From Facebook

Some of this technology came from my ā€œdeath rayā€ research :sunglasses::man_health_worker::telescope::satellite::microscope::radioactive::rocket:

https://www.facebook.com/479163965435700/posts/3118232578195479/

The Canadian Mastocytosis society will be having a webinar available on Feb 29 for people looking for some strategies for living with a rare disease. Available in both English and French.

https://mastocytosis.ca/en/rare-disease-day-2020

A new Organ?

Rydapt mailing from Inspire Advanced Systemic Mastocytosis

https://view.email.inspire.com/?qs=d48db286e9713604c532d19f4b55cb5edb338dab899626b0b673d6141532d6c0fd417246c446379be9307607ff55479e165c391e32dc924ff3ef370fd4ae316d839b2588c66b741f

A video lecture on MCAS given by renowned US clinician Dr Lawrence Afrin at NUI Maynooth on Monday the 18th of November 2019.

The lecture was organised in conjunction with Professor Bernard Mahon an Immunologist from the Department of Biology.

The first few minutes are taken up by an introduction by Prof Mahon and then there is a short introduction by Gavin Tobin the first Irish patient diagnosed under draft MCAS criteria.

Dr Afrin’s lecture starts 16 minutes into the clip and there is a Q & A session at the end.

TMS Mast Cell Disorder Primer PowerPoint presentation

From a rheumatology-immunocompromised perspective.

Happy Rare Disease Day! Here is Super T’s Mast Cell Foundation nonprofit at Rare Disease Day 2020!

Check out the Advocacy!

Virus of the week, last week type A influenza, this week bronchitis and who knows what?

Headed out to Walmart and CVS. Let us know if you need anything.

I’m up for dinner on a beach in Greece.

ā€œAsk your doctorā€ is the boilerplate recommendation in pharmaceutical ads. So, since food is medicine, why not ask doctors about which diet they recommend? That’s what Sermo (a social platform for physicians and a healthcare data collection company) recently did when it surveyed 515 US physicians across 27 specialties.