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Other various tests for diabetes

February 12, 2009 – 8:24 pm

Here are a few other tests (by far not all of them) that are important in either the diagnosis of diabetes, or if you have diabetes they are good to have to keep tabs on things.

Random glucose test – This is usually a fingerprick, or done while draining your arm/body of blood for other tests.  They test the amount of glucose (sugar) in your blood at the given moment.  Two random tests above 200 mg/dl is a diagnosis for diabetes.  That is kind of tricky for us with CFRD since illness is common and so is steroid use, which will give you higher than usual blood glucose levels.

C-Peptide test – I was told there is no real ability to measure the amount of insulin your body produces.  But when your body produces insulin it also produces a protein, c-peptide.  In theory if your body does not make enough insulin, you won’t make much c-peptide either.  Usually this means that your pancreas has given up the ghost and is no longer working properly.  I had this test done, as required to get insurance coverage (my crappy old policy) for my insulin pump.  Welllll… I failed the test… or did I pass it?? Turns out that my body makes enough c-peptide to qualify me as “normal” and not needing insulin.  Well… that is by far, not true.  The exact cause of CFRD is truely unknown to this date.  Of course our lil pancreases are on their way to complete self-distruction (which mine showed via a CT scan), but there is a study out there that claims the creation or use or something about the natural made insulin doesn’t work correctly.  Which is why I apparently have insulin dependent diabetes, but still have a normal amount of c-peptide (or at least I did last year).

Antibody test -  This is where Type 1 diabetics differ from all other types and exactly why CFRD is NOT Type 1 (although treatment is similar which is not to be confused with cause).  Type 1 diabetes is an autoimmune disease which is caused by antibodies that attack the insulin producing cells, the beta cells, in the pancreas.  If you have diabetes and have antibodies, you have Type 1.  If you have diabetes and do not have antibodies, you have a Type Other than Type 1.  A cure for “Type 1″ diabetes will not cure my diabetes and that is why I am such an advocate for the “Type Other”s.  It is possible for someone with CF to have Type 1, it is the same rate as for the “normal” population, but just because you have cystic fibrosis related diabetes and you are insulin dependent, this does not make you Type 1.

Urine Sugar tests – If you have too much sugar in your blood, it will spill over in your kidneys (which is not good) into your urine.  Usually one of the first tests they do when they suspect diabetes.

Liver function tests – For folks with CF our livers are at risk of damage from all the drug coctails we are required to take.  I am only mentioning this test because I know a few CF docs who try putting their CFRD patients on pills for treatment instead of insulin shots.  I guess pills are ok, but I would be hesitant because most diabetes pills have a high risk of causing liver issues…. Just one more thing I do not want to add to my list of things I need to deal with.

I am sure there are plenty of other tests I am not noting in this post.  Anyone else want to chime in? :)

Salty | CFRD Facts, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, Kidneys, diabetes | Comments (3)

A1c Test

February 11, 2009 – 8:49 pm

Also known as the HbA1c, hemoglobin A1c, or Glycosylated (or glycated) hemoglobin test.  This is a blood test that measures the average blood glucose levels over the past 2-3 months.  Glucose can bind to the hemoglobin which is found in the red blood cells.  This causes some sort of modification of the molecule in the blood cell which is I guess what is measured, in a percentage. What is important to understand about this number is that it is an average.  Meaning if your blood sugar is fairly stable you could get a certain resulting number, but you could also get the same exact number if you have a lot of highs and a lot of lows.  Overall, this test is used to predict if you are in good control of your diabetes or not.  A normal number could tell you that you are in good control, but a high number definitely says you are not in control and are at a much higher risk of horrible complications that are much worse than just dealing with the daily annoyances of diabetes alone.  Anytime you have bad highs it increases those risks, which is why I think the A1c test is kind of tricky.

side note: I have wondered since the extra glucose messes up the red blood cells, I wonder if it affects how oxygen, and how much of it, is carried through the blood stream (since it is also carried by the hemoglobin) which is kind of an issue for some of us cystics with messed up lungs.  I’m going to look more into that someday. But if I find that is true I am going to get even more pissed at the CF docs who put off CFRD testing (not mine luckily). *sigh*

Apparently a “normal” person would have an A1c level at about 5.0%.  My doctors suggest an A1c of 6.5% or a little lower, normal would be ideal, but that is darned hard to reach.  My docs find that above 6.5% it seems to really affect the CF lungs.  To me I really couldn’t understand what that number meant until I found a calculator online that could translate the number into something I was familiar seeing on my little meter tester thingy I use every day.  Here’s one I like, it goes both ways from A1c% to mg/dl.
http://www.accu-chek.com/us/rewrite/content/en_US/4.1.2:20/article/ACCM_general_article_2422.htm
Here’s a little chart on dLife:
http://www.dlife.com/dLife/do/ShowContent/blood_sugar_management/testing/a1c_conversion.html

154 mg/dl is the magic average number.  Personally, what I try to do is make sure I am at a safe, but lower number (preferably 85-95) through out the night since I am spending 8-9 hours at that level.  Recently with my Continuous Monitor I have found I am having a strange spike at 2:30-3am which means I am going to need to change my basal insulin rate at that time… but that is a whole different story.

Once last year I scored a 6.0% on my A1c test (yes, it went on the refrigerator)… I really doubt I am there again, it took a lot of hard work and discipline, but here is some tricks of how I did it…  Having a lower level for many hours while I am asleep made it easier to get to my goal A1c level.  When I spike at meals, I try to keep it under 200 mg/dl at the two hour mark by counting my carb intake as close as I can (IMPOSSIBLE when on evil evil prednisone), but I make corrections at the 2 hour mark if I have to (my pump figures out the calculation taking in consideration how much active insulin I already have in my system, which is why I am such an advocate of the pump, it does all the brainpower).  I have played with my numbers and found at my of 1 unit of insulin (which is an unbelievably small amount, it’s like a few drops!) for every 8 grams of carbs and my correction or sensitivity rate of 1 unit to 25 mg/dl (how much my bg number will drop with one unit of insulin), If I miss calculate my carb intake by 20 (two macroon cookies, who ever eats just two cookies?!) my blood sugar level will go up 62.5 points (mg/dl). HOLY!  That means I need to keep quite a close eye on things.  It never used to be that way when I was on shots, I was on a 1:15 ratio…. but then again, I was never in control of things on shots.

Back when I was out of control, my A1c level (at least the first one I really paid attention to) was 9.3%.  That number alone wasn’t enough to scare me.  But it should have.  The toll it took on my poor body was too much for it to handle and I have not escaped a few complications.  Nothing too scary, but annoying enough to get put on a few extra medications.  I wish I would have known then what I know now.

Salty | Challenges, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, Kidneys, diabetes, insulin pump | Comments (5)

Oral Glucose Tolerance Test

February 10, 2009 – 7:46 pm

I was about to launch off in a review about an article I read online at the American Diabetes Association regarding two diagnostic tests for diabetes.  But then I realized that it may be more important to give you a bit of a description of the tests before I go spouting off my opinion of the article.  So here goes…

The Oral Glucose Tolerance Test, OGTT, has been used as the primary diagnostic of Type 2 diabetes as well as some of the Type Others of diabetes like CFRD, (once again, CFRD is not Type 1 OR Type 2 we are Type Other go look it up on the wikipedia!).  The OGTT is time consuming and fairly painless.  Like it says, the test is done by intaking glucose oraly and they test your tolerance to it.  In other words they take a few blood draws (or fingersticks) before and after you drink something like orange soda and see how your body reacts to the sugars.  If it doesn’t react properly, then the finger points to diabetes.

Getting ready for the test… Don’t eat or drink from midnight the night before, they say 8-14 hours.  I am not sure if black coffee is ok, but it seems like caffeine has different reactions to blood sugar levels in different people, so if I were you having this test I’d drink water and only water.

Next, you show up at the doctor where they sit you down hopefully in front of a TV because this test takes two hours of basically just sitting there.  Some doctors (or nurses) use a small IV to draw blood, so they don’t have to stick you mulitple times.  Others use a finger stick blood glucose meter, which you just better learn to deal with if the test comes up positive (I have to use my fingerstick thingy 4-8 times a day, sometimes more).  I had my OGT test 7 years ago, and I think they used the fingerstick method… but my memory escapes me.  …The nurse sits you down and draws a fasting level which will show what your blood sugar level is when you have no food in your system.  This alone can be enough to diagnose someone with diabetes (as it was for me).  If your pancreas does not make enough insulin to regulate the sugars normally produced in your body, even without food, more than likely you have da ‘betes, they call that fasting hyperglycemia.  Pretty much, if you have fasting hyperglycemia, you have diabetes.

As a quick note, to explain how insulin works simply, it is like a key that unlocks the cells and allows them to take in the sugar (ie glucose) and turn it into or store it as energy to use in the future.  Without insulin (made by your pancreas or by supplemental shots) it is not possible to change the nutrients into energy.  Basically put.  Without insulin, sugar builds up in your blood which wrecks your blood vessels and does some other nasty stuff.

So… back to the test.  After they draw a fasting blood glucose level, they hand you a bottle of this sickening sweet drink that is like a flat orange soda with a little extra sugar added.  If they are nice enough, they will have refridgerated it for you which helps it go down a lot easier.  (Ooh! If you are going for this test you could make a funny out of it and bring in a swirly straw and a drink umbrella!!!  Bet the nurses would be a little nicer when they stick you for blood! Wish I would have thought about that before! hehe!)  Back to the matter…  I have heard a lot of folks complain about how sweet that drink is.  But to me, when my body wasn’t absorbing enough energy from (not enough insulin to do so) I craved sweets and other carbs night and day, the warm flat sugary soda tasted so yummy.  For those of you number crunchers, the “soda” has 75 grams of carbs in it.  Regular orange soda has 35 grams in one cup… so it really isn’t much sweeter than two cups of the real thing.

At 30 minute intervals they test the level of sugar in your blood until the 2-hour mark.  They should be able to tell you right then and there what the number is.  I stole the following data off of the American Diabetes Association website it is in reference for ANYone testing for diabetes, no matter what Type (and are also used for the diagnosis of CFRD):

Fasting Levels:
Normal Fasting <100 mg/dl (mg/dl is the unit measure used in the US and what would be shown on your fingerstick meter if you are using one)
Pre-diabetes Fasting <125 mg/dl
Diabetes diagnosis Fasting >126 mg/dl
For me, I was above 126 fasting, so we already knew at that point I was screwed.

At the two-hour mark:
Normal <140 mg/dl
Pre-diabetes 140 to 199 mg/dl
Diabetes diagnosis 200+ mg/dl  (which I hit at the first 30 minute mark)

If you really are concerned and your doctor is not listening to you, you could try the test at home if you have a meter and some decaffeinated soda (doesn’t have to be orange flavor, I would prefer grape or strawberry… ooh! or Squirt!).  Make sure you do the test in the morning though because your body makes natural steroids throughout the day which will affect your numbers.  But still, if you do the test at home, it is not an official diagnosis, but it may put your mind at ease if it’s negative and you have been worrying.  Oh! And make sure you are not taking steroids or sick.  Those two can really throw off your results.

I have been quite frustrated and disillusioned by what some of my fellow cystics have said to me.  They have shown interest in getting the test done because they are showing signs of CFRD and they want to take a proactive role in taking care of their health.  Some of their doctors say, “nah, you don’t really need it” or “go to your primary care physicain”… do these doctors have no clue in how untreated diabetes affects your health? especially your CF health?!!  I just want to shake those doctors.  It’s a simple test which could save someone a lot of pain and suffering.  Untreated and uncontrolled diabetes makes you MUCH more prone to infection, which is a cystic’s worst nightmare!  Not to mention all the other crud that comes along with it….  Come on doc’s get with the program and TEST YOUR PATIENTS!  Personally, I go with the CFF (Cystic Fibrosis Foundation) guidelines as a baseline, more can be done, but less is just irresponsible. The CFF suggests that anyone (with CF of course) who is pancreatic insufficient (takes enzymes) be tested (via OGTT) every year after the age of 12 if they show signs or symptoms.  Some docs think the A1C test is enough… but I’ll get into that later.  Next post will be about the A1C test.

Hmmm… well I think that sums up the oral glucose tolerance test.  Any questions?

Salty | CFRD Facts, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, diabetes | Comments (3)

Hot peppers on my feet

February 6, 2009 – 6:38 pm

Having been to the doctor’s about a billion times in the past few months I have learned a few new things about diabetes that I want to share.  I don’t know where I read it, somewhere said that folks with CFRD do not suffer the same complications as “regular” diabetics.  This is just bullpuckey!  I know first hand that uncontrolled sugar levels wreak havoc on your kidneys.  Now I am still not sure about DKA (I hear we can’t get it).  But I have found out recently that we CFRDers can get neuropathy as well, POO!

I’ve had a weird tingly feeling in my legs in the evenings for years now, and finally brought it up to my CFRD doc.  Turns out it could be neuropathy (nerve damage pain) which for me was caused by years of not really caring about my diabetes.  Apparently a simple treatment for the discomfort exists, over-the-counter capsaicin cream.  Yep, it is a cream made with the burnin’ hot oil that comes from hot peppers!  Who would have guessed!  I have been a bit nervous to try it.  I still have flashbacks of an old guy friend of mine who… ummmm… wasn’t so careful after cutting up peppers for salsa then went to the little boy’s room… let’s just say it wasn’t his eyes that were hurting, but many tears fell that night.  DO NOT TOUCH SENSITIVE SPOTS AFTER TOUCHING HOT PEPPERS!

My legs were super creepy crawly, driving me crazy.   The feeling is always worse when my blood sugars are bad, which they are right now thanks to the lovely Prednisone and a lack of continuous glucose monitor sensors (my refill order has been sitting on someone’s desk for the past few months, no explaination why except it is not the fault of my insurance).  I finally talked myself into giving the capsaicin cream a try.  Tried a little dab… nothing…. rubbed more in… eh, it kind of took the tingling away, a little… my feet felt like they were lathered in regular ol’ body lotion.  No cooling sensation, no burning… nothing special.  Reading the lable it sounded like it was supposed to feel like icy’hot.  Brodie, his little inquisitive doggy mind, oh boy… When I wasn’t paying attention I felt the slightest lick of his tongue on my feet.  I would have loved to see how big my eyes got when I felt that!  I was afraid his little tongue would fall off or something… I mean, what would I do if it burnt his tongue?!  then… nothing.  lick… lick…  Didn’t even faze him.  Strange… was I just duped into buying into a placebo?

The next morning when i woke up my feet were on FIRE!! Holy smoke!  Turns out that it was a bit much for my super sensitive skin.  At least I know it wasn’t just plain lotion now.  I think I will give it another try sometime possibly soon and let you know how it goes.  Definitely, I will be using much less next time.

Salty | CFRD Facts, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, diabetes | Comments (5)

What goes up, must come down, oh whyyyy?!

February 5, 2009 – 6:32 pm

That is how my life has seemed to be over the past few months… ok, maybe past few years.  After my last oh so awesome post, not even a day later, I got some bad health juju that kicked me on my arse which is why I have been on the ‘downlow’ (or what ever the cool kids call it now).  For the past oh maybe 3 months (ever since I kissed that last toad, damn him) I’ve had something stirring in my tonsils, other than that I felt ok.  Alright, I lie.  I have been EXTREMELY tired, and felt like I was obviously fighting off some sort of bug, but I try to convince myself I am ok.  The day after my big happy dance news, I was hit hard with another lung infection.  Unfortunately it was a big bad scary bug (which apparently was the root of this issue in my tonsils).  Fortunately we found medicine (freakin ex-pen-sive medicine) that kicked the bugs butts and now I appear to be free of it even though just before I was finished with two weeks dose my body decided to revolt and become allergic to it. *good grief!*

Just as I was starting to feel better from the freakin expensive medicine allergic reaction, my tonsils started to blow up again like one of those puffer fish. (geez! can’t I catch a break??!)  Back to the doctor I go.  Turns out I got ANOTHER weird bug I have never had before.  Luckily this one can be kicked by some cheep non-allergy inducing (fingers crossed) meds.  For an extra boost I agreed to do a boost of Prednisone (evil evil evil), which has given me some lovely roid rage, blood sugar numbers that go from normal to 450 in 30 minutes and a tummy monster that can not be tamed with no matter how much food I cram down.   I am afraid to say, go away bad juju, that I am starting to feel better FINALLY.

Salty | Challenges, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, Kidneys, diabetes | Comments (2)

Oh my! Did she say the “f” word?!

January 6, 2009 – 6:00 pm

Over the last week my tonsils were giving me heck.  So I stopped by my CF clinic yesterday to get some good ol’ Levoquin (antibiotic).  As tradition goes, as with any clinic visit, I did the typical blow into the machine and it spits out a number thing.  To my surprise it seemed really easy.  Usually I have fits of asthma that really makes it tough despite all the meds I take.  I asked the therapist if I could get a copy of the results and she kind of was reluctant to give them to me, which was weird, it is totally normal for us cystics to want our own proof.  But my eyes bugged out when I saw the number.  This was the best test I have had in YEEEEARS.  I haven’t been feeling all that well recently, probably my emotions getting the best of me.  Considering my throat was partially closed up to my tonsils the size of golf balls, it was amazing to me. (I am giving credit to the Inhaled Aztreonam study which I started only 28 days ago and adding a new asthma drug).

Holy smoke folks!  I never thought I would have this conversation with my docs ever.  Partially because I was reluctant to ask, because I didn’t want to get my hopes up, until I found that special someone to share my life with (yea, I am giving up on that for the time being, until time wears away some more horrible memories).  But my doc said some of the most wonderful things to me.  If I am able to get my lung function just a little bit better, which is very possible and should be easy to do, and keep my diabetes under control, my doc believes I could live a very long and healthy life, which may even include… having a FAMILY!  Oh my! She said the “f” word!  I never really considered this to be an option for me.  So hearing it makes my mind boggle!

I don’t know… maybe doc has been reading my blog and found out that I have been down in the dumps and wanted to lift my spirits about my future… who knows. (by the way, I don’t mind if you read my stuff docs and nurses.. if you are reading this)  :)   But still.  A FAMILY is something that I had never seriously dreamed of.  Much like the people I have dated, I always invisioned myself to have the “expired” stamp on my forehead.  These people have done hell to part of my self-esteem, which you could probably read into in some of my recent posts.  Making me feel like I am less worthy than someone without my genetic mutations.  I look back to see my past wasted with tears caused by people who looked up CF on the web and deemed me lesser than thou.  They hurt me because they were scared of some outdated data.  They were scared I may die (well DUH!).  It is horrible.  And despite this happy news my doctor spoke to me, the tears I have spilled over the years over what others have told me… it is very sad to realize that this cycle will go on, people believing the internet over my word, or even my doctor’s word.  I cry more tears knowing that even though I have been given a blessing of sorts, I may not ever be able to have it just becuase of this damn internet.

What brings us together can also push us apart.

But she still said the “f” word!  :)

Salty | Challenges, Cystic Fibrosis, Dating, Invisible Disease, Life in General, Support | Comments (11)

Blood sugar and memory

January 1, 2009 – 11:14 am

Over the past, oh year and a half or so, I have noticed a severe decrese in my mental ability to remember things.  Mostly affecting my short term memory, repeating things, asking the same questions over and over, not able to remember what tasks I am doing, or have completed… the list goes on.  I think this deteriation started over 10 years ago when my blood sugar control was really bad.  I origionally blamed it on stress, emotions, getting older.  But recently as my good blood sugar control has slipped a bit and I noticed it getting worse again and I started to question if there was a connection.  Low and behold today I opened the New York Times (online) and found this article I which is very interesting to me.

NYT Health

Blood Sugar Control Linked to Memory Decline, Study Says

By RONI CARYN RABIN
Published: January 1, 2009

As the body loses its ability to regulate glucose, parts of the brain involved in memory lose blood flow, researchers find. .
Link
Salty | Cystic Fibrosis Related Diabetes, diabetes | Comments (2)

Emotional Rant

December 29, 2008 – 6:21 pm

As usual at this time of year I tend to get a bit overly emotional.  To blame, at least partially, is the lack of sunshine in my life both literally and figuratively.  As the end of the year closes it is hard not to reflect back on the passing time.  This year has definitely been the hardest ever for me maybe with the exception of when I was 13 when all hell broke loose on me. But back then I didn’t have the responsibilities of what I do now, which… *sigh* I am just not going to finish that sentence.

This past year has been super hard health wise, where I have passed a few unhappy milestones and set some disappointing records for myself.  But overall I have had no decline since this year started.  But I feel now more than ever my life slipping away, I know most of it is just mental.  Not helping are the loved ones in my life who some are not realizing that I have been having a tough time, most are living in denial.  Then there are others, mostly friends or people I have dated, who don’t have a clue what I go through and then turn their backs on me because I have had to cancel some plans because I simply did not have the energy to go out of the house or because I caught yet another one of their colds.  This year has definitely shown me what makes a true friend.  I am coming to terms that CF is a very lonely disease.

From those who I dated, it hits harder than ever, the words still echoing in my head, “I looked up CF on the internet….”  now I stop them in their tracks.  I know what comes next… blah blah blah… you are going to die… blah blah… I am just not strong enough to deal… blah blah… It scares me… blah blah blah.  HELLO?! Have you come to terms with YOUR OWN morbidity?!  They make me feel like a charity case.  Wasting their time until Ms. Perfect comes strolling along.  I have heard this story from almost every single person I have dated.  I used to try to plead my case, try to get them to understand that they are mortal too, that they have no idea what their own future could bring.  Treatments are coming out by the bucket-load to help prolong my life, so goodness knows what my future will hold.  But it always falls on deaf ears, so I no longer try.

Thanks to those who have attempted to point me to the social internet sites where others with CF can bitch, moan and complain about their ailments, I appreciate your attempt… but seriously.  Knowing that others are going through the same thing really doesn’t help that much.  I want what most “normal” (as if there is such a thing) 32 year old women want.  So far, there is nothing stopping me but kismet, which I am promptly growing tired of the lack there of.  I see my friends getting married, having babies, getting divorces,  getting re-married.  Am I ever going to be able to experience those things?…  I don’t understand why I am so… second-class? disposable? undesirable?

No wonder why people with chronic illnesses end up with depression.  Not as if dealing with the illness is hard enough, but having to deal with people who are so uncaring… or maybe they are just out of touch with reality.

Physically, I feel alright, my health is stable (even though I had some rough bumps in the road), but I constantly have people are pulling me down emotionally.  I do have bad health days, but I think it is because of my emotions more often now than before.  Being sad makes me feel sicker.  Taking care of myself is taking up more of my time, but it is only because I have more of a desire to stay healthy, live longer, it is my last hope of a somewhat “normal” life.  Even if I am the only one hoping.

Salty | Challenges, Cystic Fibrosis, Dating, Invisible Disease, Life in General, Support, Year In Review | Comments (5)

Theory of CF Gas

December 12, 2008 – 6:38 pm

So if you haven’t figured it out already, Cystic Fibrosis is not a pretty disease.  If it is an icky bodily function, CF makes it worse.  I was recently asked by a CF friend about CF gas.  We cystics have it, a lot of it, and it surely does not smell like roses.  On my way home from work it occurred to me a reason for CF’s ’specially potent gas (don’t ask why it occurred to me on my way home, you don’t want to know).  Now, I have not put much thought into this theory, so it is up for your debate. I’d love to hear your thoughts and comments.

For the past several months I have had a slight obsession with the show You Are What You Eat on the BBC.  On one episode the host, Gillian, describes how intestinal gas is formed in the average digestive system.  What she said (in my confusing words) is that if you eat your slow digesting proteins before your fast digesting carbs, the proteins act kind of like a stopper and the carbs sit, digested, rotting, fermenting, and producing gas.  This is how “normal” gas, (dare I say FART! hehe!), is made.  I have no idea if her theory is valid, but it kind of makes sense to me.

Now with CF, specifically in pancreatic insufficient folks like yours truly, the digestive tract is a bit slow thanks to the lack of water between the poo and the walls of the intestines (epithelial cells, CFTR malfunction, I’ll spare you the details for another post), this could cause a longer digestive process causing the fermenting fast acting foods to ferment further and make even more rotten stinky gas.  (oh so pretty, I feel pretty!).

No idea if I am on the right track here or not.

So I will share some things that I have changed recently in my life that has helped me with my gas issues… (except for when I cheat, then all bets are off):

  • Drinking lots of water (I am never really good at that and would much rather drink coffee)
  • Not eating red meat (no idea how this is related, but there seems to be a connection for me and my body and gas)
  • Eating more fruits and veggies
  • Taking Miralax when I am starting to feel a bit backed up and bloated.

Anyone else want to take a stab at the causes of gas?  Do you have some home remidies to prevent gas?  Go ahead, it is a funny topic so be as silly as you want!

Salty | Challenges, Cystic Fibrosis, Life in General | Comments (8)

Welcome Diabetes Forecast Folks!

December 5, 2008 – 12:55 pm

I want to send a warm welcome to each and everyone who has recently found my site.  For those who have found me from my article in Diabetes Forecast, you may not be familiar with my unique type of diabetes and I want to point you to the top of the page where you can find out a little more about Cystic Fibrosis Related Diabetes, as well a little more about myself.

I send warm hugs to all of you!!!  Hope you are staying warm this winter (it is FREEEEEZING here!).

Take care!
~salty

Salty | Cystic Fibrosis Related Diabetes, Life in General, diabetes | Comments (2)