Here is another article about how young people with chronic illnesses are treated.  There is no understanding or respect.  This woman’s illness is not completely invisible.  I thing that I would notice if a twenty-three year old woman came into the ER with an oxygen tank connected to a tube that traveled up into two little prongs in her nose attempting to breathe to live a little longer.  How insensitive are we as a society that we can not understand that she may need help more than you at the moment?  I applaud this young lady for being strong and coming out to answer that woman, even if she didn’t have the strength in the beginning.


We talk about invisible diseases, and there are so many.  These are the illnesses that are not obvious from the outside.  My son would be using the electric shopping cart at the market and someone would tell him he was taking it from someone who needs it, or park in a handicap space and be told there was nothing wrong with him and needed the exercise if he would park down the aisle.  On occasion, there was the triage nurse that looked at him and said that he looked fine and he was at the ER as a drug-seeker.  And the time he was in the hospital and I wanted a referral to a doctor outside of our insurance to consult and I was told by the  woman in the insurance department that I was trying to save my son’s life, and was told that I was being dramatic and denied the referral after going to his room and looking at him. These people had no idea about his many surgeries, his permanent G-tube that had been placed for three years, his constant pain from adhesions and having been placed inappropriately on a gurney for a surgery, that just a few years ago he weighed 230 lbs and at that time was 107 lb., that he hasn’t swallowed food in years, or that he goes  sleepless every night due to his severe asthma and narcolepsy.

I do my best to bring awareness to invisible diseases because it is difficult to hear judgements constantly.  Well, I have an invisible illness also.  It is called POTS.  Here is an article that gives some facts about this syndrome.  I  found it on Patients Count at:

POTS is much more than tachycardia
39 POTS patients at Baylor Medical Center were asked to report their symptoms, and here’s how it came out:

Symptoms reported by POTS patients:

Palpitations 92%

Fatigue 90%

Lightheadedness 87%

Lightheadedness with standing 87%

Headache 87%

Sensitivity to hot or cold temperature 87%

Concentration difficulty 77%

Facial flushing or rash 77%

Hands change color in the cold 74%

Morning exacerbation of symptoms 69%

Blurry vision 69%

Pain 69%

Muscle cramping 69%

Lightheadedness with sitting 64%

Breathing difficulty 64%

Joint pain 62%

Word-finding difficulty 59%

Medication sensitivity 56%

Leg pain 56%

Fainting 54%

Memory difficulty 54%

Early-morning awakenings 51%

Tremor 49%

Night time awakenings 46%

Irritable bowel symptoms 46%

Loose joints/double-jointed 44%

Susceptibility to cold or infections 44%

Swallowing difficulty 41%

Insomnia 39%

Iron deficiency anemia 39%

Lightheadedness with laying 36%

>2 medication allergies 33%

Hearing loss 28%

Family history of low blood pressure 28%

You probably wouldn’t be able to see many of these symptoms if I was to walk in a room, but I assure you I am having at least one to a few at that time.  Thank you for reading.