<div>Hi,
</div>
<div><br />
</div>
<div>I’m raising funds for my niece in Pakistan.
</div>
<div>Rahima, is a bright, beautiful one-year-old baby with the sweetest smile. But behind that smile, she’s fighting a rare and life-threatening disease called Spinal Muscular Atrophy (SMA).
</div>
<div><br />
</div>
<div>What is SMA?
</div>
<div><br />
</div>
<div>SMA is a genetic condition that affects the motor nerve cells in the spinal cord. Over time, these cells stop sending signals to the muscles, leading to muscle weakness and wasting.
</div>
<ul>
<li>Babies with SMA often struggle to sit, crawl, or even breathe on their own.
</li>
<li>Without treatment, SMA can be fatal — especially in the most severe form, Type 1, which often affects infants before they reach their second birthday.
</li>
</ul>
<div><br />
</div>
<div>Current Treatment
</div>
<div><br />
</div>
<div>Right now, Rahima is receiving risdiplam— a medication that helps her body produce more of the protein she’s missing.
</div>
<ul>
<li>This treatment is lifelong and extremely expensive in Pakistan, costing around PKR 1.3 million (USD ~$4,500) every month.
</li>
<li>While risdiplam slows down the disease, it does not fix the underlying genetic cause. If we stop treatment, her condition will quickly worsen.
</li>
</ul>
<div><br />
</div>
<div>The Ultimate Goal — Zolgensma
</div>
<div><br />
</div>
<div>The only treatment that can address the root cause of SMA is Zolgensma — a groundbreaking one-time gene therapy that replaces the faulty gene with a healthy copy.
</div>
<ul>
<li>Cost: USD $2.1 million (over PKR 700 million) for a single infusion.
</li>
<li>Zolgensma offers the chance for a normal life without lifelong injections or medicines, but it must be given as early as possible to prevent further muscle loss.
</li>
</ul>
<div><br />
</div>
<div>Why We Need Your Help
</div>
<div><br />
</div>
<div>We are in a race against time. Every day matters.
</div>
<ul>
<li>Every penny raised will go towards keeping her alive — whether that’s continuing risdiplam to maintain her strength or moving toward Zolgensma for a permanent solution.
</li>
<li>Even the smallest donation can help us buy more time and hope.
</li>
</ul>
<div><br />
</div>
<div>Raising millions might seem an impossible challenge but together we can move mountains and save a child’s life! The biggest fundraiser on Gofundme: $45 million - Americas Food Fund! All thanks to people like you.  2.1 million is only 5% of that immense achievement. We’re starting small with £50,000 but hope to build momentum and reach our ultimate goal with providing Rahima the Zolgensma gene therapy.
</div>
<div><br />
</div>
<div>From the bottom of our hearts, thank you for giving Rahima a fighting chance. Together, we can give her the gift of life.
</div>

Nazmun Nahar

Amel Belayachi

Hajra Bibi

Anonymous

Huzaifa Mehmood

Eman Alwattar

Rae Adams

Help Rahima get a chance at Life - urgent SMA treatment need

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Help Rahima get a chance at Life - urgent SMA treatment need

Still £49,341 to go. Help us build momentum.