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The Aplastic Anaemia Trust

The Aplastic Anaemia Trust

Non-profit OrganizationsFlag of GBUnited Kingdom11-20 Employees

Company overview

HeadquartersUnited Kingdom
Website
NAICS813
SIC832
Keywords
Charity, Research, Health, Fundraising, Patient Support, Aplastic Anaemia
Founded1986
Employees11-20

Key Contact at The Aplastic Anaemia Trust

Flag of GB

Joe Kirwin

Chief Executive Officer

The Aplastic Anaemia Trust Email Formats

The Aplastic Anaemia Trust uses 2 email formats. The most common is {first name}{last name} (e.g., johndoe@theaat.org.uk), used 66.7% of the time.

FormatExamplePercentage
{first name}{last name}
johndoe@theaat.org.uk
66.7%
{first initial}{last name}
jdoe@theaat.org.uk
33.3%

About The Aplastic Anaemia Trust

About us The Aplastic Anaemia Trust is the only UK charity providing information, advice and support to people affected by rare disease Aplastic Anaemia. Our vision is that everyone affected by Aplastic Anaemia in the UK should feel empowered and have access to the best possible treatment, care and support so they can lead full and healthy lives. We support our community through one of life’s toughest challenges – diagnosis with a rare bone marrow failure. We currently support around 1,400 people and have around 50 volunteers. In this rare and life-threatening disease, the bone marrow fails to produce healthy levels of our blood cells. Aplastic Anaemia can affect people at any age. However, children, young people, and people aged 60 and above are most vulnerable. In the UK, around 150 people are diagnosed with Aplastic Anaemia every year. It can be inherited or caused by an autoimmune reaction Recently, several cases of Aplastic Anaemia have been confirmed to be as a result of a Covid-19 infection. However, in many cases the causes are as yet unknown. Aplastic Anaemia has a serious and long-term impact on a person’s life and health. Symptoms include extreme tiredness, frequent infections, bruising and bleeding. In very severe cases it can be life-limiting. Diagnosis usually involves a bone marrow biopsy, which many people find traumatic. Treatments can be aggressive and include blood transfusions, drugs, immune-suppressive treatment, and stem cell transplant. In some cases, people – especially children – will need a Bone Marrow Transplant to be cured. Hospital appointments, tests and treatments can span years. Our aims Our aim is for people affected by Aplastic Anaemia to have better treatment, better information and better networks.

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The Aplastic Anaemia Trust revenue & valuation

Annual revenue$1,711,100
Revenue per employee$86,000
Estimated valuation?$5,500,000
Total fundingNo funding

Employees by Management Level

Total employees: 11-20

Seniority

Employees

Entry
C-Suite
Manager

Employees by Department

The Aplastic Anaemia Trust has 6 employees across 5 departments.

Departments

Number of employees

Funding Data

The Aplastic Anaemia Trust has never raised funding before.

The Aplastic Anaemia Trust Tech Stack

Discover the technologies and tools that power The Aplastic Anaemia Trust's digital infrastructure, from frameworks to analytics platforms.

reCAPTCHA

reCAPTCHA

Security

Cloudflare Bot Management

Cloudflare Bot Management

Security

Royal Mail

Royal Mail

Shipping carriers

Microsoft 365

Microsoft 365

Email

Cloudflare

Cloudflare

CDN

Stripe

Stripe

Payment processors

jQuery

jQuery

JavaScript libraries

HSTS

HSTS

Security

MailChimp

MailChimp

Email

Google Analytics

Google Analytics

Analytics

Microsoft ASP.NET

Microsoft ASP.NET

Web frameworks

Google Tag Manager

Google Tag Manager

Tag managers

Frequently asked questions

The Aplastic Anaemia Trust is located in GB.
The Aplastic Anaemia Trust was founded in 1986, making it 40 years old. The company has established itself as a significant player in its industry over this time.
The Aplastic Anaemia Trust has approximately 11-20 employees. The company continues to grow its workforce to support its business operations and expansion.

4.8

40,000 users

top 50
high performer
most used
tier 1 accuracy

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