Hi all, I’m Molly my mums daughter. She’s had ms for 12 years and unfortunately has now got advanced ms now all ms is different and I’m not writing this to scare or hurt anyone. I would just really like some advice please We’re looking at a rig or peg feeding tube for my mum as she really struggles with choking. We’ve spoken to doctors but they’ve said usually they do it for people who are in the earlier stages of ms I just wondered if anyone had one and can share there experience or give us any advice. It would be very appreciated. I hope whoever’s reading this is having a amazing day, thank you