Spondylitis

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Medical marijuana, cbd use

Medical marijuana, cbd use

I am looking for alternative treatments for my AS. Will be on pure Medicare this next year and I’m very doubtful that I will be able to afford my humira. If you are using or have tried using either the full product or the cbd (without thc) I would love the feed back. Also if you know a source for good cbd, product descriptions are sketchy online. ( I can buy from 9 to 120 and they all read the same) thank you!

A MySpondylitisTeam Member said:

Pray kansas soon get med. Marijuana. They were but the police thought it would make crime higher. I have prescription pain med sometimes that doesnt… read more

posted about 21 hours ago

Fired by surgeon

Fired by surgeon

has anyone ever been fired by their surgeon because their office staff decided to tell me that I had no confidence in the doctor I had confidence in the doctor. I did not have confidence in his staff. I caught her in several lies regarding my insurance because I was calling back and forth. And just I have now Blue Cross found me another surgeon in and she got me an urgent office visits and. And they are going to make it like an urgent appointment like I'm going to go in there he's going to have… read more

A MySpondylitisTeam Member said:

I was diagnosed in 2006. My surgeon stated that he could do surgery, but guaranteed the procedure would not be beneficial due to the constant changes… read more

posted 1 day ago

I cannot stand on my feet. How many feel so alone?

I cannot stand on my feet. How many feel so alone?

I cannot stand on my feet an longer than 15-20 minutes before they are absolutely killing me. My diagnosis are AS, Fibromyalgia, sjogrens, Raynauds, and neuropathy. I hear how people describe neuropathy as pins and needles but I don’t have that. I never know how to explain it but my feet just hurt and the longer I’m on them the more swollen and red and hot they become. I have to literally plan each day around my feet, meaning I have to decide what hideous shoes to… read more

A MySpondylitisTeam Member said:

I hear you! Don't despair. We are much more than a number on the scale, or blood pressure cuff! No "fat shaming" here. There are multiple reasons… read more

posted 1 day ago

Has Remicade helped anyone?

Has Remicade helped anyone?

Hey Guys,
I am currently on Cimzia right now. My options are very limited due to me still nursing my 10 month old little girl. My rheumy said that Remicade is another option that has been seen to be safe while nursing. Every time I do one of my Cimzia shots they seem to last less time and I am really only getting 50% relief. I was wondering how anyone has done while on Remicade? This would be my last try on a TNF inhibitor because if it doesn't give the relief needed then my Dr. would… read more

A MySpondylitisTeam Member said:

They always want to go another round. That's why after 6 rounds I said no more
Not helping making things worse. Had to change Drs. After that.

posted 4 days ago

I have As and my symptoms seem to be getting worse my question is does anyone else experience worsening memory as time goes on?

I have As and my symptoms seem to be getting worse my question is does anyone else experience worsening memory as time goes on?

Also maybe finding it harder to come across words?

A MySpondylitisTeam Member said:

You are certainly not alone
Even on Percocet 10mg 2x day in constant pain. Does not seem to matter much to anyone who has.not been involved with it.… read more

posted 5 days ago
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