Does anyone in lupus group have Hashimoto's Encephalopathy? Help please

Hi, I need help here please, nobody has been able to answer me. I have been just recently dx with Hashimoto's encephalopathy. Also have UCTD with features of lupus and scleroderma, have Hashimotos disease, microscopic colitis, Raynauds, Photosensitve, Myositis, myopathy, neuropathy, high blood pressure, allergies, just to name a few, lol. But now this. I looked it up and feel very fortunate that I have a neurolgist that was on top of things and dx this for me. But still scares the hell out of me, being so rare is weird, I though being dx with scleroderma was rare, yikes lol. But would love it if someone knows someone who has this, that I can talk to the forum groups have been such a great help for me through all the rest of this mess I am in. 

Thank you in advance.

Bobthe builder54 

Joy, oh thank you for answering my post. I certainly do appreciate it.

Let me ask you this if I may? Is your Hoshimoto's also the encephalopathy kind? I have have been hypothyrod for a long time, and figured it was hoshimotos because of all of the autioammune stuff but not this, YIKES.
You sure have yourself a load full of trouble too. LOL> They kept telling me I had asthma also, but when i started to see my pulmologist he said no.
So who knows right? Why is it if you get one dang autioammune you get more, we should all go see Dr. House. LOL.

Thank you again for your reply,
perfect, or bob thebuilder what ever lol I sign boy ways.

Joy, you are so right they are all frustrating and if people do not have anything like that going on in their health world they just dont get it because usually we do not look sick.
Susie

Peggy,
thankyou so much for responding to my post. It sure sounds as if you have had your fair share of problems, Wow. I am so sorry to hear.

Yes you are so right when you say doctors have egos that is a understatement. I have a few very excellent specialists who are disagreeing on a few things, not the new dx but some old ones. I have decided I am going to go with my gut. If I trust a doctor, then that is it. I am so tired of being poked, tested, questioned, etc, and when you go to a new one they do all there own tests because they do not trust another doctors tests or inturpations.

Are you loosing your hair because of the plaqunel? or from the lupus its self? There were two to three years I lost all my hair from my arms, legs, underarms, I was not on any meds at this time. It seemed when I started on plaqunel the hair started to come back, so I do not know if it is just the timming or was it the meds. I have noticed that the hair on the back of my head is breaking off, I do not know why, but I can see it, so I do not know if it is something comming on, I am under extreme stress (seems to be my middle name) lol, and now with this new dx it just adds more stress, Ikeep saying the doctors are going to convince me yet that I am sick, lol.
Perfect54 just so you know sometimes i sign by accident bobthe builder or susie, all the same lol

I'm sorry, Nadia, I'm having a hard time reading all capitals. Vision issues are common with our condition. Can you please retype this in lowercase?
Also in internet ediquett writing in all capital letters is considered yelling.