Monday, December 28, 2009
As for the biopsies of my small intestines...well they were apparently "within normal limits" also. What does that mean? Apparently they have ruled out Celiacs disease, and are unsure of what could still becausing my malabsorbtion. At this point the doctors want to do a few more tests and continue with IV therapy. I can't do it anymore. I'm out of money and short on hope these days. Before I was diagnosed with cystic fibrosis I was frustraited, I was sick and I had no reason for it all. When I was diagnosed I was relieved to have an answer. Now I feel as if I am going through it all again, only this time I get to drag my husband and daughter down the "unknown" path.
I just feel overwhelmed. I mean why can't they figure out what is going on? When I don't get IVs my CK goes up; when it gets high enough it causes kidney damage. When my vitamins and minerals are low I'm tired, get headaches, muscles cramps, get confused and forgetful...I just sometimes feel as though I am being set up to fail. With the CF I at least know what the possible outcomes can be, with my mitochondrial mutations...I have no clue. I ask if the malabsorbtion has something to do with my "unknown" mutation and I get told, "maybe". Why doesn't anyone care? I thought with a new mutation maybe I'd get some attention for my other problems... HA...
What the hell was I thinking. I'm not upset that they don't give a sh*t about what happens to me; but rather that my husband, daughter, friends and family have to sit there and watch it all. I'm sure they have all at some point questioned the validity of my problems; it's not like I have any answers. Hell even the GOVERNMENT FUNDED hospital isn't interested in figuring me out.
Monday, December 14, 2009
All of my life I have had battles with depression, and I have one a few with out medication or counseling. The last Christmas that I had a problem with was right after my Grandmother has a stroke a few years ago; and before that one it was when My Grandfather (on my Mom’s side) was dying of cancer.
This Christmas will be the first with out Grand Donald (on my Dad’s side); we are loosing my Grandmother’s house (she bought it the year I was born); several people from the cystic forums have been sick and we have lost some too. I am still not feeling well; I don’t think I have felt good in a while. Maybe a day or two here and there; but this year has been an eye opener for me. I don’t think my life is worthless or anything and I am not suicidal, but I just can’t get myself out of this funk.
Now Christmas is coming and we are broke; my usual answer to this would be “so what we have each other”. This year…I can’t seem to get it out. It seems to get caught in my throat. I don’t want to be around people, well truthfully I do…I just don’t feel like I’m good company. I have to prepare myself, go over conversation ideas in my head…normal stuff I would have talked about before all of this crap.
On Thursday I go in for my second EGD, and I’m having a difficult time finding someone who wants to go with me. I guess I can understand; who wants to take off work to sit in a waiting room all afternoon and then help a sedated Chrissy into the car? My Dad said he’d take me; but he had a cow when I asked him about it. I need someone who can come back to recovery and listen to what the doctor says because it might be important. So I’m a little concerned about it. Wednesday my piano is being moved from my Grandmothers house to mine. My Aunt is helping to cover the cost, and the rest of the money is coming from our Christmas cash. Frank and Kate knew I’d be devastated if I lost the piano and both thought this was worth it. I love them so much.
Monday, November 23, 2009
She called the nurse in and had me lie down. She took me blood pressure and pulse; she had me sit up and she took BP and pulse again; and finally she had me stand and got the info. The nurse helped me sit back down and left the room to go talk to the doctor.
In comes the doctor and she is talking, but honestly my head was pounding and I couldn't pay attention. Really all I could make out was "you have POTS Chrissy" and "new medicine to help".
So I came home and looked it up...
What is Postural Tachycardia Syndrome?
Postural orthostatic tachycardia syndrome (POTS) is one of a group of disorders that have orthostatic intolerance (OI) as their primary symptom. OI describes a condition in which an excessively reduced volume of blood returns to the heart after an individual stands up from a lying down position. The primary symptom of OI is lightheadedness or fainting. In POTS, the lightheadedness or fainting is also accompanied by a rapid increase in heartbeat of more than 30 beats per minute, or a heart rate that exceeds 120 beats per minute, within 10 minutes of rising. The faintness or lightheadeness of POTS are relieved by lying down again. Anyone at any age can develop POTS, but the majority of individuals affected (between 75 and 80 percent) are women between the ages of 15 to 50 years of age.
Doctors aren't sure yet what causes the reduced return of blood to the heart that occurs in OI, or why the heart begins to beat so rapidly in POTS, but the current thinking is that they are the result of abnormalities in the sympathetic nervous system (which is responsible for decreasing muscle tone and increasing heartbeat in reaction to situations of stress or emergency) or the parasympathetic nervous system (which does the opposite) or both .
(taken from http://www.ninds.nih.gov/disorders/postural_tachycardia_syndrome/postural_tachycardia_syndrome.htm)
The symptoms of POTS are life altering and debilitating at times. POTS patients use about three times more energy to stand than a healthy person. It is as if these patients are running in place all the time. Activities such as housework, bathing, and even meals can exacerbate symptoms (Grubb, Kanjwal & Kosinski, 2006). Research shows that POTS patients' quality of life is similar to those with congestive heart failure and chronic obstructive pulmonary disease (Benrud-Larson, Dewar, Sandroni, Rummans, Haythornthwaite & Low, 2002) Twenty-five percent of people with POTS are disabled and unable to work (Goldstein, Robertson, Esler, Straus, & Eisenhofer, 2002). Most patients will have to make some lifestyle adjustments to cope with this disorder.
So...that explains a lot for me! December 1st I have a colonoscopy and endoscopy scheduled. I'm a little worried but they say it will help my digestive problems be diagnosed. My problems are too different from "standard" (their words not mine) CF digestive problems; and with my mitochondrial disease...well they just don't know. So getting these tests done will help figure out the puzzel that I am! (HA!)
Thursday, November 5, 2009
I don't like to constantly complain because I feel like I could be doing so much worse. And honestly, complaining does not help me to feel better. However, for those who read this...I don't feel well. I'm not deathly ill or anything and I don't have H1N1 (knock on wood); its the same old same old. I am super tired, lacking energy, forgetful, achy and sad. All of these things can be attributed to my inablility to digest and absorb, except for the sad part. I am sad because I'm sick all the time (it feels like it) but mainly because I can do nothing for the people suffering around me. So I'm going to do what I can, which is pray.
Most of you know I am a spiritual person so praying is something I think I might be good at!
I have been praying for peace and healing for sometime. As a matter of fact I have a list so far it includes:
Scott's Dad, RR, Lauren and her family, Ginger and her family, my Grandmother, Chel, Deborah and her children, Jessica and her Dad, my brother Pete, Piper...and several others.
But I want to ask you who read this to give me names too, I want to gather a litany of them! I know there are people out there who need prayers, and you'll be helping me to feel somewhat useful durring this down swing of mine. So just leave a post on here whether you know me, or you just happened on my blog...whatever reason...tell me who and why. Those who have passed, those who are healthy but struggeling, anyone you think I might be able to help; if only a little bit.
Wednesday, August 26, 2009
My friend Chris and I talked and I won't be watching Devin on a regular basis for a while. In actuality I think it will be longer than just a while...I didn't do anything wrong but found out from my husband that he talked with Chris about me watching Devin. I didn't get upset like he thought I would, he was worried about me and I guess he told Chris about it. I don't know how I really feel about the whole thing. I miss Devin like crazy; but I know that not watching him has allowed me to rest.
I always worry about what people think of me; you know the stuff they don't say to your face. The last thing I want is for people to feel sorry for me, or pity my life. I say things like "I don't care what so-and-so thinks"...but I do care; if only a little bit. (Not like cry myself to sleep and change my life care...but...enough to put up a front about how I feel) So when Frank sat me down and told me about his talk with Chris and his feelings on me watching Devin, I was a little surprised and hurt. It hurt because I knew he was right. I would have never given up watching the baby if I could help it. Not that I would watch him while contagious or unable to take care of him, and I think (hope) that everyone knows that I would put him before myself. I was actually able to go over to Devin's house to play D & D (Yeah...I play D & D) and I got to hold him and play with him, if only for a little bit. He has gotten so big! And still adorable ;o)!
My sister in law has 3 boys. Nick, Anders and Finn; I used to watch Nick when he was a baby. Nick is close to the same age as my daughter and I really miss having him around. I haven't really gotten the chance to know Anders or Finn that well, and Nick and I have grown apart... Which breaks my heart. He is such a great kid and he is funny, witty and smart. I know he doesn't need me to tell him those things; but I wish I could more often. His Mom is having a birthday party for Anders tonight, and I can't go. I wanted to but I'm not driving myself often because my muscles are so bad, so I need my husband to drive me to these things. Unfortunately he has to work.
I really wanted this year to be the year that I strengthened all of my relationships, however, my body doesn't seem to want to cooperate! I guess since this year isn't over yet I still have time...
For my next blog entry I want to answer questions and say things that I probably should have said already (thanks CG)...so feel free to email me a question or post it on here and next time I'll compile it and answer...
~ The adoption day came, and despite being emotional it was my husband who told a story that made everyone cry. For once...it wasn't me!!! ;o)
~ My husband and I celebrated our 11th aniversary on the 22nd of August. We went on a weekend trip to Washington DC. Kate came with us, we always celebrate our anniversary with her.
~ My brother Pete turned 28 on the 23rd! He is doing well, I think. I always worry that he isn't. I guess that's the big sister in me. We are having Pete over this coming Friday for a birthday dinner! No matter how old he gets he'll still be my little brother, even if he is taller than me!
~ Kate is getting ready to start school next week and she is really excited about it! She went school shopping with her Nana and she had to get clothing from the juniors section...my little girl isn't so little anymore!
All in all this past week has been good, I had a NIH visit last Wednesday and my PFT's went up to 82% (FEV1) They were very concerned they would continue to trend down because of my inability to exercise lately. YAY!
Thursday, August 13, 2009
I guess I'm just worried that when I'm gone Kate will need help remembering the good times when she is sad, same with my husband. I want people to be able to say, "Hey do you remember the adoption?" I guess I'm being silly...
I got my lab work from the 4th of August this past Tuesday. I called my doctors office to discuss the results with my nurse as usual. You know brain storm ideas and new medicines...but instead I got a call saying the doctor wants to speak with me about them. So I had to make an appointment for Friday. We all know what it means when they want to talk with you about it in person. LOL
However; with the adoption being Monday there is nothing she can say to bring me down.
Thursday, August 6, 2009
My Grandmother will not be at the adoption hearing. She won't be able to tell the judge that I am a good mom, that I have been a good mom since day 1...she'll only get to look at pictures. This is something she wanted to see so badly. She and my Grandfather. He passed away earlier this year and I came to terms with the idea that he would never see it. But I had somehow managed to *not* think about how much it meant to me that she wanted to be there; to see it.
So tonight, because this is all I can think about. Because I can't stop crying, and because I love them all I will share a secret. I know what suffering is. It's not what you think...it isn't what I thought...
My Mom's Mom, Grandma--she passed away in 1995. Pre-Kate...I know had she gotten to meet Kate she would have loved her.
My Mom's Dad, Grandfather--passed away when Kate was younger. He and Kate got along great. He started her collecting dolls and coins! Back then we had no idea how badly things would go down hill with Kate's birthmother. I had always wanted to adopt Kate, but her BM was in the picture back then...trying to be Kate's mom...just not trying very hard...
My Dad's Dad, GrandDaddy--I never met him. He died in a plan crash when my dad was a boy. I often wonder if he'd be proud of me, if he would approve of Frank...but I *know* he would have loved Kate.
My Dad's Step Father--GrandDonald--He adored Kate! He was tickled when he heard about the plan for adoption. I only wish this was done sooner for his sake...Kate was devistated when he passed. She missed a whole week of school and we just couldn't believe he was gone. Some days I forget.
My Dad's Mom, Grandmommy--The only Great Grandmother on my side that Kate got to meet. She had a massive stroke a few years ago....the adoption was going to be a surprise but we told her. We wanted her to have something to look forward to. But we know now that she is not coming home. She is paralyzed on her right side, she's unable to speak or eat...
Her husband GrandDonald passed while she was stuck in that nursing home...
You know when I found out about my CF and then about the mitochondrial mutations...when they told me the odds of making it to 4o...with my motor functions in tact...I cried and I couldn't understand why I was the sick one. Why I had to suffer...but life went on. I dealt with it. But when she had the stroke I learned what it was to truly suffer. It is watching someone you love suffer...to watch her try to move---to say something. Anything. Nothing. For the life of me I still can not figure out why this happened to her...
That is why from this night on...I will not cry for what CF or mitochondrial mutations will take from me, but for what they will take from every one I hold dear. Because I know how they feel watching me struggle.
Tuesday, August 4, 2009
Kate has been staying with Frank's parents this week; I miss her terribly, I can't wait for her to come home! I have no clue what I'm going to do when she goes off to college...my plan is to move with her. lol
The IV center drew blood today so I'll be getting my results again. I can't wait to see what they are now. In other news I have a theory about my CK. My doc thinks it is related to my over all cholesterol, but I don't think it is. I've been charting and mapping my results for months and I think it has to do with my HDL (good cholesterol) So I showed my doctor at my appointment yesterday and she agreed there might me something. So it looks like we are going to try to raise my hdl. Obviously we can do it through food or IVs because I don't absorb those well enough. So she wants to try estrogen patches. That's right! My doc said estrogen is a high densitiy lipid protien, so...the plan is to try to sneak it in with the patch...
but shhhh....if my body finds out it may not work. You know it does not like to absorb anything; let alone HEALTHY stuff.
PS-If you want to look back at the test results I have posted...check out the cholesterol, hdl, ldl and CK...you'll see what I'm talking about!!
Wednesday, July 29, 2009
My First . . .
Diagnosis- 21 years old. I had a positive sweat test but the doc wanted to be absolutely sure. They called with the blood test results (kinda, they wouldn't tell me over the phone) the day after my wedding.
CF Doctor- The same one since I was diagnosed, Dr. Churnick. Head of the Cystic Fibrosis Clinic in the National Institutes of Health (NIH) in Bethesda, MD
PFT- I'm pretty sure it was before my DX, when I was 16 or so. I did a lot of test in an effort to DX my muscle disease.
Nebulizer treatment- I was young...maybe 9? I was DX'd w/ chronic bronchitis and asthma as a child.
Vest treatment- 27Dose of Pulmozyme- 27
CF Sibling: None
Non-CF Sibling: Pete; my last entry was all about him!
"Clean out": My first Tune up/Clean out was right after my 30th birthday. My doctor was very happy that I made it to 30 before needing one. My PFTs had droped to 77%, they had always been in the 90's or above. It's ironic because now my base line is low 80s, high 70s...
Bad memories: Vomiting, sitting on the cold bathroom floor in tears alone, because everyone in the house was asleep. I didn't like to wake anyone up, so I sat in there alone--sometimes in the dark so I didn't wake anyone. (This actually happened several times until they figured out a had gall bladder issues/pancreatitis) My mom woke up when she heard the bath water running. It always made the pain better, or maybe it just relaxed me to be in a hot bath. I'd only be in it for 15 or 20 minutes before the pain would come back. Then I'd put my pajama's back on and my mom and dad would drive me into the hospital. They NEVER figured out what the problem was.(until I got away from my pediatric doc and started seeing someone else. She said gall bladder and sent me to the best GI in town, he was amazed I was only 15. The next time this type of thing happened my mom called him at 3 in the morning. He met us at the hospital and told them to check my amylase and lipase levels. The were so high...he stood there with his mouth open staring at me...)
Good memories: Any with my daughter in them!!!
Real Friend- When I was in kindergarten I made my first real friend (non imaginary). Carlolyn Coelho; sadly we have lost touch over the years.
Dose of Tobi- Durring my first tune up I had an IV of Tobi, but I have never had the inhaled Tobi (tobramycin)
Read: "One Fish Two Fish", as a tween it was "Are You There God, It's Me Margaret."
Started thinking about mortality: I think I always thought about it. But I started to think about my own at 15 and was fixated on it for a while.
Started realizing I'm gonna live through this chapter and then the next one too: When I was DX'd at 21, I couldn't see that but gradually afterwards I realized I could make this work. I realized I had to.
First loss: CF related it was a girl I had only made a few comments on her blog and didn't really know. Her name was Debbie, the first CF death that hit me hard...
First time I really remember FEELING sick: It is one of my first memories as a toddler. I guess I was 3 or 4 and I was laying under the Christmas Tree holding my ear. (Ear infection) I recall thinking that Santa was coming and he would made me feel better.
First hemoptysis: Not happened yet
First major bleed (later diagnosed as Pulmonary Endometriosis): None
First home IVs: Never had them, we have an IV center that my primary dr likes to send me to
First home IVs with no hospital time: None yet
First time I freaked out about my fertility: I never had a problem getting pregnant. Just one staying that way. It took 5 miscarriages for the doctors to figure out that I had a blood clotting problem as well, my blood clots too much. At that point I made the decision that with my medical history and terrible genes, and the fact that Kate needed a mother who wasn't going to come and go but one who would stay around...I had a tubal ligation.
First time as public advocate for CF Adult issues: Battle for The Cure, Amtgard. I think I was 24?
First time a relationship changed dramatically during/immediately following big changes in my health: 21, I was DX'd right after my wedding. I told him he could leave since it would only get worse and he said, " Chrissy, don't be stupid." He still tells me that!!
First time without health coverage: I didn't have it when I was a kid which could be why I was DX'd so late. Luckily I am in a life time study for adult CF patients at the NIH, so even if I loose insurance I won't loose NIH. All my meds are free, except for extras from my primary and my GI. My tune up was paid for as well.
First PICC line: Have not had one yet
The First time it hit me: 23
When I was DX'x the only part of CF I understodod was the dying part; then with no time to stop reeling from the news...they told me I had two mitochondrial mutations. After a little while it hit me that I had two progressive disease and I educated myself about them. One effected my lungs and digestive sustem and the other would more than likely take my ability to walk one day and possibly more than that.
I had a choice; I could sit around and be angry and feel sorry for myself or I could teach my daughter and others around me that no matter what the odds are you can deal. These diseases will probably take my life. I know that and I'm OK with it...but no one will say that CF beat me, or that "I lost a battle"...no way.
Saturday, July 25, 2009
He is sweet and kind, he has a good heart and sense of humor. Pete is a caring guy. He works hard, and when he isn't working he is doing things for our mom and dad.
Pete worries about me a lot; although he won't tell me he does. I know it, I can see it when he looks at me and I can hear it when he talks to me. I can usually tell with most people; a talent I picked up a few years after my diagnosis. He lies about things to protect me, nothing big...all small little white lies or not telling me everything...but I can tell when he does it. Again it's a talent after years of dealing with doctors concerning my unknown mitochondrial mutation an CF. However with him I think I know because, we are connected.
I don't know if he read's my blog...but that's ok. I'm not really writing this for him, or for me. I'm writing this to tell those who read how lucky I am to have him for a brother. Sure he electrocuted me...twice; and yes he flushed my My Little Ponies hair brushes and ribbons down the toilet; no doubt he hit me over the head with a Tonka truck; and he totally hit me in the head with a wrench and a mop too. I can imagine the list of things I did in retaliation or to start the fights were just as rough! HAHA!
He is a great brother, and I could not ask for a better one. No matter what mistakes he has made or will make he will always be my little brother.
I figured that I'd blog about him today because I'm sick of blogging about me! I don't have any news anyway!!
Friday, July 24, 2009
The question was, "Would you choose CF?" I'm going to post a link to his blog response because it was amazing.
Before I was diagnosed I was a different person, I think. The birth of Kate changed me, made me more responsible and made me less bitchy. (LOL) When I finally got the diagnosis; I feel as if I shut myself away. Went into a cocoon so to speak: I picked fights with the people close to me, and I didn't take very good care of myself. I was depressed a lot. It took me a while but when I "emerged" I was different. When I did, I had a respect for everything; nature, life, my family, my friends and myself. I started to be more understanding with people who had different opinions than me, started to pay more attention to the world, and really looked at myself as a person. I became the mother I knew my daughter needed, a better friend...it all made sense to me. I appreciated everyone around me; all the plants and trees--the blue skies and the gray ones as well.
Sure I still have depressed days. Sure some days I wake up and wonder why me...we all do. But would I change my life and give up what I have now to be born healthy? No. I regret nothing. I don't want to go back and change anything. Cystic Fibrosis shaped my personality and life...the crappy part but most importantly all the good parts. I'm still working on me...being compliant... not pushing myself... being a positive influence... taking things at a slower pace...
I guess that this question may depend on the day you ask, because some days I wish I was healthy. Not for me but for all those around me who suffer because of my illnesses. But today is not one of those days.
So yesterday my hubby had his doctors appointment; we have the same doctor so he asked me to go with him. He has trouble with doctor speak...
We are sitting in the room and she comes in. She looks over at me and says, "I can't believe the IV center wants me to admit you." I nod and say "yep. I'm fine with being admitted...I feel like crap." Then my doctor explains that FMH and every hospital have viruses and bacteria that run wild and she doesn't want me exposed to it because my immune system is crap. I mean I know those bugs were there, I'm very aware of the crap floating around at the hospital. But it just never occurred to me that she would be afraid to admit me. I don't know why I didn't think of that reasoning. I feel so dumb! So it looks like I get to spend the next two weeks at home. Resting...Blah...how do I do that!?! LOL (she is in talks with the IV center to get me back in next week, but the isolation would be for my protection...)
Frank got his test results, a prescription, and then was off to Rose Hill for his CT scan. I'm not sure what happened but he went in happy and came out a bear! We think it was some sort of reaction to the contrast dye. Neither of us are sure, but that is the only thing we could think of. When we got home he worked on the website for a bit and then took a 3 hour nap. He was so upset that he was so tired. He wanted to work on Shot stuff all day since he had off to get his scan and see the doctor. But I made him take that nap, I was afraid he'd fall asleep at the computer!
Kate and her friends (Molly and Bethany) are in the other room playing Rock Band. It's nice to have them here; they are good kids. But don't tell them I called them kids. HA HA! I'm trying to convince them to be a chick band. LOL Molly is drumming and Kate is the guitar and Bethany is singing....they aren't half bad.
Tonight I am planning to make a beef roast for dinner. This will be my second attempt at a roast that Frank will like. He is not a beef person, unless it is ground up or chicken fried! He choked on a piece of steak years ago...and it scared him for life.
I'm off to rest...whatever that is...
Tuesday, July 21, 2009
"Before the blisters are crusted over, the virus can be spread to anyone who does not have immunity to chickenpox through vaccination or previous infection. " (http://www.medicinenet.com/shingles-rash/article.htm)
All of my blisters are dried up and scabbed over. They are not oozing, it is covered up on my back and under my arm...out of sight... But the nurses have to do what the FMH infectious disease people say. No matter how dumb. Oh and no one even looked at the rash. Not a soul, so I'm not sure why the conclusion could be made that I would need to be in isolation. But whatever...
They did not give me the name of who it was that said I need isolation. So they sent me to my Dr's office. I go in and my dr is not even there! So I sat and waited...and waited...and then my dr came in and said she would see me. HUH? Just admit me so I can get the IV's!
I'm totally freaked out about what she said yesterday about my immune system. About being at a higher risk for certain things...so why would they make me wait? I'm so upset right now and my pain meds just don't seem to be helping much.
So she says she'll see me. FINE. So I wait and wait....and wait and wait....finally I wrote her a note apologizing for being a problem. I just asked her to call me today and tell me what to do. I would like to be admited so that I can get my IV's as they are uber important right now.
But right now I get the feeling they'll just tell me to rest at home for 2 weeks!!
My doctor always uses the analogy of a car and gas. She says I am the car and right now I'm on E, just barely hanging in. If your car runs on E constantly eventually it starts to cause damage.
The vitamins, minerals and lipids are the gas and it just goes out just as quickly as they put it in.
So what happens when I run out of gas completely?
Monday, July 20, 2009
Say what mom and dad? Shingles? Huh?
I know what they are; I just didn't expect that was what I had. So today I went in to see my doctor. She took one look and was like, "yep. That's Shingles." That wasn't all she had to say though. She gave me prescripts for pain and for the virus itself. The whole time she was a FLURRY of activity. Upping my dose of multi vitamins at the IV center, entering things into the computer, asking my what seemed to be random questions...then I recognized a few of them and it dawned on me as she pulled up my blood test results. My vitamin levels have basically gotten so low--I have no ability (or it is a weak one) to fight off infections and such.
She explained to me that her flurry mode was because I can't fight stuff off...my vitamin levels are so low...and then she mentioned the C word...
I don't have cancer; but am considered at risk; and if I do develop it...I can't fight it off. I'm not planning on bringing it up to Frank right now. He has a lot on his plate, including his own medical problems...The C word would just scare him like it did me. There is no point in that. I just have to take care of myself...resting, drinking lots of fluids, and not missing IVs.
Tuesday, July 14, 2009
Vitamin K went from 3.6 to 3.9; up is good! lol
Morning Glucose was 82
Calcium was 8.9 which is the same as it was before. If it doesn't go down I'm happy.
AST the 23rd it was 120 and on the 30th it was 156...
Gamma GT last time was 86 and on the 30th it was 106
ALT was 110 and went down on the 30th to 103
CK has gone up from 1165 to 1690
Cholesterol has dropped again! This time I am at 73. hdl dropped to 12 and ldl is at 44
Vitamin B12 652.6
Vitamin B2 listed as repeat test needed again?
B6 dropped to 11
Vitamin C is listed at .13
Vitamin E 3.9
Apolipoprotein A1- 77
Oh they have been checking vitamin d too, but since it doesn't come back flagged I hadn't noticed it. Vitamin D 1 is 20 which the lab says is low.
Other than that everything has been going OK. I'm getting better about saying everything is fine, or good...but its been baby steps. I just never think people want to hear me whine. lol
Over the weekend we went to a good bye for now party for my best friend Jessica. Her dad is really sick and she is going to stay with him in Las Vegas. She says she isn't planning to stay...I really hope not. I lost touch with her several years ago; so even if she doesn't come back...I'm not letting that happen again.
On my way home from Iv's I heard a song that makes me think of Frank and how hard it is for him to be married to someone who is sick. It's by Rob Thomas and it's called "Her Diamonds"
Wednesday, July 8, 2009
Morning Glucose was 101 this time
Calcium was 8.8 and has gone up slightly to 8.9
AST last time was 181 and the 23rd it was 120
Gamma GT last time was elevated at 92 but has dropped to just above normal range at 86
ALT was 84 which is an improvement from 110.
CK has gone down from 2762 to 1165 on the 23rd
Cholesterol is still 76. hdl went up from 5 to 14 and ldl droped from 56 to 43
Bun/CREA 8.3, down from 10
Vitamin B12 was 625.7
Vitamin B2 listed as repeat test needed.
B6 has continues to trend upwards and was 18 on the 23rd.
Vitamin C was .47 but droped to undetectable again at < .12
Vitamin E 3.8 down from 4.8
So my cholesterol hasn't improved but it hasn't decreased again, which is good. My CK has dropped but so have vit c and e...
What can I say? Really not much. I am always so freakin' tired now, not that it is new. Thats been going on for a while. I just hate to show it. I don't want my family to remember me as lazy and no fun...lol...I am at least fun!
Tuesday, June 30, 2009
Vitamin K was 3.7 which was barely within the normal range listed. These results came back this time at 3.4 just under the normal range.
Morning Glucose was 105 before breakfast and this time it was 135 before breakfast. The 135 came back marked as high this time...not really sure what that means! HA!
Calcium was 8.6 on the 9th; again just above the labs "normal range" and on the 16th it was 8.8
AST last time was 124; well above the normal range of 10-40; and on the 16th it was 181.
Gamma GT last time was elevated at 136 but the 16th it was 92. Which by the way is slightly higher than the normal range. So yay for improvement!
ALT was 124 on the 9th; and this time it was 110. Again yay for improvement!
Alright this is the biggest disappointment for me. My CK level last time was 1516; normal range is 21-232. Elevated yes but two weeks prior to the 1516 it was 2064 or something around there...so it went down; which is good. This number coincides with my muscle pain level and fatigue. So when I say that I pratically burst into tears when I read that the 16th I was at 2762...
It always freaks me out a little to see the numbers; even though I new my pain had gotten worse I casually put it off as pushing myself to hard for Kate's surprise birthday party...guess not, huh?
Next to update on is my second dissappointment. My cholesterol. This time my result is....drum roll please...76! Yep it has droped from 83 to 76...my hdl dropped from17 to a woping 5, while my ldl went from 48 to 56. I started a new medicine that we hoped would help me absorb fat and transport it properly...so far it doesn't seem to be doing much.
Bun/CREA went up from 7.5 up to a 10
Vitamin B12 was 631.8 and has gone up a little to 628.7! (YAY)
Vitamin B62 was a 13.6 on th 16th which has also gone up from 7.8
B6 was < 2 on the 9th but has improved to be a 5. (YAY)
Vitamin C was low but has risen up to be within the normal range at .47...yay!!
Vitamin E has improved to just below the normal range at 4.8
My Apolipoprotein A1-78 went down a litlle bit more to 69
My vitamin levels have all improved a bit...except for my vitamin K; so I'm hoping they continue to trend up. Today I had an appointment with a new GI doctor and he is planning an endoscope and a colonoscopy so that he can biopsy my tissue (Esophagus, intestine and stomach) to attempt to discover what is causing the malabsorbtion. He is also worried about my liver and for the second time in three years someone has thought that I have NASH (Nonalcoholic steatohepatitis).
So he also wants to review all of my liver tests from the last 5 years and he is talking about a liver biopsy...I hope he changes his tune because I do NOT want one of those! LOL
For those who are unsure of NASH check out:
So for those of you who are wondering how I'm feeling today--I could be better. But I'm not going to complain...
My husband went to his new doctor today too, and he seems to really like her so far. My daughter is planning a camping trip with her brother next week; and she has been supper excited about it! My car blew a tire today, on my way to IV's this morning...But I made it in with out being stranded on the side of the road! So today I am just thankful for the small things!!
Saturday, June 27, 2009
Tuesday, June 23, 2009
Labs from 6/9/09
Vitamin K- 3.7 according to the lab it is barely within normal range (3.5-5.1)
Morning glucose (before breakfast) 105 (not sure if that is good or bad!!)
Calcium-8.6 also told by lab it is just in normal range (8.4-10.2)
AST-124 normal is 10-40
Gamma GT-136 normal is 5-85
ALT-124 normal is 30-65
CK-1516 down from the last number which was like 2064 or something normal is 21-232
(CK is the number associated with my muscle problems. They are almost always checking...I haven't gotten the results from last weeks blood work but am hoping that it is continuing to trend down. ALT AST and the Gamma GT all all something to do with my liver. My numbers have always been a little elevated; they think it has something to do with my CK # being high also...but as with all things Chrissy they just aren't sure.)
Cholesterol- 83 normal is listed as anything below 200. However this # according to my doctors is too low. Go figure. 83 is up from 80 which is what it dipped to last month. Keep in mind that I am receiving IV lipids too raise it.) The breakdown is LDL 48 and HDL is 17 (hdl should be above 40)
BUN/Crea-7.5 normal is 12.5-18.7
Vitamin B12-631.8 normal is 239-931 (YAY)
Vitamin B2-7.8 normal is 6.2-39.0 (this is improved from my last blood work)
B6 <2 normal is 2.1-21.7 ( This one is always a struggle for me to maintain.)
Vitamin C- <.12 normal is .20-1.90 (this result is up from my last test...before it was undetectable)
Vitamin E-3.3 normal is 5.7-19.9
LDH-349 normal is 100-200
Apolipoprotein A1-78 normal is 101-198
So I have been getting IV therapy for months now, and a few weeks ago started going in 3x a week instead of 2. Why am I doing it? Well because if I don't get multivitamins and lipids directly into my blood steam; everyone is scared of what will happen. But really...it isn't making much of a difference. I keep getting my blood work results and hoping; praying that the numbers will be great. They should be...not only do I get IVs but I take a multi vitamin 2x a day extra B6, C, D, E and B complex(100). Can someone please tell me what the hell I'm doing this for? Why can't they just FREAKIN' FIX ME???
I am so sick of feeling like it's not fair for me to ask for others to adjust because I don't feel well...but apparently NO ONE (except my husband and a select few) cares about whether I adjust for them. At least that's how I feel.
Oh...I just got a call from the Dr's office and they are giving me a prescript to try to bump up my vitamin E...
Sorry for those who aren't used to me whining...lol...I do it a lot on my blog on cysticfibrosis.com; or at least I did. My husband says I need to stop telling people I feel fine or ok when they ask how I feel. So here it is guys...for those who want to know how I feel right now, today....like crap. I feel like crap.
Saturday, June 20, 2009
The next step is to wait for 30 days; the amount of time in which the BM could appeal, and then file for the adoption date. We are all so happy...
Also this weekend is my father in-laws birthday and as everyone knows Father's Day. So we have a pretty packed weekend. Kate has been invited to go camping with her brother Jesse and his family on July 4th week end, and I'm excited for her! She has never really been fishing and it sounds like he is going to teach her. It is just awesome that they have connected again, Kate missed him terribly. I'm not sure if my doctor will be ok with me going camping or not, so I guess we'll see...
This past week I started the Carnitor 330 3x a day, so I'm anxious to see if it has helped or looks like it will. I get bloodwork done every Tuesday so hopefully by the end of the week we'll know something!
Friday, June 12, 2009
My husband has a daughter from his first marriage; his daughter (Kate) has lived with him and I since she was 1. The birth mom had sporadic visitation by choice (Not b/c of us or the courts) Right before Kate was to turn 3 the BM picked her up for a visitation. It wasn't the BM's weekend but it was a holiday weekend (Memorial day) and since the BM had canceled the last 2 visits we thought it would be nice for Kate to get to see her. Long story short she didn't bring Kate home. We fought her in court and finally we got Kate back. This time though she had a set visitation schedule. It wasn't a particularly nasty battle in court, but she lied a lot. But Frank and I decided to keep things as civil as possible. She still did not keep her visitation schedule, she always said she was too sick to take care of Kate. (she told us on 3 separate times she was having a hysterectomy and I can't tell you how many times her car broke down) About 6 years ago or so, she stopped calling or attempting to visit Kate. She was just gone and we had no clue where or why.
After she was gone for a few years Kate's sisters father and step-mom got in touch with us. We were thrilled that Kate would get the chance to have a relationship with her sister. From them we discovered our suspicions that the BM had moved to Florida were indeed correct, and that she still maintained visitation with Kate's sister.
Flash forward to last year. The BM started to pull some stunts with the younger sister and her father some what akin to how she played with Kate and us. Kate got really nervous because the BM kept making comments to the younger sister that she would get Kate and Jesse (Kate's older brother w/ different dad) for Christmas. Somehow Tracy got a hold of Kate's email (although admittedly it is not like we were attempting to hide) She sent Kate a forward about God, and then a few days later an invite to be her friend on face-book. Kate was really upset. No personal letters, no attempts to call all of this time finally culminated.
Kate came to my husband and I and told us she wanted me to adopt her. So we got a lawyer and that is what we are doing. The original court date was in May, but the BM showed up and said she doesn't want her parental rights terminated. Um...hello? Where were you when Kate needed help with her homework, or advice about her friends? Where were you when Kate fell off her bike and scraped up her knee? What about when she celebrated her birthdays and Christmas? And now you want to come play mother to MY daughter? No. It doesn't work that way. You don't get to walk away from a 7 year old and come back when when you want. Anyhow she showed up and made no attempt to speak to Kate, or ask to see her or call her...NOTHING. Do I think for one second she's fighting because she loves Kate? Honestly, I don't. I would never tell that to Kate, but she is fighting because she hates me. This is an attempt to hurt my husband and I. Not a mother attempting to gain redemption.
So next week is the second court date (they granted a continuance so that the BM could obtain a lawyer). I'm anxious to get this over with, she is coming up from Florida and assuming she got a lawyer will be there that day. Kate is scared about what the BM may do and has requested support from friends and family.
So please support her with your prayers and thoughts!
Tuesday, June 9, 2009
I cried. Of course all Disney/Pixar movies are like that. This one was different though. This was MY movie. I wish I could explain it but all I can say is that sitting there watching the screen I identified myself with one of the characters and my husband did the same thing. We didn't even really talk about it until we left the theater. It was just one of those wierd coincidences that happen on occassion I guess.
This morning I am getting ready for a round of IV therapy in Frederick. What I really want to do is to crawl back in bed; but I know the lack of energy is a direct result of no IV's for 2 weeks. Bad Chrissy. *smacks hand*
Other than that, everything here is going well; my daughter Kate is almost out of school. My husband hasn't been feeling well lately, but the doctor prescibed some high blood pressure medicine so hopefully that will help. He has been stressed out lately with work and then more work when he gets home!
Sunday, June 7, 2009
So home we went! I had to call the DJ about the wedding, not to mention firm up everything else.
August 22, Wedding day!
August 23, That afternoon I got a call that the CF dr left an urgent message for me to call her back. I didn't return her call until the next day which was a monday.
August 24, I called the dr and she said I needed an appointment. I laughed and told her that I knew it must have been positive for them to want another appointment. She didn't deny it. So I made my first CF clinic appointment at NIH and then I hung up to call my parents. My mom and dad were both on the phone and I can't remember what I said....but I'll never forget their reactions...My mom said "no, Chrissy I prayed. It's no. You don't have it. Make them do it again." and my dad just hung up his end of the phone. He couldn't even talk to me. I found out later that it was b/c he was crying (my dad is a private guy), my brother is the same way. My brother talks about CF more now than before. Actually my mom had said that if you had mentioned it before he would just walk away.
I knew August 23rd. I knew it, and that night my new husband held me while I cried. (I was actually relieved to have a name but the tears weren't for me but for Frank and Kate.) I told him he should go. For his and Kate's sake...they didn't need me hanging on. I was sicker than either of us thought I was before we got married. I would hold them back... He brushed the hair out of my face and told me, "Chrissy, don't be stupid." (I was 21; he was 26 and Kate was 2) We told Kate August 24th together. We knew at 2 she wouldn't understand, but now we could atleast give my strange illness a name now. Today at 12 she educates her friends on Cystic Fibrosis. She leads her very own team at our Great Strides, Kate's Krusaders. My two mutations are R347 P and Delta F 508.
I also have two mitochondrial mutations, they were not identified until around the same time I was diagnosed with CF. G15995A in tRNApro and A8326G in tRNAlys are my two mutations, both are rare but one is totally unique to me. Which basically means I'm floating through life with out knowing what could be next!
For those who read this though...don't feel sorry for me. Seriously. I have a great life and the BEST supprt system!
Wednesday, June 3, 2009
I was diagnosed when I was 21, years after being misdiagnosed all of the time with chronic bronchitis and asthma. I actually got the call confirming the diagnosis while on my honeymoon with my husband Frank. I'll blog about that diagnosis next time.
Why is the title "The life and times of a mutant"; well my genetics doctor and I joked when my mitochondrial mutations were identified that I was an origonal mutant. So that is where my title name comes from. Both of my mitochondrial mutations are rare, one of them is totally unique to me and has never been seen before. So I really am a mutant, but the X men have not called me yet.