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Hundreds of children with cerebral palsy have improved spasticity, balance, speech and motor control through our two-week protocol. 89% reported quality-of-life improvement. 87% satisfied with the treatment outcome.
n=258 · See full breakdown →
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For those living with cerebral palsy, the search for effective treatments has often been met with limited options mainly focused on symptom management. Stem cell therapy takes a different approach: it aims to influence biological processes related to the underlying brain injury by supporting the brain’s repair processes and neuroplasticity, with the goal of improved function and a better quality of life (1, 2, 3).
Read on to see what it involves, who it is for, and what the evidence and our own results show.
No. Stem cell therapy does not cure cerebral palsy.
What the published studies and our own follow-up data describe is improvement in specific functions, most consistently gross motor function and muscle tone, in many children, though not in all. The gains measured in controlled trials are modest, and they were seen in children who continued their rehabilitation. Clinical benefit is not guaranteed, the degree of improvement differs considerably from one child to another, and the treatment remains experimental (2, 3, 4).
Cerebral palsy has one of the largest bodies of controlled evidence among the conditions we treat. The most careful analysis is a 2025 individual participant data meta-analysis published in Pediatrics, which obtained 498 individual data records, covering 447 children and young people, from 11 studies of umbilical cord blood. Children given cord blood scored 1.36 points higher on the GMFM-66 gross motor scale than controls at 6 months and 1.42 points higher at 12 months, with no difference at 1 or 3 months. Two findings are relevant to families. The effect grew with the cell dose and was close to zero below about 50 million cells per kilogram. The children who benefited were mainly those under about 5 years old who could already move with some independence (GMFCS levels I to III). At GMFCS levels IV and V no significant treatment effect was demonstrated (report summary, 2).
For mesenchymal stem cells, a 2025 review identified 30 published reports and 10 registered trials (1,292 people) and found a large pooled effect on gross motor function at 3, 6 and 12 months in six controlled studies, with substantial variation between them. It found no significant difference between intrathecal and intravenous delivery, or between one dose and several, although there were too few studies to rule out a difference. No phase 3 trial has been published, and almost a third of the patients in the literature were treated through compassionate access rather than in a trial (report summary, 3). A 2025 meta-analysis of 13 randomized trials of several cell types reached a similar conclusion, with the estimated effect becoming smaller after sensitivity analysis removed three studies responsible for much of the heterogeneity (report summary, 4). A 2026 updated meta-analysis of 10 controlled trials involving 621 patients also found an overall improvement in gross motor function at 12 months. When the studies were separated by cell product, the improvement remained significant in the studies of cord blood-derived mesenchymal stromal cells (MSCs), while the cord blood mononuclear cell subgroup did not reach statistical significance (5).
Real-world data are also encouraging. A 2024 compassionate-use study of 152 children treated with umbilical cord MSCs reported improvements across motor assessments, including a median 1.9-point increase in GMFM after four administrations, and younger children generally showed greater improvement (6).
Not every result has been clear-cut. A double-blind, sham-controlled trial from Tehran gave 108 children a single intrathecal dose of umbilical cord mesenchymal stem cells, cord blood cells or a sham procedure, and found significantly greater gross motor gains than sham with both cell types (10, 11). A 2026 follow-up analysis of the same trial used MR spectroscopy and found that neither treatment produced a significant overall change in the brain metabolites measured at 12 months. In the 73 children with usable scans, both cell groups improved significantly in gross motor function from baseline while the sham group did not, but the median gains of 11 and 9 points against 6 with sham did not differ significantly between groups in this smaller subgroup (report summary, 7). A 2023 Korean extension study found that gross motor gains in the year after an additional cord blood infusion were much smaller than in the first trial year (1.55 against 5.75 GMFM-66 points; 1.97 against 5.69 in children who received cord blood both times), and again that a higher cell dose did better. Because this was an open-label extension study, the finding does not prove that every second treatment will produce less improvement than the first (report summary, 8).
In summary, the trials show a modest improvement in gross motor function. It is strongest in younger and less severely affected children and at higher cell doses. There is no published confirmatory phase 3 trial and long-term evidence remains limited (2, 3, 4, 5, 8). All of our summaries are listed on the cerebral palsy medical reports index.
Suitability is decided case by case. Every enquiry goes to our medical department, which reviews the patient’s medical condition through our online medical evaluation system and only then recommends a specific treatment location and protocol. We recommend speaking to our specialists before you decide, so that you know what can realistically be expected in your case.
Send us the medical records and our team will come back to you.
Every patient is reviewed individually by our medical team before treatment is accepted. Treatment may be declined, postponed, or require additional medical evaluation when there is a condition that could increase the risks of stem cell administration, intravenous infusion, sedation, or lumbar puncture. Similar safety considerations have also been used as exclusion criteria in published clinical studies of cell therapy for cerebral palsy (10, 12, 13).
Possible exclusion or temporary deferral criteria include:
These are general safety considerations rather than absolute exclusions in every case. Some conditions may only require treatment to be postponed until the patient has recovered or become medically stable, while others may require additional investigations or modification of the treatment protocol. Final eligibility is determined individually after review of the patient’s medical history, current condition, medications, seizure history and control, laboratory results and relevant medical reports.
We do not currently publish an overall acceptance or rejection percentage. Each application is reviewed individually, and some patients may be accepted immediately, while others may require additional medical information, treatment of an existing condition, a period of neurological or general medical stability, modification of the proposed protocol, or may ultimately not be considered suitable for treatment.
Cerebral palsy (CP), also first known as Little’s disease, is the most common cause of physical disability in children (17). Its prevalence varies between populations and is approximately 1.6 per 1,000 live births in many high-income countries, with higher rates reported in some low- and middle-income settings (1).
Despite the current lack of a curative treatment, stem cell therapy has been investigated as a novel treatment for CP, with the aim of supporting repair and neuroplasticity within the injured developing brain (1, 2, 3, 4).
Stem cells have the ability to develop into different cell types. However, research now suggests that in cerebral palsy their potential benefit may come mainly from the signals and growth factors they release rather than simply replacing damaged brain cells. This is known as a paracrine effect. These signals may help create a more favourable environment for the brain to protect surviving cells, control inflammation, improve blood supply and support its own repair and neuroplasticity (3, 9, 13, 14, 15, 20, 21).
Some clinical studies have also reported improvements in motor function together with measurable changes in brain connectivity and white-matter pathways after stem cell treatment (9, 10, 11, 14).
In the case of CP and other neurological disorders, stem cells may therefore offer neuroprotective and regenerative-supporting effects through several proposed mechanisms, most of them shown in laboratory and animal studies rather than in patients (3, 9, 13, 14, 15, 20, 21):
An uncontrolled study reported functional improvements in 85% (17 of 20) of a small group of children with CP treated with autologous bone-marrow-derived cells by lumbar injection alongside intensive rehabilitation. Improvement was most often in muscle tone, limb strength or speech, and included changes reported by parents; only 3 of the 20 children improved on a standard measure of independence (19). Stem cell therapy aims to support neurological repair and reduce secondary processes such as inflammation, and it might support recovery from some consequences of the original brain injury. Controlled trials have mainly measured, and shown gains in, gross motor function (2, 3, 4, 20). Smaller, mostly uncontrolled studies have also reported changes in other areas (19), including:
Although stem cell therapy may provide significant benefits for some people with CP, it should still be used in combination with other treatment modalities rather than replace them, including physiotherapy, occupational therapy and speech therapy, all of which are available at Beike Technology, in order to support the best possible functional outcome (1, 16, 17).
Given that this might be a difficult decision to make, and you might need to weigh the benefits versus risks prior to starting this journey, we will discuss with you different factors that might affect your child’s response to stem cell therapy, and how we at Beike Technology address each factor to ensure that we provide you with the highest efficacy using the safest procedure possible.
The purpose of the treatment is to support the brain’s repair processes and neurological function. Thus, various kinds of improvement are possible after our treatment. The majority of Cerebral Palsy patients that have been treated by Beike, utilizing the combination of stem cell therapy and rehabilitation, showed visible signs of improvements, especially for these symptoms*:
Based on follow-up reports from 258 patients across 642 forms, here is the percentage who self-reported any improvement after treatment.
| Symptom | % of Patients who noticed Improvement | % who noticed a Small Improvement | % who noticed a Moderate Improvement | % who noticed a Significant Improvement |
|---|---|---|---|---|
| Trunk muscle strength | 88% | 34% | 34% | 21% |
| Head control | 88% | 31% | 32% | 25% |
| Range of movement | 86% | 34% | 34% | 18% |
| Spasticity | 84% | 37% | 31% | 16% |
| Limb muscle strength | 84% | 37% | 26% | 20% |
| Appetite | 83% | 27% | 24% | 32% |
| Involuntary movements | 79% | 38% | 27% | 14% |
| Swallowing | 79% | 33% | 22% | 23% |
| Speech (babbling for infants) | 77% | 37% | 24% | 16% |
| Mood disorder | 77% | 31% | 26% | 20% |
| Balance | 73% | 36% | 27% | 10% |
| Learning disability | 72% | 36% | 22% | 13% |
| Drooling | 69% | 30% | 22% | 18% |
| Standing up | 58% | 28% | 22% | 8% |
| Bladder control | 56% | 24% | 13% | 20% |
| Walking | 53% | 25% | 14% | 14% |
| Crawling | 46% | 24% | 15% | 8% |
Patients self-assess each symptom on a 5-point scale (Worse / No improvement / Small / Moderate / Significant) at follow-up checkpoints after treatment, comparing to their pre-treatment baseline. "Reported improvement" combines the small, moderate and significant buckets. Data is updated daily from our internal patient registry. As with any medical treatment, past results do not guarantee future outcomes — improvements vary from patient to patient.
| No | 11% |
| Yes - has slightly improved | 39% |
| Yes - has moderately improved | 24% |
| Yes - has significantly improved | 26% |
| reported quality-of-life improvement | 89% |
| No | 12% |
| Yes - small improvements | 38% |
| Yes - moderate improvements | 29% |
| Yes - significant improvements | 20% |
| reported physical improvement | 88% |
| No | 4% |
| No comment | 9% |
| Somewhat satisfied | 34% |
| Yes | 54% |
| satisfied with the treatment outcome | 87% |
Updated · 258 patients followed up · 642 follow-up forms · See full breakdown →
*It is important to remember that as for any medical treatment, improvements cannot be guaranteed. Please contact us for more information regarding the possible improvements for a particular case
Stem cell treatment has generally been well tolerated in published cerebral palsy studies, but like any medical treatment, stem cell therapy can have side effects. Many of the short-term reactions reported are similar to those that can occur after an IV infusion or injection, such as fever, headache, nausea, vomiting, temporary discomfort, breathing difficulty or a temporary fall in oxygen levels during the infusion, or an allergic or immune reaction. Intrathecal administration also involves a lumbar puncture and may cause temporary procedure-related symptoms such as headache, back discomfort, nausea or vomiting (2, 3, 4, 10, 11, 12, 13).
In the 2025 meta-analysis of cord blood, serious adverse events occurred in 16.0% of treated children and 12.9% of those who did not receive cord blood, and only one was definitely related to treatment: a reaction to the cryoprotectant used to freeze the cells (report summary, 2). In the review of mesenchymal stem cell studies, no serious adverse events were reported; the side effects of intrathecal injection were fever, irritability, headache, low back pain, vomiting, nausea and neck stiffness, all resolving within days, and 7 of the 30 published reports gave no safety data at all (report summary, 3). In randomized trials, fever, vomiting and irritability were not significantly more common than in controls (report summary, 4).
Our protocol delivers cells both intravenously and by intrathecal injection, which is performed after a lumbar puncture, a procedure with its own risks (most commonly headache and back pain afterwards), which the treating physicians go through with you before you consent. Intrathecal CP trials have also reported transient headache, lower-back pain and irritability related to lumbar puncture (3, 10, 11).
On the cells themselves: a 2020 meta-analysis of 55 randomised trials, covering 2,696 adults given mesenchymal stromal cells into a vein or artery, found no increase in cancer compared with controls (22). A 2022 review of 361 people given donor umbilical cord blood for neurological conditions, including cerebral palsy, found no serious adverse events definitely or probably caused by the infusion and no tumour (teratoma) formation (23). In randomised trials of umbilical cord MSCs given into a vein or artery in adults, no increase in cancer has been seen so far either. However, only some trials reported on cancer, most followed patients for a year or less, and longer follow-up is still needed (18).
Every batch of cells is screened, tested twice and traceable by code before it is released for use. The full process is described on our standards and certifications page.
Treatment is delivered at affiliated hospitals in Bangkok, Thailand and in Dongguan, China. It is not approved by the US Food and Drug Administration and is not offered in the United States. It is given under Thai and Chinese regulations for cell therapy, and the cells are prepared in laboratories with CNAS, GMP and ISO accreditation. The accreditation details and the certificates are on our standards and certifications page.
Beike is unlike any other stem cell treatment provider in the world, the reason? Since 2005, we have been developing and optimizing our stem cell treatment protocols with the concept that a comprehensive treatment approach may provide more individualized support for our patients. We believe that stimulation through various therapies is necessary to enhance stem cell regenerative response, therefore our protocols include daily therapies to support the stem cells. Finally, we provide a wide variety and large quantities of stem cells in order to adapt to each patient’s specific condition and deliver maximized regenerative potential.
Our stem cell therapy program for cerebral palsy consists of 6 to 8 simple and minimally invasive injections of umbilical cord-derived stem cells. The stem cells are transplanted using two separate methods: by intravenous way using a standard IV drip system, and through intrathecal injection performed after lumbar puncture. These two delivery methods allow for increased efficacy while ensuring safety and minimum inconvenience for the patient.
After a successful first stem cell treatment in Thailand in 2019, six young people with cerebral palsy travelled again from Poland for a second round of stem cells and supporting therapies. The families agreed to sit with us and tell us more about the improvements they have noticed so far and the treatment experience in general.
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Medically reviewed by
Dr. Mohammad Alzogool
Medical Director
Beike's Medical Director, Dr. Mohammad Alzogool, is a physician-researcher with a background in ophthalmology and regenerative medicine. His research contributions span ophthalmology, regenerative medicine, artificial intelligence, medical imaging, and evidence-based clinical guidelines. He brings a strong scientific and clinical perspective to the evaluation of emerging regenerative therapies.
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Find out more about patients previously treated with Beike stem cell protocols. The families participating in these blog posts talk about their stories and present their own view of the treatment, including thoughts regarding the daily therapies, the stem cell injection themselves as well as improvement noticed during and after treatment.
Patients and their families talking about treatment, recovery and the changes that mattered most to them.
Plain-language summaries of independent, peer-reviewed studies. Each one links to the original publication.
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