New doctor, new questions: We just moved to... - Cure Parkinson's

Cure Parkinson's

26,582 members27,897 posts

New doctor, new questions

kaypeeoh profile image
9 Replies

We just moved to Connecticut after 35 years with Salt Lake City doctors. They got my wife through three cancers and me through 100% obstruction of the LAD coronary artery. They're also who diagnosed me with PD. I had an appointment to be seen by a neuro here but their first opening wasn't til January 31. However the office just called, they had a cancellation and can see me tomorrow--October 27--at 8AM. Any questions you guys recommend me asking? I generally go into a fugue state and forget everything once we're out of the exam room. For that reason my wife is coming too. I know she wants me to apply for disability but I'm still not sure I actually have PD.

TIA,

kpo

Written by
kaypeeoh profile image
kaypeeoh
To view profiles and participate in discussions please or .
Read more about...
9 Replies
MBAnderson profile image
MBAnderson

You've posted a lot of insightful and informative threads. If you had to declare right now, what would you say?

kaypeeoh profile image
kaypeeoh in reply toMBAnderson

I see how much suffering there is in people in this forum. I have dominant hand resting tremor for 5 years. I have constipation controllable with ozone and minor balance problems. But nothing that is painful. I have a bad back but I've had a bad back for 50+ years. So I don't know whether I have PD. Propranolol, Sinemet and/or ropinirole don't have any effects on me other than lower leg edema. Doctors in Salt Lake City say I have PD but I guess I need this as a second opinion.

MarionP profile image
MarionP in reply tokaypeeoh

You should have a DaT scan by a neurologist. If you have PD or are on the path toward it, the scan will confirm it. If there is any question, then a subsequent scan in about 2 years will help make that more definitive. the reason you need to do this is because if you do not have pd, then your symptoms may be due to something else that may need to be treated within an accessible window, within which your treatment options and prognosis may have a shelf life which you do not want to miss or delay meeting. We called the process of tracking down symptoms that can be common (or which may mimic) to more than one condition "differential diagnosis," and it can be critically important to get to the right cause of the symptoms. I would waste no time. You should also be seen by a rheumatologist, endocrinologist, and an infectious disease specialist...perhaps even a toxicologist...and all should be asked to work and collaborate together. You could conceivably have anything from an infectious viral or bacteriological or even fungal disease to a toxic or poisoning disease, to even hanta virus or radiation poisoning (if you ever spent much time in the four corners area (you did say Utah, right?)) or industrial or agricultural chemical poisoning, as well as an assortment of other neurological disease, or even a nutritional deficiency or excess. Or nothing. Get the rule-outs done.

Despe profile image
Despe

"I have dominant hand resting tremor for 5 years. I have constipation. . ."

These are PD symptoms, especially the resting tremor.

kaypeeoh profile image
kaypeeoh

I'm back from the neuro. I have a photo. This website only allows photos on new posts. So I posted a photo of my discharge info and added a short discussion.

mgregor6 profile image
mgregor6

Who is your neuro in Connecticut, may I ask?

kaypeeoh profile image
kaypeeoh in reply tomgregor6

Elena Bortan

mgregor6 profile image
mgregor6 in reply tokaypeeoh

Oh okay. Th e Parkinson's community is smaller in CT so that it's easier to ask around in order to find out from you PD peers which neuros and/or motion specialists are decent and which to avoid. But I have yet to hear of Elena Bortan.

Godiv profile image
Godiv

I think I could really tell it when my arm stopped swinging when I walked. Even though I would tell people I had a stiff shoulder LOL.

Not what you're looking for?

You may also like...

I've been treated for PD for 16 yrs and have a new Neurologist who doesn't think I have PD because I didn't show "The Signs"

In 2003 I thought I had a severe case of arthritis through my whole body because I hurt and was...
Sugarbear67 profile image

New location, new neuro

I posted under new location, new doctor. But I can't send a photo to an existing file so had to...
kaypeeoh profile image

Am I unusual?

I was diagnosed with PD in 2013. Was an active full time worker in a very active dangerous at times...
Henry1244 profile image

You never know what tomorrow will bring. And a update on my new home.

My former next door neighbor of 33 years came to check out my new barndominium yesterday. He...

Nightmares !!!

When I was first diagnosed with PD after about 6 months I started having very very vivid...
Mally13 profile image

Moderation team

See all
CPT_Aleksandra profile image
CPT_AleksandraAdministrator
CPT_Anaya profile image
CPT_AnayaAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.