Below you can find a range of information about TTP including videos of our past events, tips for travelling with TTP, patient stories, Scholarly articles and more.
Take a look at the map for details of your local specialist centre, including (where available) contact numbers.
If you are not yet linked to a specialist centre, take a look at where your nearest is, click the pin to see the Lead Consultants name. Take this name to your GP and ask for a referral.
Specialist centres and NHS England are keen to ensure anyone with a TTP diagnoses in England, no matter how long ago, is linked in to a specialist TTP centre.
Contact us for help or support
This group is for anyone dealing with the rare blood disorder Thrombotic Thrombocytopenic Purpura. Their familes or medical professionals.
Donate at our fundraising platform, or join our shop and give scheme or our lottery. We are also keen to hear from you if you wish to fundraise on our behalf.
TTPNetwork is led by volunteers and we welcome any support, particularly if you have experience of being a trustee.
