Research and the ITP Support Association

The Association is a registered charity whose aims are to promote and improve the general welfare of patients and their families. It does this in a number of ways, by providing written information, support through the website, access to experts, mentors and other patients, and through the Conventions and small group meetings which allow patients to meet others with similar problems to discuss and share their issues. ­

The Association also has an important role highlighting the disease regionally, nationally and internationally through links with Societies and specialist groups, by organising medical seminars and by communicating with the regulators, commissioners and various NHS bodies. We have also been active in linking in with other patient groups and have strong links with the PDSA in the States and with a number of the European groups. ­ rough the latter we have been pushing recognition of ITP, as a bleeding disorder, on a wider scale.

My Success with MMF

 By Anthony Heard

As I approach my thirteenth ITP Birthday on July 28th, I can reflect upon plenty of incidents during ITP years. It hasn’t been a picnic by any means. I have been through the Prednisolone ringer five times, Rituximab twice and a horrible week or so with Azathioprine (I could not tolerate it all and withdrew from it within ten days).

I am one of those ITP sufferers who have been fortunate to respond well to Prednisolone and Rituximab. With the steroid, I have obtained about 6 months remission every time that I went on it and with Rituximab, I got about 2 years and 8 months remission both times that I had it. But in February 2016, I relapsed from the Rituximab remission that I had enjoyed since Summer 2013.

So, at that point my specialist suggested that we try Mycophenolate Mofetil (MMF). He was reluctant for me to undergo a third round of Rituximab treatment. Although I had responded well to it twice already (2010 & 2013). He felt that the long-term damage that it could potentially do to my immune system was not worth the risk. More long stints with Prednisolone were also ruled out. Although I responded well to it, the problems that it caused every time that I had used it on 5 occasions already, would just not be bearable again. 

Second Meeting of the West Sussex ITP Support Group

We welcomed two new members to the West Sussex ITP Support Group meeting which was held recently in Chichester, details of the next meeting are available at Local Support Group Meetings

June 25, 2019
-Approval Based on Positive Efficacy and Safety Data from Two Phase 3 Clinical Trials-
-Company Intends to Partner for the European Commercialization of DOPTELETDURHAM, N.C., June 25, 2019 (GLOBE NEWSWIRE) -- Dova Pharmaceuticals, Inc. (NASDAQ: DOVA), a pharmaceutical company focused on acquiring, developing and commercializing drug candidates for diseases where there is a high unmet need,

ITP Support Association Christmas Cards

Yes, we know its only early summer but we have already had a number of requests from people asking when will our Christmas Cards be available, well, here they are. To order go to the ITP Shop, click here >>>>>

First Meeting of the Scotland ITP Local Support Group

The first meeting of the Scotland ITP Local Support Group was held on 6th June 2019 in Edinburgh, a big thank you to everyone who attended.

First Meeting of the Nottinghamshire ITP Support Group

The first meeting of the Nottinghamshire ITP Support Group took place recently in Chichester, details of the next meeting are available at Local Support Group Meetings

First Meeting of the West Sussex ITP Support Group

The first meeting of the West Sussex ITP Support Group took place recently in Chichester, details of the next meeting are available at Local Support Group Meetings