MEET THE PARENTS

Bonnie McGee Broussard

Bonnie McGee Broussard came to us from Indiana and immediately stole our hearts! Very outgoing and silly, she always wants to be by your side, no matter what you're doing. A hunter, explorer, always looking for something, determined little lady. And when its time to settle down, she's never met a bed or a lap that she has not liked! She has the stare of a soft heart framed in a feminine face that will draw you toward her immediatly.

Genetic Information

Name: Bonnie McGee Broussard

Breeders: Sunshine Acres

Sire & Dam: Cameo & Luna

Breed: Poodle

Phenotype: Apricot

Sex: Female

Birth: 10/21/2024

Weight: 20 Pounds

CDDY - N/C - At Risk: Dog has one copy of the CDDY mutation. Dog is at risk for IVDD and may pass the mutation to offspring.
CDPA - N/N - Clear: Dog is negative for the CDPA mutation.
DM - n/n - Clear: Dog is negative for mutation associated with Degenerative Myelopathy.
NEwS - n/n - Clear: Dog is negative for mutation associated with NEwS.
PRA-prcd - n/n - Negative: Dog is negative for the mutation associated with prcd-PRA.
vWD1 - n/n - Clear: Dog is negative for the mutation associated with von Willebrand's Disease Type I

CAMEO (Sire)

Moyen Poodle

COLOR: Red

WEIGHT: 24 Pounds

HEIGHT: 18 inches @ shoulder

OFA (HIPS): Excellent

OFA (Elbows): Negative

ADVANCED CARDIAC EXAM: Normal

NEONATAL ENCEPHALOPATHY W/ SIEZURES (NEwS): Clear (Negative)

VON WILLEBRAND (vWD1): Clear (Negative)

DEGENERATIVE MYELOPATHY: Clear (Negative)

PROGRESSIVE RETINAL ATROPHY (prcd-PRA): Clear (Negative)

LUNA (Dam)

Moyen Poodle

COLOR: Apricot

WEIGHT: 22 Pounds

HEIGHT: 15 Inches @ shoulders

OFA (HIPS): Excellent

OFA (ELBOWS): Clear

OFA (Eye – CAER): Certified Free

ADVANCED CARDIAC EXAM: Normal

DEGENERATIVE MYELOPATHY: Normal (Clear).

OSTEOGENESIS IMPERFECTA: Normal (Clear)

VON WILLEBRAND’S DISEASE: Normal (Clear)

PROGRESSIVE RETINAL ATROPHY, PROGRESSIVE ROD-CONE DEGENERATION: Normal (Clear)

NEONATAL ENCEPHALOPATHY W/ SEIZURES (NEwS): Clear (Negative)

Clyde G McPhatter Broussard

Named after Scott's great uncle and World War ll veteran and one of Scott's favorite 1950s music artists - was originally from the sunshine state of Florida, but fit right into our Louisiana family. He is the more reserved of the two, but oh my goodness, he is one of the most cuddly, affectionate dogs we've ever owned! With his slightly thicker build and dark red coat, he is physically stunning and crazy athletic!

Genetic Information

Name: Clyde G McPhatter Broussard

Breeder: Pineapple Poodles

Sire & Dam: Chili & Hazil

Breed: Poodle

Phenotype: Red

Sex: Male

Birth: 11/26/2024

Weight: 18 Pounds

CDDY - N/C - At Risk: Dog has one copy of the CDDY mutation. Dog is at risk for IVDD and may pass the mutation to offspring.
CDPA - N/N - Clear: Dog is negative for the CDPA mutation.
DM - n/n - Clear: Dog is negative for mutation associated with Degenerative Myelopathy.
NEwS - n/n - Clear: Dog is negative for mutation associated with NEwS.
PRA-prcd - n/n - Negative: Dog is negative for the mutation associated with prcd-PRA.
vWD1 - n/n - Clear: Dog is negative for the mutation associated with von Willebrand's Disease Type I

CHILI (Sire)

Minature Poodle

Color: Red
Weight: 12 Pounds
Hip Dysplasia Finals (OFA, Penn HIP, BVA, SV, FCI) Results: normal (clear)
Elbow Dysplasia Finals (OFA, BVA, SV, FCI)
Results: normal (clear)
PawPrint Genetic Panel (Breed Specific)
Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD)
Degenerative Myelopathy
Osteochondrodysplasia
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
Progressive Retinal Atrophy, Rod-Cone Dysplasia
ALL Normal (clear)

HAZIL (Dam)

Moyen Poodle

Color: Red
Weight: 29 Pounds
Hip Dysplasia Finals (OFA, Penn HIP, BVA, SV, FCI) Results: normal (clear)
PawPrint Genetic Panel (Breed Specific):
Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD)
Results: 2 variants
Degenerative Myelopathy
Osteochondrodysplasia
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
Von Willebrand Disease Type 1, Type 1 vWD
GM2 Gangliosidosis
Results: normal (clear)
Patellar Luxation:
Results: normal (clear)
Cardia Evaluation (registered with OFA)
Results: normal (clear)