I'M SCARED!... Aspergillus Fumigatus?

[ClockworkOrange]

Spent the last 24 hours looking on the internet and getting extremely worried and I suppose scared.

Eighteen months I was diagnosed with COPD (chronic obstructive pulmonary disease).

The only time it has effected me is when I have had a chest infection. The only medication I have been taking reguarly is Seretide 125 two puffs twice a day.

Had to go back to see my consultant at hospital and after last blood test, he was pleased to tell me I did not have an allergy to birds but the blood test had shown up my reading was very high on Aspergillus Fumigatus!

So, yesteday I started taking Prednisolone 10 mg and Itraconazole 100 mg in the morning. Plus the obligatory Salbutamol and Seretide. I am also to be put on a Bone Protector...............sounds like armour for riding my bike!

HOWEVER, despite I thought I was on a relatively low dose of Prednisolone I am so worried about the side effects, facial hair, Moon Face, edema in my legs and a hump on my back and that's on a good day!..............aaaaaaaaaaaaaargh!

Is this rare, can anybody put my mind at rest with any of the above.

Clock.......................fed up cos still not well enough to ride!

[OakLeaf]

Did the doctor say you're allergic to aspergillus (very common, it's a pervasive mold), or that you're infected with it? What blood tests did they do? Did he lead you to believe that you'll need to be on Prednisolone for a long time?

[alpinerabbit]

I think therapy for aspergilloses is in the range of weeks.
I'm pretty sure the serious side effects of corticosteroids only come over the long term.

But sheesh! How on earth! I hope you are being taken care off and that this clears up asap.

[ClockworkOrange]

No, I didn't make things very clear, I kid you not, I am so worried about the outcome.

Anyway, the diagnosis has now changed from COPD to asthma and he said that this fungus thing is in the airways, he basically described it as green sticky blobs that stick to the sides?

I have to have a blood test in 4 weeks and he has written down 'Asthma and aspergillus infection' The blood test I suppose is just routine, it's has boxes ticked by Renal, Liver and FBC.

Something else I forgot to mention, I have been told I am to be on them between 6 months to 1 year.

Clock

[PamNY]

Can you talk to a pharmacist about the drugs? I don't know how your health care system differs from ours, but I have found them to be really helpful. Best wishes to you; I hope all goes well.

Pam

[Duck on Wheels]

Hi Clock! Try not to worry too much about the Prednisone. Yes, there can be side effects, but one of them is a feeling of extra energy Speaking as someone who's been on high doses for long periods of time, the side effects do go away and that energy boost one is missed when it goes.

[spindizzy]

Your dose of corticosteroid is not a large one -provided you are only taking it once a day. You should probably protect your bones though, Vit D and Calcium.

[Zen]

I am also to be put on a Bone Protector...............sounds like armour for riding my bike!

Sounds like she's been prescribed Boniva or something along those lines.

[ClockworkOrange]

Thanks for all the useful tips.

I like the sound of having more energy!

Am so trying to eat better foods, am even enjoying sardines for my lunch, I believe that is a good source of Vit D............plus sunbathing.

I am waiting to be told what Bone Protector I am to have, still not happy about that. I read something 'The Delusion of Bone Drugs'!

If I end up with a full beard, a Moon Face, humpity back and oedema in my legs making them fatter than what they are already and it is only for a year BUT I do not get this awful shortness of breath, then let's go for it!

Clock......................the bells, the bells.....Long Chaney, eat ya heart out!

[bmccasland]

Clock - I was on Prednisone therapy after my allergic reaction to something I ate (squid or octapus or squid ink). I didn't notice any "extra energy" - what I noticed was I was figidty. Didn't help that part of the time I was at a conference, sitting in lectures most of the day. I walked down to the nearest pharmacy to ask the local pharmacist if I was going insane or was it a side effect to the Prednisone. She reassured me that my sanity was safe, it was the drugs, and that once I was off them, I'd quit being so twitchy. I suppose if I was home, and had access to my bike, it would have been better. It certainly didn't help that there were raging forest fires in the area, so I couldn't exercise outside (asthmatic lungs do not like smoke filled valleys). I was only on Prednisone for a two weeks, so maybe over time I would have gotten used to the side effect, but it drove me nuts sitting in the hotel conference facilities.

At home, where you could take breaks, or go for a walk or ride, you could probably cope better than I was able to - captive in the conference. I didn't notice the side effects nearly as much on field trip days - hiking to look at stream restoration sites.

Good luck.

[spindizzy]

If you're only on pred one once a day- better to take it in the morning. Parents of kids with asthma who are having an exacerbation always complain how "hyper" it makes their kids.

[ms1]

I've been on Prednisone many times for an arthritis problem. Long term is definitely a problem and that's where the permanent side effects that you are reading about come in.

For short term use, there are some side effects, but the important thing is that they go away once you are off the medication.

Everyone is different, but for me, the worst side effect is nervous energy, but not the good kind of energy that one of the posters discussed. After about a week or two, I have trouble sleeping at night and am uncharacteristically sensitive, much like PMS. This is very unpleasant, but it goes away once I'm off the medication.

Long term use is totally different.

I hope that helps.

[Mistie]

I know a guy who has a platlet problem and goes on prednisone about 6 month out of a year. He went on them in April of last year and I didn't notice anything until we went back to school in September. He had that moon face, but he didn't gain much weight (he was on a low dose). He did tell me he had a ton of energy (soccer coach) and felt the best he had ever felt. After he took his last dose in November, it took about 1-2 weeks and he looked completely normal. I also have a young friend who takes a low dose of pred. for rheumatoid arth. She doen't have many side effects, except energy. I hope you get better soon!

[ClockworkOrange]

When I first started this thread, nearly 8 months ago I was scared but as time went on, I did not struggle with the medication too much.

Since November I have been tapering down, nobody warned me how hard that was going to be.

I started getting awful aches and pains in all my joints, putting my arms above my head was agony but that is all easing up.

Have not been on my bike properly for about 6 weeks and just as I felt fit enough, we have snow..........apparently the UK are having the worst winter for some 50 years!

Anybody else going on Prednisolone, just be wary of when you have to taper off the stuff, it MUST be very gradual.

On the funnier side, I thought I would share these Prednisone T-shirts with you.



This is the slogan on the first T-shirt. "Prednisone. The all the time eating, shaking, bone thinning, weight gaining, b*tch making, so you can never sleep again medicine"

Thankfully, I am getting back to normal.............well, sort of normal.

Clock

[tulip]

Clock, I hope your health continues to improve! Those t-shirts are very funny for those of us who have experienced prednisone. I was on it when I was in high school--what a time to get fat, mean, and scaly (my skin got sooo dry!) I had to quit the varsity basketball team and the following soccer season was terrible (I had been a very good soccer player and had planned to play in college, but prednisone took care of that, too!) Fortunately, I was on it for only a few months, but that was bad enough.

Best to you!