Tag Archives: Veterans Affairs

Advocating For My Wounded Warrior (Part 3)

I’m sorry to have been away from my blog for so long. It’s been a very, VERY, busy year. Work has been kicking my butt and by the time I get home I really don’t want to do much. We’ve had some other things kicking our butts too, but that’s another story (click to read more). I’ve also taken on a new hobby that incorporates some “me time” along with my love to share smiles and helping veterans. I joined Pinups For Patriots! YAY! Go me! If you want to check out what I’m doing in the Pinup world, please like my Facebook Page.

</selfless plug>

Anyway, what I would like to talk about today is the fact that I haven’t stopped advocating for my husband when it comes to his pain and the VA. In fact that is also another part of my busy life. So, last year in October was his last civilian Botox treatment.  He was due for another one in late December, but you know how the Holidays always throw off everyone’s schedule. So we went to schedule it in January. For the past 3 years he has been having this done, every three months, all we’ve ever had to pay for was the doctor’s visit. The Botox was covered. Well, 2016 rolls around and not any more. We will have to pay $1000 every 3 months in order for him to get his Botox. We just couldn’t afford this.

So I asked him to ask his Primary Care at the VA to refer him to VA Neurology. He had that appointment on the 3rd of February. When we explained the conditions, he said, “No problem. I can refer you to the Pain Center for that.” We also brought up the fact he wanted to try Ketamine Infusions. And the doctor said he would include that in his referral and we could discuss it at the Pain Center.

A month goes by and we never heard anything. We logged into MyHealthEVet every so often to check for an appointment. Called the VA Pain Center and they said they never received a referral. He finally found out that on the 4th of February, a different doctor went through his records and saw that he was getting care outside the VA for Botox and revoked the referral.

Joy.

Ok, two months have gone by since the original Neurology appointment. He had his first visit with the VA Pain Center, his consult, on May 6th. May 6th! And even though he’s been there before he STILL had to go through his history. Oh and it’s all right there in his medical records! But they decided to start from scratch. He had to go through a “test” procedure with steroids and lidacaine, something that he’s gone through so many times before and it didn’t work. It was documented in his VA medical records that it didn’t work. Yet they wanted to do it again since “it’s a new procedure.” Um, no it’s not. TheHubs explained to the doctor the exact procedure he went through the last time he was there. It was the same procedure the doctor was explaining to him. But, let’s try it one more time. That happened on July 5th. And guess what?! It did nothing for him.

Ugh.

So we had to wait even longer to get that Botox injection. His next scheduled appointment was 3 October. This was when he was to have his Botox. Even though we brought his civilian doctor records of the last 3 years worth of injections, the VA only does half the dose at double the time. Oh this is so frustrating. During this appointment we also found out that the VA Pain Center is not trained to do most of the areas he has been getting Botox injected into, which happen to be his worst areas. So they are writing in his notes that he needs a referral to go to Neurology to do that. We also mentioned Ketamine Infusions. They said they have done a few of those in the past but he needs a referral for that as well. The nurse instructed us to contact his PCP to get that referral.

We sent a secured message to his PCP on the 4th. We get a reply on the 11th stating that Neurology is submitting a referral to the Choice Program (where he can see a civilian doctor). Of course we haven’t heard anything. I call up The Choice Progam and they don’t have an authorization letter for me to speak on his behalf, even though we’ve sent it in multiple times over the years. Apparently they are not the VA, but work with the VA. Ok. So I finally get to talk to them and they don’t have the referral yet and it usually takes at most 3 business days to get it.

We sent another secured message to his PCP and the nurse instructed us to contact the VA Neurology. VA Neurology knew nothing about a referral. They said his Primary needed to submit the referral to the Choice Program. Emailed his PCP back, and they said, no, Neurology needs to submit the referral.

Oye ve! Can we please stop this merry-go-round? I want off!

When we emailed the PCP back, the nurse said that she will “forward this to a specialist,” whatever that means.

So, I’m still fighting for my husband for him to get the care he deserves and hopefully some relief from all the pain. It breaks my heart to see him balled up in bed, ripping at his hair, squeezing the crap out of his neck, nearly in tears all because of the pain.

This was taken outside the VA Pain Center when he went in for his procedure…the first time. I just love it!

img_20160705_102314

LadyJai

Related Articles you may like:
Advocating for My Wounded Warrior (Part 2)
Advocating for My Wounded Warrior (Part 1) 
Our Story

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The Forgotten

My father served in Vietnam in the late 1960s. When he came home, he was spit on and called a baby killer. He was one of too many. Everyone hated him and everyone that put that uniform on. That was a horrible time for our military.

As our country engages more and more across the world, spreading our military might too thin, their overall support dwindles. I watched as everyone wore their American Pride well during the First Gulf war in 1989. But the political landscape capped that quite well – “It’s all about the oil.” Everyone listens to the media.

And then one horrible day that has spread across the world, 9/11 ripped through our lives, everyone’s lives. And our national pride soared once more. For a while, anyway. And then everyone started listening to the media again. The spun any part of “The War on Terror” as a waste of money, Bush’s War, the daily death count. I was confused when the new phrases came out – “Where’s the weapons of Mass destruction?” No one could think that a plane would be a weapon of mass destruction, or bio-weapons. All they cared about was seeing the nukes. Where were the nukes? Unfortunately, we gave them plenty of time to get those out of their country. And when we couldn’t produce a cache of weapons that the media wanted and the fact that we weren’t getting out of there any time soon, the phrase changed to,  “Support our troops, but not the war.” How can you support that which engages in the thing you don’t like? It was a complete conundrum for me that still leaves me scratching my head. Just ugh.

Why do we continue to hate on our military?

According to a report released in March 2016 by the National Center for Veterans Analysis and Statistics, the greatest number of Veterans still comes from the Vietnam Era, closely followed by  peacetime only Veterans and then The First Gulf War. Yet, everyone focuses their attention, and money, on those Post-911 veterans, which only account for 13% of the total number of Veterans in that census.

Thirteen.

And yet, they are the ones who receive the attention, the focus, the help. They are the ones that all the charities gear their marketing efforts towards. In 2014, there were 19.3 million veterans living in the US and PR. Of those 19.3 million veterans, only 3.8 million have been awarded a service connected disability. Other statistics include: 7 million served in Vietnam, 5.5 million served during the Gulf War era (representing service from August 1990 to present), and 2.5 million served in Iraq and Afghanistan.

Now, when I say that 2.5 million served in Iraq and Afghanistan, I’m sure that is an accurate number in the sense that there were 2.5 million people deployed to those areas. However, it is a well-known fact that of those 2.5 million people quite a lot have been on multiple deployments. So, in essence, there aren’t 2.5 million veterans of those two wars. The RAND Association explains it best –  in troop years, rather than number of deployed. At present, I have been unable to locate the exact number of Iraq and Iran Veterans. However, RAND is stating the strength of approximately 554,000 soldiers in December 2011. The VA is reporting that it has seen approximately 860,000 Iraq and Afghanistan veterans utilizing their Health System.

As the US Veteran population ages, the older generation numbers will dwindle. This is only natural. But with our continuing efforts in Iraq and Afghanistan, the number of veterans from these two areas will undoubtedly surpass the Vietnam era.

I am in no way trying to downplay the younger generation of veterans. By no means. What I am trying to point out is that Every Veteran Matters. 

And that’s how ALL these benefits/charities SHOULD be run. But they’re not.

I lived through my husband’s combat deployment. He experienced it. Still experiences it. Every. Horrible. Moment. And how many people remember Kosovo and their atrocities?

Only those who went there in the beginning.

So why is it that only the latest veterans, those post-911 combat veterans, are the only ones to get any benefits, any assistance, anything from anyone?

We are not ones to ask for assistance or help. We are those people who would offer up our help to others, no matter how bad off we were. But this last year has put us in a bind. With my medical insurance premiums and cost going up, the services and prescriptions covered going down, we’ve pretty much wiped out our savings. The VA hasn’t paid for any of the procedures he’s gone through since they stopped working back in 2012 or so. I can’t remember the last time he went. They don’t pay for any of his pain medications. So we are forced, now, to go seek civilian help.

He’s been going to a civilian neurologist since we moved to Florida and he’s been doing Botox injections in his neck and shoulders for his dystonia. For the past two years, all we had to pay for was the doctor visit for this procedure. Now, we have to pay for the Botox and the doctor visit. At $1000 every 3 months, that’s a no go. So he hasn’t had this since October of 2015. His pain is ever-increasing.

I did some digging and found out that now the VA Pain Center can do the Botox injections for him. I also want him to try ketamine infusions, as it’s helped a couple of people with their chronic pain that no pain medications have been able to touch.

In January 2016, I called for a VA neurology consultation so he could possibly be seen for both Botox injections and get a referral for the ketamine infusions. February 3, 2016 was his appointment and the VA neurologist evaluated him and said he’d refer him over to the VA Pain Center where they do the treatments. March rolls by and so does April. OK, we knew we’d have to wait, but I had him call and check anyway. Come to find out, February 4, 2016 another neurologist revoked his referral due to “having a civilian neurologist and received Botox there.”

Um, no! Just no!

So he had to fight to get that referral reinstated and he had his fist consult with the VA Pain Center in May 2016. Despite having previously been seen there, with quite a few procedures that eventually failed, and records to show for it, the evaluating “doctor” decides to “try” a procedure he had, that failed, twice, since he hadn’t been there in several years. He kept trying to say it was “new” when it really was the exact same procedure he’s had there before. We are convinced he was fishing to get TheHubs to say, “no, I don’t want to do that” just so the VA could deny him benefits because he refused a recommended treatment. But TheHubs suffered through this treatment in June 2016, which seems to have made his pain worse. They have scheduled his Botox injections for the end of October 2016 (a full year without Botox, so it’s like starting completely from scratch.) And to top it off, they can only inject HALF of what he was getting in the civilian world. HALF! How the heck is that even going to help when his full dose only took the edge off the pain!?

Not only do we have to deal with all his VA and civilian doctors, TheBoy had to have surgery on both his feet last year. Now he’s in braces, which we are still paying on. And, of course, my medical issues. And last month, our A/C died. At 95 degrees, in Florida, you don’t want your A/C to die. I had just emptied out our savings to pay off all the medical bills and then this happened. Everyone in my support groups were great, giving me places to apply for assistance, in the hopes that someone, somewhere could help me with the payment of a brand new A/C handler and compressor.

That’s when I found just how frustrated and forgotten TheHubs REALLY feels…

Out of about 35 organizations I tried, only 2 were open to all eras. But both of them were out of money. Everywhere else, you had to be a post-911 combat wounded veteran. I was crushed. All the charities I see out there, helping people with all kinds of needs and assistance, and we don’t qualify. Just like the VA Caregiver Program or any of the “automatic benefits” these veterans get without having to fight for their compensation Retreats, discounts, even a day at an amusement park (even *if* he could go with all those people) are not an option for him. Heck, even just a simple tool box for veterans, and we were denied.

Nope, we have to fight tooth and nail for everything he deserves. He has always called it “The Forgotten War.” I understood it. But now, I am seeing it as “The Forgotten Veterans,” too. It breaks my heart. And what about my dad? He had to wait 30 years before the government would even acknowledge the fact that they used Agent Orange. Luckily, now they have automatic diagnosis that fall into the Agent Orange category. But, really, any assistance that my mom might need, like the Caregiver Program, is lost to her as well.

I just can’t believe that we are a NATION OF NOW, a reactionary force to whatever happens to be in your face at the moment. And since the Iraq and Afghanistan wars are still ongoing, because the returning and broken veterans are so young and so plentiful, more people see them, see their wounds, and want to help…them.

I want to know where we can go for ALL era veterans. I want to know why we continue to discriminate and forget about those that came before. I want to know why we can’t recognize and help them too! This is only a small portion that adds to the 22 veterans a day that die by their own hands. I only hope I can keep his hope from fading!

LadyJai

 

 

Related Articles you may like:

Our Story

VA Appeal Update

VA Appeal Update #2

VA Appeal Update #3

VA Appeal Update #4

VA Appeal Update #5
VA Appeal Update #6

VA Appeal Update #6

I contacted the VA Under Secretary, in hopes to either speed up the process or at the very least, let them know about the gobbledygook woman that did his C&P.

Again, they just “passed the buck” on the whole thing. We did get an “update,” if you want to call it that.

Here’s what we got:

STATUS OF APPEAL:  Your husband’s appeal began in July 2011 when VA received his Notice of Disagreement.

BVA VIDEOCONFERENCE HEARING:  On 07-24-14, a videoconference hearing with the Board of Veterans’ Appeals (BVA) was requested. The next step in the appeals process will be the scheduling of that hearing. Your husband will be notified in writing of the date and time of the hearing.

 A hearing is not required. The wait for a BVA videoconference hearing can be long as there are limited slots available. The St. Petersburg, FL Regional Office – which is where the hearing will be held – received many requests for BVA videoconference hearings prior to your husband’s July 2014 request. Those requests are filled based on date order.

 If your husband decides to withdraw his request for the hearing, the appeal would then go directly to BVA for their review. (provided no additional evidence has been submitted requiring Regional Office action) Please know that he is entitled to a hearing – it is his choice whether to have the hearing. If he decides to withdraw the hearing request, that written, dated, signed statement should be submitted via:

·         fax to VA’s Evidence Intake Center at (844) 531-7818
·         or mail to Evidence Intake Center at –
Department Of Veterans Affairs
Evidence Intake Center
PO Box 4444
Newnan, GA 30271-0020

APPEALS BACKLOG:  The appeals backlog is large. Regional Offices and the BVA are working those appeals based on the date they were received. I apologize for the long wait which I know can be frustrating. The Under Secretary has repeatedly requested additional resources from Congress to help VA work appeals more quickly.

EXPEDITING AN APPEAL:  However, please know that an appeal may be expedited for a veteran who is terminally ill, homeless or otherwise experiencing very serious hardship. If your husband is in one of those categories, he may request that his appeal be expedited based on such circumstances. To do so, submit that request in writing with documentation of the hardship to the VA regional office in St. Petersburg, FL. Documentation of severe financial hardship could include such things as copies of bankruptcy proceedings, eviction notice, past due bills, utility shut-off notices, etc. Submit the request and the supporting documentation via:

·         fax to VA’s Evidence Intake Center at (844) 531-7818
·         or mail to Evidence Intake Center at –
Department Of Veterans Affairs
Evidence Intake Center
PO Box 4444
Newnan, GA 30271-0020

 If your husband does not fall into one of the above categories, then his appeal will continue to be worked in date order. That means it may be a few months to many months to even more than a year before the next step in the appeal, which is the scheduling of the BVA videoconference hearing. Again, I apologize for the long wait – but I want to give you a realistic timeframe.

 CHECK STATUS OF APPEAL:  To check on the status of the appeal, please call 1 (800) 827-1000. Your husband’s representative, Disabled American Veterans, can also provide updates and assistance.

I hope that this information is helpful to you and your husband. As noted above, the next step in the appeals process will be the scheduling of the BVA videoconference hearing. Your husband will be notified in writing of the date and time of the hearing.

This waiting is expected. I grew up in the military. Everything was hurry up and wait. But this is absolutely ridiculous.

Let the “more waiting” ensue.

LadyJai

 

 

Related Articles you may like:

Our Story
VA Appeal Update
VA Appeal Update #2
VA Appeal Update #3
VA Appeal Update #4
VA Appeal Update #5

Advocating For My Wounded Warrior (Part 2)

We recently completed our annual eye exam. (You can read more about that here.)

We had to spend about $600 on TheHub’s glasses. His eyesight is increasingly bad. Every year he needs a new prescription. And glasses aren’t cheap. And since he’s become photosensitive, we decided to get him a pair of prescription sunglasses. So that tacked on to the price tag. Luckily, we used his old frames for that. I was hoping that would help him get out of the house more. But they aren’t as dark as we were hoping, nor are they as strong as he needs.

So, I’ve been trying to think of something he can do so he’s not stuck in the house all the time, something he can be passionate about again. And I posted the dilemma I have to one of my caregiver groups I’m in. I was blessed to have found it because the lady who runs it, her husband also suffers from migraines. She pointed me to the VA for their VIST program (Visual Impairment Support Team. Her husband goes through them and they have given him two pair of special glasses, one for inside and one for out.

During my research on this, I found that in our location it is called the VICTORS (Visual Impairment Center to Optimize Remaining Sight). I called them yesterday morning and they said they don’t normally see migraine patients, but they put in a referral for TheHubs to be evaluated by this program.

He now has an appointment for the end of September. I do hope this works for him, better than what we can get on the civilian market with our limited pocket-money. And allows him to get out of the house better, and more often.

Wish us luck.

LadyJai

Related Articles you may like:
VA Appeal Update #5
VA Appeal Update #4
VA Appeal Update #3
Our Story

 

VA Appeal Update #5

I’ve been trying, for two months now, to find the contact information for Secretary Bob McDonald. I’ve had one person offer help with our claim because she had his “cell phone number” and would “gladly help so no one had to go through what they had to deal with.” Yeah, after 3 attempts to contact her different ways with no response, I’ve given up on her.

I sent the second letter to Rep. Ted Yoho on 6 February 2015 and haven’t heard anything back.

On 3/4/2015 I tried sending a letter to the House Committee on Veterans’ Affairs and when I hit the submit button it returns a 404 PAGE NOT FOUND error. I also sent that same letter to the Senate Committee on Veterans’ Affairs and when I hit the submit button on their contact form, I receive “Access Denied.”

Yeah, I’m beginning to think there’s a conspiracy to cover up anything dealing with the VA. So much for their “TRANSPARENCY.” UGH.

Sent them both a tweet about it. No response.

Went to the Senate’s Facebook page but the option to post on their page has been disabled.

Went to the House’s Facebook page and asked about the 404 error there, and tagged the Senate’s account. Now we wait to see if they respond.

Yes, I’m getting very, VERY frustrated.

I went home that night and posted this in my caregiver support forum:

Today was a complete waste of time and effort. So many things I WANT to do but I spent most of it lost in google and government red tape. Someone in another offered to help with our claim issues and never followed through. I also haven’t heard back from my Representative I wrote to a month ago. So I decided to see if I could look up Secretary McDonald’s contact info. No luck there either. Then, I went to the House AND Senate Veterans’ Committees and their contact us form. One gave me a 404 Not Found error. The other, Access Denied. I thought maybe it was just the browser, so I tried another. Nope. Me thinks there is a conspiracy! I tweeted both of them. No response yet. I went to their Facebook pages. The Senate Committee page doesn’t allow posts from followers. But the House one does. I commented about their web page issue and tagged the Senate in that same post. No response yet. So frustrated. I guess we are supposed to be patient and wait, even though we’ve been doing that since 2003. I guess we aren’t meant to be lucky like everyone else. I guess pain and suffering in more ways than just what he’s going through is our lot in life. I should accept this. But I’m not going to stop. I will continue to try to get my heart hurt because that’s what I have to do. If I don’t do it. He will give up. It just reminds me of the story of Job in the bible. There’s always hope. Right?

I received an offer to help from one of the admins who was “connected.” Four emails later, and started feeling a bit better.

But that didn’t last.

I’ve sent the letters to Senator Ted Yoho, the House & Senate Committee several more times since February. I have heard nothing. What else can I do to get this going? I know I’m supposed to “Hurry Up And Wait.” That’s been the military motto my father drilled into my head since I was a baby. You’d think I would understand this by now. Logically knowing this is so very different from actually practicing this.

A few days ago, we did receive a letter from our Regional Office stating:

We have certified your appeal to the Board of Veterans’ Appeals and are transferring your VA records to the Board in Washington, D.C. The Board will notify you when it has received your records.

More Hurry Up And Wait. Let’s see, here’s a brief rundown of our latest claim with the VA:

  • 7/22/2009 – Claim Received
  • 7/29/2010 – Claim Considered
  • 8/2/2010 – Notice of Decision
  • 7/14/2011 – Notice of Disagreement
  • 10/2/2012 – Personal Hearing at the VA Regional Office
  • 1/29/2014 – VA C&P Exam
  • 7/14/2014 – De Novo Review election Received from Appellant
  • 6/22/2015 – Certified the appeal and sending records to the Board of Appeals in DC.

You can see how frustrating waiting can be!

In the mean time, I continue to advocate for him, anyway I can. But I’m running out. If anyone has any more ideas I can try, I am open and willing to listen. Please send them my way. I have finally found Secretary Bob McDonald’s phone number, which I will leave here for anyone else; but I think I might be too chicken to call him. I wouldn’t even know what to say. I write better than I speak.

http://static.c-span.org/assets/swf/CSPANPlayer.1434395986.swf?clipid=4507948

LadyJai

 

 

Related Articles you may like:

Our Story
VA Appeal Update
VA Appeal Update #2
VA Appeal Update #3
VA Appeal Update #4

Advocating For My Wounded Warrior (Part 1)

So, yesterday was a day of HOPE. Today, not so much. But I’m still advocating!

I’ve been following a the use of magnetic stimulation for migraines since 2008. eNeura, Inc. has the first FDA approved personal magnetic device for use with migraine patients. In 2013, the FDA approved its marketing. I attempted to contact the company then to see about getting my husband into a study or find out any more information. However, no one ever returned my email. Their site was basic and they only had a contact for press relations. I tried anyway.

We know from first hand experience that magnetism WORKS to relieve his migraines. When he was still in the Army, and the migraines weren’t as often, nor as bad, he would keep a neodymium magnet inside his cap and it would help. When they went to the berets, though, there was no place to keep it secured and hidden. So he went without. Every time he’s ever had an MRI he’s had a very bad migraine. This is not unusual, even, since he gets them at least 4 times a week. Every time he’s gone into the MRI machine, he falls asleep almost instantly, and then wakes up with NO MIGRAINE. So we know magnetic therapy works. But there’s no way we could get our own personal MRI machine. Plus, it would be incredibly expensive to run the thing. *shudders*

Yesterday, I went looking at it once again. This time, there was more information about the device and more contacts I could pose more questions to. I again sent a letter explaining my husband’s 15 year migraine history and asking about the device, how much it costs, and how we could get it.  This time, they responded quickly, but with rather disappointing words.

Dear Jamie –
Thank you for your inquiry regarding eNeura’s SpringTMS migraine treatment device. We are pleased to announce ours is the first clinically proven, non-invasive device cleared by the US Food and Drug Administration to relieve pain caused by migraine headaches that are preceded by an aura. The company has also received European CE mark for its SpringTMS device for the treatment of acute migraine and is currently marketing the device in the United Kingdom.
The initial U.S. availability of SpringTMS will be through a post market open-label study with leading headache specialists at a number of headache centers around the U.S. The headache centers participating in the post market open-label study are located in Arizona, California, New York, Ohio and Pennsylvania.
Please email Customer Care to request contact information for the site nearest you, or click on this link for a complete list of the sites currently recruiting for the study: https://clinicaltrials.gov/ct2/show/NCT02357381 . This link will also provide you with the list of inclusion and exclusion criteria for the study. If you husband does not meet the criteria, please still contact the study site nearest you. Some of the sites are also prescribing the device to private-pay patients who do not meet the study criteria but may benefit from sTMS (Cleveland Clinic, Mayo Clinic and Jefferson Headache Center).
The SpringTMS is rented for $750 for a three-month prescription, and we do not have a discount program in place at this time. If your husband is prescribed the device, the prescribing clinician will provide a treatment plan that is appropriate for him.
Best regards,
eNeura Inc.
Sr. Director of Customer Care

Seven hundred fifty dollars EVERY. THREE. MONTHS! Oh man oh man oh man. And this isn’t even something that insurance will probably pay for right away, I’m sure! Let alone the VA.

Speaking of the VA.

This got me thinking and doing a little more research. I found out that the VA has a research and development team within their organization. So I thought I’d contact them. With the eNeura device still in studies, I thought maybe the VA would consider this. I know there are more veterans out their who suffer migraines than just my husband. And I wonder how many of them are in the same situation where nothing has worked for them to relieve the pain and severity and the number of them. TheHubs has exhausted the VA Pain Center’s capability to help him. Last year was his last appointment with them and they pretty much told him that they can no longer help him.

I am hoping beyond hope they will consider getting into the study and offer it up to my husband. But this is the VA we are talking about. I don’t know what else to do, where else to go for help. Their “Contact Us” form is generic and done by a 3rd party (UGH) rather than contacting R&D directly. And now I wait.

Please pray.

LadyJai

Related Articles you may like:
VA Appeal Update #4
VA Appeal Update #3
Our Story

 

VA Appeal Update #4

I guess it’s about time to update you on our VA Claim/Appeal process. Last time I wrote about the VA Scandal and where it got us. I was so excited to see that Washington actually took our story and made movement on it. My veteran was getting all kinds of calls for a week or so and each time they told him that they couldn’t do anything until such-and-such department made their decision.

Well, I guess that department made their decision because we got a letter from the Director of the C&P office. Here’s what they said:

We received your letter regarding your Compensation and Pension (C&P) exam
with <EXAM DOCTOR>. <CHIEF OF C&P DOCTOR>, Chief of C&P, reviewed the letter
received, the C&P exam notes from <EXAM DOCTOR>, and met with the examiner to get their
input.
<EXAM DOCTOR>’s professional opinion is based on objective evidence and a
thorough review of available resources, to include: service treatment records,
electronic medical records, Disability Benefits Questionnaires (DBQs), and Veteran’s
statements. The diagnosis was reached through a forensic disability psychological
exam. This is standard practice across all Compensation & Pension services within
VHA.  reviewed the examination notes and supports ‘s
rationale behind her professional opinion. <CHIEF OF C&P DOCTOR> mentioned that during his call
with you on December 3, 2014, your concerns were discussed and you indicated you
were currently going through the appeals process with VBA.
We apologize for any misunderstanding that may have been caused.

If you have been following our Appeal Updates, you might remember that the C&P examiner only saw my veteran for no more than ten minutes and rushed him out, saying his memory is fine if he can remember all the meds he takes every day for the last 7 years and that his nightmares are nothing more than “gobbledygook”. How is gobbledygook “objective evidence?” 

Why do they continue to only focused on the PTSD portion of his claim? He’s been told he missed the PTSD qualifications by 2 points. Ok, fine. He doesn’t qualify for PTSD. BUT, the VA found, during that C&P exam that there is evidence of depression and mood disorder and his VSO clearly defined the precedence in his NOTICE OF DISAGREEMENT SUBMITTED ON 7/8/2011.

July 8th, 2011!

That was 2 and a half YEARS ago! And they STILL ignore it.

I also applied for the VA Caregiver Support Program in May of last year. Some caregivers told me it took them a month, while others told me it took them a year. I’ve given it a while now, somewhere in the middle, and decided to check up on my request. After many calls to many different people, we found that the national office had attached it to my file but never emailed the Caregiver Support Coordinator. When she found it, she apologized profusely and said she’d do what she can to get this pushed through as fast as she could. A few days later, we had our eligibility appointment. I just received a call from the VA Caregiver Support Coordinator telling me that we qualify based on his mental health. However, there is no record that it’s service connected. I proceeded to explain to her that it’s still in the claims/appeals process that we’ve been fighting for years over. She informed me that if/when we receive that service connection, to contact her and she will get this pushed through again.

This is just our luck. What a kick in the teeth.

So now the scramble again, to get this ball rolling. I’ve contacted Rep. Ted Yoho again with a second letter. We’ll see how that goes. And TheHubs is trying to contact his VSO about this. Since he’s always so busy, he had to leave a message.

And the waiting game continues.

LadyJai