Learn more about us

 Golden Beauties. . . Driven to Doodles, LLC was officially founded in 2009. We began Obtaining breeding stock in 2005 and actually began Breeding in 2007.  

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About Us

goldendoodle cream colored, adult medium goldendoodle

Exquisite Goldendoodle, Labradoodle & Golden Breeder

Stacy Lynn Parks Fleming, M.S., CBCC-KA, CBST is the President & Breeder of Golden Beauties Driven to Doodles, LLC (www.goodlepups.com).

Stacy obtained credentials from Animal Behavior College in 2002 [ABCDT], attended the APDT's 5 day conference in 2003, Stacy has written several excerpts 
and articles for dog behavior magazines over the years, including the APDT's Top Tips From Top Trainers book. Stacy has a B.S. in Psychology and has 
a Diploma from Companion Animal Sciences Institute; Dip. CBST (Canine Behavior Science and Technology).
Stacy holds a Master's of Science [M.S.] in Psychology, a Bachelor's in Science [B.S.] in Psychology, has successfully passed the CCPDT’s Certified Canine Behavior Consultant exam. Stacy has been a trainer since 2002, a behavior consultant since 2004 years and a breeder since 2007. Stacy is educated through courses as well as plenty of hands on experience in canine behavior modification, veterinary assisting and canine breeding as well as human and animal psychology. 


goldendoodle puppies, goldendoodles, doodle puppies

Excellent Therapy DoGs!

 Many of our dogs have been homed with families as therapy dogs for Autism and physical disabilities. Goldendoodles have been shown to  be a very loyal and obedient which is why they do well in homes requiring a therapy dog. Both poodles and Golden Retrievers have been  successfully utilized in the past as therapy dogs.   

F1 medium goldendoodle shaved, goldendoodle

We are the breeder you have been seeking!

A Good breeder is going to have you sign a contract to spay/neuter your pet; a great breeder is going to offer a guarantee; an excellent breeder with great faith in their breeding stock is going to offer a 4 year health guarantee as we do!

We health test our dogs, we select the best mate for our girls and we select our breeding stock as puppies and raise them to our high standards! As 
you can clearly see here at Golden Beauties Driven to Doodles we truly care about our dogs and puppies and want to provide you with the best possible 
pet for your family!

We are licensed and inspected by NYS; PD # 638
We are a preferred breeder with the CKC (Continental Kennel Club) and a member of the exclusive Goldendoodles.com owner recommended breeder list!

Goldendoodles.com owner recommended breeder; premium breeder with goldendoodle-labradoodle.org

What is a Goldendoodle?

A Goldendoodle is much like a Golden Retriever but does not shed like a Golden Retriever and can be bred to be smaller than a Golden Retriever. 
They are also much smarter than an average dog because they are a combination of two very intelligent breeds! Goldendoodles coat colors can range from Jet Black to White! Health and longevity are excellent when the perfect breeding stock are chosen as we do here at Golden Beauties Driven to Doodles!

What Happens while your puppy is with us?

Microchip

Stacy administers a Microchip in the withers area when your puppy is between 2 and 3 weeks of age. This is proof of ownership and excellent to bring your dog home if ever lost! 

Vaccinations!

@ 6 weeks Stacy administers the core vaccine covering Distemper, Adenovirus, Parvo & Parainfluenza and a second series at 8 weeks prior to going home; IF your puppy is in our custody longer we will administer the next core vaccines.

Other added vaccines are available upon request and for a small fee.

DE-Worming

Stacy Deworms puppies starting at 3 weeks of age, using Pyrantel Pamoate, cocciguard, Safeguard & occasionally sulfadimethoxine.


Exclusive Vitamins and Food puppies for sale

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Health Testing

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ALL of our dogs are tested for all of the below PLUS more

   

We Health Test for ALL of the below Plus More!

We test for over 160 known genetic health conditions in 16 different areas, per displayed below:

Clinical

MDR1 Drug Sensitivity (MDR1)Alanine Aminotransferase Activity (GPT)

Blood

P2Y12 Receptor Platelet Disorder (P2RY12)Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)Factor VII Deficiency (F7 Exon 5)Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)Thrombopathia (RASGRP2 Exon 8)Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)Von Willebrand Disease Type II (VWF Exon 28)Von Willebrand Disease Type III (VWF Exon 4)Von Willebrand Disease Type I (VWF)Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3)Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)Canine Elliptocytosis (SPTB Exon 30)Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20)Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)May-Hegglin Anomaly (MYH9)Prekallikrein Deficiency (KLKB1 Exon 8)Pyruvate Kinase Deficiency (PKLR Exon 5)Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)Pyruvate Kinase Deficiency (PKLR Exon 10)Trapped Neutrophil Syndrome (VPS13B)Ligneous Membranitis (PLG)

Immune

Complement 3 (C3) deficiency (C3)Severe Combined Immunodeficiency (PRKDC)Severe Combined Immunodeficiency (RAG1)X-linked Severe Combined Immunodeficiency(IL2RG Variant 1)X-linked Severe Combined Immunodeficiency(IL2RG Variant 2)

Hormones

Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)

Eyes

Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A)Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9)Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1)Progressive Retinal Atrophy (CNGB1)Progressive Retinal Atrophy (SAG)Golden Retriever Progressive Retinal Atrophy 1(SLC4A3)Golden Retriever Progressive Retinal Atrophy 2(TTC8)Progressive Retinal Atrophy - crd1 (PDE6B)Progressive Retinal Atrophy - crd2 (IQCB1)Progressive Retinal Atrophy - crd4/cord1(RPGRIP1)Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1)Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)Autosomal Dominant Progressive Retinal Atrophy(RHO)Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11)Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2)Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant)Primary Lens Luxation (ADAMTS17)Congenital stationary night blindness (RPE65)Macular Corneal Dystrophy (MCD) (CHST6)

Multisystem

Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC)Primary Ciliary Dyskinesia (CCDC39 Exon 3)Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5)X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8)Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)Canine Fucosidosis (FUCA1)Glycogen Storage Disease Type II, Pompe's Disease (GAA)Glycogen Storage Disease Type IIIa (GSD IIIa)(AGL)Mucopolysaccharidosis Type I (IDUA)Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)Mucopolysaccharidosis Type VII, Sly Syndrome(GUSB Exon 5)Mucopolysaccharidosis Type VII, Sly Syndrome(GUSB Exon 3)Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Whippet and English Springer Spaniel Variant)Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant)Lagotto Storage Disease (ATG4D)Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8)Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4)Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2)Neuronal Ceroid Lipofuscinosis 1 (CLN5 Border Collie Variant)Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7)Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2)Neuronal Ceroid Lipofuscinosis (MFSD8)Neuronal Ceroid Lipofuscinosis (CLN8)Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)Adult-Onset Neuronal Ceroid Lipofuscinosis(ATP13A2)GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)GM1 Gangliosidosis (GLB1 Exon 2)GM2 Gangliosidosis (HEXB, Poodle Variant)GM2 Gangliosidosis (HEXA)Globoid Cell Leukodystrophy, Krabbe disease(GALC Exon 5)

Kidney and Bladder

2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis(APRT)Cystinuria Type I-A (SLC3A1)Cystinuria Type II-A (SLC3A1)Cystinuria Type I-A (SLC7A9)Hyperuricosuria and Hyperuricemia or Urolithiasis(SLC2A9)Polycystic Kidney Disease (PKD1)Primary Hyperoxaluria (AGXT)Protein Losing Nephropathy (NPHS1)X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35)Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3)

Other Systems

Autosomal Recessive Amelogenesis Imperfecta(Italian Greyhound Variant)Persistent Mullerian Duct Syndrome (AMHR2)Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS)Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP)

Brain and Spinal Cord

Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)Alexander Disease (GFAP)Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)Cerebellar Hypoplasia (VLDLR)Spinocerebellar Ataxia, Late-Onset Ataxia(CAPN1)Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)Degenerative Myelopathy (SOD1A)Fetal-Onset Neonatal Neuroaxonal Dystrophy(MFN2)Hypomyelination and Tremors (FNIP2)Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)L-2-Hydroxyglutaricaciduria (L2HGDH)Neonatal Encephalopathy with Seizures (NEWS)(ATF2)Polyneuropathy, NDRG1 Greyhound Variant(NDRG1 Exon 15)Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4)Narcolepsy (HCRTR2 Intron 6)Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)Juvenile Laryngeal Paralysis and Polyneuropathy(RAB3GAP1)Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10)Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2)

Heart

Dilated Cardiomyopathy (PDK4)Long QT Syndrome (KCNQ1)

Muscular

Muscular Dystrophy Cavalier King Charles Spaniel Variant 1Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)Centronuclear Myopathy (PTPLA)Exercise-Induced Collapse (DNM1)Inherited Myopathy of Great Danes (BIN1)Myostatin Deficiency, Bully Whippet Syndrome(MSTN)Myotonia Congenita (CLCN1 Exon 7)Myotonia Congenita (CLCN1 Exon 23)Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)

Metabolic

Hypocatalasia, Acatalasemia (CAT)Pyruvate Dehydrogenase Deficiency (PDP1)Malignant Hyperthermia (RYR1)

Gastro-intestinal

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)

Neuro-muscular

Congenital Myasthenic Syndrome (CHAT)Congenital Myasthenic Syndrome (COLQ)Episodic Falling Syndrome (BCAN)

Skin & Connective Tissues

Dystrophic Epidermolysis Bullosa (COL7A1)Ectodermal Dysplasia, Skin Fragility Syndrome(PKP1)Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)Ichthyosis (PNPLA1)Ichthyosis (SLC27A4)Ichthyosis (NIPAL4)Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)Hereditary Footpad Hyperkeratosis (FAM83G)Hereditary Nasal Parakeratosis (SUV39H2)Musladin-Lueke Syndrome (ADAMTSL2)

Skeletal

Cleft Lip and/or Cleft Palate (ADAMTS20)Hereditary Vitamin D-Resistant Rickets (VDR)Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever)Osteogenesis Imperfecta, Brittle Bone Disease(COL1A2)Osteogenesis Imperfecta, Brittle Bone Disease(SERPINH1)Osteogenesis Imperfecta, Brittle Bone Disease(COL1A1)Osteochondrodysplasia, Skeletal Dwarfism(SLC13A1)Skeletal Dysplasia 2 (COL11A2)Craniomandibular Osteopathy (CMO) (SLC37A2) 


Certifications and Credentials

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