Tag Archives: anemia

I’m Bacckkk!

Hello everyone!  I hope everything is going well your way!  I took a bit of hiatus but I am back again!  I just wanted to catch ya’ll up on what’s been going on for the last several months I have not been in touch…

Well, after the major hemorrhage that I had back in April, I had a couple more, however, not quite as major.  For some reason that the doctors still can’t figure out, my RBCs (red blood cell) counts keep dipping on the low side.  I have been either admitted to the hospital or been in the ER at least two to three times after I had the big one.  I just can’t seem to keep my bone marrow producing the blood cells like it should be!  There was this last instance when I was outside planting bushes and my doctors kept calling me and telling me that I should get to the ER and get a blood transfusion because my level was at a 7.3. (The normal level is 12-15) way lower than it should have been.  I thought the reason I was feeling dizzy was due to being dehydrated because of my Crohn’s Disease.  Anyhoo, I told the doctors they would have to wait until I finished planting my bushes or they would die!  It really had gotten that routine it was just a nuisance every time I had to drop everything and go!

I do have some great news for a change…I just got my catheter out last week!  I had mixed feelings before I departed with the catheter because it had been a part of me for 2 1/2 years and kept me hydrated and well.  I still have a little anxiety over this ordeal but I am going to only try and think positive thoughts and I can do this, I know I can!  I was thinking the other day that now I will be able to shower instead of bathe, I can wear bras with straps instead of my strapless bras and I will be able to continue doing yoga!

About 2 weeks ago, my father had a bad wreck so I was down there helping him out.  The day I was to leave and go back home, I changed my bag that morning.  It later turned out to be a big mistake!  Anyhoo, I had been on the road for about an hour when I had to pull over at a gas station and go to the bathroom.  When I got in there, I noticed that my bag had busted because the paste from changing my bag earlier hadn’t cured yet and my seatbelt had been on top of it causing the bust.  I drained the bag and prayed that I could make it home without too much of a mess.  When I got about 30 minutes down the road, my bag was really getting full and I knew I was going to have to pull over and change the whole thing..never done this in public before.

Likely I had brought a couple of extra bags just in case.  I pulled over and brought a couple of things to the bathroom with me.  My plan was to pull my bag off, clean myself up and hurry up and put another one on.  Well, it didn’t go as planned unfortunately.  As soon as I pulled my bag off, the bag overflowed all over the floor and toilet!  I hurried up and put the bag in a ziploc and threw it in the trash.  Then I had placed some supplies where I could get to them to wipe myself off and before I could get there, I was pooping everywhere!!  All over the floor again, my pants and my shirt!  I was literally freaking out at this point!  I hurried up and put the new bag on then had to clean up the mess.  When I walked out, I felt like everyone was staring at me…I figured I pooped on myself and missed something while cleaning it up.

I went straight to my car and didn’t get out again until I was home.  I called and warned my family beforehand that I was going right to the bathroom and clean myself up and put another bag on and get in the bath!  I immediately took my clothes off and put them in the wash and I was a whole new person afterwards.  It did, however, wear me out because I couldn’t rest after that 3 1/2 hour drive.

I’m not sure I will ever change my bag in public again but I do know not to change my bag before going on a long trip!  I should have just waited til I got homeAnother lesson has been learned!  After almost 5 years with my colostomy bag, I still have to take it one day at a time and learn from my experiences what to do and what not to do.  I just hope this helps someone who may be new to all this ostomy stuff not to panic, and they are not out there alone.  We all have troubles and feel down at times, even the people who have had ostomies for a while.  I tell you one thing, I have to laugh at my mishaps because if i didn’t, I would cry.  I may not laugh when it is actually happening, but after I think about it for a bit, and think of how I could have done something differently and how it probably looked like, I have to find some kind of humor to it but learn from it too.

Chow for now!

 

Ringing In The New year

Hello everyone, I hope the holidays went well for you!  Mine was great but my health wasn’t too great..I would like to blame it on all the great food I ate during that time but something else had reared it’s ugly head.

In my last post I had told you the blockage pains had come back and I am now taking the Entecort (steroids).  About one month later, I still wasn’t feeling great but couldn’t figure out just what it was.  I was feeling very fatigued on top of all this.  One day while my Home Health nurse was at the house, I was telling her my symptoms and how I was feeling.  When she took my vitals, she found that my heart rate was 50 bpm.  It is normally 75-80 bpm and she acted alarmed that it was this low.  She told me that this was probably the reason why I was feeling fatigued.  She then called my primary doctor and told her what was going on.

The primary doctor ordered some blood work and told me she would like for me to wear a heart monitor for two days to record what is going on with my heart.  The blood work showed that I was moderately anemic and that I definitely had something going on with my heart.  My heart rate during the two days ranged from 41-144 bpm. I’m still not sure what they are going to do with me about that – I haven’t heard from them regarding a game plan yet. For the anemia, they told me to put more red meat in my diet.  That’s kind of ironic due to the fact that I gave up eating red meat this past summer because it is the hardest meat to digest with my Crohn’s.  I didn’t think about losing iron because of it.  I’m still not eating red meat but I found at the pharmacy this “shot” of iron called Pur Absorb.  It is literally a shot of water infused with iron.  It taste like drinking water from a rusty pipe but if it helps and keeps me out of the hospital, I’m willing to do it!

Just this past week, the job I had before I was laid off in 2012 called me out of the blue.  They offered me another position, full-time and told me they would consider my medical condition.  For 3 days I was really considering going back because it would have been for a lot more money and we could get some bills paid off and go on some great vacations!  I considered the pros and cons and in the end, I had to decline the offer.  I had to consider my health of course, the surgery hanging over my head, my heart thing and the fact that if I did go back to work, I would lose my disability.  The way my health is now, I could be fine for a day, a month or even a year and then one day before you know it, I’m in the hospital for some reason, having surgery or just not able to get up off the couch.  I would then be out of a job and have lost my disability.  It was so nerve wracking for those 3 days though..my brain was telling me one thing as my body was telling me another.  I really would love to get back to work one day but this just isn’t the time.  I still have some kinks to work out!

On the other hand, I am a very spiritual person and firmly believe that everything happens for a reason..this is another reason why I struggled with this decision.  I pray to God all the time to open my eyes and ears and let me see/hear what he wants me to do for my future.  Then all the sudden, out of the blue, this job offer lands at my feet.  Was this some kind of sign or something or was I thinking too much on this?  Also, the same day I declined the offer, I got a phone call from Mercy Hospital in St. Louis inviting me to one of their job fairs for lab personnel!  I did tell God that he would probably have to hit me on top of my head for me to get it as I don’t get subtle hints very well – they kind of fly right over me!

I do feel a little better now but still fatigued.  My heart rate is back in the 70-80s bpm.  I did however just get some more blood work done and I am waiting on those results.  It did feel good that my old job is still thinking of me.  Maybe one day I will able to go back to work and live like a normal person.  I have to take this disease one day at a time and work toward the goal of getting better!

 

Chow for now!

Kelly

Blockage Problems and Then Some

Hello everyone, I hope things are going well with you.  I am sorry you haven’t heard from me in a while – I haven’t been feeling in tip top shape here lately.  My blockage problems have came back and I have some other mishaps along the way.  Here are some details on what have been going on since I last posted.

11/28/2016. After we had Thanksgiving and festivities at my family’s, we came back up to O’Fallon, IL on Saturday.  Saturday night, my husband and I went out to eat at Hooter’s because I was craving chicken wings and we hadn’t been there in a while.  I noticed when I got up the next morning that I hadn’t filled up my bag any throughout the night.  I thought it was weird but I didn’t think much about it.  That next day, we were to have Thanksgiving at the Tyberendt’s house.  I had my fair share of food that day and still did not fill my bag any.  Early the next morning around 2 am, I woke up with severe pains that came and went in waves.  That night, I didn’t get any sleep and was doubled over in a fetal position all night.  Later that morning, I took the Entecort steroids that my new doctor told me to take if the blockage pains ever returned.  I mustered up the strength to take my daughter to school then crashed on the couch the rest of the day.  I didn’t eat or drink anything all day until around 6 pm.  I decided I would try a little chicken noodle soup.  That was not a good decision, I could not keep it in for very long after eating.  That day I took a total of 2 pain pills, 2 advil and my steriods and was still not doing well.  I emailed my doctor to let her know what was going on.  I also had the hydration saline bags hooked up to me so I wouldn’t dehydrate.  The doctor told me I was doing the right things but if I kept having the pains I should see about going to the hospital.  I would rather do everything at home than sit in the hospital room for 3 -4 days doing the exact same thing I’m now doing at home.  The next morning, I didn’t have any blockage pains but I could still feel something wasn’t right.  I did find the courage to eat one scrambled egg that day and a little bit of water.

12/13/16.  So I am now not feeling well but not sure what is going on.  I just feel blah.  At one point I am thinking it may be my blood pressure.  Every night around 6 pm I just crash.  I start getting a huge headache and my face gets flushed.  Last week when I went to the doctor, my BP was 120/73 which is perfectly normal for other people but it hasn’t been that high in ages for me.

12/15/16.  Still not feeling well. I wake up with a headache and go to bed with a headache and have a headache in-between and I’m not a headache person! I have been taking beau coups amounts of Tylenol just to subside it a bit. I also found out from my home health nurse that I have a low heart rate (50).  She called my primary doctor and let her know my symptoms I have been having and that my pulse is usually around 80 but now it is 50 for some reason.  My primary told me to get some blood work done and to go to Mercy’s Heart Hospital in St. Louis and get a heart monitor put on me. I feel tired all the time, hence the heart rate I guess.. All this right before Christmas! Also, my food isn’t tasting right either. Unless I have a lot of salt on my food to taste or it is very sweet, I don’t taste it.

12/16/16.  I did get some information back on my blood work from the doctor..I am moderately  anemic.  This has gotten worse from the slightly anemic that I was.  The nurse told me to eat more red meat!  I told her that I cut red meat out of my diet this past summer due to blockage problems.  Obviously I should have compensated for taking the red meat out of my diet.  Now I need to increase my iron in my diet.  Damned if I do, damned if I don’t!  Also, my magnesium was on the low side so she wanted me to get some over- the- counter magnesium topical cream. This cream is suppose to soak through your skin.

Please say a little prayer for me as I am going through all this stuff.  I haven’t yet found out what the heart monitor reads, I guess my doctor will call and let me know the results.  I will keep ya’ll informed of any new news. I know I have to take this disease one day at a time but sometimes it is so difficult to remind myself.  I need all the encouragement I can get right now, so please send me a shout out and let me know I’m not alone with this disease..

Chow for now!