2017 has been a good year for me this far!
For those that remember my story from last year and all the doors that have been slammed on my face, I am finally, finally! getting some progress with my journey.
I changed GPs this Feb and I am so glad I did!
So far this year....
I have seen a rhuemy twice, the dermatologist at the University of Alberta Lupus clinic and will be seeing the neurologist in July/August, and go for exploratory surgery for cervical cancer.
doc at the hospital started to give me injections on my head (but had to stop as I passed out lol), then put me on Plaquinel (however you spell it). Finally some relief!!!!
Just came back from Rhuemy and it is entirely confirmed I do NOT have SALE...yay! But I have mixed connective tissue. But that's OK.
At least I know what I have and that I have a treatment plan and a bunch of doctors who are here to help me and not ignore me!
2013: Discoid Lupus
2016: Pernicious Anemia
2017: Fibromyalgia and MCTD
I know one this post may sound weird but pop pop fizz fizz oh what a relive it is to know I am finally getting diagnosed and help is on its way