We currently have two open chocolate male puppies at this time.
Please, see future litter page for upcoming litters.
Updated: 10/13/2019
Babe and Moe had a litter on 8/6/2019
The following are open puppies in the litter.
Chocolate male second pick
Chocolate male third pick
Puppies in this litter are $1800.00 Limited AKC ask about Full AKC
Deposit of $300.00 is required to reserve a puppy.
Balance of $1500 is due before the puppy is released to go home.
Contact Wendy Mabry at mabrywendy@gmail.com or call/text 618-521-5719
You can place a deposit to hold on of the chocolate males by using this link.
These pups are guaranteed to not be affected by the following:
Coagulation factor VII deficiencyElliptocytosis
Leukocyte adhesion deficiency, type III
May-Hegglin anomaly
P2RY12 receptor platelet disorder
Prekallikrein deficiency
Pyruvate kinase deficiency
Von Willebrand disease
Renal cystadenocarcinoma and nodular dermatofibrosis
Amelogenesis imperfecta
Multidrug resistance 1
Cone degeneration
Congenital stationary night blindness
Dry eye curly coat syndrome
Early retinal degeneration
Hereditary cataracts
Juvenile Laryngeal Paralysis and Polyneuropathy
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Primary lens luxation
Primary open angle glaucoma
Progressive retinal atrophy, Cone-rod dystrophy
Progressive retinal atrophy
Progressive rod-cone degeneration
Progressive retinal atrophy Rod-cone dysplasia 3
Progressive retinal atrophy, generalized
Complement 3 deficiency
Primary ciliary dyskinesia
Trapped neutrophil syndrome
Gallbladder mucoceles
Glycogen storage disease IIIa
Adult-onset neuronal ceroid lipofuscinosis
Glycogen storage disease IIIa
Glycogen storage disease Ia
Glycogen storage disease VII
Mucopolysaccharidosis I
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Pompe disease
Pyruvate dehydrogenase deficiency
Pyruvate kinase deficiency
Juvenile Laryngeal Paralysis and Polyneuropathy
Adult-onset neuronal ceroid lipofuscinosis
Congenital myasthenic syndrome
Degenerative myelopathy
Exercise-induced collapse
Glycogen storage disease IIIa
Juvenile Laryngeal Paralysis and Polyneuropathy
Mucopolysaccharidosis I
Musladin-Lueke syndrome
Myotubular myopathy 1
Osteochondrodysplasia
Pompe disease
Skeletal dysplasia 2
Adult-onset neuronal ceroid lipofuscinosis
Benign familial juvenile epilepsy
Congenital myasthenic syndrome
Degenerative myelopathy
Episodic falling syndrome
Exercise-induced collapse
Juvenile Laryngeal Paralysis and Polyneuropathy
Late onset ataxia
Mucopolysaccharidosis I
Musladin-Lueke syndrome
Narcolepsy
Neonatal cerebellar cortical degeneration
Neonatal encephalopathy with seizures
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Sensory ataxic neuropathy
Spinocerebellar ataxia
Startle disease
Primary ciliary dyskinesia
Primary ciliary dyskinesia
Anhidrotic ectodermal dysplasia
Dry eye curly coat syndrome
Dystrophic epidermolysis bullosa
Ectodermal dysplasia
Epidermolytic hyperkeratosis
Hereditary nasal parakeratosis
Renal cystadenocarcinoma and nodular dermatofibrosis
Fanconi syndrome
Hyperuricosuria
Persistent Müllerian duct syndrome
Primary ciliary dyskinesia
Primary hyperoxaluria
Renal cystadenocarcinoma and nodular dermatofibrosis
Puppies come with the following:
AKC papers
Vaccinations, we give vaccines weeks, 4, 6 and 8.
De-wormed from day three until they leave. 11 intestinal worms (including roundworm, whipworm, hookworm, tapeworm and hydatid tapeworm)
Given prevention medication for Giardia and Coccdia
Pet insurance for 30 days included for free, pays out 90% of bill with a $250 deductible starting the moment you leave with your puppy. This is a new insurance beginning January 2019.
One year congenital guarantee
36-month guarantee
EIC, CNM,PRA, PKD, DM, HU, DILUTE, RD/OSD, AND HNPK unaffected
Socialized
Access to water for swimming when weather allows.
Microchip with no fee
Puppy food, collar, blanket, reusable tote, microchip, shampoo, leash, treats, toys, puppy information packet
Basic commands started such as sitting to wait on food and treats.
City sounds, fireworks sounds and thunderstorm sounds are started from two weeks old.
Introduced to other animals and people.
Puppy culture from day one
Housebreaking started prior to leaving.
We are here to answer any questions before and after the sale of the puppy for life of the puppy. Pedigrees of parents will be provided.
All AKC registration papers will be handed over at the time of puppy pick up.
Thank you for looking at our website and we hope to see you soon for your next labrador puppy. We can guarantee that in Illinois we do the most work for our adults and puppies. No other breeder comes close to do all this. We have some attempting to copy us, but if you go to their kennel you will see not one is a real kennel like ours. Garages, basements, living rooms, bedrooms are not a real kennel and those breeders that have bred more than five years with multiple litters should invest the money into a kennel to house their adults better than dog houses or back rooms! lab puppy, lab puppies for sale, akc lab puppies for sale.
THREE YEAR HIP GUARANTEE AND A ONE YEAR CONGENITAL HEALTH GUARANTEE!
Coagulation factor VII deficiencyElliptocytosis
Leukocyte adhesion deficiency, type III
May-Hegglin anomaly
P2RY12 receptor platelet disorder
Prekallikrein deficiency
Pyruvate kinase deficiency
Von Willebrand disease
Renal cystadenocarcinoma and nodular dermatofibrosis
Amelogenesis imperfecta
Multidrug resistance 1
Cone degeneration
Congenital stationary night blindness
Dry eye curly coat syndrome
Early retinal degeneration
Hereditary cataracts
Juvenile Laryngeal Paralysis and Polyneuropathy
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Primary lens luxation
Primary open angle glaucoma
Progressive retinal atrophy, Cone-rod dystrophy
Progressive retinal atrophy
Progressive rod-cone degeneration
Progressive retinal atrophy Rod-cone dysplasia 3
Progressive retinal atrophy, generalized
Complement 3 deficiency
Primary ciliary dyskinesia
Trapped neutrophil syndrome
Gallbladder mucoceles
Glycogen storage disease IIIa
Adult-onset neuronal ceroid lipofuscinosis
Glycogen storage disease IIIa
Glycogen storage disease Ia
Glycogen storage disease VII
Mucopolysaccharidosis I
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Pompe disease
Pyruvate dehydrogenase deficiency
Pyruvate kinase deficiency
Juvenile Laryngeal Paralysis and Polyneuropathy
Adult-onset neuronal ceroid lipofuscinosis
Congenital myasthenic syndrome
Degenerative myelopathy
Exercise-induced collapse
Glycogen storage disease IIIa
Juvenile Laryngeal Paralysis and Polyneuropathy
Mucopolysaccharidosis I
Musladin-Lueke syndrome
Myotubular myopathy 1
Osteochondrodysplasia
Pompe disease
Skeletal dysplasia 2
Adult-onset neuronal ceroid lipofuscinosis
Benign familial juvenile epilepsy
Congenital myasthenic syndrome
Degenerative myelopathy
Episodic falling syndrome
Exercise-induced collapse
Juvenile Laryngeal Paralysis and Polyneuropathy
Late onset ataxia
Mucopolysaccharidosis I
Musladin-Lueke syndrome
Narcolepsy
Neonatal cerebellar cortical degeneration
Neonatal encephalopathy with seizures
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Sensory ataxic neuropathy
Spinocerebellar ataxia
Startle disease
Primary ciliary dyskinesia
Primary ciliary dyskinesia
Anhidrotic ectodermal dysplasia
Dry eye curly coat syndrome
Dystrophic epidermolysis bullosa
Ectodermal dysplasia
Epidermolytic hyperkeratosis
Hereditary nasal parakeratosis
Renal cystadenocarcinoma and nodular dermatofibrosis
Fanconi syndrome
Hyperuricosuria
Persistent Müllerian duct syndrome
Primary ciliary dyskinesia
Primary hyperoxaluria
Renal cystadenocarcinoma and nodular dermatofibrosis
