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DiscussionMy sister is undiagnosed and I'm scared
Autoimmune Diseases | Last Active: Apr 6, 2016 | Replies (7)Comment receiving replies
Replies to "Hi Colleen, just wondering if there any physician's that reads and respond or at least give..."
Thank you so much Colleen, sorry, take your time reading or just file. It<br />
is just hard to stop writing. I am 65 and have had autoimmune since 22, so<br />
there have still been great gifts<br />
No she was diagnosed with crohns in 2005. Then vasculitis, then RA,, lupus.<br />
I don't think it is ever just one. Nov 2008 she was blessed with a perfect<br />
baby girl. For nine months she was in remission. She has ostenecrosis with<br />
bone death in left foot and has lost back teeth in the last year.<br />
She received Full Social Security Benefits at 26. Her case manager worked<br />
so hard and saved her life emotionally from all the doctors, family and<br />
friends that just thought it was drugs, alcohol, lifestyle etc. It Never<br />
was.<br />
She went from Miss Teen Alabama, working pagents for Donald Trump.<br />
World Champion Baton , Miss Majorette of Alabama, University of Alabama<br />
Crimsonette (majorette) and Miami Dolphin NFL Cheerleader.<br />
Then in a blink she was on a feeding tube and months of hospital. Yes I<br />
fired my share of doctors. Dr. David McClain and Dr Treason were the 2<br />
doctors saved her life but we moved and it has not been the same.<br />
So she has been working on her degree in integrative medicine, nutrition,<br />
and natural healing . I just know she will make a difference. She already<br />
has for her and me.<br />
Just one last thing. My mother, her grandmother, died 3 yes ago from<br />
complications of crohns,<br />
My son, her brother, died at 37 , from a heart emulsion from respiratory<br />
infection, 12 yes after being released from ER that documented slow<br />
respertory from drugs!. Again no truth. But the assumptions will never get<br />
my Son back to me and his babies.<br />
<br />
Like everyone on this and other groups, I could write a book. A few weeks<br />
ago my 1st post was my Sarcoid in 1973, my baby boy was 6 months old and<br />
because my diagnosis was skin, lungs and more in 1973 I was the only white<br />
female that the university of Alabama Birmingham Alabama had ever treated.<br />
Therefore they said 6 months to live or remission. Weeks in the hospital<br />
because a teaching hospital, treatment was only steroid and<br />
antidepressants. Looking back I spent all of those weeks and months with<br />
doctors of all fields testing and absorbing and I don't think we are<br />
anymore knowledgable in the medical field.<br />
Good question @mswanda.
Connect is a place where you can find people like you, with similar questions and concerns. As part of the online community, you can talk with others and share your health challenges, experiences and wellness goals. Sometimes it can simply help to know that you're not alone. I bet your message was helpful to Michelle despite the medical situations of your family members being very different. It is so hard to watch a family member suffer and to not be able to do anything.
A diagnosis from a physician is impossible online. However, people can request for a Mayo Clinic department/physician to review their case by contacting us here: http://mayocl.in/1mtmR63 Additionally our physicians and other health care providers host webinars on a variety of topics and answer questions live or following the presentation. However, here again, a personal diagnosis cannot be made without a complete medical history and personal consultation.
How awful it must have been to be told that your daughter's suffering was all in her head. Did you have to insist on a biopsy and blood tests? Thank goodness you finally have a diagnosis and can seek treatment. How is your daughter doing now?