Disease-modifying therapy, done right, first
High-efficacy disease-modifying medicines, relapse management, symptom control, rehabilitation, and MRI surveillance stay at the center of every plan we build with you.
A precise, physician-led path forward
If MS is limiting your life, our Istanbul program combines AHSCT and MSC protocols with expert neurology oversight, precise cell dosing, and full aftercare — built around your phenotype and goals.
Conceptual biological visualization
Evidence status
High-efficacy disease-modifying medicines, relapse management, symptom control, rehabilitation, and MRI surveillance stay at the center of every plan we build with you.
Our transplant partners deliver AHSCT against the best available high-efficacy therapies for treatment-resistant relapsing MS, with careful selection and experienced center oversight driving safety.
We won't tell you a generic MSC or exosome infusion rebuilds myelin or reverses fixed disability. We focus on what current cell therapy can responsibly deliver for relapsing and progressive MS.
A direct answer
Our Istanbul program is built around two proven directions: autologous hematopoietic stem cell transplantation (AHSCT), an immune-reset procedure backed by randomized trial evidence in highly active relapsing MS, and MSC-based protocols for patients seeking supportive, physician-monitored care. Every plan starts with your phenotype, disease activity, and prior treatment history, matched to the right pathway by our neurology team.
Start with the phenotype
Relapse activity, MRI inflammation, accumulated disability, and progression independent of relapse all shape which protocol our physicians recommend for you.
Every Istanbul evaluation starts alongside expert MS care — never in place of an effective disease-modifying therapy that is already working for you.
Distinct relapses and new inflammatory MRI activity create the clearest setting for disease-modifying treatment decisions.
Progression is present, but recent relapses or new MRI lesions may still indicate treatable inflammatory activity.
Gradual worsening without inflammatory activity is biologically different and has weaker evidence for immune-reset strategies.
Progression begins without a relapsing phase, and evidence from selected relapsing-MS transplant trials cannot be transferred automatically.
Product and route matter
"Stem cell therapy" covers several distinct protocols with different goals, delivery routes, and evidence bases. Our team matches you to the one your case supports.
Chemotherapy suppresses the immune system before the patient's collected blood-forming stem cells are returned.
Evidence boundaryThe aim is to control inflammatory disease activity, not to replace neurons or directly rebuild myelin.
Bone-marrow or other stromal-cell products are studied for immune-modulatory and neuroprotective signals.
Evidence boundaryThe large MESEMS trial did not improve its primary MRI inflammation endpoint.
Some early studies deliver selected cell products into cerebrospinal fluid to explore neuroprotective outcomes.
Evidence boundaryLumbar puncture adds route-specific risks, and findings do not transfer to IV products or commercial exosomes.
Laboratory and early clinical research investigates oligodendrocytes, neural precursors, and repair-promoting molecules.
Evidence boundaryThis is not an established method for reversing fixed MS disability.
Indexed evidence ledger
We read every trial by MS phenotype, comparator, conditioning regimen, product, route, and outcome — never grouped under one generic stem-cell label.

Measure what changes
A precise baseline lets us distinguish real inflammatory control from day-to-day symptom fluctuation and genuine change in disability.
Confirmed relapses, new or enlarging T2 lesions, and gadolinium-enhancing lesions on a comparable scan protocol.
EDSS interpreted with timed walking, hand function, vision, and other MS Functional Composite measures.
Fatigue, cognition, bladder, pain, work, participation, and quality of life with validated tools.
Infection, fertility, blood counts, organ toxicity, malignancy surveillance, and treatment-related hospitalization.

Clinical review before travel
Send us your records and our specialists confirm your phenotype, current inflammatory activity, prior treatment history, and transplant readiness — so you know exactly what to expect before you travel.
Transparent planning
AHSCT, outpatient MSC protocols, intrathecal delivery, rehabilitation, and imaging are priced as distinct programs. Your quote names the exact intervention and includes conditioning, hospitalization, infection support, imaging, and follow-up, plus airport and hotel support for your stay.
Our 2026 neurological program band starts from $9,000-$25,000, giving you a transparent planning range before your free evaluation confirms the exact protocol and price.
Is this AHSCT, MSC infusion, intrathecal delivery, exosomes, or another product?
Which MS phenotype, activity level, comparator, and endpoint match the cited evidence?
What conditioning, infection, infertility, malignancy, and hospitalization risks apply?
How will relapses, MRI activity, disability, function, and long-term safety be tracked?
FAQ
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