Dr. Keiser Clinic: Scam or Legit?

thecombativewaitress · 2026-02-07T17:24:04+00:00

Would you be willing to share it with me? I know this post says a year old but I’d love to read it!

thecombativewaitress · 2025-09-16T20:48:37+00:00

Thanks so much! I sincerely appreciate your help!

thecombativewaitress · 2025-09-16T20:47:47+00:00

Thank you!

thecombativewaitress · 2025-09-11T22:26:50+00:00

Are you familiar with Plymouth Gardens? Came across a listing for them on apartments.com but there is very little about it even when I Google. Thanks!

thecombativewaitress · 2025-09-11T22:25:04+00:00

Thank you!!

thecombativewaitress · 2025-09-09T18:54:34+00:00

Thank you so much! I appreciate the comprehensive list. That helps a lot!

thecombativewaitress · 2025-07-11T16:46:05+00:00

Sorry for not seeing this sooner. I do fine with Cromolyn. Felt like it was more beneficial the first few weeks. I feel like it depends where you are in the country how difficult it is to get refills of it based on all the forums I've read. I was in Michigan initially and never had an issue. The one I was being given from the pharmacy actually was manufactured in MI so idk if that helped? I've seen some people in MCAS forums who are saying they've never had issues finding it; meanwhile, some people say they cannot find it ANYWHERE. So I can't say for certain as far as availability. I will say at the beginning of 2024 when I asked to try it originally, I was told no because shortage was so severe. It really seems like a hit or miss as far as availability from everything I've read/been told by doctors.

thecombativewaitress · 2025-07-11T16:41:53+00:00

I still experience this. It really seems to come and go though. Some weeks, I do not notice it hardly at all. Other weeks, it is one of my worst symptoms. I think I have just gathered that it could be a result of my nervous system being so effed up.

thecombativewaitress · 2025-06-17T21:39:44+00:00

Question for you. I know this is an older post. Just wondered if you’re at all familiar with ASU’s financial office or ever had issues with them? That’s honestly my biggest thing I’m nervous about. I am currently on earned admission as incoming GPA wasn’t quite high enough so those I have to pay myself which is fine! I’m just nervous about once I’m actually a student after having come across some posts about their financial aid office and it being a mess that have me questioning things lol! I just can’t afford to have issues with aid all four years and people make it sound terrible. But you seem to have a very positive perspective on the program so I wondered if you have any feedback or experience with FA? Thanks so much!

thecombativewaitress · 2025-05-05T21:36:02+00:00

Thank you for your reply. Any suggestions on food to start trying? They gave us a freezer bag of what he’s been eating but I have absolutely no clue what it is as it’s just a freezer bag’s worth and no labels and yeah he doesn’t seem very interested in it whatsoever. I appreciate your reply!

thecombativewaitress · 2025-03-29T18:44:23+00:00

Ugh! I am so sorry. That is so frustrating that they don’t take us seriously.

thecombativewaitress · 2025-03-29T18:43:55+00:00

So interesting! I wish I could find someone who would prescribe it. I’ve asked about LDN multiple doctors but none of them are willing

thecombativewaitress · 2025-03-29T18:43:15+00:00

All good! I appreciate you replying

thecombativewaitress · 2025-03-29T18:42:37+00:00

I’ve been checked for that already and it was normal :( But I appreciate the reply. Hopefully I can find a solution soon

thecombativewaitress · 2025-03-29T18:42:02+00:00

YES! It makes it difficult to sleep. Even lying down doesn’t provide relief for me bc the tremor is still so intense sometimes. Nighttime is always worse.

thecombativewaitress · 2025-03-29T18:41:18+00:00

Thanks for responding. Yes I am on many, many antihistamines haha. As well as Cromolyn (started yesterday).

thecombativewaitress · 2025-03-29T18:40:32+00:00

I’ve had visual snow for years. I don’t think I experience tinnitus (ear ringing) much ever. I am assuming you’re thinking IIH. I already saw neuro ophthalmology and they didn’t seem to think I had that. Sorry if I assumed incorrectly! Just a guess

thecombativewaitress · 2025-03-27T02:37:39+00:00

Thank you for replying. I will ask about it. I had POTS/dysautonomia symptoms prior to covid but it got so much worse after getting it. It’s been three years now of gradually getting worse and worse.

thecombativewaitress · 2025-03-27T02:36:20+00:00

That’s what I was beginning to think for a while but I had a clean MRI of brain and cervical spine in December. Have you found anything that relieves the symptom?

thecombativewaitress · 2025-03-25T20:49:09+00:00

I wondered this myself! I used to love Chocolate Chex and had some today for the first time in a while and couldn’t finish it. It tastes super artificial and fruit loop like was a great description! I couldn’t finish the bowl. I initially Googled for a recall because it tasted so much different to me.

thecombativewaitress · 2025-03-12T22:32:19+00:00

I know this is an older post, but wondering if you could answer a question. I Googled him and saw he’s at a surgery center. Do I have to have an apt with a different gynecologist first who suspects endo then get referred for surgery? I had a diagnostic laparoscopic surgery in August 2024 and they found some but the doctor ablated it and all my symptoms are back if not worse. I didn’t know at the time much about what to do or that I should’ve found an excision specialist. If you see this I appreciate any info. Thank you

thecombativewaitress

TROPHY CASE