Showing posts with label Chron's. Show all posts
Showing posts with label Chron's. Show all posts
Wednesday, February 15, 2017

Medical Supplies - Full Time Job


I seriously wish I could be paid by the hour for the time I spend advocating for medical supplies for my children. I normally like to keep things upbeat and chill on FB but today has been a beating, this week has been a beating ...

Children with lifelong chronic illnesses should not have to fight for the medically necessary equipment that keeps them alive. No one should!

How hard is it? 

And I fear things are only going to get worse all the way around --- fighting for their medical needs and their federally protected rights is exhausting.

Today I am tired. More than just sleepy. Just tired of the bullshit. And let's be clear ---- it is all bullshit. 





Friday, October 7, 2016

A New Hope - Humira




On Friday, September 23rd, we began a new chapter in Sophie's Crohn's Disease story.  After we got the results back that told us she had built up antibodies to the Remicade we immediatly began the insurance battle for Humira.  It was a long and heated battle but in the end we came out victorious and the Humira was delivered while Ian and I were still in Hawaii.  As soon as it arrived, I made plans with Sophie's doctor to come into the hospital to learn how to administer the meds.  We had heard and read absolute horror stories about Humira.  About the pain that it causes after the injection.  Sophie had heard them too.  We both had a lot of apprehension and fear about this new chapter.  Sophie's doctor recommended that we see the GI Peds Psychiatrist before coming in for the 1st injections.  

I am so glad we were able to do that!  She worked through both of our fears, gave Sophie some great coping skills, and a few tips for getting through the injection without it being quite so terrible.  It was good for us both to be able to have someone to talk to about it and calm our fears. 

On the 23rd we made our way to the hospital, all a bit nervous for what was about to come but we had a plan, and there was a calmness --- there was also a promise of Chick Fil A and the rest of the day off from school!  SCORE! 

Here is what I posted on Facebook after we were done.  I meant every word.  She is so strong, so stoic, and so very brave:

We did it. She is so brave. I do not take bravery lightly --- she was so strong and brave and fierce. 

She didn't want any distractions (ice, candy, numbing cream) --- she wanted to just do it. 
Y'all I love her brave self so much!!

The nurse gave the 1st shot and I did the 2nd one. She tried so hard not to cry but I told her it was totally fine if she wanted to do so ---- so we cried together.  My mommy heart broke to pieces watching her be so brave and endure such pain while trying to keep her brave face on. 

She said it was worse than she thought it was going to be --- pain level 10 out of 10. She did so great! 

We will begin to taper the prednisone and should know if the Humira is working by mid-October. 








This is being posted on Friday, October 7th, it has been 2 weeks since her 1st injections.  Today she gets her 2nd dose but we do it at home.  On our own.  

Stay tuned for my next post.  Things have been hard.  Harder than expected.  Mostly for me.  It is so difficult watching Sophie deal with so much.  I fear I have fallen back years.  She is doing so much better than I am.  I have been dreading this day, yet here it is . . . 


Wednesday, October 21, 2015

Seven Days

After 3.5 years of remission - it took 7 days for a full blown flare.  Seven Days.

I am not going to go into what a full blown flare looks like again.  If you are having trouble remembering or you are new to HWHAP - you can read: The Sh*t that is Crohn's Disease here! I don't mince words in that post.

Last Monday, the 12th was her Remicade appointment date but we found out the Friday beforehand that there was a lapse in her coverage and we were having trouble getting answers.  There were words like:  pre-existing condition, pre-authorization and you need to call financial services but ultimately they canceled her appointment and would not allow us to cash pay.  I was frustrated but not OVERLY concerned. #Mistake

I honestly had no idea she would get this sick so fast.  After 3.5 years you forget. You forget how completely awful it is.  It is so awful! I was even brazen enough to allow myself to believe that she would be ok.  Maybe she doesn't even need Remicade anymore!  Maybe, just maybe she can stay in remission without it!  Her doctor has told me countless times that they do NOT take children off of biologics - it just does not happen.  Why would I allow myself to think Sophie would be the exception? I don't know why.  I just know that it is hard, hard to know that your child will need this for the REST OF HER LIFE. It hit pretty hard. Again.  Which seems ridiculous but this disease is ridiculous so I think it is only fair that my emotions can be ridiculous too!

I left Sophie for a few minutes this morning to run to the gift shop and cafeteria.  While in the gift shop my emotions got the better of me and tears started flowing. Being here is hard. Coming through the ER was so hard.  We were in the same room that we had when Nate was diagnosed.  Being back on the GI floor brought back so many feelings.  Just ALL OF IT is hard.  Another mom came up to me and asked if she could hug me.  Not is a creepy, stalker way! She had tears too.  The mom bond is strong.  Being the mom of a chronically ill child somehow, if possible, makes the bond even stronger.   I didn't even get her name, or her story, but I could see the sadness in her eyes too. We are same same.

And now here we site in her comfy suite at Children's Medical Center Dallas overlooking downtown, an IV in her arm -- she is receiving the Remicade that was previously denied and we are hoping this kick starts her little body right back into remission.  She wants to go home and although her doctors wanted to observe her for one more night, they are granting her wish and letting her go home tonight! As long as everything goes well, of course.  She will miss school for the rest of the week as she rests and allows her body to recover.

2.5 years of hell was forgotten in the 3.5 years of remission but it only took 7 days to bring it all back and now I am hoping 7 days to get her back into the remission bubble.  It may take mommy a little longer to forget and will certainly take a while for the guilt to go away.   This sweet girl pays the price when things go wrong, when balls are dropped, and denials are made.  It hurts every fiber of my being to see her suffer.




This girl though is fierce, she is a fighter, a warrior and she will warrior on.
I am so honored to be this warrior's mom.  #SuperSweetSophie #CrohnsFighter #WarriorOnLittleOne

Thank you all for your calls, texts, and messages!  Thank you also for always allowing me to come here when times are tough.  When things are good I easily forget what comfort I find here, it is nice to always be able to come back when it is needed.



Tuesday, November 5, 2013

Brand New Me



To say that I hate the above picture is a complete understatement.  UGH!  That photo was taken a few years ago along with some other really great photos of my littles but I never shared the one above with anyone! My kids are adorable - duh!  If I could crop myself out it would be perfect!

When this photo was taken I was still spinning from both diabetes and Crohn's. Although you cannot tell it in this photo, Sophie was very, very sick and I believe we ended up in the hospital for a week just a few days after this was taken!  I knew the photo shoot was coming up and it was all I could do to get clothes picked out for the minis.  I didn't even give myself a 2nd thought.  I remember the morning so clearly getting everyone ready and then thinking ---- what the hell am I going to wear? Do I even own makeup anymore? Do any of my clothes even fit right now?

The answers were:

Who the hell knows!
Not much makeup!
Nope, nothing fits!

I knew I didn't feel comfortable with my looks that day but it wasn't until we got the proofs back that I really took a look at myself and wondered who I had become.  Since the birth of Ms. Emma Leigh my weight had gone up and down -- that will happen when you are pregnant every 2 years or so!




I think the above picture is my heaviest ---- Size 14.  Yes, size 14.
Did I just admit that here? 


I'll add a few cute photos of Emma here because she rarely gets any FaceTime on HWHAP:





Ok, back to my point . . . had I gotten to that yet?  I started looking at old pictures and got totally distracted!

This post is supposed to be about me.  So, my weight has fluctuated a lot since having kiddos but I had gotten down to a comfortable size 6 after I lost the Nate weight.  I was totally happy at a 6.

Until . . . . dun dun dun . . . Nate was diagnosed.  You all know how hard that was blah blah blah -- I've blogged that to death.  Then Sophie was diagnosed with Crohn's and blah blah blah it was hard again.  My point being after those 2 major life changing events I totally lost myself.  I no longer cared.  I gave up on me.  I was just trying to survive the day to day of raising 3 kids along with diabetes and Crohn's in the mix.  I think my weight went up to an 8 and then a 10 again which isn't a huge deal to some but I am 5'2" and fluctuated between a size 2 and 4 before I had Emma.

Then last summer I lost a lot of weight due to stress and other factors that are not bloggable but then as soon as I got happy again I started gaining and gaining and before I knew it I had yo-yo'd back up!



Same photo shoot as above.  I call those my lunch lady arms! 
(No offense to lunch ladies or their arms!)


Then in January of this year I turned forty! FORTY! Why do I keep admitting these things?! 

I started trying to lose weight again in March when during spring break I couldn't fit into any of my clothes. What the what?!?!?! 
So, I started dieting hard in March and was feeling totally frustrated and depressed by the end of April with NO results. Had my metabolism changed so much so quickly?? UGH!
Meanwhile, my friend Shay had started taking a supplement called Plexus Slim to help her lose weight. When she started I scoffed at her for trying it and down right laughed in her face when she tried to persuade me to take it too. Until, she lost 8 pounds on a two-week trial. She had me at 8 pounds...
I started taking the Plexus Slim and an Accelerator pill each day the 1st part of May and was down to where I wanted to be within 30 days. It sounds crazy but I promise it worked that fast for me. I didn't weigh but I had a pair of shorts that sat on my bathroom sink and I would try them on each week until they fit. They'd been sitting there since spring break!!
After 30 days on Plexus I decided to do another 30 days to maintain and now I just take the pink drink because I love how healthy I feel.

I need to add that I have NEVER felt better in my life. My energy level is off the charts...it is crazy. I also feel like it has helped my anxiety level so much. I am just happy! I know it sounds crazy. I am actually still taking the Plexus Slim drink, not the accelerator, because it makes me feel so great.

To recap --- I was needing a size 8 when I started, my goal was size 4 and now I am wearing a size 2. Being the shortie that I am it's not too small or to thin. I still carry some meat in my butt and thighs but that is just how I am built.

I feel like it helps curb my appetite and gives me an extra boost of energy each day. It's really taken away my snack cravings and I can always use the boost after a night of checking blood sugars. #DMommaProblems
I was already working out and running before I started Plexus - I didn't change anything there but my results after starting Plexus are quite noticeable. I've read many testimonials where people say they changed absolutely nothing and still lost weight.
After I lost the weight people kept asking me how I had gotten so thin so fast . . . I sent Shay so many customers! I would give them Shay's web site and they would order. Finally, she convinced me to become an ambassador and start sharing the products with others since I, and so many people we knew, were having great results and loved it. I told her I am not at all "high pressure" and feel totally uncomfortable trying to get my friends to buy something from me. 
She stressed it was more like sharing a great secret than selling and asked me to commit to putting it on Facebook just once a day. Reluctantly, I did, and now my business is blowing up! I know I am driving most of you crazy with my FB posts! But . . . it truly does sell itself . . .because IT WORKS! Also, it has become a valuable source of income for me so that I can continue to stay home and care for my minis. Working from home is a true blessing as I am able to be at the school with the children whenever they need me.

So, if you want to give it a try for yourself, you can order at my web-site or message me for more information.
My web site is: www.pinkdrinktexas.com
The best part is the products are all natural with no stimulants!







Just a Mom

I am NOT a doctor, nor do I play one on this blog.

I AM a wife.
I AM the mom of 3 wonderful children.
I AM my son's pancreas.

The information provided on this blog is from our personal experiences with Type 1 diabetes. Because something works for us does not mean it will work for you.

Please consult your doctor if you have any questions or concerns about your health care options.

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