Muñiz School of Filipino Warrior Arts

Mabuhay! This message is to all The Kapatid, fellow brother Warriors and practitioners of the Arts of Mayhem
( https://www.merriam-webster.com/dictionary/mayhem ),
please consider helping me financially in me battle with Cancer:

https://gofund.me/05f4da860

https://gofund.me/6fd76ef81

Donate to Support our fight against Cancer, organized by Donald Muniz Hello myname is Donald, and I’m facing one of the hardest battles of my life. I've been … Donald Muniz needs your support for Support our fight against Cancer

https://gofund.me/7bda1ab0c

Donate to I have Cancer: Please help Eliseo & Margaret not to suffer, organized by Donald Muniz My name is Donald, and I’m facing one of the hardest battles o… Donald Muniz needs your support for I have Cancer: Please help Eliseo & Margaret not to suffer

It went down something like this 🌲🕯️🦌⛪

Kids Explaining The REAL Meaning of Christmas😂🤣 #Jesus #nativity #merrychristmas #biblestories

I've studied and sung Opera Arias, Classical Art Vocals in Italian, French, German and some English music. BUT I can't sing this song ALABASTER BOX. My emotions build up and I choke up on my own tears. Hopefully some day. I hope this song blesses you as much as it blesses me 🙏😇🦖

Lillie McCloud - Crowd-Surprising Cover of CeCe Winans' "Alabaster Box" - THE X FACTOR USA 2013 Lillie is here to win it all and to prove that it's never too late to give up on a dream.Subscribe now for more THE X FACTOR USA clips: http://bit.ly/TXF3_Su...

Listen... the Pope got this one RIGHT!

Pope Leo Declares Jesus Alone Saved the World, Rejects Title of Mary as 'Co-Redeemer' A decree from Pope Leo's office firmly rejects the claim that Mary, Jesus' mother, helped save the world from damnation,

Hot tip……if you get into a committed relationship with someone that has chronic health issues please please please understand that that person may not be able to do anything for themselves for weeks to months at a time and a large burden is going to fall on you. Take the time to make sure you're able to handle it before you commit.
I didnt ask for my body to fail.
My favorite quote from my doctor was, “it can’t really be that bad if you are still working and doing everything you do. “ I told him I didn’t know I had a choice. 🤷🏻‍♀️
Years in pain, tired and the many changes in me for no reason or apparent reason ... Hiding everything from someone else, pretending to be doing better than you are; until it no longer works. No matter how strong you want to be.

Then the moment comes when they tell you what you have ... You have mixed feelings: you finally know what you have, but how do you deal with it?
Lack of encouragement, wanting to lie down, taking medication frequently; having a whole pharmacy on top of the nightstand.

Then, the daily responses, "Why did you get so fat?" “I have this great diet, if you just go out and exercised.
That once beautiful hair of yours now awful and it falls out.
What happened to you??....
This is all true and that's why I'm sharing it!

Silent and invisible diseases do exist ...
When you have an invisible disease it is difficult to argue from your perspective with ignorant people.
Life takes a lot of turns !!!

Tired of being told:
* Did you go to the doctor?
* Have you tried this?
* Have you tried that?
* I don’t know what else we can do for you...

Yes! I tried and still try everything !!!
Doctors say this disease is forever. That I will not heal. However, I am not giving up, but I want to make others realize:
* A nap will not cure me but it will help me ...
* I am not lazy, I take medication and it sometimes makes me sleepy.
* I am not angry but sometimes cranky with pain.
* I struggle daily with pain, mobility problems, fatigue, the criticism of my environment.

Most frustratingly, people look at me and say, "It can't be that bad; you look good "
Despite the fact that my body is experiencing excruciating pain everywhere, of course I look good, I always try to look good, it is an "invisible" disease.

This disease affects me physically, mentally and emotionally. Because rare autoimmune diseases cannot be seen, but we feel them.

And they are there ... Silent attack but extra painful.

I AM LOOKING AT THOSE WHO TAKE TIME TO READ THIS POST TO THE END.

The following request is sent to the post:
Please, for me and in honor of someone who fights against:

-Sicklecell Disease SS & SC etc..
-Ankylosing Spondylitis
-Lupus
-MS
-POTS
-Dysautonomia
-Crohn’s Disease
- Ménière’s Disease
-Addisons Disease
-Hashimotos Disease
-Graves Disease
-End stage liver disease
-FND
-Depression
-Anxiety
-Autoimmune disease
-Sjogrens syndrome
-Polycystic o***y syndrome.
-Kidney Desease
-Rheumatoid arthritis.
-Chronic pain
-Endometriosis.
-IIH
-migraines
-Multiple sclerosis.
-Myasthenia gravis.
-Pulmonary hypertension.
-Epstein Barr syndrome.
-Chronic fatigue syndrome.
-Diabetes
-Fibromyalgia.
-Raynaud and Scleroderma.
-Neuralgia of the trigeminal
-Epilepsy
-Cancer
-Hypothyroidism
-Arachnoiditis
-NEAD
-Vasculitis
-Neuropathy
-Ehlers-Danlos syndrome
Lymphedema
- Psoriasis
-Alpha 1 antitrypsin deficiency
-BPD
-Traumatic brain injury
-MOGAD
or some other disease you can’t see

I would like 5 of my friends to post (not share) this message to show that you are always there when that someone needs to talk.

In support of a friend, a family member who is fighting any of these diseases. Just say
" Done " 💜