September is
Interstitial Cystitis (IC) Awareness Month.
IC is a debilitating bladder disease that there is no cure
for at this time. Whenever I read
articles written about IC I am so frustrated at how inadequately they describe
the disease. So many times it is called
a chronic pain syndrome. That hardly
comes close to what an IC patient experiences day to day year after year. I do like the line on Wikipedia that
describes IC this way: “IC/BPS
can result in a quality of life comparable to that of a patient with rheumatoid arthritis, chronic
cancer pain, or a patient on kidney dialysis.” IC is life
changing. It takes the food, the
physical activities, the day to day energy, and most of all it is so very
difficult to see a light at the end of the tunnel with this disease.
My bathroom cabinet has 4 baskets filled with medications
that have been tried on me to hopefully get me better. There is only one FDA approved medication for
IC and that’s Elmiron. Elmiron is
thought to repair the lining of the bladder but the pharmaceutical company that
produces it is honest and says they don’t know what it does. But it does help some of the people who take
it. I took Elmiron when I first got
diagnosed. I was violently ill for almost
a week after taking it and after I stopped taking it. The list of side effects of the medication is
long but if it helps and you don’t have those great! I just wasn’t that lucky. After Elmiron I’ve been put on over 25
different medications trying to control some of my symptoms. Some were compounded some were medications
for other illnesses but help control some of my symptoms. All in all only one of the medications
actually helped at all and that was hydroxyzine. Hydroxyzine helps because it lowers the
histamines in my body that the mast cells in my bladder are sending out from
the disease. Everyone with IC has an
overabundance of mast cells in their bladder that have been activated and are
pouring histamines into your system. But
even this medication doesn’t get me totally out of pain. So this week I’ve started on a new medication
called Cystoprotek. Cystoprotek is sold
online and was first suggested by my urogynecologist. Cystoprotek is supposed to work similarly to
Elmiron but without all the side effects.
The biggest side effect with Cystoprotek seems to be stomach upset which
is helped greatly by freezing the pills for at least an hour before you take
them.
Alkaline Diet
For over 2 years I’ve been on an alkaline diet with only
whole foods. I can’t eat prepackaged
foods that have chemicals in them which pretty much knock them all out for me
except for one brand of saltine crackers and some Amish styled pasta. I buy and drink only Mountain Valley Spring
Water which is very alkaline at a pH of 7.8.
I eat fish grilled or baked with
only real butter and I can eat these other foods and that’s it:
v Blacked
eyed peas
v Carrots
v Celery
v Cucumber
v Green
beans
v Homemade
bread
v Potatoes
baked, stewed or mashed with sour cream &/or real butter
v Red and
yellow peppers
The diet is a healthy diet except for the fact that it
won’t allow me to eat a wide enough variety of food and to get enough B
vitamins. So I give myself a B12 shot
every Wednesday. This diet is
monotonous. I have blogged before about
my diet and how I understand how the Israelites felt in the desert eating the
same food day after day. It truly is
maddening. But the diet decreases the
pain further. So I stick with it and I
never cheat. I could NEVER have said
that before IC. I was the least
committed dieter out there but pain is a wonderful motivator.
Medical Procedures
Many patients with IC have various procedures done to
help cope with the pain. None of them
completely stops the pain but the hope is that it makes the pain more
manageable. I’ve had my bladder
repeatedly numbed with medications. I’ve
had bladder instillations which means a cocktail of medications were put into
my bladder with a catheter and then I held the medicine in my bladder for an
hour. Many patients get relief from
bladder instillations. I wasn’t one of
them. I had 6 instillations but each one
increased my pain more and more. For
those patients that these help your urologist may teach you how to do these at
home which would be more convenient than having to run to the doctor once a
week or however often your doctor suggests you have them. I had them once a week for 6 weeks.
Invisible Disease
People occasionally ask how I’m doing and then comment on
how good I look which is a nice product of eating such a clean diet. Your hair and skin will look so much better when you are eating whole foods than
if you are eating a diet laced with countless unknown chemicals. I often complain to my friends who also have
IC that I wish for one day other people could feel what I feel or see my
damaged bladder so they would know that I’m not eating this way because I want
attention. I’m eating this way and
trying new medications on an ongoing basis to get out of pain. I could live on prescription pain medications
for the rest of my life but they do nothing to help IC in fact I’m convinced in
the long run they would actually make my symptoms worse. So I press on every day researching the
latest study for the disease and hoping and praying for the day that there is a
light at the end of the tunnel. This
disease is hard for those of us suffering with it but it’s also hard on our
families who have to watch you go through all the suffering, who want to help
but don’t know what to do, and who just want everything to go back to the way
it used to be. I’m thankful that I have
God to walk with me through this painful journey. HE whispers to me when I cry out…”this is
only for a little while” and I cling to that and know that HE is making me
stronger in the meantime.
“And
we know that in all things God works for the good of those who love him, who
have been called according to his purpose.”
Romans 8:28


