Sooo over this!

Always_Believe · 05-08-2015, 09:22 AM

Quote:

Originally Posted by LIT LOVE

If you're having side effects or a bad reaction to a medication, than by all means, make an appointment and discuss it with your doctor. But stopping all your meds at the same time makes it difficult to even determine where the problems lie. Are dosages too low? Too high? Are there interaction issues?

Same thing with the pt. Is it the wrong therapist? Or the wrong type of therapy?

Regardless of SS, there is little point in you going to a doctor you don't trust or communicate with. There is nothing wrong

If you are unsuccessful with your SSDI application and your Date Last Insures expires, you can always apply for SSI benefits later on, so long as you meet the savings and resource test.

Therein lies a lot of the problem...my PCP isn't listening.
Gabapentin: Prescribed dose - 400mg TID...gained 15 pounds in 2 weeks...no noticeable difference in pain, in fact, I had more flares while taking it. Previously prescribed (May-June 2014) dose - 600mg TID...gained 15 pounds in 3 weeks...no noticeable difference-doc discontinued. Discussed all of this with PCP...she agreed there has been significant weight gain and suggested I use a rowing machine. SERIOUSLY??? The med is NOT effective, my issue is with my knee & foot - how exactly am I supposed to use a rowing machine?
Wellbutrin: Prescribed for smoking cessation so what difference does it make if I no longer take it? (I am doing well with my smoking cessation on or off this med)
Fosamax: Combined with the GI issues from D2, and projected bone density being slim, why continue? I also need dental treatment that carries detrimental effects while on fosamax. I unfortunately didn't realize this before starting (have taken 5 doses) and doc recommendation is to NOT take the med until after dental treatment.
D2: Constant heartburn/nausea. I have chewed copious amounts of tums to counteract the D2 to no avail. Have talked with doc and am taking D3 instead per doc recommendation.

Therapy: Both of my therapists seem knowledgeable of RSD, however, my issue with therapy is the physical pain. I can EITHER do PT exercises OR function beyond trips to the bathroom/back to the couch. This is limiting my progress. Therapy stated their concern is that without PM, there is limited progress and without the progress, more visits will not get approved. They suggested holding off the remaining visits until I am seen by PM and have some measure of relief. Due to the 6 weeks we have been attempting to FIND PM that accepts my insurance, let alone the appointment wait time, it would seem likely that were I to postpone my remaining visits, I won't be in therapy until Christmas. Unless I pay out of pocket for PM or visit medical marijuana.

LL...I so appreciate your point of view with this! My apologies for simply venting and not clarifying my decisions in earlier posts.

Similar Threads
Thread	Thread Starter	Forum	Replies	Last Post
I am sooo getting these..	cindi1965	Reflex Sympathetic Dystrophy (RSD and CRPS)	2	01-09-2011 08:46 PM
sooo many questions	draggin'	Myasthenia Gravis	5	01-15-2010 10:23 AM
Sooo frustrated...	Chazen18	Multiple Sclerosis	19	04-17-2009 06:56 PM
I'm sooo in the doghouse!!	Jodylee	The Stumble Inn	36	01-08-2009 09:21 PM
Sooo....	Sweet Sunshine	Weight Loss & Healthy Living	18	12-12-2006 01:26 PM

Site Navigation

NeuroTalk Online Support Groups

Sooo over this!

NeuroTalk Forums