I just wanted to start a blog to stay up to date with my customers and keep them informed but most importantly introduce myself. My Name Is Sharee. I am a wife, and a mother to 4 beautiful children. We Live in Washington State. I love it here. OK so i wanted to give you a little insight to what inspired Next Level Luxuries. Back in 2015 me and husband finally bought a house! We were beyond ecstatic. So we were wanting to grow our family and wanted a little boy so bad we at the time had a 6 year old girl. So in January of 2016 we found out we were pregnant. We were on cloud 9. We did a blood test at 9 weeks to find out the sex of the baby and indeed was a little boy. you could wipe the smile off our little families face. Until that 18 week doctor appointment and ultrasound. The tech doing the ultrasound was very quiet and not all smiles and kept focusing on one main thing which i noticed to be his head and I told my husband i feel like something isn't right and it wasn't your typical ultrasound setting. so she gets done and asks us to sit tight and the doctor comes in and told us to follow her and takes us to her office and says I am sorry to have to give you this news guys but this baby appears to have some major brain malformations. Our world crumbled at that moment in time. They gave us no hope for any positive outcome. So they sent us to a ultrasound Specialist. We had to sit and wait a week and half before being seen. That was the longest time in the land I cried all day everyday. so we finally go to our appointment where this doctor tells us that our little boy has half of a brain and to abort my child that we was gonna die anyway and it was bad for my health to carry this child and his diagnosis was hydrocephalus. I refused to abort my child and he kicked me outta his office and said he wouldn't see me anymore that I was ignorant. So we were referred to a specialist in Seattle WA 4 hours from home. That's where we would continue our care thru out the rest of the pregnancy. After tons of testing and tons of doctor visits to many specialists we were giving a diagnosis of Holoprosencephaly and Hydocephalus. and a very grim survival chance. only 3% chance my little boy would make it to live birth. So i was putt on complete bed rest had to quit my job and hope for the best but i never lost my faith it was stronger than ever i would give anything to hold my baby in my arms even if it was for a couple mins like they intended. so they had us prepared to be setting up a funeral not long after a due date. My body kept going into labor and they were able to stop it until 32 weeks. i was dilating to much and i was at a 4 so they lifeflighted to Seattle so i could deliver my son with the specialist who had been caring for us and so my baby would have a better chance at survival. I ended up having to have an emergency c section and Carter Dell Sweet was born July 1st 2016 8 weeks early and weighted 4 pounds and 1 ounce. He was perfect. The most beautiful little thing you would ever see. Doctor didn't give me a chance to name him because they anticipated for Carter to pass but my little guy had other plans he was thriving and breathing and eating and doing all these wonderful things they said he wouldn't and i knew my prayers were being answered. We stayed in The ICU for a month and i got to bring Carter home. Every doctor there said expect the worst pretty much and said the baby i left with would be the same baby in a year if he was even alive. Well i am happy to report that we just celebrated 4 years old this July. i am not saying those 4 years haven't been rough but they have brought more joy than anything else. The rough part is watching your child have 9 brain surgeries in a year be on life support twice and seize sometimes for a hour or more. but he is my hero and he fights everyday to be here with us and as long as he is fighting i am fighting right beside him. So i care for him around the clock and stay home and its been a dream of mine to own a business and i thought how cool to start a online clothing store to help supplement my lost income from staying home to help care for our child. So carters diagnosis are terminal and i hope he is here with me for many many years to come. Everyday i get with him is a gift and that why everyday is so special and i want to be able to stay home and make my store work because that more time spent at home with him as our days our numbered. So there the story of how next level Luxuries came to be. So Now You know when you purchase from me your supporting a dream and a hope to be able to stay home and spend the time i have left with my son. I dont want to have to go drop him off at a babysitters and miss any precious memories or time spent with my little guy. Thanks for reading my blog and choosing to support a mother trying to support her children.