Thursday, March 29, 2012

18 and feeling better than ever

Not much to update on. I turned 18 on Monday the 26th and I am 5 weeks out of surgery today. I am ready to graduate in less than 3 months. I WILL get to walk with my class. :-)
I am feeling better than ever in three years.
I still do have the kidney stones, but I will see the doctor next week to see what to do. They do hurt, but the pain is minimal compared to what I have been through.
I am started having rib pain about a week ago again in the same area where they did the rib graph. That pain completely went away a few weeks after my fusion surgery in December, but suddenly came back. It hurts! My primary doctor thinks its inflamed from allergy's and a sinus infection. I am on antibiotic and if it does not help, I will go back for the next option.
Thanks for the support.


Monday, March 12, 2012

Feeling GREAT!

First off THANK YOU to everyone who donated, helped or came to the spaghetti dinner. It was a HUGE success and it was great to see everyone! I posted some pictures from the day below.






I am two weeks out of surgery. This Thursday will make three. I am taking NO PAIN MEDICINE for the first time in three years. Yes, I do have a very high pain tolerance, but I can truly tell that I am pain free. I am feeling better than ever. The past three years have physically and emotionally drained me in so many different ways. I am finally back to my old self. I do know that Chiari and EDS are always going to be a part of me and sometimes will be more difficult than others. It is just who I am and I am going to have the make the best of it. I am not tired all the time and I can make it through the whole day without a nap. For once I actually feel like doing stuff with my family and friends. It is the best feeling in the world. I can not wait to graduate and get a fresh start. I finally feel like I am reaching the end of the tunnel and seeing a bright future.
Thank you for all your thoughts and prayers. They mean more to me than you will ever know.

Thursday, March 1, 2012

What a February

I am so glad to say that the month of February is OVER! It was not a good month at all for me. So with that being said, I have not been able to update because I have been so sick and in and out of the hospital and doctors offices. I am going to go back and try and piece it together the best I can.

February 14th was the two month marker from my last surgery. We left to go to Bethesda that day so we could see Dr. Henderson for my 6 week post op visit on Friday of that week as well as a Urology appt. that I had on Thursday.

I had my Urology appt. first. They did a urodynamics test to see if I have neurogenic bladder. It was a HORRIBLE and PAINFUL test. The test came back positive for neurogenic bladder. There was no denying it. There sat the paper on Dr. Murdock`s desk that said it. It was so bad....It was off the chart. I did not only find out that I had neurogenic bladder, but that I have MULTIPLE kidney stones in my right kidney. The doctor says both of these things are very normal for Ehlers Danlos people. He prescribed medicine for both. Now to Dr. Henderson on Friday.

We sat in the waiting room to see Dr. Henderson for forever as usual (he was 2 hours behind), but trust me it is so worth it! We are called back. I tell him I'm doing good, but a few things had been bothering me.....my hardware was protruding out, my back and I was starting to get random headaches behind my eyes.
Now in a perfect world he would have said "Lets fix the hardware....No big deal and Oh yeah, I can do tetherd cord surgery and you will be set for good." but, it so did not happen that way to say the least. He can not fix my hardware due to the fact that my bones have not fused completely and it would mess the graphed up, so the hardware still remains. He also was not sure I had tethered cord because it was not showing up on the MRI and X-Ray that I had. So he would not do surgery anytime soon, until he was positive that was the problem. I do appreciate that he is not just going to do surgery unnecessary, but when you are desperate and feel horrible its not what you want to hear. If I did have it, it was considered a colt which means its there, but not showing up. So since I was having pressure headaches behind my eyes he thought that I could have Inter cranial Hypertension. He said it can cause back problems too. So unwillingly I went back on the horrid drug of diamox. I was SO upset. I knew I had tethered cord, but I could not challenge him about it because it was not showing up on the scans. :( I was not a very happy person.

All of that weekend I stayed on my uncles couch complaining I did not feel good. I did not want to do anything. We set for home on that following Monday and I made it as far as Alexandria, Virgina from Chevy Chase, Maryland. I got this god awful headache and as much as I did not want to admit it was behind my eyes and it felt as if fire crackers were exploding in my head. I immediately started sobbing and vomiting. (That is not like me at all. I usually tough it out and don't complain, because if I did not all I do would complain.) We headed to the ER to meet Dr. Henderson.

The ER was a horrific experience and I refuse to ever go back. I swear everyone with a hang nail was in there. It was ridiculous. Not an empty seat in the room and I could barley sit up. After hours of waiting in the waiting room we finally got called back. I was losing it. I was given an IV which took 8 sticks to get and I mean digging around to get. I finally said you have to find someone else. I'm going to black out. My veins are completely trashed from everything throughout the years. Dr. Henderson came in and ordered tons of stuff (I'm not even quite sure what all because by that point I was on some strong medicine). He did admit me though. Again, I was not happy, but I was SO VERY VERY sick.
After being admitted and finally getting a room at 2:30am, neither mom and I were very happy people. By the second day of being there he finally thought I needed tethered cord surgery. I WAS THRILLED! Not that I wanted surgery, but I just knew that's what I had and I wanted to be better and out of there. So tethered cord surgery got scheduled for Thursday. I was going crazy. I wont deny it though, Mom and I did get some good laughs while being in there.

That next day leading up to surgery seemed to last forever. Every thought of 'what if' came to mind. It was finally surgery day. It was scheduled to start at 3:30....yeah right! ha Anyway, I got prepared and cried and then cried some more. Mom was the only one able to be at this surgery. Everyone said it was going to be the easiest surgery you will have ever had.....NOT! I was preped and finally got down to surgery holding and the IV gage was not big enough. I was freaking. I knew they were not going to be able to get another one in me, So they ordered a PICC line. Then I was freaked about that, but looking back the  best decision I ever made and will never not have one again. Surgery started at 5:30. Mom sat in the waiting room alone. Our dear friend Jean White showed up to sit with her. It was suppose to take two hours and it did but I was in recovery a while. I remember being in the operating room and in the recovery room and carrying on conversations with the nurses and doctors. Dr. Henderson went to confirm the surgery went well with my mother. He said the normal filem around your spinal column is .2, well my was 6! I go big or go home, that's all there is to it. My incision is only about 2 inches, but very deep. He also at that time told her my angle when he did fusion was the worst he had ever seen at 99 degrees. A normal angle is 150 degrees. Its a wonder I survived. PRAYER that's all I can say about that!  While in surgery he also did a lumbar puncture to check my pressure.....its a part of the surgery. My pressure was dangerously high. It was 41 and the high end of a normal pressure is 15. Again, I go big! He removed spinal fluid to make the pressure normal. I was in very little pain and had to lay completely flat for 3 days. That is harder than it seems. I was basically spoon feed. I was discharged on Monday even though I had a headache. Dr. Henderson said drink some coffee you will be fine. I did just that and I was okay.

We left and headed for my uncles house in Chevy Chase about 30 min. away. Not even 5 minutes of being in the car I got that god awful headache again that put me in the hospital the first time, but 10 times worse. I was trying so hard to hold it in. I was NOT going to that ER. I was denying it, but I could not take it any longer. We showed up at Jeans house begging her to take us in. I could not of made it to Chevy Chase.

I literally layed flat on her couch in excruciating pain crying, screaming, vomiting, and holding my head. It took everything I had to get to the bathroom and once I was there I had to lay on the floor before I could leave. BLESS! Mom called Dr. H and said I refused to go back to the ER and what did he want me to do. Again, he said drink some coffee and lots of fluids and stay flat. He said its probably a low pressure headache because he reduced my pressure and then I took spinal fluid reducing medicine, so I did not have enough spinal fluid and it could last anywhere from two days to a week. I did not know what I was going to do. I so thought I was dying. Out of everything I have been though that was the worst by far. By day 3 I was better! Thank gosh, I literally thought I could have died at any second and did not know what was going to happen.

We stayed at Jeans through Wednesday and left Thursday Morning. I had a follow up with Dr. H Wednesday and believe me I was FIRED UP! That is not like me at all, but I knew I could NEVER handle that pain again, plus I did not want to have a lumbar puncture or take diamox in the first place. I was really challenging him and he was probably wishing I would shut up. I was throwing questions at him left and right and was telling him what I was and wasn't ever doing again. He just sat there and listened and took it all in. He even had his arm around me while I was ranting! I felt bad once we left and told mom I needed to text him and apologize, but she assured me by the look on his face he was trying not to laugh. I was so out of character. In saying all of that. I really do trust Dr. H and it was just a little mistake that was missed. I'm not mad at him. I was frustrated, yes, but I still love him and trust his opinion.

We made it home Thursday evening after 17 days of living a nightmare and ate dinner out as a family. So happy to be home and cant wait to see all my friends. I appreciate all the support. This was not a great experience, but I did make some amazing Chiari friends out of all this while I was up there. No one knows what it is like until they have lived it and it was nice to have people around who have. I know this was such a long post, but February was a long bad month that I don't want to meet up with again like that, but I would not have changed it......maybe just a few things!  ;)
March has already started off amazing! Next weekend is my spaghetti dinner fundraiser and a bunch of family comes in and then I will be 18 in just 24 short days!

Wednesday, February 1, 2012

Long Night

Last night was very long, to say the least. My back (lumbar area) and hip were KILLING ME! It felt as if I was being stabbed with a knife and there was so much pressure. I could not get comfortable to save my life. Two lortab did nothing for me. I was up until all the alarm clocks in the house were going off this morning. It is due to my tethered cord.

Today was much better. I slept most of the day, due to the fact that I got NO sleep last night. My new medicine for my cortisol level seems to be working. I have only had two doses and will take the third tonight.

I hope the rain does not kill me tonight. Please pray that it does not kill my head or any other chiarians head. The barametric pressure really bothers most of us with Chiari. Thank you!

Have a great night!

Tuesday, January 31, 2012

If it`s not one thing it`s another...

Believe me when I say I would love to share good news, but unfortunately that is not always the reality. The 20 mg upped dosage of prednisone by Doctor Henderson made me itch like a dog with fleas within an hour of taking it last night. I was miserable all night. I had to take two benadryl to make the itching stop and it only helped some. I was to the point of  wanting to go to the ER to get an IV so everything in my system would be flushed out.

Today I went to preschool for most of the day. It was so good to be back and the kids know just what to say to make you smile and laugh even on your worst day. The itching just kept getting worse. I had to leave. I came home took benadryl again and was out within 15 minutes. Mom talked to Doctor Henderson's office and they said it would be very rare if I was allergic to prednisone, but to start at my primary care doctor.

So off to Salisbury Pediatrics we go. My results from the cortisol testing came back and they are still low. That is what the prednisone is suppose to be helping. So here we have two issues with prednisone. It turns out I REALLY AM ALLERGIC TO PREDNISONE! Yep, I'm rare what can I say. My whole life is one big rare case and I have finally come to terms with that. I knew all along that it was the prednisone, but was trying to give it a chance. I just felt like I knew my body, and that was the cause. I have been through enough to know when somethings wrong. I`m not new at having medical issues and I`m not four.

So I am now on medicine for itching, and a different cortisol (cortisol is the hormone that controls your energy and helps manage stress) medicine. Lets hope this time I don`t get any of the rare side affects.

I am not allowed to go back to preschool for a while because of my low immune system. Just when I thought things where going to get back to semi normal....

Please pray these next few weeks until the 28th of February pass very quick. I can feel my legs and back getting worse everyday and it is harder to walk as each day passes.

Much love and hoping everyone has a pain free Wednesday!

Monday, January 30, 2012

Just another Monday


This song 'Praise you in this Storm' has become my new favorite song! It fits my life perfect right now. I seem to find myself listening to it every time I'm struggling.

I am still having a reaction to something. We are still not sure what it is. I really wish we knew so, I could stay away from it or stop using it. Dr. Henderson upped the dosage of my prednisone to 20mg from 1mg. He says that it will help the itching. We shall see if it really does. I hope it does, but I'm not getting too hopeful. ;-)

Hope everyone had a great Monday and has a terrific Tuesday.

Thanks for all your prayers,
Em

Sunday, January 29, 2012

What a weeked!

(Lily doing her full split...impressive)


Friday night I went and saw my sister Lily, cheer at her game. She was awesome, as always. Click on this link to watch them do their dance routine: http://youtu.be/o3-jgIdYZ4E. Lily is the one doing the straddle split. Lily and I got that special talent. haha!  I was so glad to get out. Its just what I needed. We then went out to dinner at Monterrey. That was fun and my first time eating out with the family since surgery. :)

Saturday I slept in. It was a lazy day. Later that night I got in the tub. I then got a headache very suddenly after feeling AMAZING all day long. Soon after the headache, I started to get very itchy and swollen. I had gotten an allergic reaction from something that was in the tub. I used nothing new, but Lily was in there before me and she used something I had never used before. I took some bedadryl and bleached the tub and got back in to get whatever was on me off! I put wet tea bags on my eyes which helped a lot. Thanks Sherri for the suggestion! The benadryl made me fall asleep fast and the itching finally stopped. That was the best nights sleep I had gotten in a long time!


(One of my new best friends)
Today I woke up and was feeling fine, just tire. I skipped church and slept in. I ate lunch with my family and then went and got in the tub so I could get dressed for the day. Well, once again I got another reaction from being in there, even after I cleaned it very thoroughly. This time Lily had not been in there before me. She was not even home. So I have NO clue what is causing it. I once again got a rash, was swollen, and this time it felt hard for me to breath. It was as if a 300 pound man was sitting on my chest. I took more benadryl  and  put more wet tea bags on my eyes and the itching stopped, but not the hard breathing.


(And another new best friend)
I have NO CLUE what is causing all of this. I have no new medicine and have had no dietary changes. It is so weird. It remains a mystery! I'm glad the benadryl is helping and I have not ended up in the ER. Please pray that we figure out what is causing this and that it does not get worse. Thanks!

I hope everyone is having a good weekend and has a great pain free week!

Thanks for reading my blog,
Emily