Just wanted to say, I'm sorry I haven't been round much-well posting much anyway, this week.
I just thought I'd let you know, even though you haven't seen me posting, I am still doing daily spot-checks on the forum, to make sure there's no actual modding that needs doing.
Cody you seem to be doing an excellant job of responding and welcoming people, and Abbs it's nice to see you're still around and posting too.
I'm just not 100% at the minute, physically and definately not mentally. I'm not nearly as strong as you lovely lot. Add that too being busy with college and stressed out like the big numpty I am (my tutor keeps telling me there's nothing to stress at, but I can't help it)
Anyway, I just wanted you too know.
Hugs to everyone, and I promise to try and get back to my normal self in the near future.
PS: Cody, this does not mean you can go crazy, and get drunk on the forums........I will still be watching.
Moderator of the Cystic Fibrosis Forums
Cystic Fibrosis, Asthma, ABPA, Clinical Depression, Mild Liver Cirrohsis, Mild Osteopenia, Erythema Nodosum. Waiting for final diagnosis on Muscular Dystrophy type symptoms.
Medication: Creon 10,000, Vitamins A,D+E, Serevent, Salbutamol, Paracetamol, Tramadol, Nefopam, Ursodeoxycholic Acid, Trazodone, Slow-Sodium, Azithromycin, Metachlopromide, Omeprazole, Tobi Ineb, Fresubin Liquid Feed, Skandishakes. I use PEP device as my physio. Had a Port-a-cath fitted on chest wall since Nov 04
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Sometimes, I feel that I should go and play with the thunder - then I get scared and run away.I'm from the UK!!!!! If anything I say makes no sense to you, let me know so I know how not to be so English.
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