Home / Health Conditions / Hypotonia (Low Muscle Tone)
Hypotonia (Low Muscle Tone)
Hypotonia means low muscle tone — a baby or child who feels “floppy”. It is a sign that something is affecting the brain, nerves or muscles, not a diagnosis on its own. Finding the cause matters, because some causes have effective treatments and therapy can start right away.
A baby who suddenly becomes floppy needs emergency care. Call 911 or go to the emergency room if a baby or young child suddenly turns limp or floppy, is very sleepy or hard to wake, stops feeding, or has trouble breathing. These can be signs of serious illness such as meningitis (NHS (opens in a new tab)) or sepsis, where breathing may be very fast or difficult, with grunting or the tummy sucking in under the ribs (NHS (opens in a new tab)).
Infant botulism is another cause. In babies it can cause constipation, poor feeding, drooping eyelids, a face with less expression and a weak cry that sounds different (CDC (opens in a new tab)), as well as a limp or floppy head, neck, arms or legs (NHS (opens in a new tab)). All kinds of botulism are medical emergencies; CDC says to see a doctor or go to the emergency room right away and not to wait (CDC (opens in a new tab)). Never give honey to a baby under 12 months (NHS (opens in a new tab), MedlinePlus (opens in a new tab)).
If your child already has hypotonia, get prompt medical help for new trouble swallowing, coughing or choking with feeds, or any breathing difficulty. Weak muscles can affect swallowing and breathing in conditions such as spinal muscular atrophy (NINDS (opens in a new tab)), and in congenital myasthenic syndromes, fever or infection can trigger episodes of severe weakness or breathing problems (MedlinePlus Genetics (opens in a new tab)). Ask your child’s team for a written plan for illness and breathing problems.
What is hypotonia?
Hypotonia is the medical term for decreased muscle tone. It can happen when the brain, spinal cord, nerves or muscles are damaged (NINDS (opens in a new tab)). Healthy muscles always keep a very small amount of contraction, even at rest, which gives them a springy feel and some resistance when someone else moves the arm or leg. Hypotonia is not the same as weakness, although the two can happen together (NINDS, archived (opens in a new tab)).
Most important, hypotonia is a sign, not a diagnosis. It is seen in conditions as different as Down syndrome, muscular dystrophy and cerebral palsy, and sometimes no cause can be found (NINDS, archived (opens in a new tab)). Finding the cause can be hard, but it matters: it shapes the outlook, related health problems and the chance of it happening again in a family (Sparks, Clinics in Perinatology, 2015 (opens in a new tab)). Low tone on its own does not affect intelligence (NINDS, archived (opens in a new tab)), although some of its causes do.
The “floppy infant”
Babies with hypotonia can have a floppy, “rag doll” quality: their arms and legs hang by their sides and they have little or no head control (NINDS, archived (opens in a new tab)). Doctors may notice a “frog-leg” posture from low tone and few movements (Morton et al., JAMA Neurology, 2022 (opens in a new tab)), and parents may notice that the head lags when the baby is picked up from lying on the back (NINDS (opens in a new tab)). Some floppy babies also have trouble sucking and feeding, or with breathing (NINDS, archived (opens in a new tab), NICHD (opens in a new tab)).
Brain (central) causes and nerve-and-muscle (peripheral) causes
Doctors first look for common secondary causes, such as low blood sugar, heart disease or a serious infection (sepsis). If none is found, they consider primary causes, which fall into two groups (Morton et al., 2022 (opens in a new tab)):
- Central hypotonia starts in the brain or spinal cord and accounts for about 60 to 80 percent of primary hypotonia in newborns. Genetic examples include Down syndrome, Prader-Willi syndrome and inherited metabolic conditions; non-genetic examples include brain injury from lack of oxygen, infection, bleeding in the brain and injury (Morton et al., 2022 (opens in a new tab)).
- Peripheral hypotonia comes from the motor nerve cells in the spinal cord, the nerves, the junction where nerves meet muscle, or the muscles themselves, and accounts for about 15 to 30 percent. These babies often have hypotonia as their first sign, along with weak or absent reflexes and marked weakness (Morton et al., 2022 (opens in a new tab)). Many of these neuromuscular disorders are genetic (MedlinePlus (opens in a new tab)).
Some conditions that cause hypotonia
- Down syndrome — weak muscle tone in infancy is one of its features (MedlinePlus Genetics (opens in a new tab)). See our Down Syndrome guide.
- Prader-Willi syndrome — in infancy, weak muscle tone, feeding difficulties, poor growth and delayed development; extreme hunger begins later in childhood (MedlinePlus Genetics (opens in a new tab)).
- Cerebral palsy — some infants with CP have low tone that makes them seem relaxed, even floppy, while others are stiff (NINDS (opens in a new tab)). See our Cerebral Palsy guide.
- Spinal muscular atrophy (SMA) — a genetic disease that damages the motor nerve cells controlling movement. Type 1, the most common, usually shows before 6 months, with severe weakness and trouble breathing, coughing and swallowing (NINDS (opens in a new tab)). Newborn screening and treatment are covered below.
- Muscular dystrophies and related muscle diseases — congenital muscular dystrophies are present at birth or appear before age 2, and weakness may first be noticed when children don’t meet movement milestones (NINDS (opens in a new tab)). Our Muscular Dystrophy guide is coming soon.
- Problems where nerves meet muscle — congenital myasthenic syndromes cause weak muscles that tire easily (MedlinePlus Genetics (opens in a new tab)); infant botulism is an emergency (see the alert above).
- Metabolic and other genetic conditions — for example Pompe disease, where a sugar builds up in muscles (MedlinePlus Genetics (opens in a new tab)), Zellweger spectrum disorder (MedlinePlus Genetics (opens in a new tab)) and biotinidase deficiency (MedlinePlus Genetics (opens in a new tab)). In one international study, rapid genetic sequencing found a cause in 60 percent of tested newborns in intensive care with unexplained hypotonia (Morton et al., Neurology, 2025 (opens in a new tab)).
- “Benign” congenital hypotonia — a label for babies whose tone improves and in whom no other cause is found. A long-term study of 41 such children confirmed a good outlook and noted that many of their parents had loose joints (Carboni et al., Pediatric Neurology, 2002 (opens in a new tab)). Still, school-age children with this history had weaker gross motor skills than classmates, so follow-up should continue (Parush et al., Dev Med Child Neurol, 1998 (opens in a new tab)).
If your child has developmental delays, our Developmental Disabilities guide covers services and rights; see also our Angelman Syndrome and Autism guides. Spina Bifida and Smith-Magenis Syndrome guides are on the way.
Signs at different ages
CDC’s “Learn the Signs. Act Early.” milestones describe what most babies can do by each age. Missing movement milestones like these is a reason to talk with the doctor:
- By 2 months: holds head up when on tummy (CDC (opens in a new tab)).
- By 4 months: holds head steady without support when held; pushes up onto elbows or forearms when on tummy (CDC (opens in a new tab)).
- By 6 months: rolls from tummy to back; pushes up with straight arms on tummy; leans on hands to support herself when sitting (CDC (opens in a new tab)).
- By 9 months: gets to a sitting position by herself and sits without support (CDC (opens in a new tab)).
- By 1 year: pulls up to stand and walks holding on to furniture (CDC (opens in a new tab)).
At any age, low tone can bring problems with movement and posture, breathing and speech difficulties, loose ligaments and joints, and weak reflexes (NINDS, archived (opens in a new tab)). Children with significant, ongoing hypotonia are also at higher risk of hip problems that standard newborn checks may miss (Livingstone et al., Dev Med Child Neurol, 2025 (opens in a new tab)). A child who keeps losing movement skills needs prompt evaluation: steady loss of skills may point to a genetic or muscle disease, a metabolic disorder or a tumor rather than CP (NINDS (opens in a new tab)).
How doctors find the cause
Evaluation usually starts with a neurologist checking movement and sensation, balance and coordination, mental status, reflexes and nerve function. Tests may include a CT or MRI scan of the brain, an EMG of nerve and muscle function, or an EEG of brain activity (NINDS, archived (opens in a new tab)).
- Genetic testing looks for changes in genes and chromosomes; genome or exome sequencing checks all or the protein-making parts of a person’s DNA (MedlinePlus (opens in a new tab)). An international group of newborn specialists recommends rapid genome or exome sequencing as a first test for babies in intensive care with unexplained hypotonia; it found a diagnosis in more than half and often changed care (Morton et al., 2022 (opens in a new tab)). For SMA, a blood test for changes in the SMN1 gene finds at least 95 percent of types 1 to 3 (NINDS (opens in a new tab)).
- Blood tests can show muscle injury: a raised creatine phosphokinase (CK) level is typical of congenital muscular dystrophy (Morton et al., 2022 (opens in a new tab)).
- EMG and nerve conduction studies help tell whether symptoms come from a muscle or a nerve problem; the needle can cause brief discomfort and some soreness (MedlinePlus (opens in a new tab)).
- Muscle biopsy, removing a small piece of muscle, may be used when gene testing for SMA is normal, to look for other conditions (NINDS (opens in a new tab)). Fast genetic results can spare some babies invasive tests such as EMG and biopsy (Morton et al., 2022 (opens in a new tab)).
Hypotonia can be lifelong, but in some children muscle tone improves over time (NINDS, archived (opens in a new tab)).
Side by side
Six approaches compared
For every condition we look at the same six approaches: what each involves, what it typically costs, and what a patient can realistically expect.
| Approach | What it involves | Estimated cost | What to expect |
|---|---|---|---|
| Conventional medicine (AMA) | Find and treat the cause first; then physical, occupational and speech or feeding therapy, early intervention, braces and equipment as needed. Some causes have specific treatments, such as nusinersen, onasemnogene abeparvovec and risdiplam for SMA. | Early intervention is free or reduced-cost for eligible children under 3; Medicaid EPSDT covers medically necessary care for enrolled children under 21. Genetic tests, specialist visits, private therapy and SMA medicines: cost estimate being researched. | Depends on the cause. Some babies’ tone improves over time; for others it is lifelong. Early SMA treatment tends to help more than later treatment. |
| Chiropractic | No role. We found no studies of chiropractic care for hypotonia. | Not applicable. | Not a treatment for low muscle tone. Loose joints and possible neck instability (for example in Down syndrome) make spinal manipulation a real safety concern in these children. |
| Acupuncture | Little research. Two small Chinese trials in babies with cerebral palsy and sitting problems (some with low-tone CP) reported gains when acupuncture was added to sitting training; no trials in other causes of hypotonia. | About $125–$230 for a first private visit and $90–$185 for follow-ups; community clinics about $50–$90. | Unproven for hypotonia. If you try it, use a licensed practitioner experienced with children and keep up therapy. |
| Herbal medicine | No herb or supplement has been shown to improve muscle tone. A few rare causes (such as biotinidase deficiency) are treated by specialists as part of medical care. | Not applicable. | Give a child supplements only with your clinician’s agreement. Never give honey to a baby under 12 months. We don’t list doses. |
| Massage therapy | Gentle infant massage by parents, for comfort and bonding, alongside — not instead of — therapy. | Learning to massage your own baby is free. Cost of instruction: being researched. | Small studies, mostly in babies with Down syndrome, suggest gains in tone, development and vision; for other causes of hypotonia the evidence is thin. |
| MBHA Wellness Coach | Family support: getting early intervention started, therapist-guided tummy time and play, feeding support, safe sleep and home safety, tracking milestones, and care for caregivers. | Cost estimate being researched. Early intervention evaluations, CDC milestone tools and Parent Centers are free. | Supports — never replaces — your child’s doctors and therapists. |
Approach 1 of 6
Conventional medicine (AMA)
Treatment begins with a thorough evaluation. Once a diagnosis is made, the underlying condition is treated first, followed by therapy for the low tone itself (NINDS, archived (opens in a new tab)). For newborns, the main treatments are physical, occupational, speech and feeding, and breathing therapy (Sparks, 2015 (opens in a new tab)). We name treatments but never doses.
1. Treating the cause
- Secondary causes such as infection or low blood sugar are treated directly (Morton et al., 2022 (opens in a new tab)).
- Genetic causes: a genetic diagnosis changed the care of most babies who received one in a five-hospital study (Morton et al., 2025 (opens in a new tab)). Effective treatments exist for some conditions, such as congenital myasthenic syndromes and SMA (Morton et al., 2022 (opens in a new tab)).
- Prader-Willi syndrome: growth hormone, exercise and dietary supervision can help build muscle and control weight (MedlinePlus (opens in a new tab)).
- Muscular dystrophies: there is no cure (MedlinePlus (opens in a new tab)); care aims to keep people independent and prevent complications, with physical therapy, stretching, medicines, surgery and supports such as splints, braces and wheelchairs (NINDS (opens in a new tab)).
2. Spinal muscular atrophy: screening and treatment
Where newborns are screened for SMA, it can be diagnosed in the first week of life (Morton et al., 2022 (opens in a new tab)). That matters, because treatment early in life tends to help more than treatment later (NINDS (opens in a new tab)), and early treatment can help prevent the most severe symptoms and early death (California Department of Public Health (opens in a new tab)).
- Newborn screening: each state chooses the conditions it screens for (NICHD (opens in a new tab)); some include SMA (MedlinePlus (opens in a new tab)), and California screens every baby for it (California Department of Public Health (opens in a new tab)). If a screen is positive, follow up quickly (MedlinePlus (opens in a new tab)).
- FDA-approved treatments named by NINDS are nusinersen (Spinraza), given by lumbar puncture to children and adults; onasemnogene abeparvovec (Zolgensma), a gene therapy for children under 2; and risdiplam (Evrysdi), taken by mouth from 2 months of age. They preserve motor nerve cells, improve muscle function and extend lives, but they are not cures (NINDS (opens in a new tab)). The FDA approved onasemnogene abeparvovec in 2019, with a boxed warning about serious liver injury (FDA (opens in a new tab)), and risdiplam in 2020 as the first SMA drug taken by mouth (FDA (opens in a new tab)).
- Supportive care includes therapy, braces, nutrition support and breathing support during sleep (NINDS (opens in a new tab)).
3. Therapy
- Physical therapy can improve motor control and overall strength; occupational therapy helps with everyday activities; speech-language therapy can help with breathing, speech and swallowing (NINDS, archived (opens in a new tab)).
- What the research shows: a review of therapy for young children with central hypotonia found good evidence for treadmill training to help children with Down syndrome walk; evidence for most other approaches was weaker (Paleg et al., J Pediatr Rehabil Med, 2018 (opens in a new tab)).
- Feeding and swallowing: a speech-language pathologist can treat swallowing problems; changing foods or head position while eating can help, and in serious cases a feeding tube may be needed (MedlinePlus (opens in a new tab)).
4. Braces, equipment and hips
Orthotics (braces) improve foot alignment in children with hypotonia who walk, but in babies who are not yet walking they may hold back motor development, so timing matters (Paleg et al., 2018 (opens in a new tab)). Because children with significant, ongoing hypotonia are at higher risk of hip problems, one review recommends a hip ultrasound between 6 weeks and 6 months and yearly orthopedic checks for those with persistent low tone (Livingstone et al., 2025 (opens in a new tab)). Ask your team about a plan.
5. Early intervention and school
Early intervention is free or reduced-cost for eligible children, and you don’t need a doctor’s referral: call your state’s program and ask for an evaluation. From age 3, ask your local public elementary school for a preschool special education evaluation (CDC (opens in a new tab)). Early intervention is Part C of the Individuals with Disabilities Education Act (IDEA), which serves infants and toddlers from birth through age 2 under an Individualized Family Service Plan (IFSP); from 3, services are planned in an Individualized Education Program (IEP) (ECTA Center (opens in a new tab)).
What it costs
- Early intervention: free or reduced-cost for eligible children (CDC (opens in a new tab)).
- Medicaid: EPSDT covers comprehensive care for children under 21 enrolled in Medicaid, including medically necessary services to correct and ameliorate health conditions (Medicaid.gov (opens in a new tab)).
- Genetic testing, specialist visits, private therapy, braces and SMA medicines: cost estimate being researched.
What to expect
Finding treatable conditions early lets treatment and early intervention begin sooner (Cicala & Mercuri, Dev Med Child Neurol, 2026 (opens in a new tab)).
Approach 2 of 6
Chiropractic
Chiropractic care has no role in treating hypotonia. A PubMed search in October 2026 for chiropractic or spinal manipulation and hypotonia or the “floppy infant” found only one unrelated study, of adults with low back pain, and no studies of children with low muscle tone.
Safety concerns are real. Children with low tone can have loose ligaments and joints (NINDS, archived (opens in a new tab)). In Down syndrome, misshapen bones at the top of the spine can press on the spinal cord (atlantoaxial instability); NICHD warns that certain movements during anesthesia or surgery could cause permanent injury (NICHD (opens in a new tab)). A review in a chiropractic journal warned that adjusting the neck of a person with Down syndrome can have potentially fatal consequences (La Francis, J Manipulative Physiol Ther, 1990 (opens in a new tab)).
- In children under 10, most reported side effects of spinal manipulation are mild, such as more crying or soreness, but a rib fracture in a 21-day-old baby has been reported, and the risk of moderate and severe side effects is unknown (Corso et al., Chiropractic & Manual Therapies, 2020 (opens in a new tab)).
- Serious problems after spinal manipulation are very rare, but people with underlying health problems may be at greater risk (NCCIH (opens in a new tab)).
- MBHA’s advice: do not have a floppy baby or a child with loose joints or a known genetic syndrome manipulated. Spend the time and money on the evaluation and therapy described in the Conventional section.
Approach 3 of 6
Acupuncture
We found little research on acupuncture for hypotonia.
What the research says
- Two Chinese trials, each of 120 infants and young children with cerebral palsy who had trouble sitting, reported better sitting scores when acupuncture was added to sitting training, with larger gains in spastic and low-tone (hypotonic) CP than in other types (Zhang & Du, Zhen Ci Yan Jiu, 2013 (opens in a new tab), Zhang et al., 2015 (opens in a new tab)). The 2015 trial compared two acupuncture styles rather than acupuncture with no acupuncture. Both were published in Chinese, and their abstracts don’t say whether assessors were blinded.
- We found no trials of acupuncture for hypotonia from other causes, such as Down syndrome, genetic or muscle diseases. See our Cerebral Palsy guide for the wider research on acupuncture in CP.
Safety
Relatively few complications have been reported, but problems have come from non-sterile needles and improper treatment; in the U.S., needles must be sterile and single-use (NCCIH (opens in a new tab)). If you consider it, choose a licensed acupuncturist experienced with children, tell your child’s doctor, and don’t let it replace evaluation or therapy.
What it costs
Published examples run about $125–$230 for a first private visit and $90–$185 for follow-ups; community clinics about $50–$90 a visit (The Pricer (opens in a new tab)).
Approach 4 of 6
Herbal medicine
No herb or supplement has been shown to improve muscle tone. A PubMed search in October 2026 for herbal or dietary supplements and hypotonia found case reports, genetic studies and one laboratory study, but no trial of an herb or supplement for low muscle tone in children.
A few rare metabolic causes, such as biotinidase deficiency, where the body can’t recycle the vitamin biotin, need lifelong treatment (MedlinePlus Genetics (opens in a new tab)). That is specialist care after a diagnosis, not something to try at home.
Safety first
- Many dietary supplements haven’t been tested in children, “natural” doesn’t always mean safe, labels don’t always match what’s in the bottle, and supplements can interact with medicines. Ask your child’s health care provider before using any (NCCIH (opens in a new tab)).
- No honey before 12 months, including in “natural” remedies: honey can contain the bacteria that cause botulism (NHS (opens in a new tab)).
- Give a child supplements only with your clinician’s agreement. For feeding and growth worries, ask for a dietitian through your child’s care team. We don’t list doses here.
Approach 5 of 6
Massage therapy
Gentle massage can be a calm, close time with your baby. Most of the small body of research is in babies with Down syndrome.
What the research says
- A systematic review of therapies for young children with central hypotonia gave massage its top rating for improving muscle tone, motor development and use of vision in infants with Down syndrome, but rated it only “possibly effective” for other groups (Paleg et al., 2018 (opens in a new tab)).
- In a Spanish study of 32 babies with Down syndrome, daily parent massage for 5 weeks led to short-term gains in developmental scores (Pinero-Pinto et al., 2020 (opens in a new tab)). In a small Italian pilot trial, babies with Down syndrome who received massage developed sharper vision sooner (Purpura et al., Early Hum Dev, 2014 (opens in a new tab)).
- In a small U.S. trial of 28 children under 4 (14 with Down syndrome), parent- and trainer-given qigong massage improved gross motor scores (Silva et al., Am J Occup Ther, 2012 (opens in a new tab)).
- These studies are small and short, and most are in one condition. Massage works best as comfort and bonding alongside therapy, not as a replacement for it.
Safety
The risk of harm from massage appears low, though rare serious problems have been reported, some with vigorous deep-tissue massage. Don’t use massage to put off seeing a health care provider (NCCIH (opens in a new tab)). Use gentle strokes, avoid stretching or twisting the neck (especially in Down syndrome; see the Chiropractic section), and ask your child’s physical therapist to show you safe techniques.
What it costs
Massage you give your own baby is free. Cost of classes or instruction: being researched.
Approach 6 of 6
MBHA Wellness Coach
Waiting for answers about a floppy baby is hard. An MBHA Wellness Coach can help with everyday care — alongside, never instead of, your child’s doctors and therapists.
Act early
- CDC’s “Learn the Signs. Act Early.” program offers free milestone checklists and a Milestone Tracker app for ages 2 months to 5 years (CDC (opens in a new tab)), with milestones listed by age (CDC (opens in a new tab)).
- If you’re concerned, don’t wait: bring a completed checklist to the doctor, ask about developmental screening, and contact early intervention (CDC (opens in a new tab)). A coach can help you prepare for these calls.
Tummy time and play, guided by therapists
- Supervised tummy time, while baby is awake and watched, helps strengthen the neck, shoulder and arm muscles needed to sit, crawl and walk. NICHD’s Safe to Sleep campaign suggests short sessions after a diaper change or nap, a rolled-up towel under the arms for support, and a toy or a familiar face in front of baby (NICHD (opens in a new tab)).
- If your baby struggles with tummy time, ask your physical therapist how long and how often to practice and which positions and supports suit your child. A coach can help you fit the home exercises your therapists recommend into the family’s day.
Feeding support
- Weak sucking and feeding difficulties can come with low tone, for example in Prader-Willi syndrome, where nearly all infants need feeding help (NICHD (opens in a new tab)). A simple log of feeds, coughing and weight helps the care team.
- Ask for a speech-language pathologist if feeding is slow or your baby coughs or chokes; they treat swallowing problems (MedlinePlus (opens in a new tab)). New swallowing or breathing trouble needs prompt medical attention (see the alert at the top of this page).
Safe sleep and home safety
- Place all babies — including those born preterm and those with reflux — on their backs to sleep, for naps and at night, until they are 1 year old, and never on soft surfaces such as couches, pillow-top mattresses, quilts or thick blankets (NICHD (opens in a new tab)). Ask your doctor if your baby has a breathing condition.
- Limit time in car seats, bouncers, swings and carriers where the head rests against a surface, and hold baby upright for “cuddle time”; NICHD suggests both to help prevent flat spots on the head (NICHD (opens in a new tab)).
Finding services and caring for caregivers
- Parent Centers — nearly 100 across the U.S. and territories — work with families of children and youth with disabilities from birth to 26 (Center for Parent Information and Resources (opens in a new tab)).
- A coach can help you plan questions for appointments, organize reports and test results, share care with family and friends, and protect time for your own sleep, meals and rest.
Another approach
Questions to ask your child’s doctor
These questions can help you make the most of appointments:
- Do you think my child’s low tone comes from the brain (central) or from the nerves or muscles (peripheral)? Why (Morton et al., 2022 (opens in a new tab))?
- Which tests do you recommend — genetic testing, MRI, CK blood test, EMG or biopsy — and in what order (NINDS, archived (opens in a new tab))?
- Did my baby’s newborn screen include SMA (MedlinePlus (opens in a new tab))?
- Should my child’s hips be checked, and when (Livingstone et al., 2025 (opens in a new tab))?
- What signs mean we should call you, and what signs mean we should go to the emergency room?
- Can you help us contact early intervention today (CDC (opens in a new tab))?
Member stories
Living with Hypotonia (Low Muscle Tone)? Share your experience
Real experiences help others choose. Tell us what you tried — conventional medicine, chiropractic, acupuncture, herbs, massage or coaching — what it cost and what changed.
Sources
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- NINDS — Cerebral palsy (opens in a new tab)
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- Pinero-Pinto et al. — Effects of massage therapy on the development of babies born with Down syndrome, Evidence-Based Complementary and Alternative Medicine, 2020 (PubMed) (opens in a new tab)
- Purpura et al. — Effect of early multisensory massage intervention on visual functions in infants with Down syndrome, Early Human Development, 2014 (PubMed) (opens in a new tab)
- Silva et al. — Qigong massage for motor skills in young children with cerebral palsy and Down syndrome, American Journal of Occupational Therapy, 2012 (PubMed) (opens in a new tab)
- NCCIH — Massage therapy: what you need to know (opens in a new tab)
- ECTA Center — The Individuals with Disabilities Education Act (IDEA) (opens in a new tab)
- Medicaid.gov — Early and Periodic Screening, Diagnostic and Treatment (EPSDT) (opens in a new tab)
- Center for Parent Information and Resources — Find your Parent Center (opens in a new tab)
This page is for education only and is not medical advice. Costs are typical U.S. ranges and estimates; yours will depend on your provider, location and insurance. Talk with your doctor before starting, stopping or combining any treatment. In an emergency, call 911. See our disclaimer.
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