Looking forward to speaking to Antony tomorrow morning on ⁦BBC Tees⁩ about our small charity in memory of our son David & #rarediseaseday2023 wonderful.org/fundraisers/nV…

Tomorrow morning I will be chatting to Antony on the amazing #localradio BBC Tees 📻 Talking about #rarediseaseday2023 & what our small charity TheDavidAshwellFoundation does to raise funds & awareness for #ACD #research ACDA

I’m wearing my 👖 for #RareDiseaseDay2023 Are you?

Remembering our precious boy David who would be 12 today. Not a day goes by when we don’t remember you or wonder what you would be doing. #babyloss #grief #fordavid #RareDisease ACDA

Remembering our precious boy David who would be 12 today. Not a day goes by when we don’t remember you or wonder what you would be doing. #babyloss #grief #fordavid #RareDisease TheDavidAshwellFoundation ACDA

ATS/Alveolar Capillary Dysplasia Research Grant from American Thoracic Society (ATS) is funded together with the ACDA and TheDavidAshwellFoundation to support researchers working on the rare disease ACDMPV. research.thoracic.org/grants/partner… Applications close on January 8, 2024. #ResearchFunding #scientifyRESEARCH

#waveoflight2023 remembering David & too many precious babies taken too soon #babylossawareness #raredisease ACDA

Remembering my son David & so many parents going through the unimaginable grief of child loss #waveoflight2023

It is coming up to rare disease day 2024! Rare Disease Day is on Thursday 29th Feb. If you’d like to support our small charity The David Ashwell Foundation & wear jeans for genes… please do get in touch! You can donate here wonderful.org/fundraisers/384 #ForDavid💙

It’s rare disease day on Thur 29th Feb Please support our charity & wear jeans (or blue) to school or work raising awareness of rare diseases & heping us fundraise for research into this rare disease that took our newborn baby David. 👖💙 wonderful.org/fundraisers/Nl…

What an absolute privilege to put on my jeans 👖 and stand up in front of Yarm School Prep & Pre-prep pupils to talk about #rarediseaseday and the fundraising they are going to do for our small charity the #Davidashwellfoundation wonderful.org/fundraisers/Nl…

Amazing questions from the students! Thank you for supporting our small charity and giving me the opportunity to talk about my biggest boy David. wonderful.org/fundraisers/Nl…

It was a pleasure to welcome Prof Amelia A Lake to school to talk about #RareDiseaseDay which we will be supporting with our 'Jeans for Genes' fundraiser this week. Looking forward to breaking out the denim and supporting the brilliant TheDavidAshwellFoundation. Yarm School Joanne Speight

It’s #RareDiseaseDay2024 We have our 👖💙 on remembering baby David & raising money for ACDA #research Please donate 👇🏼 wonderful.org/fundraisers/Nl… & send me pictures of you in your jeans 🤳📸 #babyloss #RareDisease

We are wearing our 👖 & denim today remembering my baby boy & fund raising for research in his memory. Please support us wonderful.org/fundraisers/Nl…

It’s #RareDiseaseDay2024 Remember to support our small charity TheDavidAshwellFoundation wonderful.org/fundraisers/Nl…

The school is awash with denim as part of our Jeans for Genes fundraiser in support of #RareDiseaseDay2024 and TheDavidAshwellFoundation. Many thanks to all members of our community who have supported such a valuable cause. #SchoolValues #responsibility #Compassion Yarm School Joanne Speight

So gorgeous to see so many children remembering David today on #RareDiseaseDay2024 & fundraising for #ACD research!👖💙 Thank you Yarm School Joanne Speight Bill Sawyer ACDA #ForDavid💙 wonderful.org/fundraisers/Nl…

13 years ago today our first baby was born. David - a gorgeous boy! Joy was overtaken by the worst possible nightmare when David became seriously ill only 48hrs after birth. We got a diagnosis of #raredisease #ACD & on day 15 we said goodbye. #ForDavid💙 TheDavidAshwellFoundation

13 years ago we said goodbye to our beautiful baby David. Today his magnolia tree has one flower open, as if acknowledging his special place here - but not here. Miss you every single day my biggest boy #david💙 TheDavidAshwellFoundation #babyloss #raredisease #ACD