A Cambuslang mum said she got “no answers” from the Scottish Parliament after appealing for help to establish a clinic that can treat her young son’s rare condition.
Jennifer Mellin tried to spread awareness of young Finlay’s condition at a meeting last Wednesday but branded the experience as “frustrating”.
The two-year-old has Poland syndrome, a rare limb difference which has left him with a shorter left hand and arm, a sunken chest and a missing shoulder tendon.
Parents Jennifer and Chris recently spoke to Lanarkshire Live about how, due to there being no clinic in Scotland, they were forced to travel to Birmingham to consult a specialistThe Lanarkshire Live app is available to download now.
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