Alyssa MPS1
Baby Alyssa continues her brave fight against MPS1. We are rallying to find a life-saving bone marrow donor and raise crucial funds for her urgent treatment.
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Go Fund Me | Donate to Save Alyssa – A Baby’s Urgent Fight Against Hurler Syndrome
Go Fund Me | Donate to Save Alyssa – A Baby’s Urgent Fight Against Hurler Syndrome
Help Save Alyssa in Time Alyssa Aldworth is a joyful and cur… Jo Porter needs your support for Save Alyssa – A Baby’s Urgent Fight Against Hurler Syndrome
ALLY IN THE NEWS
Noel Johnson: Baby Alyssa Aldworth Campaign - Cassette Radio
Noel Johnson: Baby Alyssa Aldworth Campaign - Cassette Radio
Baby Alyssa’s parents spread awareness on Hurler Syndrome - The Drive By
Baby Alyssa’s parents spread awareness on Hurler Syndrome - The Drive By
DKMS Africa
DKMS Africa
KZN-pa ná dogter se skokdiagnose: ‘Dis seer in ons binneste, maar ons is sterk vir haar’ | Huisgenoot
KZN-pa ná dogter se skokdiagnose: ‘Dis seer in ons binneste, maar ons is sterk vir haar’ | Huisgenoot
Dis hulle dogter se glimlag wat hulle in die donker en moeilike dae aan die gang hou. Wanneer baba Alyssa Aldworth vir haar ouers glimlag asof niks verkeerd is nie, is dit amper asof hulle vergeet dat sy ’n seldsame genetiese siekte het.
Community rallies around baby Alyssa | Northglen News
Community rallies around baby Alyssa | Northglen News
Alyssa was recently diagnosed with Mucopolysarcharidosis (MPS I) also known as Hurler Syndrome, a rare and serious genetic disorder.
Every rand counts for baby Alyssa | Tabloid Media
Every rand counts for baby Alyssa | Tabloid Media
The Durban North News is part of the Tabloid Newspapers Group of Community newspapers - distributed FREE to 32000 homes in Umhlanga, La Lucia, Avoca, Effingham, Seacow Lake, Redhill, Greenwood Park, Riverside and surrounding areas weekly on a Wednesday
Alyssa's fight: Parents launch campaign for urgent treatment of rare condition | IOL News
Alyssa's fight: Parents launch campaign for urgent treatment of rare condition | IOL News
A young couple from Somerset Park, KwaZulu-Natal, is fighting against time to secure life-saving treatment for their daughter Alyssa, diagnosed with the rare genetic disorder MPS I.
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