Reposted from a friend on Facebook:
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.
My favorite quote from my doctor
was, “it can’t really be that bad if you are still 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.
Please, for me and in honor of
someone who fights against:
-Lupus
-MS
-POTS
-Dysautonomia
-Crohn’s Disease
- Ménière’s Disease
-Addisons Disease
-Hashimotos Disease
-Graves Disease
-FND
-Depression
-Anxiety
-Autoimmune disease
-Sjogrens syndrome
-Polycystic ovary syndrome.
-Rheumatoid arthritis.
-Chronic pain
-Endometriosis.
-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
-Alpha 1 antitrypsin deficiency
- Paroxysmal Nocturnal
Hemoglobinurina
or some other disease you don't
see.
In support of a friend, a family
member who is fighting any of these diseases.
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