
CALL/TEXT US: 828-748-1250

(NO PUPPIES ARE SOLD BREEDING RIGHTS. SPAY/NEUTER ONLY)
Dads
Mitchell: ALAA-078272
Multi-Gen Mini Australian Labradoodle- 30lbs
DOB: 12/2/18
(Matilda X George)
Lives in a guardian home with the Lewis'
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- Cddy (1 copy) Cdpa (Clear)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated GOOD
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: Ff
Shed: sd/SD
Curl: +/-
KLocus: Kb/Kb
ALocus: At/At
BLocus: bb
ELocus: ee 9/10 intensity
DLocus: DD
SLocus: N/S

Hank: ALAA-086039
Multi-Gen Mini Australian Labradoodle- 28lbs
DOB: 11/27/19
(Loretta X Mitchell)
Lives in a guardian home with the Martin's
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- Cddy (2 copies) Cdpa (Clear)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated EXCELLENT
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/sd
Curl: +/-
KLocus: Kb/Kb
ALocus: At/A
BLocus: bb
ELocus: ee 7/10 intensity
DLocus: DD
SLocus: N/N

Cedar: ALAA-089006
Multi-Gen Medium Australian Labradoodle- 36lbs
DOB: 7/11/19
(Trinity X Dundee)
Lives in a guardian home with the Pritchard's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated EXCELLENT
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/SD
Curl: +/-
KLocus: Kb/Kb
ALocus: Ay/A
BLocus: bb
ELocus: Ee 5/10 intensity
DLocus: DD
SLocus: N/S

Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- Cddy (1 copy) Cdpa (Clear)
Waylon
Multi-Gen Petite-Mini Australian Labradoodle- 19lbs
DOB: 12/2/19
(Willow X River)
Lives in a guardian home with the Ayers
Genetic Disease Testing:
Embark
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- Cddy (2 copies) Cdpa (Clear)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated GOOD
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/sd
Curl: +/-
KLocus: Kb/Ky
ALocus: At/At
BLocus: bb
ELocus: Ee 4/10 intensity
DLocus: DD
SLocus: S/S

Pickles- AKC
AKC Toy Poodle- 10lbs
DOB: 5/14/19
(Bella X Toby)
Lives in a guardian home with the Nichols
Genetic Disease Testing:
-Embark
-Animal Genetics
-Pawprints
Degenerative Myelopathy: CLEAR
GM2 Gangliosidosis (Poodle Type): CLEAR
Neonatal Encephalopathy with Seizures: CLEAR
Osteochondrodysplasia: CLEAR
Progressive Retinal Atrophy, PRCD: CARRIER
Von Willebrand Disease I: CLEAR
Multiple Drug Sensitivity (MDR1): CARRIER
IVDD: Clear (Animal Genetics)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated EXCELLENT
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/sd
Curl: +/+
KLocus: Ky/Ky
ALocus: At/At
BLocus: Bb
ELocus: Eme 9/10 intensity
DLocus: DD
SLocus: N/N

Moms
Maya: ALAA-087885
Multi-Gen Mini Australian Labradoodle- 24lbs
DOB: 2/25/20
( X )
Lives in a guardian home with the McGraw's
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD: Clear (Animal Genetics)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated EXCELLENT
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/SD
Curl: -/-
KLocus: Ky/Ky
ALocus: At/At
BLocus: bb
ELocus: Ee 5/10 intensity
DLocus: DD
SLocus: N/S

Heat Cycles
1. 12/30/21
2. Skipped 9/2/2022
3. EST March '23
Emma
AKC Poodle
DOB: 4/7/20
(Ruby X Gunner)
Lives in a guardian home with the Nelon's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated FAIR
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: SD/SD
Curl: +/-
KLocus: Kb/Kb
ALocus: At/A
BLocus: Bb
ELocus: ee 10/10 intensity
DLocus: DD
SLocus: S/Sp
Genetic Disease Testing:
-Embark
-Animal Genetics
​
Degenerative Myelopathy: CLEAR
GM2 Gangliosidosis (Poodle Type): CLEAR
Neonatal Encephalopathy with Seizures: CLEAR
Osteochondrodysplasia: CLEAR
Progressive Retinal Atrophy, PRCD: CLEAR
Von Willebrand Disease I: CLEAR
Multiple Drug Sensitivity (MDR1): CLEAR
IVDD: Clear (Animal Genetics)

Coco
Mini Australian Labradoodle
DOB: 7/21/22
(Emma X Mitchell)
Lives in a guardian home with the Moore's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated GOOD (Dr Wallace)
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: PENDING
Thyroid: PENDING
​
Coat Testing
Furnishings: Ff
Shed: sd/sd
Curl: -/-
KLocus: Kb/Kb
ALocus: At/A
BLocus: bb
ELocus: ee 9/10 intensity
DLocus: DD
SLocus: N/N
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD: PENDING (Animal Genetics)
