R.I.P WESLYNN PICKARD

—””””””””””””””””””””””””””””””””””””””””” We are heartbroken to announce the passing out WESLYNN PICKARD on MAY 3rd2020 -Weslynn, you touched so many hearts you will always be loved by many. Your smile was so beautiful and your cute little faces; now as those turn into memories; my heart starts to hurt, both good and bad hurt. I hurt because I love and miss you, and also because I will have to wait too see your smile, hear your voice, play with you like I do with Wyatt your brother; btw he loves you with his whole entire heart ♥️ you will always live on within him. You are and always will be a blessing to our family, even though the time was short; We would never lose one minute of the time your family spent with you! It was worth every second W.P ♾ Love now, always & forever ♾ ALL OF YOUR FAMILY _____________-uncle-loves you kiddo-______________ R. I. P. WESLYNN PICKARD ————————————————————- ——————This is going to be very hard for a lot of people in our family. This is one of the worst nightmare our family has been faced with. We have just recently found out that my brother and sister-in-law‘s daughter , a niece, a granddaughter and a great granddaughter who is only five months has been diagnosed with Spinal Muscular Atrophy type 1 (SMA Type 1). This is the worst type with this genetic disorder. They do not have a cure for this and it is heartbreaking.
 
My brother and his girlfriend have already went through a premature birth with their first son who was born at 30 weeks but is a striving, healthy young boy. Wyatt Pickard is a wonderful brother to This little girl named Weslynn Pickard, she only come into our lives a short time ago but has impacted us all in more ways than she will ever know.
 
We are trying to help them relieve a bit of stress in this time of need and sorrow as we try to figure out a plan for them as they are both in their early 20s. They will need all the support mentally, physically and financially that is available. We as a family are trying to pull together for them to do our best and show them the love and support they show this beautiful baby girl ❤️
 
She has had the testing done and the  blood work confirms that she is Type 1. There will be a Lifetime of treatments, if the treatment works for her in London at the children’s hospital . The mother is on maternity leave and the father has chosen to stay home so they can be together as a team  to support  their  family. The parents have decided for her to be a part of a treatment program. There will be a  team of 10 medical professionals. Treatment will start next week but is not guaranteed to work.
This fund will go towards transportation as well as medical needs, any special equipment that they might need and as well as financial burdens at this time, so she at least can try to enjoy her time here with her family and on this beautiful earth. Any help is very much appreciated from the bottom of our hearts we will forever be thankful for all and amy support!! 
 
Thank You for taking the time to read this. This has been a heartbreaking diagnosis for our family, let alone Dustin, Nancy and Wyatt 

 
The Pickard Family xo