Premature babies often develop anemia (a low red blood cell count) because they grow fast, make fewer new red cells for a while, and have blood drawn for tests. Mild anemia is watched and often improves with iron and time. When it is more significant or the baby has symptoms, a blood transfusion can safely restore healthy red cell levels. The team decides based on the counts and how the baby is doing.

Introduction: why this question matters for your family

Families often arrive at this question during or soon after the NICU stay, when a new term, test, or piece of the medical picture raises questions. This article is written for parents of a preemie with anemia or needing a transfusion and explains what the question really means, what to expect, and the next steps other families have found most useful.

What this really points to

Behind the question are patterns that a NICU and neonatology team can recognize quickly. The specific thing parents typically describe is a low red blood cell count (anemia) on routine NICU blood tests. One observation rarely answers the question on its own; a clear picture comes together from what parents notice, the history, and a focused evaluation [1].

The most useful next step is usually an evaluation by a NICU and neonatology team, often with routine blood counts to track the red cell level [3].

Example 1: A preemie’s red cell count drifts low and she seems tired with more breathing spells, so a transfusion restores healthy levels.

Why early action makes a real difference

Acting early matters because this is most manageable when it is caught and treated promptly. Timely evaluation and treatment by the care team help your baby stay stable while the underlying issue is addressed [3].

If any developmental concerns come up later, Early Intervention (Part C) offers free evaluations for eligible children under 3 [5].

Decision flow: from observation to support
Step 1Note the finding and keep the records
Step 2Bring it to your pediatrician
Step 3Ask your care team about next steps
Step 4Follow the care plan
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What usually lies behind it

The most relevant contributing factor here is the normal dip in red blood cell production in a fast-growing premature baby, plus blood drawn for tests. This is the underlying mechanism behind what parents notice: a low red blood cell count (anemia) on routine NICU blood tests [2].

The specific cause depends on the condition and your baby’s history. Your care team can explain what is driving it in your baby’s case and how they are treating and monitoring it.

If you also notice this, here is what to consider next
New breathing pauses or a color change
Consider: Emergency care now – call 911
Poor feeding or feeding intolerance
Consider: Prompt review by your pediatric or NICU team
Fever or temperature instability
Consider: Same-day medical evaluation
Slow weight gain
Consider: Pediatric and dietitian review
Questions about the NICU course
Consider: NICU follow-up clinic visit
Any developmental delays later on
Consider: Developmental check, and Early Intervention if needed

How a real evaluation works

A typical evaluation here combines a careful history, a focused examination, and the tests that fit the concern. Where useful, the team adds routine blood counts to track the red cell level [4].

Therapy referrals frequently happen at the same evaluation, before any formal diagnosis is finalized.

What each therapy actually does
PTPhysical Therapy
Helps with gross motor: rolling, sitting, crawling, standing, walking, gait, balance, tone management.
OTOccupational Therapy
Helps with fine motor, hand use, feeding, self-care skills, sensory processing.
SLPSpeech & Language Therapy
Helps with speech, language, communication, oral motor coordination, swallowing, AAC.
FTFeeding Therapy
Helps with bottle/breast feeding, swallowing safety, transition to solids, oral aversion.
DTDevelopmental Therapy
Helps with cognitive, social, adaptive skills – milestones across all developmental domains.
VTVision Therapy
Helps with visual tracking, focusing, and eye-hand coordination when vision is affected.
~10%U.S. newborns admitted to NICU [5]
Until age 3EI Part C eligibility [4]
Up to 24 moTypical NICU follow-up schedule [2]
38U.S. states CP Family Help works in
“Discharge from the NICU was supposed to be the end. It was really the start of two years of follow-up visits no one prepared us for.”
– Father of a NICU graduate, California

Mistakes families often make

The most common mistakes we see: waiting too long on a quiet ‘let us wait and see,’ comparing one child to another, skipping NICU follow-up visits, and not requesting the full medical record.

Trusting your own observation is one of the strongest tools you have [3].

Example 2: A baby’s mild anemia is managed with iron and nutrition and improves as he grows.

Step-by-step: what parents can do next

If the patterns described above match what you are seeing, here is a practical sequence other parents of a preemie with anemia or needing a transfusion have found useful.

1
Gather and keep the key records and results (NICU discharge summary, imaging, and any lab values), and note any new concerns about your baby’s breathing, feeding, muscle tone, or development.
2
At your next visit, describe your concern in concrete terms and show one or two videos if you have them. Ask whether a referral to a NICU and neonatology team is appropriate now.
3
Keep every NICU follow-up and pediatric appointment, and raise any new breathing, feeding, or development concern promptly.
4
Request the records that matter: NICU discharge summary, imaging reports, MRI or cranial ultrasound, and labor and delivery flow sheets.
5
Follow the care team’s plan, and keep up with the monitoring and follow-up they recommend.
6
For major decisions, get a second opinion at a children’s hospital with subspecialty depth in your child’s area of concern. Bring all reports.
7
If a birth event may have played a role, schedule a free, no-pressure case review with CP Family Help.
Print-friendly checklist
Tear-off summary to bring to your next pediatric or therapy visit. Use the Print button below.
  1. Gather and keep the key records and results (NICU discharge summary, imaging, and any lab values), and note any new concerns about your baby’s breathing, feeding, muscle tone, or development.
  2. At your next visit, describe your concern in concrete terms and show one or two videos if you have them. Ask whether a referral to a NICU and neonatology team is appropriate now.
  3. Keep every NICU follow-up and pediatric appointment, and raise any new breathing, feeding, or development concern promptly.
  4. Request the records that matter: NICU discharge summary, imaging reports, MRI or cranial ultrasound, and labor and delivery flow sheets.
  5. Follow the care team’s plan, and keep up with the monitoring and follow-up they recommend.
  6. For major decisions, get a second opinion at a children’s hospital with subspecialty depth in your child’s area of concern. Bring all reports.
  7. If a birth event may have played a role, schedule a free, no-pressure case review with CP Family Help.
Find your state’s Early Intervention (Part C) program
CP Family Help works with families in 38 U.S. states. Click the button below to see all states we cover.
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When to get help quickly

Some symptoms are emergencies. If your baby has a seizure, stops breathing or has breathing pauses, turns blue or very pale, becomes very hard to wake, or suddenly goes limp or unusually stiff, call 911 or go to the nearest emergency room right away. For non-emergency concerns, such as poor feeding, a change in your baby’s usual pattern, or anything that worries you, call your care team or pediatrician the same day.

What to bring to every follow-up visit

Bring three things: a short list of what has changed since last time, one or two phone videos, and a single specific question.

How CP Family Help supports families

CP Family Help works with families across 38 U.S. states whose children were diagnosed with cerebral palsy, HIE, or other birth injuries. Every initial consultation is free and confidential.

Worried something was missed?

A free case review can clarify whether the standard of care was met.

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Important exceptions and case-specific factors

Every child’s situation is different. Factors that can change the picture include your child’s gestational age, NICU history, imaging results, family history, your state’s Early Intervention eligibility rules, and statute of limitations.

Reviewed by CP Family HelpContent reviewed for accuracy by our editorial team. Last reviewed: July 15, 2026.
Why experience, verification, and case-specific guidance matter
  • Experience: CP Family Help works exclusively with cerebral palsy, HIE, and birth-injury cases across 38 U.S. states.
  • Expertise to verify: Information like this should be cross-checked with CDC, NIH/NINDS, AAP, and ACOG.
  • Professional guidance: Confirm medical decisions with your pediatrician and, where appropriate, a NICU and neonatology team.
  • Case-specific: Your child’s gestational age, NICU history, MRI findings, and state-specific rules all shape application.
Fact-Check Notes

High-confidence information

  • About 1 in 10 U.S. newborns receives care in a NICU (March of Dimes).
  • NICU teams follow a clear treatment and monitoring plan tailored to each baby’s condition.
  • Most newborn and NICU conditions are managed with close monitoring and follow-up.
  • If developmental concerns arise later, Early Intervention (Part C) offers free evaluations for eligible children under 3.

Case-specific information

  • Whether a low red blood cell count (anemia) on routine NICU blood tests reflects a lasting difference or an expected, temporary pattern depends on the individual child and is best judged by the care team.
  • Early Intervention eligibility rules vary slightly by state.
  • Statutes of limitations for birth-injury claims vary by state and child’s age.
  • Therapy access, Medicaid waivers, and insurance coverage vary by plan and state.

Related reading for parents

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