clinic

Family First Medical Group - Evergreen Park, Illinois

5 Stars (10 Reviews)

Family First Medical Group is a clinic in Evergreen Park, IL offering Concierge Pediatrics, with 1 physician on staff.

1 Doctor | Website
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About Family First Medical Group
Address

9730 S Western Ave suite 700 700, Evergreen Park,
IL 60805

Modes of Payment

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Providers
David Beckmann - 9730 S Western Ave suite 700, Evergreen Park, IL 60805, USA, Evergreen Park, Illinois, 60805
David Beckmann, MD
Family First Medical Group
Concierge Pediatrics
(10)
Fee N/A
Max no. of Patients: N/A
Accepting New Patients: NA
9730 S Western Ave suite 700, 700, Evergreen Park, IL 60805
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Reviews
Posted by FMDD User
July 29, 2024
Enlightened me about my condition.

Review For David Beckmann

Posted by FMDD User
July 22, 2024
Guided me in choosing the best treatment option.

Review For David Beckmann

Posted by FMDD User
July 15, 2024
Very professional care and consult.

Review For David Beckmann

Conditions Treated
  • Truncus arteriosus
  • Generalized anxiety disorder
  • Dermatitis
  • Atopic dermatitis
  • Eczema
  • Sepsis
  • Hiatal hernia
  • Back pain
  • Multiple sclerosis
  • Nausea
  • Stroke
  • Sarcoidosis
  • Diabetes
  • Cardiomyopathy
  • Congestive heart failure
  • Cystic fibrosis
  • Liver disease
  • Gallstones
  • Inguinal hernia
  • Pulmonary embolism
  • Scleroderma
  • Hemangioma
  • Lupus
  • Skin cancer
  • Melanoma
  • Canker sore
  • Pityriasis rosea
  • Vitiligo
  • Rosacea
  • Ear infection
  • Swimmer's ear
  • Chronic fatigue syndrome
  • Concussion
  • Depression
  • Insomnia
  • Lactose intolerance
  • Irritable bowel syndrome
  • Ulcerative colitis
  • Umbilical hernia
  • Deep vein thrombosis
  • Hydrocele
  • Rectal prolapse
  • Harlequin ichthyosis
  • Cellulitis
  • Kawasaki disease
  • Diphtheria
  • Smallpox
  • Osteomyelitis
  • Meningitis
  • Molluscum contagiosum
  • Scurvy
  • Sjogren's syndrome
  • Narcolepsy
  • Kidney infection
  • Strep throat
  • Torticollis
  • Cerebral palsy
  • Restless legs syndrome
  • Strabismus
  • Testicular torsion
  • Tourette syndrome
  • Croup
  • Roseola
  • Scarlet fever
  • Asthma
  • Adhd
  • Upper respiratory infection
  • Allergies
  • Pneumonia
  • Measles
  • Apert syndrome
  • Beckwith wiedemann syndrome
  • Aphantasia
  • Brachydactyly
  • Cafe au lait spots
  • Cornelia de lange syndrome
  • Cri du chat syndrome
  • Crouzon syndrome
  • Cystinosis
  • Apraxia
  • Cerebellar hypoplasia
  • Dandy walker syndrome
  • Dravet syndrome
  • Duchenne muscular dystrophy
  • Medulloblastoma
  • Caput succedaneum
  • Congenital diaphragmatic hernia
  • Cystic hygroma
  • Congenital heart disease
  • Ebstein's anomaly
  • Blount disease
  • Clubfoot
  • Choanal atresia
  • Congenital adrenal hyperplasia
  • Digeorge syndrome
  • Birthmarks
  • Craniosynostosis
  • Intussusception
  • Juvenile dermatomyositis
  • Juvenile idiopathic arthritis
  • Kabuki syndrome
  • Krabbe disease
  • Kwashiorkor
  • Lazy eye
  • Lesch nyhan syndrome
  • Maple syrup urine disease
  • Munchausen syndrome by proxy
  • Nephrotic syndrome
  • Pityriasis alba
  • Add adhd
  • Micrognathia
  • Pfeiffer syndrome
  • Poland syndrome
  • Progeria
  • Sotos syndrome
  • Stickler syndrome
  • Tay sachs disease
  • Treacher collins syndrome
  • Aarskog syndrome
  • Adams oliver syndrome
  • Patent ductus arteriosus
  • Adenosine deaminase deficiency
  • Gastroschisis
  • Neonatal abstinence syndrome
  • Omphalocele
  • Plagiocephaly
  • Rhabdomyosarcoma
  • Selective mutism
  • Stork bite
  • Sudden infant death syndrome
  • Temper tantrums
  • Uncombable hair syndrome
  • Undescended testicle
  • Wilms tumor
  • Abo incompatibility
  • Acrodermatitis enteropathica
  • Rheumatic fever
  • Noonan syndrome
  • Tetralogy of fallot
  • Ventricular septal defects
  • Erb's palsy
  • Fragile x syndrome
  • Holoprosencephaly
  • Hydranencephaly
  • Hypotonia
  • Lennox gastaut syndrome
  • Lissencephaly
  • Microcephaly
  • Moebius syndrome
  • Myelomeningocele
  • Pompe disease
  • Spinal muscular atrophy
  • Sturge weber syndrome
  • Tuberous sclerosis
  • Acute flaccid myelitis
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Alexander disease
  • Encopresis
  • Esophageal atresia
  • Food allergy
  • Hirschsprung disease
  • Necrotizing enterocolitis
  • Knock knees
  • Osgood schlatter disease
  • Osteogenesis imperfecta
  • Pectus carinatum
  • Pectus excavatum
  • Polydactyly
  • Syndactyly
  • Laryngomalacia
  • Microtia
  • Otitis
  • Otitis media
  • Acute otitis externa
  • Growth hormone deficiency
  • Phenylketonuria
  • Precocious puberty
  • Albright's hereditary osteodystrophy
  • Gingivostomatitis
  • Mumps
  • Noma
  • Parainfluenza
  • Pertussis
  • Rubella
  • Fanconi anemia
  • Hemolytic uremic syndrome
  • Hemophilia a
  • Hermansky pudlak syndrome
  • Purpura
  • Thalassemia
  • Ewing sarcoma
  • Neuroblastoma
  • Newborn jaundice
  • Ectodermal dysplasias
  • Encephalocele
  • Epicanthal folds
  • Epispadias
  • Esotropia
  • Exercise induced asthma
  • Galactosemia
  • Head lice
  • Henoch schonlein purpura
  • Hydrops fetalis
  • Hypophosphatasia
  • Hypospadias
  • Rett syndrome
  • Craniotabes
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Pituitary dwarfism
  • Infectious mononucleosis
  • Eec syndrome
  • Ellis van creveld syndrome
  • Emery dreifuss muscular dystrophy
  • Fanconi syndrome
  • Fetal hydantoin syndrome
  • Floating harbor syndrome
  • Foxg1 syndrome
  • Fraser syndrome
  • Freeman sheldon syndrome
  • Frontonasal dysplasia
  • Fumarase deficiency
  • Glucose 6 phosphate dehydrogenase deficiency
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Infant botulism
  • Hallermann streiff syndrome
  • Juvenile myoclonic epilepsy
  • Landau kleffner syndrome
  • Myoclonic epilepsy
  • Hemihyperplasia
  • Periventricular leukomalacia
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Rasmussen encephalitis
  • Cytomegalovirus infection
  • Meningococcemia
  • Neonatal conjunctivitis
  • Heterotaxy syndrome
  • Holt oram syndrome
  • Neonatal sepsis
  • Duodenal atresia
  • Hepatoblastoma
  • Imperforate anus
  • Infantile pyloric stenosis
  • Cyclic neutropenia
  • Hemolytic disease of the newborn
  • Hemophagocytic lymphohistiocytosis
  • Hypochondroplasia
  • Jacobsen syndrome
  • Koolen de vries syndrome
  • Hereditary spherocytosis
  • Ganglioneuroma
  • Rhabdoid tumor
  • Lowe syndrome
  • Rhabdomyosarcoma embryonal
  • Kohler disease
  • Pfapa
  • Eisenmenger syndrome
  • Grass allergy
  • Menkes disease
  • Meconium aspiration syndrome
  • Newborn transient tachypnea
  • Pulmonary atresia
  • Endocardial cushion defect
  • Menkes syndrome
  • Interrupted aortic arch
  • Miller dieker syndrome
  • Pulmonary valve stenosis
  • Ear tag
  • Metopic ridge
  • Enlarged adenoids
  • Evans syndrome
  • Miller syndrome
  • Exstrophy of the bladder
  • Dystrophic epidermolysis bullosa
  • Epidermolysis bullosa simplex
  • Giant congenital melanocytic nevus
  • Hypohidrotic ectodermal dysplasia
  • Hypomelanosis of ito
  • Incontinentia pigmenti
  • Linear nevus sebaceous syndrome
  • Mongolian blue spots
  • Neonatal herpes
  • Scalded skin syndrome
  • Apnea of prematurity
  • Atrioventricular septal defect
  • Benign rolandic epilepsy
  • Bronchopulmonary dysplasia
  • Bulging fontanelles
  • Childhood disintegrative disorder
  • Chondrodysplasia
  • Cleft lip and palate
  • Cleft palate and cleft lip
  • Cloacal exstrophy
  • Congenital hyperinsulinism
  • Muenke syndrome
  • Myotonia congenita
  • Nail patella syndrome
  • Nemaline myopathy
  • Neuronal ceroid lipofuscinoses
  • Niemann pick disease
  • Pierre robin sequence
  • Pitt hopkins syndrome
  • Potocki lupski syndrome
  • Propionic acidemia
  • Roberts syndrome
  • Robinow syndrome
  • Rubinstein taybi syndrome
  • Saethre chotzen syndrome
  • Seckel syndrome
  • Hemophilia b
  • Laryngeal cleft
  • Meatal stenosis
  • Meningocele
  • Nasal flaring
  • Otitis media with effusion
  • Potter syndrome
  • Prune belly syndrome
  • Retinopathy of prematurity
  • Short stature
  • Delayed growth
  • Spinal muscular atrophy type 1
  • West syndrome
  • Acute cerebellar ataxia
  • Bilirubin encephalopathy
  • Congenital mirror movement disorder
  • Diencephalic syndrome
  • Door syndrome
  • Dopa responsive dystonia
  • Early infantile epileptic encephalopathy
  • Intraventricular hemorrhage of the newborn
  • Torch syndrome
  • Toxocariasis
  • Congenital cytomegalovirus
  • Cytomegalic inclusion disease
  • H influenzae meningitis
  • Tracheoesophageal fistula
  • Childhood pancreatitis
  • Arginase deficiency
  • Colonic atresia
  • Congenital hepatic fibrosis
  • Congenital sucrase isomaltase deficiency
  • Gastroesophageal reflux in infants
  • Intestinal pseudo obstruction
  • Juvenile myelomonocytic leukemia
  • Congenital mesoblastic nephroma
  • Embryonal tumor with multilayered rosettes
  • Ganglioneuroblastoma
  • Aspartylglucosaminuria
  • Beta ketothiolase deficiency
  • Slipped capital femoral epiphysis
  • Sprengel deformity
  • Congenital radioulnar synostosis
  • Stereotypic movement disorder
  • Toxic synovitis
  • Juvenile temporal arteritis
  • Tracheobronchomalacia
  • Acute bronchiolitis
  • Congenital central hypoventilation syndrome
  • Congenital tracheomalacia
  • Idiopathic pulmonary hemosiderosis
  • Infantile apnea
  • Lung agenesis
  • Supravalvular aortic stenosis
  • Total anomalous pulmonary venous return
  • Transposition of the great arteries
  • Tricuspid atresia
  • Aortopulmonary window
  • Congenital anomalies of the heart
  • Congenital heart block
  • Double outlet left ventricle
  • Lactate dehydrogenase deficiency
  • Endocardial fibroelastosis
  • Severe combined immunodeficiency
  • Small for gestational age
  • Sunken fontanelles
  • Twin to twin transfusion syndrome
  • Single palmar crease
  • Sirenomelia
  • Velopharyngeal insufficiency
  • Aural polyps
  • Congenital nephrotic syndrome
  • Smith lemli opitz syndrome
  • Duplication of urethra
  • Smith magenis syndrome
  • Spondyloepiphyseal dysplasia
  • Infant hearing loss
  • Baller gerold syndrome
  • Bannayan riley ruvalcaba syndrome
  • Giant congenital nevus
  • Infantile digital fibromatosis
  • Infantile myofibromatosis
  • Junctional epidermolysis bullosa
  • Kerion celsi
  • Kindler syndrome
  • Tetrasomy x
  • Thanatophoric dysplasia
  • Triple x syndrome
  • Trisomy 14 mosaicism
  • Vacterl association
  • Von gierke disease
  • Wagr syndrome
  • Weaver syndrome
  • Zellweger syndrome
  • Acalvaria
  • Achondrogenesis
  • Acrodysostosis
  • Adenylosuccinate lyase deficiency
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Alpha mannosidosis
  • Andersen disease
  • Argininosuccinic aciduria
  • Arterial tortuosity syndrome
  • Asphyxiating thoracic dystrophy
  • Behr syndrome
  • Chromosome 22 duplication
  • Classic galactosemia
  • Dubowitz syndrome
  • Fanconi bickel syndrome
  • Feingold syndrome
  • Femoral facial syndrome
  • Fetal cystic hygroma
  • Fg syndrome
  • Fryns syndrome
  • Gaba transaminase deficiency
  • Galactokinase deficiency
  • Galactosialidosis
  • Galloway mowat syndrome
  • Gangliosidosis
  • Gaucher disease type 2
  • Gaucher disease type 3
  • Geleophysic dysplasia
  • Glutaric acidemia type 2
  • Hennekam syndrome
  • Holocarboxylase synthetase deficiency
  • Icf syndrome
  • Isovaleric acidemia
  • Jackson weiss syndrome
  • Johanson blizzard syndrome
  • Kaufman oculocerebrofacial syndrome
  • Kniest dysplasia
  • Knobloch syndrome
  • L1 syndrome
  • Lambdoid synostosis
  • Leri weill dyschondrosteosis
  • Mandibuloacral dysplasia
  • Neonatal hypothyroidism
  • Pediatric obesity
  • Pinealectomy
  • Puberty disorder
  • Childhood hypophosphatasia
  • Opsoclonus myoclonus syndrome
  • Periventricular heterotopia
  • Beta mannosidosis
  • Post traumatic epilepsy
  • Primary amebic meningoencephalitis
  • Satoyoshi syndrome
  • Visceral larva migrans
  • Neonatal hemochromatosis
  • Atresia of small intestine
  • Berdon syndrome
  • Platelet storage pool deficiency
  • Childhood acute myeloid leukemia
  • Pediatric brain tumors
  • Pleuropulmonary blastoma
  • Primitive neuroectodermal tumor
  • Congenital contractures
  • Peer relationships
  • Neonatal onset multisystem inflammatory disease
  • Mitral atresia
  • Cold induced sweating syndrome
  • Pulmonary atresia with intact ventricular septum
  • Right ventricle hypoplasia
  • Ring chromosome 18
  • Short philtrum
  • Marden walker syndrome
  • Marinesco sjogren syndrome
  • Sternal cleft
  • Subvalvular aortic stenosis
  • Anomalous left coronary artery from the pulmonary artery
  • Arterial calcification of infancy
  • Penoscrotal transposition
  • Arrhinia
  • Newborn head molding
  • Newborn polycythemia
  • Paroxysmal cold hemoglobinuria
  • Marshall smith syndrome
  • Premature infant
  • Marshall syndrome
  • Tracheal agenesis
  • Transient erythroblastopenia of childhood
  • Visceromegaly
  • And breastfeeding
  • Asphyxia neonatorum
  • Childhood iron deficiency anemia
  • Childhood volvulus
  • Mass phenotype
  • Mckusick kaufman syndrome
  • Meckel syndrome
  • Meier gorlin syndrome
  • Perianal streptococcal cellulitis
  • Pili torti
  • Pilonidal sinus disease
  • Pityriasis lichenoides et varioliformis acuta
  • Rothmund thomson syndrome
  • Scalp ear nipple syndrome
  • Sjogren larsson syndrome
  • Beare stevenson cutis gyrata syndrome
  • Cockayne syndrome type 2
  • Medium chain acyl coa dehydrogenase deficiency
  • Mosaic trisomy 7
  • Mosaic trisomy 8
  • Mosaic trisomy 9
  • Mucolipidosis type 4
  • Mucopolysaccharidosis type 1
  • Mucopolysaccharidosis type 3
  • Myhre syndrome
  • Nicolaides baraitser syndrome
  • Nijmegen breakage syndrome
  • Ohdo syndrome
  • Opitz g bbb syndrome
  • Pallister hall syndrome
  • Pallister killian mosaic syndrome
  • Peho syndrome
  • Pentasomy x
  • Perlman syndrome
  • Peters plus syndrome
  • Popliteal pterygium syndrome
  • Prekallikrein deficiency
  • Progressive myoclonic epilepsy
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Rapadilino syndrome
  • Renpenning syndrome
  • Russell silver dwarfism
  • Schimke immuno osseous dysplasia
  • Schindler disease
  • Schinzel giedion syndrome
  • Schwartz jampel syndrome
  • Sea blue histiocytosis
  • Severe congenital neutropenia
  • Short chain acyl coa dehydrogenase deficiency
  • Short qt syndrome
  • Sialidosis
  • Simpson golabi behmel syndrome
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spondylocostal dysostosis
  • Spondyloepiphyseal dysplasia congenita
  • Stuve wiedemann syndrome
  • Temple syndrome
  • Tetra amelia syndrome
  • Tetrasomy 9p
  • Thrombocytopenia absent radius syndrome
  • Townes brocks syndrome
  • Van maldergem syndrome
  • Vici syndrome
  • Wiedemann rautenstrauch syndrome
  • Anophthalmia plus syndrome
  • Ballinger wallace syndrome
  • Benign familial neonatal seizures
  • Bowen conradi syndrome
  • C syndrome
  • Carey fineman ziter syndrome
  • Charlie m syndrome
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Coloboma of eye lens
  • Congenital aplastic anemia
  • Yunis varon syndrome
  • Diffuse mesangial sclerosis
  • Hereditary hypophosphatemic rickets
  • Infant hyperglycemia
  • Isolated growth hormone deficiency
  • Neonatal severe hyperparathyroidism
  • Transient neonatal diabetes mellitus
  • Congenital fiber type disproportion
  • Congenital muscular dystrophy type 1a
  • Cytoplasmic body myopathy
  • Epilepsy with myoclonic atonic seizures
  • Horizontal gaze palsy with progressive scoliosis
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Infantile onset spinocerebellar ataxia
  • Oculocerebrocutaneous syndrome
  • Oppenheim dystonia
  • Congenital fibrinogen deficiency
  • Congenital mumps
  • Cryptosporidium enteritis
  • Congenital hemolytic anemia
  • Rubella or measles
  • Congenital nonhemolytic jaundice
  • Omphalomesenteric cyst
  • Primary intestinal lymphangiectasia
  • Congenital femoral deficiency
  • Congenital lipoid adrenal hyperplasia
  • Developmental expressive language disorder
  • Congenital microcoria
  • Developmental reading disorder
  • Congenital pulmonary lymphangiectasia
  • Cystic adenomatoid malformation of lung
  • Congenital mitral stenosis
  • Fetal edema
  • High blood pressure in infants
  • Partial atrioventricular canal
  • Pulmonary atresia with ventricular septal defect
  • Exstrophy epispadias complex
  • Palatopharyngeal incompetence
  • Fetal and neonatal alloimmune thrombocytopenia
  • Hygroma cervical
  • Neonatal ovarian cyst
  • Congenital plasminogen deficiency
  • Paris trousseau thrombocytopenia
  • Craniofacial deafness hand syndrome
  • Cytochrome p450 oxidoreductase deficiency
  • Dehydrated hereditary stomatocytosis
  • Desbuquois syndrome
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Encephalocele anencephaly
  • Familial glucocorticoid deficiency
  • Familial hypopituitarism
  • Congenital herpes simplex
  • Cranioectodermal dysplasia
  • Farber lipogranulomatosis
  • Filippi syndrome
  • Gorlin chaudhry moss syndrome
  • Hemangioma thrombocytopenia syndrome
  • Nonbullous congenital ichthyosiform erythroderma
  • Phacomatosis pigmentokeratotica
  • Phacomatosis pigmentovascularis
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial porencephaly
  • Fetal akinesia sequence
  • Fountain syndrome
  • Frank ter haar syndrome
  • Galactose epimerase deficiency
  • Gemss syndrome
  • Genetic epilepsy with febrile seizures plus
  • Genital dwarfism
  • Hardikar syndrome
  • Hemophilia a or b
  • Histidinemia
  • Homocystinuria due to mthfr deficiency
  • Hyperlysinemia
  • Inborn amino acid metabolism disorder
  • Increased head circumference
  • Microcephalic osteodysplastic primordial dwarfism type 1
  • Microcephalic osteodysplastic primordial dwarfism type 2
  • Mucolipidosis 3
  • Mucopolysaccharidosis type 3a
  • Mucopolysaccharidosis type 3b
  • Mucopolysaccharidosis type 4
  • Mucopolysaccharidosis type 4a
  • Mucopolysaccharidosis type 6
  • Mucopolysaccharidosis type 7
  • Mulibrey nanism
  • Ornithine translocase deficiency
  • Orofaciodigital syndrome 1
  • Orotic aciduria type 1
  • Overhydrated hereditary stomatocytosis
  • Pena shokeir syndrome type 2
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Phosphoglycerate kinase deficiency
  • Phosphoglycerate mutase deficiency
  • Pmm2 congenital disorder of glycosylation
  • Potassium aggravated myotonia
  • Toriello carey syndrome
  • Trisomy 12 mosaicism
  • Trisomy 17 mosaicism
  • Trisomy 3 mosaicism
  • Walker dyson syndrome
  • X linked infantile spinal muscular atrophy
  • X linked intellectual disability
  • X linked severe combined immunodeficiency
  • Biliary atresia
  • Reye syndrome
  • Hmpv virus
  • Fetal alcohol syndrome
  • Properdin deficiency
  • Bowlegs
  • Caudal regression syndrome
  • Klippel feil syndrome
  • Legg calve perthes disease
  • Rickets
  • Langerhans cell histiocytosis
  • Horseshoe kidney
  • Anencephaly
  • Cutis marmorata telangiectatica congenita
  • Gianotti crosti syndrome
  • Netherton syndrome
  • Aec syndrome
  • Bartsocas papas syndrome
  • Idiopathic neutropenia
  • Secondary immunodeficiency
  • Donnai barrow syndrome
  • Nephronophthisis
  • Wiedemann steiner syndrome
  • Chromosome 8p deletion
  • Fucosidosis
  • Hemimegalencephaly
  • Marcus gunn phenomenon
  • Megalencephaly capillary malformation syndrome
  • Pik3ca related overgrowth spectrum
  • Congenital generalized fibromatosis
  • Curry jones syndrome
  • Langer mesomelic dysplasia
  • Mucopolysaccharidosis type 2
  • Primary carnitine deficiency
  • Short syndrome
  • Trisomy 2 mosaicism
  • Congenital afibrinogenemia
  • Fetal thalidomide syndrome
  • Hypochondrogenesis
  • X linked creatine deficiency
  • Transient tic disorder
  • Seizures
  • Tinea versicolor
  • Psoriasis
  • Celiac disease
  • Milia
  • Hand-foot-and-mouth disease
  • Fifth disease
  • Autism spectrum disorder
  • Asperger's syndrome
  • Tongue tie
  • Hypoplastic left heart syndrome
  • Multicentric castleman disease
  • Pediatric myocarditis
more..
Treatments & Procedures
  • Pediatric urgent care
  • Ear tubes
  • Well child visits
  • Vaccines
  • Circumcision
  • Immunization
  • Lumbar puncture
  • Tetralogy of fallot repair
  • Tof repair
  • Prematurity and low birth weight
  • Pediatric laproscopy
  • Pediatric thoracoscopy
  • Pediatric sleep problems
  • Food challenges
  • Vaccination
  • Medical ear piercing

Frequently Asked Questions

Where is Family First Medical Group located?

Family First Medical Group is located in 9730 S Western Ave suite 700 700, Evergreen Park, IL 60805.

What are the various modes of payment does Family First Medical Group Accept?

Family First Medical Group accepts Card | Cash.

What are the doctors who practice in Family First Medical Group specialize in?

Currently there are around 1 providers practice in Family First Medical Group who specialise in Concierge Pediatrics, etc

How can I make appointments with doctors in Family First Medical Group?

You can take appointments for doctors who practice in Family First Medical Group online on their website or by calling them.

Location