Name: Rudy
Size: 17 Pounds/15" Tall
Hips: Normal
Elbows: Normal
Cardiac: Normal
Eyes: Normal CAER
Genetic: Completed/CBP
Lives With Guardian Pawrents:
Rachel & Brad!
Size: 17 Pounds/15" Tall
Hips: Normal
Elbows: Normal
Cardiac: Normal
Eyes: Normal CAER
Genetic: Completed/CBP
Lives With Guardian Pawrents:
Rachel & Brad!
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 3-4 times to have a litter of puppies. Visit our 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:
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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Bailey is a Multigenerational Mini Goldendoodle. She was born and raised at Red Spring Farm, and is the daughter of Rudy and Daisy, granddaughter of our Stella and Teddy, and niece to Addie. Bailey's guardian family are first time dog owners and can't imagine their life without their sweet, goofy girl! Bailey is a big-boned girl who is "stocky and block" like a little retriever, which makes her extra huggable. She is a pretty laid back pup. She likes to go on walks and romps around the yard, but settles down quickly after and is ready for some couch potato time with her family. Like most doodles, Bailey is very attached and loyal to her family. Bailey absolutely LOVES belly rubs!
General Information: DOB: 10/14/19 Breed/Mix: Goldendoodle Weight: 30 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 |
Addie
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Addie is one of our home-grown petite sized Double Doodle girls (3/4 Goldendoodle and 1/4 ALD Labradoodle). She was born and raised at Red Spring Farm, and is the daughter of Rocky and Stella, half sister of Daisy and Bailey's aunt. Addie's joined her guardian family when she was a few months old, and even though she had not previously lived with children and toddlers, she fit right in and has a special bond with the youngest members of the household. She has never met a stranger, and greets everyone with a wagging tail- she is always a hit at the vet's office! Addie is quite the snuggle bug and loves nothing more than spending quality time cozied up with her guardian family on the couch!
General Information: DOB: 8/23/19 Breed/Mix: Double Doodle! (Goldendoodle x ALD Labradoodle) Weight: 15 pounds (petite weight range) Height: 14.5 inches (petite height range) Color: Apricot Coat: Curly Coat Color/Coat: A Locus: --/--, B Locus: B/?, Cu Locus: +/+, E Locus: e/e, Furnishings: F/F, K Locus: --/--, S Locus: S/S, SD Locus: --/-- |
OFA Testing:
OFA Hip Prelim: NORMAL (FAIR) OFA Elbows Prelim: NORMAL OFA Patellas Prelim: NORMAL OFA Cardiac Echo: NORMAL CERF: 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:
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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Holly - Upcoming Mom
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Maple - Upcoming Mom
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Oliver - Upcoming Dad
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