Posted by Rob Thomas wife, Marisol, will appear on the next video by the popular singer. He wrote a song inspired on her. He wrote the song while her wife was struggling with an auto-immune disorder. Rob Thomas wife illness is rare.
According to the Jacksonville Observer:
The first single, “Her Diamonds,” was inspired by Thomas’ wife, Marisol, who in recent years has struggled with a lupus-like autoimmune disease. Her battle isn’t specifically addressed, “but it’s about how something like that makes you feel empathy. I like to write about universal emotions. Everything has a base emotion; it’s just what triggers it that’s different for everyone.”
Those were the news on Rob Thomas wife.
Tags: marisol maldonado, marisol thomas, rob thomas, rob thomas bio, rob thomas wife, rob thomas wife illness
Many autoimmune diseases are rare; these diseases are interesting and scary there are approximately 80 to 100 with another 47 waiting for a name. Medical science cannot explain why and has not found a cure for even one. You can trigger one of them just by having an auto accident, taking aspirin, medication or by starting a new exercise routine, even too much stress says latest research. Have you changed anything in your life, “Look for the root, it is in the basics beginning with what is on your fork, what toxins are in your body, what exercise do you do, what stress is in your life, what is your spiritual base”. Scientific arrogance has led us down the wrong path we better stop and take a close look at what is happening. This month 144 new chemicals which are part of the Lupus problem will be added too industry with no oversight control at all. Autoimmune disease is the worst kind of contradiction; for a Lupus sufferer you are attacking your own body with your immune system, a world upside down. Here is a challenge, on a piece of paper write down as many diseases as you can think of then put them as a search on Google with the word epidemic, you will see that almost all of them are. Is anyone in modern medicine awake?
Sincerely
Paul
I hope and pray each day that more celebrities with an autoimmune will speak out. We desperately need to spread awareness about auotimmune diseases. They are debilitating, completely life changing, disabling, cruel, excruciating, chronic and deadly in some cases.
I have been battling what is best explained as severe MCTD (Rheumatoid arthritis, polymyositis,Lupus and several associated syndromes) for several years and I nearly died from complications in 2007. My whole body is under attack, in my earlt 20’s I suffered heart damage and my lungs and kidneys are under attack. My bone marrow is even diseased. It is pure hell to live like this, I am bed ridden for the most part and home bound. My contact with the outside world is through my computer. I am merely existing most days, this is no life. I have tried so many dangerous drugs, you name it, I have tried it, even chemotherapy to no avail. Some of these treatments were over $7,000.00 for one dose!
So much more must be done! AWARENESS-RESEARCH-HOPE-CURE
I am deeply touched by your stories. Stacey, your strength amazes and inspires me. Thank you so much for sharing your touching stories and sparking awareness. Hopefully, by putting your stories out there, more will be done to find a cure. You are all in my thoughts and I hope for your peace to come very soon!
The sad thing is that a lot of these mysterious disease are triggered by a childhood vaccines or flu vaccines. do the research
well im a part of a very LARGE community of people suffering w/an illness…its called lyme disease….MANY of us were misdiagnosed….told we had something else…something rare…..etc…
Please consider looking into this disease….many that were misdiagnosed finally got a diagnosis of lyme and are being treated….if you need any info about tick borne illness PLEASE contact me…my doctor says its a tsunami and many are suffering….this could unlock the mystery for her…God Bless
btw…my contact info….blwhite@atlanticbb.net…please dont hesitate….most of the medical community will never address this illness and its REAL…we must depend on one another and a handful of doctors willing to treat us
I am a 32 year old, single female living in the Seattle area. I still feel 21 but in my soul, not in body but in my soul. My illness has taken over a decade from me. At first it was pain, severe fatigue, narcolepsy, by 25 I was being fired from my job and unable to hold another one due to being unable to control falling asleep and staying awake. I lost everything. My things my home, my health insurance, my child, all of the people in my life went away as though they had already lost me. It was as though they grieved the loss of who I was and they had no interest in being apart of who I became as a result of my illness. I wish they could all understand I am exactly the same person under an abnormal amount of stress with this and all that comes with this. The illness has been locust in my life, eating the years away. I am determined to overcome this and stop living in the shadows of this disease. The pain became much more severe at 28 to 30, and from 31 I began having trouble swallowing, the pain is crippling, my hands are almost leathery at times, my knuckles and joints almost suck all the fluid out of the rest of my body. I can’t breathe a lot, my toes turn blue, my chest hurts, my jaw, my shoulder these episodes have been terrifying. I see angels a lot now, and other things that would be otherwise invisible have become visible, and terrifying. So I have 2 illnesses, one has been unidentified mixed connective tissue, 10 of the 11 diagnosing criteria for lupus sle, but I have no insurance and the PCP is a triage for the specialists and my ana has always been negative so rheumatologists won’t see me. However that’s only a marker for Lupus not a way to rule it in or out. 95% of people with Lupus are said to have a positive ana. That means less than 5% are diagnosed w ana negative lupus. I believe more people have ana negative lupus than 5% but drs are just unwilling to make the diagnoses so it is reorder that it is rare so it is viewed upon as a zebra not a horse in the medical community and they are trained not to look for the zebra. When you don’t have money it can be and for me has been impossible for me to get them to take a closer look. Even though I have severe photosensitivity, with butterfly rash, a hallmark of this disease, the only tell tale sign. From what I understand it all in and of itself is enough for definitive diagnosis. Especially accompanied by raynauds, polyarthritis, myalgia, fatigue, ulcers mouth and esophegous and so on. I can’t be under fluorescent or halo gen lights, computers get me really bad really fast, I’m beginning to feel more and more like I don’t belong in this world. I feel like my body is having a natural response to things that are unnatural, such as the global change in the electromagnetic field since ac/dc then radio towers then cell towers everywhere and everybody now carries one or more cellular or wireless devices changing the field where they are, giving off emf radiation, uva and b from the devices etc. Its like the gentleman said above from the tip of your fork, taking a medicine, exercise and I believe answers lie with in technology and our devices, something almost impossible to escape. My other illness is Morgellons now that’s a hoot! This one I first noticed when I was 26. I saw dr after dr. They had never seen anything like it, while they could see it with their own eyes, they dismissed me saying this doesn’t exist bec it wasn’t in text books …yet. Desperate I wrote to the CDC, they wrote back and I wrote back and I still have the letters. Well apparently there were about a thousand other people world wide having the same problems and symptoms and also writing to the cdc and senators to help. The people with this mystery disease gave it a name, well one woman, Specifically and it was adopted by all of us who have it, Morgellons. So when people typed in Morgellons in the CDC website it first redirected you to dilusional parasitosis, a psychiatric condition. As concerns grew, as more people became ill, the cdc finally decided to investigate. Research is conducted at Oklahoma City University headed by Dr Randy Winemore (I believe that is his name) he and his team of scientists and experts have determined this is a real disease unlike anything they have ever seen. The CDC finally changed their site to show Morgellons as an unknown dermopaathy possibly systemic still under investigation as to what it is exactly.They have hired merk to develop medications but it will be many years before I am ever treated. I think now the number is up to 12000 and growing. Seems this is environmental somehow. I have to say I lost faith in doctors when they looked right at me right at my very loud symptoms and said they see it but it doesn’t exist bec its not in their text books. Anyway, that’s my story. I hope more celebrities try to use their celebrity to raise awareness like Rob has too. He has always touched me like he was reaching right into my heart, singing healing and comfort into my soul. My son who is now going on 10 was listening to Rob Thomas with me, and when he heard her diamonds he said He (rob) feels just like I do mom. Rob reaches people, from my baby to me, I don’t know anyone who doesn’t appreciate his music and his ability to connect in a way like he is speaking to you so specifically. Anyway, I love that he loves his wife the way he does. Makes me feel like maybe somebody can still love me even though I live with this demon. Can’t wait to see him here in Snoqualmie. Peace and God Bless
BARBARA – I have been diagnosed with Lyme Disease also & definately feel that it was the trigger for the onset of my Fibromyalgia. In addition, I have Addison’s Disease, which is adrenal insufficiency. One of the main issues with autoimmune conditions seems to be that one begats another, & they all affect and/or are affected by the endocrine system, which in turn sets up yet another chain reaction. “All-Consuming” is how I refer to my illnesses…
Angela, have you been tested for scleroderma. You should read up on it. Sounds like you have a lot of the symptoms. Good luck to you, don’t give up.