<div>Hi, my name is Yvonne, and as some of you may know, I was diagnosed with multiple sclerosis in 2019 at 25 years old.
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<div>MS causes the immune system to mistakenly attack the nerves protective layer, leading to many unpredictable and sometimes permanent symptoms.
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<div>Although my diagnoses is relapsing remitting MS, the attacks I've had have been aggressive, leading to permanent loss of vision in my right eye, slight decreased vision in my left eye, weakness in my right leg, and extreme fatigue.
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<div>In April, I suffered another attack which caused further weakness in my leg and a loss of balance. I can no longer walk unaided, and require a crutch to get around. I've suffered several falls, some worse than others.
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<div>Unfortunately, the treatments I've previously tried were unsuccessful and my condition continues to deteriorate. Both treatments included, what I can only describe as, horrific side effects. Sickness, constant nausea, hair loss, headaches, increased risks of cancer and serious brain infections, amongst many more.
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<div>Although there is no cure for multiple sclerosis, the current treatments in Ireland are designed to slow down progression, but not stop it.
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<div>I have recently been accepted for a HSCT treatment in Mexico. This treatment has a high success rate and is designed to halt MS and, essentially, stop it in it's tracks, along with the possibility of repairing some of the damaged nerves. 
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<div>Unfortunately, due to funding issues, this treatment isn't available to MS patients in Ireland.
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<div>This treatment will completely destroy my immune system, and 'reboot' it. It is a long and aggressive treatment that includes freezing of my eggs before going due to increased risk of early menopause, a wide range of testing on arrival, the collection of stem cells, 4 rounds of chemotherapy, and then reintroducing the stem cells to my body. The process takes between 28-30 days.
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<div>Although this seems like a very invasive treatment, it is currently my only hope of living a somewhat 'normal' life.
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<div>When I was diagnosed, it changed my life in more ways than I could have ever imagined. I try to remain positive, but the reality is that I'm currently living on edge of what could or will happen next.
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<div>The money raised will help pay for the following:
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<div>• The treatment cost.
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<div>• Travel costs.
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<div>• Wigs.
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<div>• Medical travel insurance.
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<div>• Essential items needed throughout the month.
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<div>• Further testing, pre and post Mexico that may not be covered by the HSE.
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<div>• Basic home adaptions needed upon arrival home to accommodate weakness.
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<div>If for any reason, the treatment doesn't go ahead, the money can be returned or donated to a similar cause, but I'm hopeful that with your help and support, we can make this happen!
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<div>Thank you for taking the time to read my story. I would truly appreciate any donations, big or small, or any fundraiser ideas you might have.
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<div>Yvonne x 
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Sitholumusa Ndlovu

Anonymous

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Paula Corcoran

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Louise Ryan

Una Adams

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Avril Coakley

Patrick Ray

Support Yvonne's HSCT Journey

Support Yvonne's HSCT Journey

Still €54,806 to go. Help us build momentum.