Have you been tested for iron deficiency (anemia)?

Have you been tested for iron deficiency (anemia)? And if so, were you deficient?

*edit*
According to this article, Anemia can be seen by performing a CBC (complete blood count) which is about the most common lab test performed. If you've had a CBC done, they've checked for anemia. Two of the levels checked with a CBC are hemoglobin and hematocrit; if they're low, that is a sign of anemia, although there are many different forms of anemia. If your MCV (another reading from the CBC) shows your red blood cells are smaller, that could be a sign of iron deficiency anemia. Your doctor may perform tests to check serum iron and serum ferritin levels which would help confirm iron deficiency anemia.

Sarah was tested post op and was Iron deficient and also Folate deficient.

Matt has been tested, and continues to be monitored, and is not deficient in either.

Dusty.

pre op with an abscess I was deficient post op i'm not

I'm not anemic, but doc said, according to my blood test results, I was almost anemic at the time. Much better now, though!

yes... I was weak as a kitten, white as a ghost, so they checked my red cell count. Came back @ 24... which they thought was an 'error'... so they tested me again.. same number. I was told it should fall in a range of 160 - 240 ... took almost a year to get it close to 160 Not a good time, the iron supplements and high iron foods I was on to get there was extremely hard on my system. But, slowly it worked. Wouldn't want to go thru it again.

My iron was so bad, while I was sitting for Remicade infusions, I had to sit with an iron transfusions in the other arm. It was awhile ago though, and I haven't been tested lately so I'm not sure if its still low or not.

90% of the time I'm iron deficient. My consultant says that the majority of crohns patients struggle with iron absorption and are often anaemic. Seems it's true I've been anaemic since diagnosis and when my haemoglobin hits 9 or below I get an infusion (tablets irritate my stomach). Mum and my 2 sisters don't have crohns but all have severe anaemia. The DRs think there may be some genetic disorder affecting us all. Hmmmm.

Been tested twice in my life. Both times confirmed deficiency (before and after resection but many years apart).

Was tested a while ago my iron storage was almost depleted, and my iron count was low. I went for iron infusions that the doctor wanted each week, then it became two. Now she wants me back every week n half to two. I have had so much go on lately I have not been there since mid july. It is a trip to go into that part of the city. I am exhausted half the time. Also going there is like a day trip. I spend hours when I go there.
Years ago they wanted me to take iron pills. They make me so sick. My doctor now told me no one with an inflamatory digestive condition should take iron pills. Too hard on the system. Iron infusions are easier on the system.

My anemia was the only reason my gi ever thought to test me for crohn's. Finally after being anemic for most my adult life. I am not thanks to Asacol , hillarously started Humira after (for other issues). Now i don't faint on the subway any more!

As four people reported not being tested, I've edited testing information into the original post. I should have explained that originally. My apologies!

Hi David,

for me its seems to be a bit of a moving target. I'm quite regularly tested with various different results. For me this all started through anemia. After taking a course of iron tablets, my heamoglobin returned to normal, but I was B12 deficient. After then sorting out heamoglobin and B12 I was then low in ferritin. The B12 continues to be an ongoing issue, but I'm off the B12 tabs to see how things go as they think now that the crohns is under control, I may not need the B12.

Finally after a very recent period of tiredness and feeling generally unwell, I got my blood checked again. The doc told me everything was ok, but later when I asked the nurse what the results were, she told me all was ok apart from the hematocrit, which was low, so I'm not sure what this means. Quick search on google told me this was a form of anemia, so I'm slightly surprised the doc never mentioned it. I intend to ask about it next time I attend the surgery.

Anemia was the catalyst for the eventual diagnosis of my CD. After being diagnosed as having IBS, I developed anemia but my GP insisted on my taking high doses of iron to combat it and didn't want to do further testing to determine why I was anemic. I then went to one of the top GI Drs in the area, who started by doing a colonoscopy and managed to get a little ways into my small instestine. He found quite a bit of damage, which led to a cat scan of my SI, and the CD diagnosis. And, of course he followed with a B12 test and of course that was low also. In the words of my GI Dr -- "Of course you are anemic -- you have Crohn's." Everything is now in balance.

Always have been deficiant since I could remember. It got so bad my iron dropped to a 7 when for a regular adult female is a 12-14. The doctors fought with each other as it if I needed a transfusion or not. I had one say I needed it, the other told me I was young enough to pull through(ok thats great and all but while I spew more blood out the a$$ and get closer to death that will be on you idiot!) Eventually 2 pints were administered to me...and promptly after being admitted the nurse checking the blood bag dropped it on the floor and the bag exploded...man that was a crazy night

My hematocrit always hangs around the low side of normal, but my ferritin was below 20 both times it was checked last. My dermatologist just had it rechecked last week and I am waiting on the results.

Have struggled with Iron def since dx age 11. they insisted on many iron tablets over the years and GI wouldn't accept that they hurt me like hell but that was back when they were only getting to grips with things. I have had many muscular iron injections over the years but thats not ideal as each time its injected it weakens the muscles around the hips, just got my first infusion in May and happy days, no pain, no muscle iron stains and instant boost.

I was always a bit on the low side with my Hemoblobin - due to girl issues. I had a emergency hystercetomy and my HB went down to 89. I begged for a blood transfusion(am in the medical field so I knew exactly what I was asking for) Dr said no, it really wasn't low enough. He sent me home with iron pills. It was a long tough fight out iron deficiency - about a year before my HB was normal( I didn't tolerate iron pills orliquid very well)
My Ferritan remained low for so long - GI mentioned doing iron transfusion if I could not get it back up.(offered just as it was only slightly below normal) Well then I blew up at her - you mean you had a way to help me feel better faster but choose NOT to offer me that option!!! She said the procedure had a small chance of causing an allergic reaction. I was so pissed off, I'm feeling like crap and you think the chance of an allergic reaction would put me off this(like a 1% chance)

First I was pissed that they wouldn't transfuse me - now I am really pissed they wouldn't offer an iron transfusion esp after my Crohn's diagnosis. I went through months of needless exhaustion. Perhaps my Crohn's would be under better control if I hadn't spent the 2 years trying to make red cells and up my iron stores instead of using that energy to fight the Crohn's!!!!!

And since all the girl issues are resolved giving me transfusion(either one) was going to have lasting effects as I wasn't losing blood at all anymore!!!

I am sorry if my language offends anyone. I get so hot under the collar about this as I am a very proactive kind of person - just tell me what will fix this the fastest and let's get on with it, no waiting to see if it get's better on it's own - let's jump on it. I think what I went through was so needless - it just makes me angry.

kllyeve said:

I get so hot under the collar about this as I am a very proactive kind of person - just tell me what will fix this the fastest and let's get on with it, no waiting to see if it get's better on it's own - let's jump on it. I think what I went through was so needless - it just makes me angry.

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I don't blame you for feeling that way at all, I was put on some many iron tablets / liquids over the years for them just to rip the insides out of me, but I think it's sometimes about the money, I shiver if I see the GI write with a medical company pen, chances are I'm going to get a prescription for that drug before I leave the office even if I don't need it!!!

Ah, thanks for the edit, David: I was one of the four. GP told me I was borderline anemic when I was first diagnosed but didn't prescribe a supplement. Today Gi said my haemoglobin level is good.

Iron levels have always been low. Should be over 80 and I am consistently around 20 or lower. Iron tabs and that's it. B12 is low too. Never had injections for either.

David said:

As four people reported not being tested, I've edited testing information into the original post. I should have explained that originally. My apologies!

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My bad. I voted that way because I have never been tested specifically for anemia (at least that I know of). I have had plenty of CBCs and have never been told I am deficient.

diesanduhr said:

My bad.

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Nope, it was MY bad. I should have provided information upfront. My apologies.

I didn't vote because I wans't sure what to say - I have been iron deficient a number of times over the last 6 years, but they test for it with every blood test (which I have before every appointment) and I wasn't last time. Will be having a blood test tomorrow for Friday's appointment and hope it will say the same .

Have been tested but long after I felt like I did have deficiency but no, it was ok and I am not a bleeder. Just low on B12.

I have been iron deficient due to bleeding from the small bowel and this helped with my diagnosis. I had blood and iron infusions and my hb had been fine for the last few months.
A recent adventure with a serious leg infection has caused a flare and so my hb has gone from 142 in june to 93 last week, even on oral iron. So booked in for 3 more iron infusions starting tomorrow.
My bloods today show it has dropped again to 82 so may need some blood, but am hoping to avoid that.
My GI says that often iron absorption is much poorer whilst you are flaring as the bowel inflammation prevents absorption. I seem to absorb it ok when my Crohn's is under control.

Was tested by my GP and my Hemoglobin was 10.9 (should be 11.5 to 15), Iron Serum 28 (suppose to be 35-155) and Iron saturation 8 (suppose to be 15-55) I am on iron supplements now (27 mg 2/day) and will take a blood test again next month to see what happens. Right now very very fatigued and running a low grade fever almost part of every day. Sigh. Taking a couple days off work to chill and see if I feel better.

I haven't voted because I have been tested a few times- the first time I was deficient but after a 3 month course of iron (and also started azathioprine and got my flare under control) my levels improved and have been normal every blood test since.

For the record, when I was iron deficient I barely showed any signs of anaemia (I had symptoms like fatigue but it turns out they were unrelated!) and my haemoglobin was only 0.2 lower than normal. However my ferritin levels were 7 or 8 (12 is absolute minimum, but 20 is better).

Johnny was iron deficient but the doctor said it was because he was taking Prevacid. Once he could stop the Prednisone, he could stop the Prevacid and then he could stop taking his Iron supplement. So he is off all three now and labs are normal.

Supposed to take iron pills 3x a day, but their way too harsh on my stomach so i don't take them, by the way, yes i am iron deficient

Carey, do you take them with or without food?

And have you discussed this with your doctor? There are other forms of iron out there that might be easier on your digestive system.

Iron deficient since I was in teens but probably from young. Can give way most of time, only have to take if having child which the answer no chance or major flare.

I'm border line anemic, but my doc says that my number has been stable borderline anemic. Not sure how to take that, but I supplement with iron every other day. Until the next CBC.

Sarah was anemia at dx. She is no longer anemia. But her iron levels have remain low.

I just had full blood work and my iron and B12 were fine. Could be a couple of reasons for that - I don't have constant diarrhea (just the opposite) and I take liquid multi vitamins and hair/nails/skin vitamins.

I have been anemic in the past, but it was completely unrelated to this. Anyway, I would know the signs now.

i have to much Iron in me

I am usually borderline anaemic, my doctor seems to think this is okay, and the pills upset my stomach too much too supplement it anyway. I was severely anaemic while I was pregnant, however, and required weekly iron infusions.

This thread is very old - from 2011.

I suggest that if you have a question on this topic that you start a new thread.

All the best.

Patricia56 said:

This thread is very old - from 2011.

I suggest that if you have a question on this topic that you start a new thread.

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We're ok with people bumping old threads here

Just answer, yep and was anemic, had to take iron pills for a year