Achoo!

It’s rare to find a good team of doctors that work together. I’ve finally found a good team at Oregon Health & Science University. It took several years , but I finally have doctors that understand Wegeners. 

Just one of the many downsides to having a chronic illness is when you get a cold or the flu. It’s like a double whammy. The doctors you see for your chronic illness aren’t likely going to fit you in  just because of a sore throat and back pain. This always stresses me out. I am super lucky that all my doctors are at OHSU. they all have access to each others chart notes. Usually, if I’m sick and they schedule me with an on call doctor, but I just decline. What’s the point? They do odd tests and give meds that conflict with my other meds. I’m always told I have allergies, but it’s actually a Wegener’s flare. I usually suggest my treatment and they are happy to ablidge. 

The past week or do, we’ve been passing a nasty cold around. Travis had it, then Kenna, and then I got it. I also had pain from a UTI, the pain became too much, so I opted to get in with an on call doctor. 

He ran several tests. At first he’d said all was fine. A half hour later he called and said that he thought we should do antibiotics just on case.  Now, nearly a week later the results are back, and I’m so glad he have me those antibiotics because I have a kidney infection. This isn’t good with having Wegener’s. I was able to get a shot and start even more antibiotics man do hope it’s under control. On Monday, I’ll go and follow up with my doctor. I believe they are planning an ultrasound to make sure my kidneys are okay. 

My hearing tests came back good,so now we wait for the MRI and appointment with a neurologist. I’ve been saying for months that something is just not right with my brain. I feel very off. Luckily those darn accents have disappeared. Lol

I’m lucky to have the doctors at OHSU. Before we found them, my care was subpar. The doctors weren’t connected and things that needed to be done, weren’t. Don’t get me wrong. I had a few amazing doctors, they just didn’t communicate with each other. 

Just catching up

I’ve had a rough time finding time to blog lately. I apologize! I have just been so busy being busy. When I’m not busy, I’m exhausted. I feel that I should just do a quick update of this past week. Hopefully I can find time to blog about something more interesting this week too!

Last week I was dealing with severe dizziness and brain zaps. I still am this week, although the brain zaps aren’t as bad. On Friday I went in for vestibular testing, which was four hours of hearing type tests. The worst was when they put hot air into my ear and recorded my eyes reacting to the severe dizziness it caused. Then they did this with cold air, on each ear. It was horrible. On Monday I went to the doctor to get the results. He said that my hearing is find. Everything came back normal. This means the dizziness, headaches, and such are not caused by my ears. The next step is an MRI on Thursday, and following up with a Neurologist. In the mean time, I’m dealing with a UTI, which of course has them concerned since I just had an infusion, and it can cause Kidney’s to fail. I am going in tomorrow to make sure it’s just a run of the mill UTI, like I think it is, vs some dramatic issue they think it could be. I know it’s better to be safe than sorry, I just get tired of going to the doctor!

One thing I’d like to celebrate is that I didn’t get whatever it was Kenna had on Tuesday of last week. She was so sick. I was terrified I’d get it on Friday or Saturday and I had made commitments I couldn’t back out on. Luckily, I still haven’t gotten sick! Yep, knocking on wood.

Friday after my appointment, Kenna went to the fair with a friend. Travis and I took the time to drive around Forest Grove and look at the house we put an offer in on.

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Travis, Kenna, & I at the wedding.

Saturday we went to a wedding. It was a beautiful, fun, country wedding. I took the photos for them. It was so much fun! It was hot, but honestly, I was distracted with taking all the pictures, that the head didn’t bug me a bit. I took pictures from noonish until 9pm. I was hurting, but it was totally worth it. I really enjoy taking pictures. I had a few moments that were rough, but mostly because my camera decided to stop focusing, so I had to auto focus each picture! I did fairly well, and took 988 photos! What a fun time!!!!

Sunday we decided to go to the beach and meet our dear friends who were there for a dance competition. It was kind of cold so we didn’t stay long. It was fun though. We ate at Mo’s in Cannon Beach, then sat on the beach for about an hour. We stopped for ice cream on the way home. It was fun and low-key.

Today everything has caught up to me. However, I didn’t have a moment to rest. Well, I did sleep in a bit, but I got ready and Kenna and I ran errands. This blog is super boring I know. I promise it’ll get better. I just needed to get this all out and decompress from my busy week.

Oh, and before I forget, let me update you on my cousin. She is doing much better. She’s had 7 surgery’s this past week. They finally were able to pack and suture her leg. I stopped in and saw her yesterday while I was there to get my hearing test results. I loved getting to see her looking so much better! I’d stopped in on Friday before my testing, and she was in surgery. Thank you all for your continued prayers. Please if you can, go to her gofundme.com site: http://www.gofundme.com/8z6ena2x6e and donate.

I feel strange, don’t ya know? 

So I feel like I should start this post like this: Patients log 6156880, today things are worse than they’ve been in a while. 

All joking aside, something is wrong. Neurologically I’m messed up. I don’t know of it has anything to so with Wegener’s Granulomatosis or not? I’m dizzier than ever. I slur words. He’ll, I’ve even picked up a Northern accent. Not even being silly. I’ll be talking and all of a sudden someone from Wisconsin comes out of my mouth. It’s happened slowly over the past year. We always laugh, but now it’s really scaring me.  

As I write this, my arms and hands are twitching. As if I have gotten a chill, but it’s constant. I don’t know why? I’ve asked the doctors and they suspect WG, but unless it’s attacking my brain, I haven’t heard of it presenting that way. Most of my symptoms resembles MS, but the doctors say that isn’t it. 

In any case, I’m scared. I feel crazy and alone. Even though I know I’m not alone, I’m the only one experiencing these things my body is doing and without answers.  It’s very frustrating. 

Ramblings 

I hate just blogging about my illness.  I don’t mean to just bitch all the time. I am very happy and love life. I have great friends and family. I have lost several friends throughout this battle, but it’s their problem, not mine.  I have tons of other interests. I love photography, especially getting action shots. It’s a thrill for me. I love animals, traveling, and adventure. I miss my Harley. I miss my truck. I miss my horse.  I want to be that girl again. I love watching my kids grow, and experience life.  I thoroughly enjoy our cheer life, all the practices, competitions, and chances to take lots of action shots! I am aware of the world around me.  I’m aware of the good and the bad. I try to pay attention to the good though. I miss working.  I miss making lots of money and not stressing about it. I enjoy helping others. I like to bring awareness to things that are ignored. I don’t like bullying. I am pretty relaxed and layer back. I love to laugh.  

This illness has tried to take all of that. It’s stolle not my focus, but it’s so huge that it’s hard not to. So dear readers, I don’t mean to write sold about my illness, and how shitty I feel.  It just has seeped into every aspect of my life, despite how hard I’ve tried to not let it. Hence, Chronically Susan…. I’m Susan, and boy oh boy is my life chronic now.  

A New Way of Living 

Yesterday, my youngest, McKenna and I drove two hours east to The Dalles, my hometown. Almost all of my family still live there, plus the majority of my close friends. It was great to go back and visit. We originally went there to sell raffle tickets and event tickets to my daughters all star cheer fundraisers. The plan was to get there around 11am, and leave around 6pm. We ended up not leaving until well after 9pm. I was, and still am exhausted. I couldn’t just stay the night, because all of my meds were at home. In order to drive, I couldn’t take my pain pill.  It was a tough few hours towards the end, but we managed. 

You see,  I’ve had to learn to listen to my body. Even though I like to ignore that I’m sick, I have to strategize my plans around my illness. I had planned ahead for yesterday’s trip. I knew I had to rest the day before. Sometimes, for bigger events, I have to rest up for a few days to prepare. Then, depending on how the event goes, and what it is, I have to plan a few days, and even on some occations, weeks to recoup. It sucks, it sucks bad. 

Luckily, yesterday I just drove in to town, dropped my dog at the Pink Poodle to get groomed, and stopped at my my bothers house and visited a while. Then we went to my moms for dinner,  and then my daughters to visi. It was pretty low key. I had only gotten three hours of sleep the night before, (I was still pissed about the comments made to me on Tuesday about if I’d just be more active my disease wouldn’t be so bad. I had a rough time letting this go. I deal with so much guilt already, I don’t need other people making me feel like crap too. Plus I was excited to see my family and friends.) so I was very tired by late afternoon. Once we got home last night, I was still wound up, and in pain. I didn’t fall asleep until about 2am this morning, but I had the luxury of sleeping in until 10 am this morning. I am still hurting today, but we made it to the library (aka my new office). McKenna is diligently working on her math, and I am blogging. 

Due to this disease, I do try to plan my weeks with just one or two events. When we have big events, like our recent trip to Anahiem for All Star Cheer Nationals and Disneyland, I rested up for a week, and then crashed for a few weeks after we returned. The same thing happend at a Christmas. Now that I know this, I plan for it.  I just get so tired and fatigued after a big event. I really push myself to be as normal as possible. I want to keep up with everyone. I don’t want to hold anyone back because I have to take it slow. This new way of living has been an adjustment for our entire family, but we are learning to make it work.  

One of the best  things that I have found helpful to help others understand is The Spoon Theory. If you haven’t heard if it, I highly suggest googling it and reading the story. It really resonates with people suffering from all kinds of illnesses. 

I would love to hear from other people how they handle plans and big events. Please leave your ideas in the comments. 

Here it goes…

First off, I feel like I should have some sort of music of anticipation playing as I write this. Instead, I’m sitting here quietly in the library. How the the heck did we get here? Another lifetime ago, I’d never see myself sitting in a library to use their wifi. I’ve always been a hard working, active person. In fact, when I was single, men used to tell me I was to intimidating to date. I had my own successful real estate business, my own house, a new Dodge Ram, a new Chevy Aveo for my daughter, and a Harley Davidson. I had three kids that were very independent. We traveled all the time, and had a lot of fun. I didn’t really need a man, but I was lonely. I wish I knew then, what I know now. I’d not have been in such a rush to find someone and leave my happy lifestyle. However, I was in a rush. I was lonely. I joined eharmoney.com, match.com, and any other .com’s I could. I went on a few dates, but kept talking to this one guy in Idaho. He was a christian, and I liked that. We dated a short while before deciding we wanted to live together. However, he didn’t want to live in sin. I was on board, so we got married. This was a huge mistake for both of us. Just after the first few weeks I knew it was a bad thing, but I’d given my house and business up.  I couldn’t go back.  For the next three years, we lived a very boring, sad life. Unfortunately, my kids did too. I lost all my things, my bike, my truck, my daughters car, and my self esteem. I finally a had enough and decided to end the marriage.  

After I moved out, I met someone, my husband now.  He has saved my life. Literally, and figuratively. Travis and I met after he finished going to Northwest Lineman school in Meridian, Idaho. He was working with a company that had him traveling a lot, and so we only saw each other once a month or so.  I’d never believed in love at first sight, but that is what it was with us. Just within the first week we knew each other, we both knew we were meant to be. Both of our marriages had recently ended, and so the timing was right for us to start our new life together.  He got a job that transferred him to Texas. He moved down in January of 2012, and I followed, along with two of my kids in March. We lived in West Texas for the next two years. It had it’s ups and downs.  We were only able to see his son once during that time, which was very tough on both Travis and his son. I was diagnosed with a rare, serious autoimmune disease called Wegener’s Granulomatosis.  I had to undergo surgeries, and chemotherapy. My mom, and my oldest daughter had to come stay with us a few times to help out. It finally was very clear that we needed to move back to the Pacific Northwest to be closer to our families. 

Even though Travis was making a good income in Texas, the cost of living was taking it all. I was working for Aflac, and doing very well, for as sick as I was. When Travis got the opportunity to move to Idaho, we jumped at it.  It took all of our savings to move back. His new job was not what it was said to be, which is what we’ve found to be true with most jobs in the Lineman field. We were back to square one, and a bit scared. Within a few weeks, my super-husband had a found his new career path, in his old career field as glazier and installing automatic doors.  We made plans to move again, from Idaho to Oregon. 

I’m so glad we did. Although things are bit different than we’d planned, we are finally on the right track. I have a great team of doctors at OHSU. To save money, we bought a new RV to live in. One of my best friends let us park it at her place, and we did that for nine months. When she moved, we moved it to Travis’ best friends place, and are currently there. We are waiting to buy a fixer-upper this summer. This will be our new fresh start. Once again we will have a home of our own. Eventually, will have our dream cars/trucks/toys again. We will rebuild our lives together. I try to think of it like an adventure. It may not seem glamorous, but it will interesting.