinc, vit c/d, humidifier. Warm shower or cool wash cloths. No fever reducers etc. sister used peppermint oil on one of her school kids feet when she babysat her so her dad could work.
Yeah, they look too red to be berets but I can’t tell. Yes berets are more maroon but poor quality pic I thought they could be. I saw another pic with soldiers with Maga hats which it may be from the same place. I love it either way! My son once used my brothers army gear for Halloween and I just know pictures can distort color 🤷♀️
Picture isn’t super clear but those aren’t airborne are they? Almost looks like they could be berets. Is this from some idiot that doesn’t realize airborne army have red berets? My brother was airborne infantry. Again not a super clear photo.
Glenn Beck once did a report on this, in his explanation (which I liked being a history major made the most sense to me). The US is the only country that has ever truly known freedom as we do. We are the only country guaranteed our rights from God/born with them. So left and right means control or anarchy essentially. The more left you go in America the most totalitarian the more right total anarchy meaning no government or not enough to sustain peace like the articles of confederation. Left and right in countries that don’t have the guaranteed rights there is always some form of government. Is that government aligned with the people or with religion or with corporate. It’s the ideology of what kind of totalitarianism there is going to be left or right but it’s all some sort of repressive government. It doesn’t mean the same thing in our country.
Thanks I’ll check that out! Person asked for one link, but I don’t know what would get me kicked off I’ll try this
I wish I would have gotten her info! It was the peak of covid, husband and I went into grocery store maskless. She stopped us in the parking lot and thanked us for being two of the few who wouldn’t comply. She said she had been a NP for however many years and she says “look I’m a nurse practitioner, I know vaccines don’t cause autism…but I don’t know if vaccines cause autism”. I had trusted everything up till the start of covid for the most part…it’s what got me to question everything and actually led me here. Now I just want to protect my kids and especially my son most vulnerable in the world.
Thank you for all the info, I definitely am always willing to look into things that can help my son progress. My husband and I also don’t like to stress him out, he hates going to any type of doctor now. That is also part of the reason why I would be reluctant even subjecting him to a blood draw. Getting haircuts and going to the dentist are difficult enough.
Yeah that is my concern. I ran into a nurse practitioner during covid who actually works for this hospital. One of her concerns was the jab, she told me the list of kids considered “high priority “ for the jab were kids like my son but my son is extremely healthy and not at risk. She said red flags went off because it was a list of kids eugenicst would want to take care of first.
We have thought of that, I have many friends here who have suggested that. He is a picky eater but we did start protein smoothies to help balance. I will definitely look into this.
We realized when he was 15 mos old he was not progressing. He is 9, developmentally like a toddler, extreme hyper mobility, he can’t hold a pen/pencil like kids his age. His oral motor/tongue is immature and we believe there is motor planning issues. He is happy, loving, tries to communicate through some sounds and gesture and is learning to use a speech device. We have him in speech and OT privately and in an amazing school. We also work with him trying to learn sign language. Unfortunately with developmental delays it is at their pace, they have to do it. We don’t know what the future holds but we accept that he will likely always need to be taken care of. We have accepted he may never talk. I just don’t know that an answer will make any difference in our lives. Is it worth it to trust this children’s hospital with my sons dna? Especially when it will likely never make a difference. We are blessed that he is extremely physically healthy, no allergies, even amazing oral health. He is a joy to have in our home even with his challenges. He has the most amazing laugh.
We have a regular doctor, I don’t have a regular pediatrician I trust so we are sticking with just a regular doctor. He is not a baby, he is 9 y and we have been dealing with doctors and clinics since he was 15 month old. The geneticist said technology will have to catch up, he went as far as tech would take us- he was released from the neurologist, he was released from the cardiologist, he was released from the ortho clinic, he was told he doesn’t need Pt anymore. We are in Ot and speech. there is no treatment available from a developmental Ped because he has no behavior problems, they medicate and he doesn’t need that. We did ABA until moving states but he doesn’t really need it because he is in school full time and doesn’t have behavioral problems, he is potty trained. He is sweet, loving, happy and physically healthy. There are no medications to help his delays, he is developmentally delayed not physically ill. I could take him for a blood draw to enter him into a database not knowing what they would use it for and hope to someday get an answer. I don’t trust this children’s hospital, that is my dilemma. He is my youngest of 6 kids, I’m not new to this. We searched for answers for years, he has been put under general anesthesia for MRI’s, we have done blood tests, over 5 years of searching, Ultrasounds, many many hospital visits till we ran out of places to go. He can only do what he can do and like I said previously I absolutely love him for who he is and accept the amazing spirit God has granted me the the privilege to raise. I just don’t know that it’s worth it to enter him into the database.
Yes, we have been happy so far with his progress at school. My question was more “am I crazy not to enter him into a genetic database to try to find an answer when I know the hospital doing the database is known for doing questionable things”. We know there is no magic fix, he is delayed and he can only do as much as he can. We do private therapies and we have him with the best teachers and services. We just don’t know why he isn’t like his peers. We would never let him participate in research because he is extremely healthy, just developmentally delayed.
That is not one I’ve heard of before thank you! I will look into that!
Thank you! We are connected with other families and definitely have sought out homeschool families too- this was something new that I’m unsure of just didn’t know if I was right or wrong…still not sure. My oldest son says stay far far away from that hospital. I haven’t dealt with their genetic clinic so I don’t know anything about them. It’s just that I have no idea where his info would wind up at in the end.
My point is he is 100% healthy, the hospital is questionable, they recently were in the news for medical kidnap because parents distrusted what they were doing. Girl wound up going blind temporarily from meds parents didn’t want. We will gain nothing from it right now, we would have to trust them to use his genetic info for good. I don’t trust the hospital, I had a good relationship with the other children’s hospital in my previous state. It’s ridiculous to question this hospital that takes away parental rights for questioning them? There is no “treatment” for my son, he is absolutely healthy which is what I said. He is developmentally delayed. We were cleared from every clinic, neurology, cardiology, genetics, orthopedics. I said that, my son is healthy and happy actually the happiest person I know. So you would enter your child’s dna into the database. Thanks for your advice but please don’t misconstrue - there is no “treatment” for him other than what we are doing- this would be a worldwide database that maybe might give us a label. That’s it, there is no magic fix
If he is practicing and a temple holder yeah probably will do the right thing. One of the requirements to be worthy to enter the Lords temple is being honest with our fellow man. This is good news!