Howdy Hydrocephalus

Understanding my unique gyroscope

Pieces of a Puzzle

2 Comments

I had been meaning to go to my GP doctor since September, but that all fell by the wayside as we scrambled to deal with cast boy, then holidays and of course I forgot. Finally last week I went to the doctor. Ever since being in the hospital with SJS, my skin has been so sensitive, very itchy and has had a slow healing rash that has been present on my back, shoulders, arms, fingers, and ankle. These were getting to be annoying as I had finished my cream that somewhat kept everything at bay. I had mentioned symptoms to my specialist since June, but she seemed distracted and didn’t think it was anything.

I show him the rash and get a new batch of cream prescribed. Then I tell him about my disrupted days and nights by having to pee all the time. I mean all the time if I am hydrated and not so bad when I dehydrate myself. I told him that the dry mouth and this I thought were side effects of my meds, but I wasn’t too sure but this has been going on since June and I have had enough. I know I live in a perpetual dehydrated state…or at least it feels like it for me.

So today I went for my MRI for the hydro clinic then had blood and urine testing as well. We are trying to figure out what my body is doing. Right now the symptoms are:

itchy skin, round blistery rash that doesn’t go away, cuts take forever to heal, peeing every 15 minutes, hair falling out and always a dry mouth that makes me thirsty.

My hubby had stated that my symptoms could be diabetes. I went to my computer and followed up with Dr. Google with these common symptoms they all point to Cancer (LOL) nope it was Diabetes. Unfortunately, I do not have the profile of  someone who is a type 2 diabetic. I am not obese; do not have high blood pressure (low); do not have high cholesteral or hypertension.

I did know that there was a risk of diabetes inspidus and other endocrine disorders after brain surgery and with a new TBI/ABI. I did not know that they still can potentially occur long after initial brain injury. So now I wait for results so we can put the pieces of the puzzle together.

 

 

 

Advertisements

2 thoughts on “Pieces of a Puzzle

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s