{ bloom city plant night | jessop 3 fundraiser }

on march 28th we will be hosting a special bloom city plant night to support our very own jessop 3 and the other pkan warriors. 
click here to sign up
 in addition to creating your own beautiful succulent garden we will also be raffling off some amazing prizes and have delicious food provided by padre canyon foods.

all 3 of the jessop kids have been diagnosed with pkan{pantothenate kinase-associated neurodegeneration} a rare neurological disease with an average life expectancy of 10-12 years.  

on january 25th, 2018, at their appointment at ohsu hospital in portland, lester and noreen were told research results had come in that could change the lives of their children. not only had they found something that could stop the progression of the disease but could start the healing process, not only for their 3 children but for over 200 more children in the u.s. that are suffering from this disease. 

now we are joining the journey to get this medication to the clinical trial stage. in order for the medication to be made and the trials to take place, the spoonbill foundation, headed by dr. hayflick and dr. hogarth, needs $2 million in donations. so, we ask you to please search your heart and join us in our give so they can live, fundraiser. if you would like to find out more information about pkan and these wonderful doctors who have dedicated their lives to finding a cure, please visit http://nbiacure.org/learn/nbia-disorders/pkan/ & http://nbiacure.org/spoonbill-foundation 

all proceeds from the night will be donated to this very important cause.

if you are unable to attend or would like to donate directly

a gofundme page has been set up with all proceeds going towards the spoonbill foundation and the quest to get this treatment funded.

if you would like to donate to our raffle or help out with our event please call the shop 435.652.0870 or email contact@bybloomers.com

we loved having daron and his mom at our mommy and me - bloom city plant night

{flowers for minda}

our dear friend minda was diagnosed with alport's syndrome in 2007.  after a year of dialysis and waiting on the transplant list she found a living donor.  she will be undergoing the kidney transplant next week.  to show our support and help with her medical expenses we will give a free $50 arrangement to anyone who makes a donation of $50 of more from august 25 - august 29 {redeemable in 2014}  you can make your donation or find out more information at 

{help for a kindey} on gofundme.com