Showing posts with label meds. Show all posts
Showing posts with label meds. Show all posts

Wednesday, November 6, 2013

Crazy Nightmare Week

I have had the absolute WORST week.

First, let's talk medication. Princess was just about out of the beta-blocker she's on. So I called in the refill on Friday. They said it wouldn't be ready until after 1pm on Monday. Okay, so I wasn't entirely sure we would make it all the way to Monday as she gets this medication 3 times a day, but I figured we would be close because the last time it was filled was on the 4th and it would be ready on the 4th. I usually have at least two or three doses beyond a month in the bottle. Okay, so no big deal. We get to Monday fine. I go down to pick up her prescription and they ask for a new insurance card. I haven't received it because it JUST went into effect on Friday. So I have to pay for her prescription. Thankfully this is the only one and it's not TOO expensive. They told me that once I get a new card, to just bring it in and they'll reimburse me. Okay, God will take care of this.

I had about 4 cans of formula left. I was going to call on Monday to place my new order. On Thursday, the provider had called me for a recent length and weight because they needed a new authorization. So I wasn't too worried. Until we went out to town on Saturday. When we got home, we found ONE can of formula on the floor. The other three cans had been taken outside by the dogs! Two of the cans were destroyed and one had teeth marks in it. Now, here's the thing with her formula, WIC does NOT cover it. It has to be done by prescription, otherwise it costs $45 a can! The cans are only 14.5 ounces too, so they aren't big. There is no place to get it locally, so we have to get it delivered. So I called on Monday to order a new shipment. They said it could take 3-5 BUSINESS days. Oh great! So that means I MAY not have enough formula to last until it gets here. Thankfully I was able to stop by the cardiologist's office and pick up a can. Hopefully we'll make it to our shipment date. God's going to take care of us.

Oh, and welfare/food stamps has been stupid too! I called on Monday to see where I was at in the process. Tuesday, my worker called me back to say that her supervisor had kicked it back to her because there were these 3 deposits on the one account. So I explained it to her that those were from my (ex)-hubby and his job, but he had since quit depositing those checks into that account, which is a joint account. So I had to DRIVE down there and write an affidavit to that effect. So hopefully it's going to go through here really soon, as I have no money to pay anything!

Then today, oh today. I just want to crawl back into bed. So we are now 2 hours away from the nephrologist. Being this appointment was set up at 9:20 in the morning, we have to leave before 7am, just in case we run into traffic. Thankfully, not very much traffic at all! We get there, get coffee and then head over to their office. That's when the nightmare begins.

See, we're in California. We have a specialized medicaid program called Medi-Cal. Well, Medi-Cal JUST changed on Friday to "managed Medi-Cal." Essentially, they are partnering with bigger insurance companies. I think it's to cut down the cost, but whatever the reason, it has been nothing but a huge headache for me!

First of all, I had to choose what insurance I wanted. I was advised by the cardiologist to pick Anthem Blue Cross. Okay, so that's what I picked. Well, like I said earlier, I haven't received a card yet, that's why I had to pay for the prescription. So today, I find out that they want a pre-authorization for the nephrologist visit! WHAT? We've had this appointment on the books for 3 months now! And on top of that, THEY picked our primary care physician. So I got information from the receptionist and I called them. I go the PCP changed so I'll actually be getting 2 cards here soon. So then I went on to tell them the problem of us being at the nephrologist's office and them saying they can't see her. Well, while I'm on hold with Blue Cross, we get called back for essentially a consult. See, since Princess was diagnosed with PHA2, the ONLY ONE who can answer any questions I have is the nephrologist. PHA2 is a kidney disorder. So I get back there and while I'm waiting and feeding Princess, Blue Cross calls me back. They tell me they'll cover the visit today, but when I poke my head out the door, I can't find anyone! (Isn't that always the case!) I let them know our situation with the prescription and the Synagis shots and the whole thing. They were VERY understanding and said they would take care of everything! So, I may end up getting a bill for this visit, but I have already talked to Blue Cross and they said they would cover it, so I'm not worried about it. God will take care of the faithful.

As frustrating as this whole thing has been, we're doing okay. I found out what I can feed Princess. I found out what to do if she gets really sick. We got a decent blood pressure. We did labs. I called the pediatrician and got them going with new referrals/pre-authorizations for both the nephrologist and the cardiologist. I spoke to the cardiologist's nurse and she said that they are having just as many problems with it, but that since Princess also has CCS, we should be fine for next week's visit. So I'm just trying to decompress after all this chaos! As if things weren't going crazy enough as is! One of these days we'll be okay and things will be normal, or as normal as they can be.


Tuesday, October 8, 2013

Medicating My Child

Earlier this month, I posted my Medication Woes. Well, now that we have transitioned to our new pharmacy, I think things will be easier. I love our new pharmacy. For one, they are ONLY a pharmacy and not one of these chain drug stores. So what does this mean? They actually have precise dose syringes! These are the same ones the hospitals use.


When, Princess was first put on medication and we left the hospital, they sent me home with two of these one milliliter syringes. Well, they only last so long before all the markings start wearing off. When I had picked up her medication for the first time, the pharmacist at the drug store only had a 5ml syringe and that wasn't going to be accurate enough for dosing Princess. At one point, (ex)-Hubby brought home these 1ml syringes from the drug store he works for. I hated them. They felt like they had no pressure to them, so I couldn't tell if I was drawing anything into it. So I got some 1ml syringes from Dr. K's office. The only problem with them is that they weren't "for oral use." I worked with what I had.

When Princess was placed on the diuretic for her PHA2, we had to change pharmacies to the same store that (ex)-Hubby works for. I had to renew her prescription every 14 days because it had to compounded and it would fall out of suspension. The last time I filled it there, they put one of these little toppers in it that is made for hospital-grade syringes. The only syringe I had that fit it was either the last one I had left over from the hospital or a 3ml syringe that wouldn't have given me an accurate dosage that the pharmacy had given me.

Before the next refill, we moved up to my mom's and I had to find a compounding pharmacy. The one recommended to me was a pharmacy that was ONLY a pharmacy. Like the previous pharmacy, they put one of those little toppers in, but they had 1ml syringes!


I love our new pharmacy. I don't have to refill the diuretic every 14 days. It's been 3 weeks already and we're still going strong! I hope things get worked out with the doctor's office so that when it gets called in, it's there and I don't have to call around to make sure it's taken care of.

Thursday, October 3, 2013

Medication woes

Sometimes I feel like all I do is call doctor's offices.  And lately it's been about Princess's medication. She's on two of them currently. One is just a beta-blocker for her high blood pressure. The other is a diuretic that will help with the high potassium AND the high blood pressure. Our current plan of attack is to let her outgrow the current dosage of the beta-blocker and then keep her just on the diuretic. Okay, no big deal, right? Well, it just seems like every time I need a refill I end up call the doc's office.

The past two refills for the diuretic have required me to call the doc's office at least once. It seems that it never gets to the pharmacy's computer. Then there's the beta-blocker. I don't have anymore refills on it and am literally almost out. So I took it in to the pharmacy because I wanted to transfer it anyway if we were going to stay on it. They e-faxed on Tuesday. They then resent the e-fax today. I spoke to the gals there and they said I should call the doc's office. So I did. They said they hadn't received anything! But they were going to send it to the pharmacy.

I don't get it. Why is it not getting to the pharmacy or vice versa? Is this the world conspiring against me? Or maybe just everyone's programs aren't compatible with everyone else's? I know, depending on who I asked right now, someone would probably try to blame Obama-Care. I don't really care what the problem is, I just want it fixed so that I don't have to go through this EVERY time I need a prescription refilled.
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