Updates: Doctors Appointment, Multiple Sclerosis, and Everything Else


I had a doctors appointment on Monday June 8th and I wanted to write a short update about that appointment and also an update about how I have been feeling lately.  I also decided as I was writing this post that I wanted to include just a general life update because  I am truly struggling with things right now.  I can’t tell everything that is bothering me but I will tell what I can and maybe I will still write what is going on and password protect those posts and if you want to check them out you can email me and I will give you the password for them.  Anyway lets get on to the MS update because that is the easiest and quickest part of this post.

As I said before I had a doctor’s appointment Monday afternoon with my neurologist.  I hadn’t had an MRI or anything since I saw her last but she does like to see me every so often because of the medication I am on and things like that.   I haven’t been feeling the greatest lately but there is nothing that can really be done about that because I just don’t feel well.  My headaches are getting bad again which totally sucks because I went so long without having them or at least not having super bads one.  I know that the reason I am having them is because of allergies and also just the stress of life.  I have an MRI in August and I don’t have to see the doctor again until December so that will be nice.

Now on to the life crap that I am willing or able to talk about.  I have no idea where to start or what I even want to say.  I guess the first place to start is with the fact that the daughter I placed for adoption will be 10 this year and I am honestly not sure where the time went.  It has also been a hard year this year when it comes to dealing with the adoption and I am not sure why this year has been so hard for me.

Another thing that has been hard for me this year is family things and usually I don’t really care what goes on with family members but this year that has changed for me.  What is funny about it all is that what I am sad about didn’t even happen this year and to be honest I am not sure why it is now bothers me like it is.  I am sure it is because of everything else going on that is making all the little things in life that usually don’t affect me hard for me to deal with right now.

Anyway that is all I can think of right now so I am going to leave it like this.

How are things going for you???

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Frustrated With Multiple Sclerosis

Frustrated With Multiple Sclerosis

I guess it is time that I write about what is going with me and the Multiple Sclerosis because I haven’t really done an update in a while.  If you were to look at my you wouldn’t be able to tell that anything is wrong with me because everything that is going on is on the inside or at least if I don’t tell you anything is wrong then you won’t know anything is wrong.

For the last 2 or 3 months I have been exhausted to say the least.  I wrote a post earlier this week about how I am not sleeping but this exhaustion is so much more than just not sleeping.  It is so hard for me to explain the difference between being tired because of lack of sleep or being exhausted because of the MS.  I don’t think there really is away for me to explain it other than saying I am so tired that if I could stop breathing I would because that takes more energy than I have.

I know that my lack of sleeping isn’t helping the situation any either so that gets to me as well.  I just feel like I am falling apart and we have no reason as to why I am feeling this way.  I had an MRI done at the end of August and when I went to get the results my scanned showed that the disease hadn’t been active in the last six months.  Which should be a great thing but I felt confused and pissed off by it.  I really wish the scan would have shown something so that there was some sort of reason for why I am feeling the way that I am.

After my last appointment  I started on a new medication and I have taken it for a month and haven’t seen any change in how I am feeling so I don’t know if it is working or not.  She did say that I could take it twice a day and I haven’t done that yet because I already take so many pills that I hate taking more but I think I am going to try to take it twice a day for a couple of weeks and see what happens.

It is so hard having something like MS because it sucks when you can’t figure out what is wrong in order to try to fix it.  I have to wonder if I am going to have an MS relapse soon because this is usually how you feel before you have one or it is at least how I have always felt before one.  As of now I am “stable” but I don’t think I truly am.  There has to be something going on and it just isn’t showing up on the MRI.  My next MRI is in February and I see my doctor again at the beginning of March so we will see what happens in the next few months.

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Multiple Sclerosis Update

It has been a long time since I have written a post about Multiple Sclerosis and I really want to keep everyone in loop on what is going on with my health and all that fun stuff. Most of you know that I have an infusion once a month for my MS treatment. I take a medication that is called Tysabri. It is super expensive and can be dangerous but that is going to be another post. I was supposed to receive my infusion on the 23rd of September. That didn’t end up happening because the company I work for changed health insurance companies and I had to wait for a preauthorization to come through before I could get my treatment. So I show up on the 23rd and they send me home because of the whole insurance issue. For those that know a little bit about my job and what has been happening the the last 4 months or so you know that I can only take one day off a month because they have no one to cover the phones since they let go Misti who used to be my boss. So I knew I was going to have to wait a few weeks before I could take time off to go in and get the treatment once they got the approval that they needed.

My next infusion is on the 21st of October, which means that I have missed a whole month. Let me just tell everyone I have no idea how I used to live like this because I feel like crap. I always knew Tysabri was helping but I had no idea that it was helping so much. For the last 6 months or so I have had headaches and I also haven’t been in pain. Well since missing one month I hurt I have headaches and am exhausted. I literally slept almost all of Saturday because I was so exhausted from a normal week of work. I had to call my doctor and have her call in more pain pills because I was out and hadn’t need them so I didn’t bother getting a refill when I saw her last time. I feel so bad for people with MS that fill like this all the time. I am so glad that I have found an MS treatment that works for me and allows me to be a somewhat normal 26 year old. Also my hands are super numb right now and I am not sure if that is because I missed my treatment or just how the disease is acting right now.

I can’t remember if I wrote about my last MRI and doctor’s appointment so I am going to do a quick recap of all that information. I had my latest MRI in August and also saw the doctor after the results came in. According to the scan I am still stable and have been for about 2 years or so. They haven’t scanned my neck in a few years so when I go for my next MRI in February they are going to scan my brain and neck areas which means that it will be a super long and super expensive scan. I am interested to see if there have been any changes in the neck area. If there hasn’t been any changes that means I have been stable but if there are charges that means that I really haven’t been stable all this time. I hate the not knowing that goes along with having MS.

That is all there is for now. If anyone has any questions please leave them in the comments and I will answer them for you.
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Idiots Are Taking Over!!!!

So I was told at the doctors that I need to get in and get my infusion done as soon as possible so that I don’t get sick and I stay stable.  So I had grandma call because I am at work and don’t have time to hold on the phone with places.  Once they finally called her back they said that they now needed all my records from Julia’s office.  When she told me this I just about lost it because I was just there yesterday why in the hell didn’t they tell me this when I was calling them last week. 
I guess Julia’s nurse called my grandma back and said if we don’t hear from them tomorrow that we should call Monday and she also gave us a name of someone to talk too.   I am just so tired of getting the run around from this infusion place.  It can’t really be that hard to do you job can it?  Hell I think I could do their job better than they could.  This is the worst place yet that I have ever had to work with.  Even the insurance company’s are easier to work with and that is sad.
I am hoping I will get my infusion in the week or so.  Keep your fingers crossed for me!

Fursday’s With Elinore & Sylvia. . . But First An Update On The MS

It is Fursday and that means it is time for me and Sylvia to post our thoughts and rants on what mom and the rest of the humans have been doing.
This is Sylvia speaking.  I was ready to kill mom the other night because she kept bugging me when I tried to sleep.  How hard is it for her to get that when I am sleeping I expect to be left alone!  I guess mom is “slow” because she doesn’t seem to get the fact that when I hiss at her that I don’t want to be bugged.  Last time I checked I thought it was pretty straight forward but maybe I am just smarter than the humans are.  Oh well at least they feed me and the gray haired man plays with me all the time.  I even get to supervise him while he is working outside in my yard.  It is a great life!
I had my doctors appointment yesterday to get the results of my MRI that I had in February.  Well right when she saw me I got a lecture and was basically told to get over the issues with the new infusion site and go.  I asked her about what the MRI I had said and for the first time since I have been diagnosed I am totally stable.  There were no new lesions on my brain!!!!!!!!!!!!!!!!!!!!!!  This is huge for me because I have always had a very active disease and I always have had new lesions.  So after hearing that I am going to suck it up and do what I have to do to stay on the medication.  Even if that means jumping through hoops for the stupid drug company.