Friday, July 19, 2013

Food Allergies

A couple of weeks back when I was getting willingly poked 50 times in my arm to determine my indoor and out door allergies I also did a quick blood draw to check for common food allergies. I had to wait a week for the results, but finally got the news yesterday. The conversation went something like this...."Well, you have a LOT of food allergies!!" Me; "WHAHUH????" "Yea, two of the worst are Milk and Eggs" ::Takes the gluten free egg product out of my mouth:: (J/K). But I had almost finished a bag of gluten free cookies that contained both of those products just 40 minutes earlier haha. I made my appointment for Monday this coming week.... I don't know what I should eat at this point. I am praying she doesn't say peanuts are out... I love peanut butter and need it like oxygen!!!! Ya know... just having a day where I can wake up without feeling like there is a brick sitting on my forehead would be wonderful! If I could breathe out of both my nostrils at the same time... that may just qualify for a happy day in my book. Onward and upward!

Tuesday, July 16, 2013

Updated VNG test results as well as allergy testing

I went back for another VNG test (caloric testing where they blow warm and cold air into each ear to induce vertigo as a pair of electronic goggles that you are wearing records your eye movements). I hated the test more than any of the tests they do there. I went for a follow up the very next day and was surprised to hear that my left ear is almost back to normal and my right ear (the very bad one) still had some damage, but was looking a lot better. It seems the head shake exercises are working. That same week I had an appointment for the vestibular rehab and was mentioning how panning movement from tv, video screens at church, and sometimes moving cars can make me start to feel off balance. She told me to buy a disco ball with different colors, one that rotates around projecting the moving images on the wall and do my exercises with it going. So far so good. It actually mimics the same movement that makes me dizzy. this will help aide in training my brain. I am feeling beter and more confident that one day I will be able to drive without any more issues. We are going on vacation in October to the Keys. I usually have no problems as a passenger other than the feeling that we are going too fast. I make my husband stay at 70 mph and remind him every few minutes when he tries to go faster. :) On another note: The same day I did the caloric ear tests I had to do a slew of allergy testing, shots in the arm (about 50 for outside allergens) and a blood draw (for food allergens). I got the results instantly for the outside allergens, but had to come back the next day to see if I had any delayed reactions. I am allergic to 3 types of grass, 6 types of mold, some weeds, cats and dust mites. I had a very long reaction to the cats and most of all the dust mites. My arm is still red and raised in both of those areas and that was from early last week. I was told that allergies can cause migraines and dizziness and that I should get allergy shots to see if it helps. I am waiting to hear back regarding the food allergies and then I will start the shots. So, that is all I have for now. I had been trying to save up to see an osteopath so I could go through Igenex to get another Lymes test done. They say its hard to get a positive Elisa on the Lymes test and since I did, I should go through Igenex. It would explain the thyroid issues, migraines, dizziness, muscle twitching, etc. I would just love to get an answer. Any who, yea, I had been trying to save up, but it seems once I have the money, I have to spend it on some other bills. This has been life......

Bilateral Vestibular Hypofunction - Updates

Well, It's been a while. I didn't think anyone read my blog, but apparently others do because I've been contacted a few times. I know usually my posts on here are updates, just like this one. I have been dealing a lot better with my migraines - They now only come close to my period and during. I had taken verapamil for about a year and after stopping it I was down to just the few migraines a month. I started getting new symptoms however within a few months of stopping the med. The road ahead me, specifically on the interstate would appear to be bending downward. I also started feeling like I was sitting still, on one of those simulated ride where you are watching the screen move in front of you (like a roller coaster ride). Some call this depersonalization, but I know what DP is and this is not it. This is my brain getting confused with what my eyes are seeing, no doubt. I went to a neurotologist for testing and had a VNG study done. The Caloric testing (tubes in the ears and hot and then cold air blown into the canal) revealed Bilateral vestibular hypofunction. A "rare" (getting used to these diagnoses) condition that causes damage to both inner ears resulting in balance issues. This is usually caused from certain antibiotics ending in cin, like Azythromyacin, which I took a lot of in my lifetime due to ear infections and other illnesses. He said this was most likely causing the issues for me with driving. I also started noticing that when in coversation with people, certain head movements, primarilly up and down shaking in a "yes" head movement" I would get a quick zap of being offbalance. This too would be from the vestibular damage. Then there was also the case of while read something, say my computer screen, anything in my peripheral vision would start to shake a little, or bounce. This too is my vestibular system. Anywho, long story short I had been doing VERT, Vestibular Rehab since January 2013. I feel a little better, not a whole lot, still have the same symptoms to a degree. I did the VNG study again yesterday and got the results today. I have regained back most of my balance, with the exception of my right ear still being bad, but it has improved as well!!!! Great news!! I am going to keep up with the VRT exercises to see if some of these annoying symptoms will go away. I want to enjoy road trips agan :) On another note some other symptoms which seem to be migraine related have popped up. I do have visual snow, which I have talked about before on here... I am used to it now BTW, but this could be the contributing facot, maybe MAV which is vestibular migraine by the way (basilar migraine was my diagnosis). When I pass cross walks while driving (the ones with lines on them) the lines will appear to be moving to the right or the left. Also, cross walks made out of brick pavers will do the same. So anything with a type of pattern to it will move. Yippiee!!! I am also getting more sensitive to movement in my peripheral vision! I seem to be getting migraine symptoms without the pain too. I can always feel it in my eyes and neck. While at church viewing the big creen, once the camera starts panning left to right or if a pattern is flashing on the screen during the music playing, I will get izzy. My VRT specialist suggested getting one of those table top disco balls lights with all the different colors to see if exposing myself to this will help retrain as other therapists have suggested it to her. I am going to give it a shot :) Now there is teh case of support... I have zero support outside of my Dr's office appointments. I attribute this to years of complaining, many diagnosis' and not getting better. My husband listens, but not really. I feel as though I have to throw in the word boobs, to get his attention. You can hear the buzzing in his brain after he lets me unload on him. Quite sad. I guess somewhere in my imaginative brain I figured my husband was the best man in the world who would give me support every time I needed it. FAIL! Unless I am crying or dying... I get zero!!! All I wanted from him today was to ask me how my Dr's appointment went. He told me he was busy and couldn't talk. I told my support board, but sometimes I feel like most would be envious for hearing of others good news, because they want it to be them. I dunno... I guess that sounds crazy. I am such a nurturing type that I just don't understand how my own husband could sit back and let me go through all of this on my own. If it were him who had these issues I would be spending every bit of free time researching and contacting people. Now I know I am a very strong headed person... a Driver if you would call it that, and maybe he feels if anyone can do it it's me... but the truth is, at the end of the day I am just as human as him. I keep holding on to the dream and the vision that one day I will be back to normal. The old pain in the butt girl I was before all of this. The free spirited girl who had a dream to travel the world and see as much of it as she could. I can still feel it deep inside soul that this is going to happen. That is what keeps me going.