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

Natalie joins me to talk about her 1 year old daughter Esme and her Hirschsprung's journey so far, including how the family copes with hospital visits and surgeries. Within this episode Natalie gives us an insight into juggling hospital and family life.Natalie also talks about how strong and resilient her daughter is and how, even at the age of 1, she knows her own body incredibly well.

In this episode we chat about Katie's sons Hirschsprung's story. We start with Katie, who was diagnosed at birth with PKU which affects 1 in 10,000 people and made her pregnancy high risk.After her son was born, Katie had an unfortunate time with misleading care, which led to confusion and increased anxiety. Later in the episode we talk about how having a community and support around can really help.

A very moving and varied Hirschsprung's journey, as Andrea shares all about her son's Total Colonic Hirschsprung's. During the episode Andrea talks about the complexities of having a child with a weakened immune system and how she navigates public places to give him the most 'normal' life possible.Follow Andrea - @andrearguse

Jodie talks about her son Ollie, who has long segment Hirschsprung's Disease. In this episode we talk about plenty of challenges that Ollie has faced over the last 10 years, including multiple bouts of enterocolitis and stoma issues. Later on we talk about how Ollie is getting on with his ACE stoma and how it has improved his quality of life.
Follow Jodie - @jodie_mulrainey28