JoanDublin
Senior Member
- Messages
- 369
- Location
- Dublin, Ireland
Thanks for that info Abha. Im storing it all up. I'll see what the Childrens Hospital suggest next week and take it from there. Its good to have other avenues and recommendations for next steps if needed though so thanks a million. I had to look up PTHP. Its very interesting and not something I had even considered.Joan....As you are in Dublin ,I think it might be a good idea to take your son to see Professor Thompson(Beaumont) as he is an expert on PTHP(pituitary issues too).That GP(mentioned above) who dealt with me all those years ago was an Irish Rugby player(pre War?).I have also contacted an endocrinologist to rule out/or in PTHP, in my case.I now believe I have the latter.According to the Daily Mail article in May and other articles that I have read since, many people being diagnosed with ME/CFS probably have PTHP(and no one has recognised that).NICE seemingly have ignored it and I believe in Scotland a Group there are fighting to get it recognised so, that the patient can get the treatment(hormones etc) that their case may require.It is much easier(cheaper?) to send patients off to Psychiatrists/Psychologists.
I attend Beaumont Hospital myself so I will check this guy out. There may be an issue because my son is a Paediatric case though, but no harm in checking it out