Read's Blow Me Away Windy Sky

WALA No: WALA00040145

Lacey is just like her mom (Hope) and grandfather (Sur) she is... personality, personality, personality! She is a beautiful parchment and white tuxedo mini with a great wavy fleece coat. She was Windy out of our amazing Hope and Nova, out of our "Sky Litter". She is bubbly, outgoing and adores everyone...especially children. She loves water, lounging on the couch, going on car rides and just can not resist a game of fetch! She reminds me so much of her grandpa "Sur" who is now retired and service as a Service Dog to a young man who needed him so much. She is athletic and has amazing agility, yet knows when to calm down and relax. She is such a cuddle bug. She has such a strong desire to please and is super smart. She has such a sweet, laid back, loving and gentle demeanor. Lacey's first litter will be sired by our amazing Jay and will be this summer. We just can't wait! I know she will be such an amazing mama like her mom, sisters and grandma were!

  • Sire: Barksdale Nova Scotia  - Nova ALCA Registration No: 278-02132018-005-D,  ALAA Registration: ALAA-067085 & WALA: WALA00010702

  • Dam: Read's A Lil Bit of Hope - Hope  ALCA Registration No: 278-10072017-002-LB1 & WALA: WALA00010700

  • DNA PROFILE: Completed On file with PAWPRINT Genetics

  • Color: Parchment & White Tuxedo 

  • Coat type: Silky Wavy Fleece

  • Size: Large Mini, 21 LBS

  • OFA Hips: Good

  • OFA Elbows: Negative for dysplasia R and L

  • OFA Patellar: Normal

  • OFA Eye: Normal L&R

  • OFA HEART: Normal

  • Centronuclear Myopathy : Normal 

  • Cystinuria: Normal 

  • Degenerative Myelopathy: Normal 

  • Exercise-Induced Collapse: Normal (carrier) 

  • Familial Nephropathy: Normal 

  • Glycogen Storage Disease VII, PFK Deficiency: Normal

  • Hereditary Nasal Parakeratosis: Normal 

  • Myotubular Myopathy 1: Normal  

  • Narcolepsy: Normal

  • Neonatal Encephalopathy with Seizures: Normal 

  • Progressive Retinal Atrophy, Cone-Rod Dystrophy 4: Normal 

  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration: Normal 

  • Retinal Dysplasia/Oculoskeletal Dysplasia 1: Normal 

  • Skeletal Dysplasia 2: Normal 

  • Von Willebrand Disease 1: Normal 

  • IC Locus: CLEAR (not a carrier)