Our Dogs
We are proud to offer fully health tested Goldendoodles to family homes across the United States. Our adult dogs are health tested and kept in an indoor family environment- NOT in a kennel. Most of our dogs are raised in Guardian Homes, where they live out their lives as a family pet, only coming back to Red Spring Farm 3 times to have a litter of puppies. Visit our Goldendoodle Health Testing page, where we break down all of the important tests that the parents of your Goldendoodle pup should have prior to breeding. We are committed to producing high/ quality puppies and we back this up with our Health Guarantee. We have Upcoming Litters planned now!
Females:
Harper
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Harper is a Petite/Mini Multigenerational Australian Labradoodle. She is lean and lanky (legs for days) which puts her in the petite weight range and the mini height range. This girl was born gold with tuxedo-style white markings and lightened to her current cream color as she reached adulthood. Harper is such an intelligent, gentle soul who does well with other dogs but much prefers the company of a special human companion. We say that she has "people eyes" because she will look right at you when you are talking to her and seems to know exactly what you are saying. She has a silky-soft coat that is to die for!
General Information: DOB: 01/26/18 Breed/Mix: Multigenerational Australian Labradoodle Weight: 20 pounds (petite weight range) Height: 17 inches (mini height range) Color: Cream Abstract Coat: Wavy Fleece Coat Color/Coat: A Locus: at/at, B Locus: B/B, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: ky/ky, S Locus: S/sp, SD Locus: SD/sd |
OFA Testing:
Pennhip (09/18) Right DI: 0.30/Left DI: 0.36 OFA Hip Prelim (09/18): NORMAL (GOOD) OFA Elbows Prelim (09/18): NORMAL OFA Patellas Prelim (09/18): NORMAL OFA Cardiac Prelim/Ausc (09/18): NORMAL CERF (09/18, 02/20): NORMAL Genetic Testing: Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Daisy
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Daisy is a Mini Multigenerational Goldendoodle. She was born and raised here at Red Spring Farm, and is the daughter of Stella and Teddy (both now retired), and half sister to Lila, Lucy, and Layla. This gal is a goofy, happy sweetie pie. Daisy doesn't walk, she prances! She has a beautiful gait and moves with ease and grace, almost as if she is dancing. She is one of the larger dogs that we have here at approximately 30lbs, but she doesn't know her size. Just like her daddy, Teddy (now retired), this girl is an extreme CUDDLER! She wants nothing more than to share her love and give you hugs. She inherited a retriever smile and a curly poodle tail.
General Information: DOB: 04/06/18 Breed/Mix: Multigenerational Goldendoodle Weight: 30 pounds (mini weight range) Height: 18 inches (large mini height range) Color: Faded Red/Apricot Coat: Tight Curly Coat Color/Coat: A Locus: unknown, B Locus: B/b, Cu Locus: +/+, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: S/sp, SD Locus: SD/SD |
OFA Testing:
Pennhip (5/19): Right DI: 0.36/Left DI: 0.30 OFA Hip Prelim (5/19): NORMAL (GOOD) OFA Elbows Prelim (5/19): NORMAL OFA Patellas "Prelim" (5/19): NORMAL OFA Cardiac Ausculation (8/19): NORMAL CERF (05/18, 01/20): NORMAL Genetic Testing: Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Lucy
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Lucy is a Petite/Mini Multigenerational Goldendoodle. She was born and raised at Red Spring Farm, and is the daughter of our famous Luna and Teddy (both now retired), niece to Bella, full sister to Layla, and half sister to Lila and Daisy. She is lean and leggy, with the height of a mini but the weight of a petite. This funny girl is a trip! She is quirky in the best possible way... it is not unusual to find her sleeping with all four feet in the air and her head hanging off the couch. She definitely inherited the happy-go-lucky (and goofy) demeanor of a Golden Retriever, but in a much smaller package. She loves to "dig" in water and play with other dogs... but at the end of the day she wants to cuddle on the couch with you.
General Information: DOB: 06/15/18 Breed/Mix: Multigenerational Goldendoodle Weight: 20 pounds (petite weight range) Height: 16.5 inches (mini height range) Color: Faded Gold Abstract Coat: Wavy Fleece Coat Color/Coat: A Locus: unknown, B Locus: B/b, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: S/sp, SD Locus: unknown |
OFA Testing:
OFA Hip Prelim (9/19): NORMAL (GOOD) OFA Elbows Prelim (9/19): NORMAL OFA Patellas (9/19): NORMAL OFA Cardiac Ausculation (9/19): NORMAL CERF (08/19): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): CARRIER* *As long as Lucy is paired with a "NORMAL" mate, there is 0% chance of offspring being affected by this disease :) Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Layla
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Layla is a Petite/Mini Multigenerational Goldendoodle. She was born at Red Spring Farm and raised by her fabulous Guardian Family. She is the daughter of our famous Luna and Teddy (both now retired), niece to Bella, full sister to Lucy, and half sister to Daisy. She is lean and leggy, with the height of a mini but the weight of a petite. This girl is more serious than her sister, Lucy, but still enjoys a romp in the yard and playtime with the other 3 dogs in her home. She is a serious cuddler (just like her daddy) and is very attached to "her" people, especially her human guardian sister.
General Information:
DOB: 06/15/18 Breed/Mix: Multigenerational Goldendoodle Weight: 20 pounds (petite weight range) Height: 17 inches (mini height range) Color: Faded Gold Abstract Coat: Wavy Fleece Coat Color/Coat: A Locus: unknown, B Locus: B/b, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: S/sp, SD Locus: unknown |
OFA Testing:
OFA Hip Prelim (8/19): NORMAL (FAIR) OFA Elbows Prelim (8/19): NORMAL OFA Patellas (8/19): NORMAL OFA Cardiac Ausculation (8/19): NORMAL CERF (08/19): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): POTENTIAL CARRIER *As long as Layla is paired with a "NORMAL" mate, there is 0% chance of offspring being affected by this disease :) Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Ginger
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Ginger is a Petite Multigenerational "Double Doodle." She was born and raised here at Red Spring Farm, and is the daughter of our F1B Goldendoodle, Abby (now retired) and our Multigenerational Australian Labradoodle. Charlie. She is full sister to Rocky and Sadie, and half sister to Pippa. Ginger captures everyone's heart! She loves being held like a baby, and will stay there all day (she is known to close her eyes and start snoring after just a few minutes). She is one of the smallest dogs here at Red Spring Farm and she plays very well with everyone, she will stand on her hind legs and use her paws to swat at them (she will do the same thing to you when she wants to be picked up)! Don't think you like small dogs? Spend one day with Ginger, and she will change your mind! She is very intelligent and has the best traits of both large and small dogs packed into a teddy-bear package. Her coat, like all Charlie pups, is thick and fabulous.
General Information: DOB: 07/17/18 Breed/Mix: Double Doodle! (Goldendoodle x ALD Labradoodle) Weight: 10 pounds (petite weight range) Height: 13 inches (petite height range) Color: Red Caramel Coat: Wavy Fleece Coat Color/Coat: A Locus: unknown, B Locus: b/b, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: S/S, SD Locus: unknown |
OFA Testing:
OFA Hip Prelim (10/19): NORMAL (GOOD) OFA Elbows Prelim (10/19): NORMAL OFA Patellas Prelim (10/19): NORMAL OFA Cardiac Prelim/Ausc (10/19): NORMAL CERF (11/19): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Sadie
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Sadie is a Petite Multigenerational "Double Doodle." She was born and raised here at Red Spring Farm, and is the daughter of our F1B Goldendoodle, Abby (now retired) and our Multigenerational Australian Labradoodle. Charlie. She is full sister to Rocky and Ginger, and half sister to Pippa. Sadie is the right hand gal of Ginger, rarely leaving her side. Sadie is the "omega" of the pair (Ginger calls the shots) and is playful with every dog and puppy she meets. She loves kisses and cuddles and never meets a person who isn't a friend. She is a carbon copy of her mommy, Abby, and has a the most beautiful big brown eyes that will melt your soul when she looks up at you. She is extremely smart, and doesn't miss a beat when playing fetch (she knows when you hide the ball behind your back)!
General Information: DOB: 07/17/18 Breed/Mix: Double Doodle! (Goldendoodle x ALD Labradoodle) Weight: 11 pounds (petite weight range) Height: 13 inches (petite height range) Color: Red/Apricot Coat: Wavy Fleece Coat Color/Coat: A Locus: unknown, B Locus: B/b, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: S/S, SD Locus: unknown |
OFA Testing:
OFA Hip Prelim (10/19): NORMAL (GOOD) OFA Elbows Prelim (10/19): NORMAL OFA Patellas Prelim (10/19): NORMAL OFA Cardiac Auscultation (10/19): NORMAL CERF (11/19): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Pippa
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Pippa is a Petite Multigenerational "Double Doodle." She was born and raised here at Red Spring Farm, and is the daughter of our famous Bella (now retired) and our Multigenerational Australian Labradoodle, Charlie. She is half sister to Rocky, Ginger, and Sadie. Pippa's guardian home couldn't believe how quickly Pippa bonded with her! Pippa is a cuddle bug who wants nothing more than to spend time with her people. She has the most expressive, sweet face that her eyes show how much LOVE she has to give! She has a fantastic coat (her photos don't do her justice!) just like her parents.
General Information: DOB: 03/08/19 Breed/Mix: Double Doodle! (Goldendoodle x ALD Labradoodle) Weight: 10 pounds (petite weight range) Height: 13 inches (petite height range) Color: Apricot Parti Coat: Wavy Fleece Coat Color/Coat: A Locus: unknown, B Locus: B/b, Cu Locus: -/-, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: sp/sp, SD Locus: unknown |
OFA Testing:
OFA Hip Prelim (08/20): NORMAL (GOOD) OFA Elbows Prelim (08/20): NORMAL OFA Patellas Prelim (08/20): NORMAL OFA Cardiac Prelim/Ausc (08/20): NORMAL CERF (06/20): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Scout
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Scout is a Petite/Mini Multigenerational "Double Doodle." She is 3/4 Goldendoodle & 1/4 ALD Labradoodle. She was born and raised at Red Spring Farm, and is the daughter our Rocky and Lucy, granddaughter of our Luna, Teddy, Charlie, and Abby, niece to Layla, and full sister to Holly, Willow, and Maple. Scout is genetically a red/apricot parti (spotted) but has minimal red markings. This means that the white in her coat is a true pure white, not cream. Funny enough, we expect to only have red colored pups out of this girl if bred to Rudy or Ollie (her planned "boyfriends")! This sweet, pup inherited the best of both parents. She is cuddly as can be with a sweet, silly, quirky personality like her mommy! She is a happy-go-lucky girl that ADORES her guardian mommy.
General Information: DOB: 06/13/19 Breed/Mix: Double Doodle! (Goldendoodle x ALD Labradoodle) Weight: 20 pounds (petite weight range) Height: 16.5 inches (petite height range) Color: Apricot Parti Coat: Wavy Fleece Coat Color/Coat: A Locus: unknown, B Locus: B/?*, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: unknown, S Locus: sp/sp, SD Locus: not tested |
OFA Testing:
OFA Hip Prelim (06/20): NORMAL (GOOD) OFA Elbows Prelim (06/20): NORMAL OFA Patellas Prelim (06/20): NORMAL OFA Cardiac Prelim/Ausc (06/20): NORMAL CERF (01/20): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): POTENTIAL CARRIER* *As long as Scout is paired with a "NORMAL" mate, there is 0% chance of offspring being affected by this disease :) Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Bailey
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Description Coming:
General Information: DOB: 10/14/19 Breed/Mix: Goldendoodle Weight: 32 pounds (mini weight range) Height: 17 inches (mini height range) Color: Apricot Coat: Wavy Fleece Coat Color/Coat: A Locus: at/at, B Locus: B/B, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: KB/ky, S Locus: S/S, SD Locus: SD/sd |
OFA Testing:
OFA Hip Prelim (06/20): NORMAL (FAIR) OFA Elbows Prelim (06/20): NORMAL OFA Patellas Prelim (06/20): NORMAL OFA Cardiac Prelim/Ausc (06/20): NORMAL CERF (01/20): NORMAL Genetic Testing (by parentage): Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Males:
Rocky
Rocky is not available for outside stud service
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Rocky is a Mini Multigenerational "Double Doodle." He was born and raised here at Red Spring Farm, and is the son of our F1B Goldendoodle, Abby (now retired) and our Multigenerational Australian Labradoodle, Charlie. He is a full siblings of Sadie and Ginger, and half brother to Pippa. Rocky is SUCH a laid back, love bug! You would never know that he was an intact male, as he is very docile and submissive. He loves retrieving and carrying toys in his mouth (but is extremely gentle accepting toys and treats from your hands- he inherited the soft retriever mouth)! This sweet boy has eyes that will melt your heart and is a gentle soul whose favorite spot is snoozing under the kitchen table...but only after you give him a cuddle.
General Information: DOB: 07/17/18 Breed/Mix: Double Doodle! (Goldendoodle x ALD Labradoodle) Weight: 25 pounds (mini weight range) Height: 16.5 inches (mini height range) Color: Red/Apricot Abstract Coat: Wavy Fleece Coat Color/Coat: A Locus: ay/at, B Locus: B/b, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: KB/KB, S Locus: S/sp, SD Locus: SD/sd |
OFA Testing:
Pennhip DI R.33/L.32 OFA Hip Prelims (03/19): NORMAL (GOOD) OFA Elbows Prelim (03/19): NORMAL OFA Patellas "Prelim" (03/19): NORMAL OFA Cardiac (03/19): NORMAL (Cleared w/ Echo) CERF (03/19, 01/20) NORMAL Genetic Testing: Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Rudy
Rudy is not available for outside stud service
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Rudy is a Petite F1B Goldendoodle (with a Goldendoodle mother and a Poodle father)! We waited very patiently for him to be born... it was his mothers 3rd litter before she had this perfect boy! He was worth the wait, as this sweet fella has it all. He is the constant shadow of his Guardian Mom. It is rare to find a "stocky" small dog, but Rudy has a thick, square body that is SO huggable! His docile, easy-going personality is reminiscent of his Golden Retriever heritage, and his coat is silky soft and completely non-shedding. To top it off, Rudy's big brown puppy eyes are what truly makes him irresistible!
General Information: DOB: 08/01/18 Breed/Mix: F1B Goldendoodle Weight: 17 pounds (petite weight range) Height: 15 inches (petite height range) Color: Red/Apricot Coat: Wavy Fleece Coat Color/Coat: A Locus: at/at, B Locus: B/B, Cu Locus: +/-, E Locus: e/e, Furnishings: F/IC, K Locus: KB/ky, S Locus: S/S, SD Locus: sd/sd |
OFA Testing:
Pennhip DI R.37/L.37 OFA Hip Prelims (03/19): NORMAL (GOOD) OFA Elbows Prelim (03/19): NORMAL OFA Patellas "Prelim" (03/19): NORMAL OFA Cardiac Ausculation (03/19): NORMAL CERF (03/19, 01/20): NORMAL Genetic Testing: Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): CARRIER *As long as Rudy is paired with a "NORMAL" mate, there is 0% chance of offspring being affected by this disease :) Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Charlie
Charlie is not available for outside stud service
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Multigen Mini (ALD) Labradoodle
Faded Red Caramel with a Wavy/Fleece Coat Happy, Loving, Sweetheart Charlie is a very special boy because he was the first Multigenerational Australian Labradoodle that we added to our program, specifically to produce Double Doodle puppies (a cross between a Labradoodle and a Goldendoodle). We really lucked out, because he is the whole package and the perfect foundation dog for our Double Doodle program! His puppies are stunning and we have kept several back for our program, including his son, Rocky, and daughters Ginger, Sadie, and Pippa. Charlie's coat is extremely thick and soft, giving him the ultimate teddy bear appearance (which he consistently passes on to his offspring). Charlie is a laid back boy who is treasured by his Guardian Family. He gets along with everyone he meets, and it is hard to keep yourself from wanting to cuddle and pet him all day!
General Information: DOB: 09/03/17 Breed/Mix: ALD Labradoodle Weight: 25 pounds (mini weight range) Height: 16.5 inches (mini height range) Color: Caramel Coat: Straight Fleece Coat Color/Coat: A Locus: at/at, B Locus: b/b, Cu Locus: -/-, E Locus: e/e, Furnishings: F/F, K Locus: KB/KB, S Locus: S/sp, SD Locus: sd/sd |
OFA Testing:
Pennhip DI 32/.21 OFA Hip Prelims (05/18): NORMAL (EXCELLENT) OFA Elbows Prelim (05/18): NORMAL OFA Patellas Prelim (05/18): NORMAL OFA Cardiac Final (09/18): NORMAL (Cleared w/ Echo) CERF (09/18, 01/20): NORMAL Genetic Testing: Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Boone
Boone is not available for outside stud service
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Boone is a petite Multigenerational Goldendoodle. This goofy little guy is the life of the party! He may be small, but that doesn't stop him from doing everything that the big dogs do. Boone is a master of fetch, and his Guardian Dad goes running and hiking on a regular basis... Boone has no problem keeping up thanks to his long legs! Luckily, he is just as happy crashing on the couch or under the bed (that is his sleeping spot), as long as he is with his "Dad"! Boone rarely needs to use a leash, because he is a loyal pooch who follows his Dad everywhere. This boy is a cuddler and he isn't picky- no one is a stranger and he is happy to be cradled and cuddled by all. His coat is thick and very straight with little wave, which is hard to produce in doodles this small. We look forward to Boone babies in 2020!
General Information: DOB: 06/01/18 Breed/Mix: Multigenerational Goldendoodle Weight: 12 pounds (petite weight range) Height: 14.5 inches (petite weight range) Color: Faded Gold Coat: Wavy Fleece Coat Color/Coat: A Locus: at/at, B Locus: B/B, Cu Locus: +/-, E Locus: e/e, Furnishings: F/F, K Locus: KB/ky S Locus: S/sp, SD Locus: SD/sd |
OFA Testing:
Pennhip DI R.45/L.43 OFA Hip Prelims (03/19): NORMAL (EXCELLENT) OFA Elbows Prelim (03/19): NORMAL OFA Patellas ("prelim") (03/19): NORMAL OFA Cardiac Ausculation ("prelim") (03/19): NORMAL CERF (03/19, 01/20): NORMAL Genetic Testing: Centronuclear Myopathy: NORMAL Congenital Myasthenic Syndrome (Labrador Type): NORMAL Cystinuria (Labrador Type): NORMAL Degenerative Myelopathy (DM): NORMAL Dystrophic Epidermolysis Bullosa (DEB): NORMAL Elliptocytosis: NORMAL Exercise-Induced Collapse (EIC): NORMAL Familial Nephropathy (Cocker Type): NORMAL GM2 Gangliosidosis: NORMAL Glycogen Storage Disease VII (PFK Deficiency): NORMAL Hereditary Nasal Parakeratosis (HNPK): NORMAL Hyperuricosuria (HUU): NORMAL Ichthyosis (ICH): NORMAL Muscular Dystrophy (Golden Retriever Type): NORMAL Myotubular Myopathy Type 1 (MTM1): NORMAL Narcolepsy (Labrador Type): NORMAL Neonatal Encephalopathy with Seizures (NEWS): NORMAL Osteochondrodysplasia/Skeletal Dwarfism: NORMAL Osteogenesis imperfecta (OI): NORMAL Progressive Rod-Cone Degeneration (PRCD): NORMAL Progressive Rod-Cone Degeneration Type 4 (PRCD4): NORMAL Progressive Retinal Atrophy Type 1 (GR-PRA1): NORMAL Progressive Retinal Atrophy Type 2 (GR-PRA2): NORMAL Pyruvate Kinase Deficiency (Labrador Type): NORMAL Retinal Dysplasia/Oculoskeletal Dysplasia Type 1: NORMAL Sensory Ataxic Neuropathy (SAN): NORMAL Skeletal Dysplasia 2 (Dwarfism): NORMAL Von Willebrand Disease Type 1 (VWD I): NORMAL |
Upcoming Parents:
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More Pictures Coming Soon
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Addie - Upcoming Mom
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Holly - Upcoming Mom
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Maple - Upcoming Mom
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Oliver - Upcoming Dad
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