The msg's i have recieved today has just confirmed I have made the right decition to stay as a Fibromite LOL. You are all so kind and lovely,
I will continue to try and be as helpful and kind to all you special people, we all have something in common "dam Fibro" so heres to common ground for all of us.
I havent replied to everyone today, and its not because i cant be bothered.
Ive had quite a bad day today, Up at 9am, back a sleep by 6pm, up at 8.30pm and i feel like crap...
I have swollen glands, a lump in my neck, IBS flare up and god dam now a coldsore in my top lip lol !!!!!!!! Prob a bit run down, so im going to take it easy for a few days and rest as much as I can.
I just wanted to thank you all for replying to my msg, THANK YOU YOU ARE SWEETHEARTS.
Yes i do get swollen glands occationally, Ive suffered with coldsores since i was 7, but the lump in my neck is something new.. IBS is also something regualar for me too, i can have bouts of both in the same day so taking tabs just confuses my system even more lol.
Thanks Jom, Me too i hate being poorly, especially with cold sores, they just take so long to go. Ive used Zovirax several times and i must be allergic to it, It makes my cold sores 10 x worse, and it burns so bad ive had to wipe it off and end up with them infected then..
I have crap immune system too. Just taken over 3 weeks to get over a cold, then I find out I am iga deficient and means takes me a long time to get over illnesses, even with double doses of antibiotics. No s**t Sherlock. Also waiting on repeat bloods, which I have 'sticky blood', may mean lupus or Hughes syndrome, plus hypermobility syndrome. I think someone thinks I like to collect diagnoses.
Have you tried something like blistex, might not be as strong as zouvirax. If your glands are something new, go to docs. Might be worth it, if its infected and they could also think of something else for your coldsores. Although that's one thing I don't get, my sister does get them really bad, so I see how much it affects people.
You take care and keep us posted on how you are.
Still grateful about your nytol experience, nearly tried it myself. Will stick to taking 2 antihistamines when really need it.
Oh my u do have a lot to contend with. Hope its not Lupus, Ive tried blistex b4 and yes im ok with that, thing is with cold sores u need to treat at the first signs of itching or theres no stopping them. Im prob a bit run down at min, i was the same as u with antibiotics, i always needed 2 to 3 prescrpitions for chest infections to go. Ive also always suffered with chest infections from a few months old. My dad said i had bronchitis at 2 months old and it carried on into my 30s, The last chest infection i had was 12 months ago and it took 3 weeks of antibiotics and an inhaler!! so ive gone up a notch lol. First inhaler ive ever had to have.
I couldnt get out of bed one morning for the wheezing... it was awful. We have a history of immune problems in the family, my son has Ulcerative Colitis and auto-immune hepititis (Liver problems).. Apparently M.E, which i also have, has some connection to immune problems,
Basically my once fit and healthy body, gained from years of fitness has kicked me in the teeth, big time lol. But hey i have to deal with it as do we all.
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A message from Jules- thank you for the love!
A warm belated \"HAPPY NEW YEAR\"to all my fellow fibro mites
My fibro birthing site a kind of hello again
Thank you my lovely fibro friends
My daughter found this and sent it to me. I cannot get to the end without crying. Its just perect.
