Saturday, October 1, 2011

My Life Today October 1, 2011





The photo is of my niece Verenda Teagle and myself.




It is interesting to say that my life has improved in 2 1/2 years.   Tardive Dyskinesia has not defined me.  Nor has it beaten me.  I learned that having my medication; especially my Clonizepam is essential to my physical well being.  Without this medicine, I would not be able to write, type, walk, talk, and hold my head still.  Most people think that I am an average normal person.  They see my disability card on the mirror of my car.  And they see me walk out of my vehicle and walk to my destination.  


I know that they probably think, "There's nothing wrong with her.  Why did she park there?"  In fact a woman actually confronted me once about it.  I don't agree with some people who think that I am taking tax payers money.  I worked all my life, since the age of 16.  I earned that money.  I payed my taxes and I payed my social security for such an occasion as this.  I choose to be an asset to society rather then a burden.  I do my part.  Even if its a small part.


I know that when I have an episode, my body is rigid yet constantly moving and my heart hurts.  I imagine since my heart is also a muscle that it probably tightens up and spasms much like the rest of my body.  I still have trouble sleeping without medication.  I'm on Trazadone, but on a much lower dose.  I'm on a higher does of Cymbalta.


I know that taking Qco10 helps me feel better and Caffeine is definitely not in my best interest.  But I can have small doses of chocolate in the form of chocolate covered raisins, nuts and fruit.  I have been  blessed with a wonderful granddaughter; who loves me unconditionally.  She tells me that she misses me every day.  Even though I take care of her almost every day.  She is very polite and beautiful.


My sons have also been blessing.  They help me when they can.  I don't even have to ask them. Most of time they do things on their own.  Which makes me proud.  They are all successful in their own right.  My books are not selling as much as I hoped.  But I do have my videos which are free to the public on You Tube.  Although I have made a video for the president; I feel that perhaps its time to send a letter to my Governor and/or Senator, and anyone that will listen.


I saw many people at MHMR that I suspected were trapped in their own bodies; like I was.  And that probably had some sort of neurological disorder due to medications such  as Geodone, Invega, Reglan and Seroquel.  Thankfully there has been a recall on Reglan.  I still want to raise awareness of the dangerous side effects of such drugs.   Especially Anti-Psychotic medicine.


My life is forever changed.  My opinion on the medication remains the same.   The benefits do not our the risks.  I am a 47 year old woman who still desires to become a nurse.  My heart tells me to work; but my physician tells me to keep selling my Avon.  I want to go back to college and try again.  I want to work in an office setting or admitting part-time.  I'm frustrated, but I know that right now it's for the best.  And I'm enjoying the company of my granddaughter.  


Another issue that has been on my mind is losing my sister to pancreatic cancer last month.  It's so important for people to understand that drinking too much or for long periods of time has consequences.  She was not an alcoholic.  She was a good person, kind and she suffered a great deal of her life.    I really miss her.  Sometimes we take family members for granted.  We feel they will live forever.  But that is not the reality of life.   We all choose a way to cope with our problems.  I was on the same path in my early twenties.  Now I just want to stay healthy as long as possible to be here for my children and grandchildren.  Love has not found its way to my door; but I am ever faithful that someday it will find me.  


The good news that taking Clonazipam/Klonopin twice a day has made as normal as then next person.  The downside is I cannot stop taking the medication.  After 10 days I relapse.  I'm still writing poetry, working on the third book, selling Avon as well as advertising for my two books on lulu.com.  I would be lying if I told you that I never breakdown and cry.  I do.  I even feel like giving up.  But just when I think I can't take anymore.  Someone, my children, friend or stranger offers sound advice.  To me they are the angels that God sends when I can no longer stand on my own two feet.  They give me the courage and perseverance that I need and crave to give me strength. 



With warmest thoughts of hugs and kisses to everyone.  May God bless you and keep you in safety always.  Thank you and God Bless Everyone who reads my blogs.


Donna C. Ledesma
Writer


Changing the world one person at a time, by showing compassion for others.


Copyright ©  October 1,  2011
All rights reserved 


Earth Therapeutics Anti-Stress Sinus Pillow

Wednesday, March 16, 2011

Thursday, February 10, 2011

A New Discovery


Angels
Angels Comments



It's been about 3 years since I had my nervous breakdown and developed Tardive Dyskinesia. This road has been rather bumpy, but through friends and loves one I am able to cope.


In The Magic, Rhonda Byrne reveals this life-changing knowledge to the world. Then, on an incredible 28-day journey, she teaches you how to apply this knowledge in your everyday life.Since my relapse a month ago. I am slowly returning to the beginning of my illness. That is not to say that I have lost hope or faith. I know what works for me. I know when I exercise I am better. I know that taking Clonazepam works. I am going to try to buy blue tinted sun glasses to see if I am better.


I have learned that as much as I love my sons, I have to let them live their own lives. They know that they only have one true mother. And I will be there should they call me. But I can no longer carry the burden of pain and disrespect.


I know that when I have a severe episode; I can take Benadryl. ( Don't try this if you get agitated or are allergic)  ***Consult your Neurologist.***


I was at a cricket store recently; I was trying to get a phone, because my condition has not improved much. I was so worried about communicating with my son that I didn't feel my legs giving out from under me. This is the third time in a month that my legs just don't want to cooperate.


So it's time for me to consult with my Neurologist. My legs actually turned inward and my arms as well. I looked like I had Cerebral Palsy. I was ashamed and sad all at the same time. I couldn't write my name. But I know that this illness directly connected to my emotions.


So while in San Antonio I purchased a Yoga CD at a Second Hand Bookstore for $2.00 brand new. I know that proper medication and exercise is key. Wearing dark blue glasses or light blue tinted glasses is a experiment, but worth a shot.


So I have found that when you don't use your limbs; you will lose the ability to use them properly. I say continue to try to fight TD and exercise with a family member. Take short walks at first. Find something to concentrate on. Read a book or play a game and concentrate. Practice spelling or writing,and start a journal. These are the things I found that work.


Keep believing that we will find a way to live better and pray that they find a cure.  Never give up. Never lose faith. Trust in a higher power.  And trust yourself.  Challenge yourself.  Fight for your health and well being. Search for answers to your questions and if you find something new please post it at "Grace A Mothers Journey" on Facebook.  Or leave a message here.


God bless you and yours
Donna C. Ledesma


Written by Donna C. Ledesma
Copyright (C) 2011
All Rights Reserved. 
Skylanders: Spyro's Adventure Starter Pack - Wii - Wii Games 

Monday, January 31, 2011

Blue Lenses Help People With Tardive Dyskinesia



My contacts a a slight blue tint. I wonder if that's what helping me. And another thing I really feel it's worth a try to buy a pair of glasses with blue lenses or blue tinted sunglasses. See if this helps.


Tardive Dyskinesia Tips

Saturday, January 29, 2011

Helpful Tips For Tardive Dyskinesia

Here is a short video about things you can do to help yourself get better or at least be more comfortable.
 Medifocus.com,Inc.





I feel that we really need to take a stand against companies that know that the product cause this type of neurological disorder or any ailment.  This is very serious.  My life has been turned upside down and it's taken me 4 1/2 years of therapy and many doctors to get where I am today.  Alot of it was my own determination to get better and beat this thing.  While I'm never going to be 100% the person I was prior to this; I'm functioning as normal as any other person.  I still have a few tics but they are not as predominant as before.  The following video is about this very topic.

 
West LegalEdcenter - CLE & Legal Training





Today I am 95% better through determination and hard work.  I found a herbal supplement that replaced the clonzipam.  I'm still taking cymbalta for depression and body aches.  I also take naproxin for the neck and lower back pain which is never ending.  In time I feel that eventually I will be able to function without the cymbalta.



Sunday, January 9, 2011

There IS Hope!


Here are a few videos of TD... The childs movements are more like the type I had.   In the beginning I was close to the gentlemen, I couldn't move my arms behind me.  I still grimace and blink and click with my tongue.



West LegalEdcenter - CLE & Legal Training





Medifocus.com,Inc.


Here is my personal video... I am about 95% better... Reglan, Invega, Geodone and Antipsychotic medications have been linked to this condition.  Get Physical Therapy as this is the key to recover as much as possible.  Seek a Neurologist.