Showing posts with label John. Show all posts
Showing posts with label John. Show all posts

Monday, December 12, 2011

Brother John


I have suffered from my brother not caring to admit that I exist.It is his attitude. I believe he is stressed out and suffers allergies and things as I do, but he keeps it inside and becomes cold towards all people,especially family. To those who could help him. So I have to survive and I turn away from the relationship and move on. I can not get emotional support from him, nor financial either, so it will remain a purely surface relationship for now. I admired him growing up. Admired his degrees, learning, ability to make money, security and self-confidence. But not coldness, lack of emotion, empathy, and soul. I care for him deeply. but in this latest bout with the disease of depression, I have learned that a disease that is not seen, is not understood by the unempathic and logical people of this family. But to survive, one must not hold on to the things of childhood, but cast them aside if they are in the way of moving on,



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Tuesday, November 15, 2011

Lock Up Blog-CFBH log

11/4/11
I have come to a mental hospital by Seaworld.  Scary at first. Very,very scary. locked in. Every door is under lock and key.
Residents are all sitting in a line of chairs in front of the TV. Some zoned out, other more alert and attentive.
Tough night, and possible wheat or aspartame reactions in the morning from the juice,which was .a crystallite or HONEY NUT OATS  I had for breakfast.
11/5/11
Dr. Hasheez put me Effexor .75. Dr K put me on Xanax .25x3, the singular 10mg, Xyzal by allergist.  I will cancel the allergy shots for now. It-the shots were to start the eight if Nov....I have postponed the Chiropractic for now. The chiropractor was adiment that I not take drugs. That could not not be possible and hold a job. So let that be. I suffered enough. I will maintain about as healthy a life style as I can.
11/5/11
I pray that I have a job to go back to when I get out of here. John says that he would like to help us with our finances, and wants to review how we spend our money. That sounds good right now. Eases the worry.

Poor David, he has seen the down turn in my health,  and now the separation that this lock up causes. Visits are only twice a week for one hour, phone calls are limited to only when others are not using the two phones that are set out when phone access happens three times daily. The access is shared by about 16 women.

The pencils are short golf pencils so people can no use them to stick them into themselves or others. The night I saw a TV show there at the lock up on how someone did that,  well it almost liquidifed my innards.
They won't allow me my watercolor brush, so I wrap a small piece of cloth around the tip of a pencil and use that.  With it my art survives.......it will always help me to survive.
They dose me up on the antihistamines and Ambien to help me sleep. Only thing is these antihistamines don't induce sleep.

I find that when I have a stressful allergic day, as in cleaning, the lymph glands hurt and the VNS does not keep me awake as much.   It is as if the toxins in the body are slowing the effect of the VNS. It does not physically stop it, just slow the affects on the body.  When I am away from the house with all of its dust mites, and then come to the house to sleep, then it has the affect that it gives me too much energy...as if I  drank a lot of caffeine in the late afternoon.  So I am going to try this strategy : cut it down as I can remember during the day, let it decrease it's affects during the day when the body has less to fight and then let it rip at night when I am at home.  The magnet will let me do this. It shuts off the device for that one stimulation and the device will pick up again two hours later. That is how it is set up.

11/6/11
I upped the VNS before I came to this lock up.  Thank God, for it has really helped me in many respects. I am realizing that I must come at this from a different aspect.  They have offered me to visit the therapy program that is attached to this facility. I will do it, if we can do it with out incurring more costs.  It would involve 5 hours of therapy-group therapy.

11/7/11
We work with affirmations here at the PHP side of the lock up. It is a mirror reflection of what is happening to me.. I was locked in my location in the other area in this facility, locked in the depression, hopelessness and anxiety. Here it seems that I am unlocking thoughts that caused some of the depression.


11/8/11
Most of the TV shows that are shown here in the lock up are extremely violent. Amongst the constant bouts of dramas on the phones, residents attacking staff, people in constant hideous emotional states, if one wasn't unstable when they came in,  they are now.  What ever I was going through at home, it was far less than what is going on here. Abilify started at 2.5 mg.

11/9/11
Meds now:Abilify upped to 5mg


11/10/11
Knowing how to stop the automatic negative thoughts that I have programmed into the brain over the years. ANTeaters : thought reprogramming to stop the negativity.

Monday, September 12, 2011

My Depression is back

It seems that the combination of food sensitivities and mold allergies is having its affect once again. The weather is drying out, but not completely dry yet.  It seems that any moisture in the air is triggering the mold again. Could be even the dripping in the shower that provides enough moisture to have me suffer. I know that sounds nuts, but I will say that when I visited John's house that had a flood this last week my feet itched painfully for the 10 minutes that I was in the house. I know that sounds crazy, but what else can I attribute it to? It was the same type of itching that occurred all last week when I was standing in the wet or moist weather out at work. Who can say that an itch that occurs  at one time is caused by the same condition the next time. It just occurs in the same place, or near the same place. It feels the same, same intensity and when I leave the areas the itching stops. I notice the itch stopping about five minutes after I leave the areas.
I proved to myself that it was airborne, what ever it is, pollen, mold, chemical. I can leave the area at work and go indoors to air conditioned area, and within twenty minutes the anxiety and depression leave, the itching stops. If I leave an area, like John's house, the itching stops as well. To night, even with an air purifier going in an open room (door to rest of house open) the depression returned. Tied a hanky around my face and now I do feel better. It has been about half an hour later. My house is not well sealed, but it is inside, much better than outside in the moldy air.

Next day, AM see the post for 9/13. Safflower Oil. Sometimes two different allergic reactions are going on at the same time. As I come up from the mold allergy I have a reaction to safflower oil. So, the diet must remain very simple.

thesilhouetteshop.yolasite.com

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jkmatthews100

Wednesday, August 17, 2011

Family Night

Support in my efforts to battle this problem is the main thing that I need. I get it  from all who I encounter, except one major person. This is an email from my sister and my reply:






On Aug 15, 2011, at 4:48 PM, Edna  wrote:


Dear Janet,
I did try to get to your blog but I could not get in to read any thing. I am sorry.  I did try to surf and do some research.
When I was on line trying to do some research this afternoon, Jennifer called. (Her daughter who suffers from allergies) We actually had some decent conversation for about an hour.  I do not know how much communication got through but at least it is a start for us.  That was good.
Continue to keep your food journal.  Keep the amounts of food and the times that you eat also.  I know that this sounds picky but you are looking for repeated patterns and foods that are bothering you and giving you bad reactions.  Look for daily, weekly, and monthly patterns.  Also, record your sleep patterns.  Note your moods and feelings.  Don’t obsess about all this.  If you miss something or time, get back on track the next time cycle.  Again, don’t get down on your self for looking for the why.  Perhaps, you will be able to talk to the doctor more intelligently.  Be sure to include a joke on yourself and then laugh at yourself and press on with life.  We are praying for you.
Love,
Edna
thanks, I need support. I get it from everyone except John. He seems to think it is all in my head. I have to think about what the bible said: and I don't know just what verse, but we get our esteem from the Lord, not others, even our brother. It is hard on Wednesdays. The day after Family Night. I am poisoned by the food and the doubts (caused by his unfaltering statements of this doesn't bother me, so it can't be bothering you) he causes. I am sorry, but swollen joints, lost balance, blisters in the mouth, break outs of herpes around the mouth, swollen gums, gas, bloating, itchy skin, constipation, depression, anxiety, popping in the ears, fatigue does bother me and I need support from someone I have adored all of my life. I am glad that I got that out of my system. And God be praised for your support.Glad you got to talk to Jennifer. Did you find out just what she suffers with? Both mentally, and physically?

Sunday, May 17, 2009

Letter to Edna

Hello from Orlando.
Mom (89 years old) had a problem with one of her heart medications because it caused severe hives. We are working with her doctor to rid her of this problem and still cover her heart problems. She is getting depressed that she is stuck out at John's and we are working with that. She will be brought into the city at least once a week to connect with the friends and church buddies she has. Right now I am leary of giving her money, certainly no credit card. She forgets everything so easily now and then gets up set with herself. Her memory is going. at least short term memory. One day at a time.
Booger, our feline companion, is slowly losing the battle with cancer. But we will be with him until he is in too much pain to bare. Then we will end it. He has been a wonderful little person to be around.
Dave is still plugging on, he is wonderful in his support for Booger and for me and mom.
I ended up in the hospital overnight as I had an adverse reaction to the prep meds that I was taking for my colonoscopy. Good news, they did the colonoscopy in the hospital and I do not have colon cancer! Just a routine check up.
I have had a blood test that indicated increased levels of alkaline phosphatase . I was taking cinnamon as I was fighting a high sugar level. Cinnamon can do this response increase the levels of alkaline phospatase . Only thing is it is an indication for cancer, breast or colon. I go for a mammogram,, on June first.
One day at a time.
I have gone back up on antidepressants to help fight the stress.

Thursday, November 15, 2007

Questions have shown up

John, my brother, has asked how long will the effect last.It has occurred to me that he was asking about the VNS device's length of effectiveness and I must ask about this factor. But the thought that this device is much like a heart pace maker has occurred to me as well. The device may not last as long as is profitable for the initial investment.Or will I have to come up with a large amount of money every, what, seven to ten years? Not to mention the cost of the insurance to replace the batteries every five years.
But if it gives me renewed hope for life and renewed motivation to do things. Even for just those few years. Would it be worth it? How much for a replacement device? How much for the replacement of batteries? What kind of warranty do I get. I mean if they put it in and it, God forbid, malfunctions. But a pace maker could malfunction as well. Questions to be answered.


Friday, July 6, 2007

Family's Reaction

I had hoped that of all the people in my circle that would understand my plight would be my brother, John. I love and respect him and honor the fact that more than likely he will always be there for me. He has steadily maintained that if I just eat right, exercise, and pray and learn to balance stress that everything would be OK. To a certain extent I can see his point. I have been doing that very thing for the last six months and over the years that this has affected me I,  have tried all sorts of combinations of food, meditation, medications, prayer, exercise and psychotherapies that I could afford. I am by no means perfect in following all these programs either when they are combined or separate. But, I'm going through yet another down turn at this time.
I just would like to point out if I had a viewable handicap instead of a deficient brain that it would be socially inexcusable to ask me to carry on as if everything is normal. This treatment of "just buck up","hunker down", or any such advice is frustratingly constant. I guess because I am not lying under covers and crying constantly (which did happen about three years ago) that I can cope with life, and I better well stop my quest for living a higher quality of life. Ah, that is the quest, the quality of life, the feeling of a happy memory that can be recalled at any time, an ability that most people have. It is the difference between living the life that God intended, or existing as a shell. A shell pumped full of drugs.