As an incredible high achiever, Rachel shares her story through all of the ups and down from 55 years of experience. We chat about how medicine and surgery has evolved over time, as well as the tips and tricks Rachel has used to help her over the years.

Da'Veon and his mum Vonney join me to talk through Da'Veon's incredible Hirschsprung's journey.Da'Veon shares his story from both a physical and spiritual point of view, as well as very honest recount of his school struggles.We also talk about how diet and exercise have really helped him Da'Veon in controlling his Hirschsprung's symptoms.

Fellow radio host Stephanie talks about her extremely rare Hirschsprung's diagnosis as well as how her quality of life has differed over the years.Diagnosed with TCHD+ Stephanie remains one of the rarest forms of Hirschsprung's ever known, from this she has been able to work in radio and is in the process of writing a book.

Two and a half years on from her first appearance Aimee rejoins the show to chat about everything she has achieved in that time, including new information and a global book tour!In the first part of her story Aimee shares her extraordinary life with one of the rarest forms of Hirschsprung's ever seen, which left her with just 60cm of small bowel, on the face of it, a medical impossibility! We chat about how despite her illness, Aimee runs 2 businesses and a busy home life, as well as being an inspiration to many in showing that anything is possible.Stay tuned to find out when the book will be released and which countries Aimee will be touring.

Kaytlin rejoins the podcast, a year after her first episode, to talk about her daughter Isabella and how she is progressing with her condition.A completely different episode from part 1, Kaytlin chats about the clubs that Isabella has now joined, and the need for these activities to be as inclusive as possible.We also talk about how Isabella is doing medically and look positively towards the future.

Lex talks about her son Frankie's complicated Hirschsprung's story as well as being diagnosed with short gut/intestinal failure.We also chat about surgery, as Frankie has already had 14, and the impact this can have on young children. Lex also explains her way of advocacy through her excellent social media account the documents her son's Hirschsprung's life.

After her local hospital had no idea what was wrong, Megan became increasingly concerned about her son Oaklee when he was diagnosed with Hirschsprung's Disease.We also chat about Megan and her families involvement in the Every Step Campaign, an organisation that supports patients and parents across Newcastle, and how the whole family was involved in the promotion.Megan explains that even though Oaklee's story hasn't been straightforward he is doing really well and thriving, as well as what they hope for in the future.

Jodie talks about her 8 month old daughter Libby and her variety of medical conditions, including Hirschsprung's Disease and Mowat-Wilson Syndrome.We talk about the need for advocacy and how Jodie and her husband have had to learn a lot in the first 8 months, when it comes to these conditions. Jodie also explains the importance of seeing the glass half full when it comes to seeing what Libby can achieve.
Follow Jodie - @growingwithlibby

Megha comes back on the show to give us an update on life after 18 months. Although not without its challenges, this is a wonderfully positive episode focusing on how Anya is progressing with her Hirschsprung's.

Mum of four Nicole, joins me to talk about her 6 month old son Holt and his remarkable Hirschsprung's story. Nicole talks in detail about how strong her son is and the multiple red flags missed by the hospital, as well as how her mothers instinct was critical in helping her son to receive the correct diagnosis.Follow Nicole on TikTok - @nicolevoss