I started this post in Oct. and have thought about it several times in the past 4 months but haven't had the heart to finish it. I apologize in advance if it turns into a novel.
I think it's time for a health update on Scott. So many of you have asked the same questions over and over but I have been reluctant to post many Lyme updates on our blog. Actually, I am pretty reluctant to include Scott in most of my posts. There are several reasons for this. I think my main reservation is the misconception that follows a diagnosis of Lyme Disease. If you do not have a sick friend or family member, there is no way you can understand this disease. Googling LD does not make you an expert. It was easier for Scott when his paperwork said, "M.S." because people have actually heard of and know someone with that disease. Once that diagnosis changed, people's perception changed as well.
Scott's health struggle started back in 1997 during his previous marriage. He was bitten by something (tick, spider, who knows) followed by the onset of various neurological symptoms. He recalls Bells Palsy, vertigo, extreme pain and other issues. His health went up and down while he sought answers, visited numerous neurologists, endured spinal taps, MRI's and other tests all ending in an eventual diagnosis of MS. He was too sick to work several times during his last marriage and after months of unbearable medication/side effects his disease seemed to go into remission.
Fast forward to 2004 and Scott was feeling pretty good with minimal symptoms and a less stressful home environment. He still suffered from extreme pain but overall felt better than he had in years. During the summer of 2005 Scott made a decision to go commercial salmon fishing to try and get us caught up on bills. We knew it would be tough on his body but he was determined to make a dent in our debt and push thru the pain. He left mid May and fished for 2.5 months and came home a week early due to a severe injury. We have since learned that commercial fishing has a 100% injury rate...everyone gets hurt at one time or another and his time came and he almost had his arm ripped off.
Scott cooked and worked with the nets while fishing in 2005.
While he had been in Alaska Scott had proposed and although I was freaked that he had been hurt, I was ECSTATIC that he was coming home to me a week early!! He came home the last week in July and we got married less than 2 weeks la
ter! We had been apart for 3 long months and since our pastor didn't get back home until Monday, Aug. 8th, we decided that Tuesday night sounded good! :)
ter! We had been apart for 3 long months and since our pastor didn't get back home until Monday, Aug. 8th, we decided that Tuesday night sounded good! :)This is how Scott looked when I picked him up from the airport. Tan and hairy! He definitely looked like a fisherman! I was the HAPPIEST girl in the world!
My mom took us on a wonderful family vacation in september and when we got back home we quickly fell into our old routine of work, work, work. In December, Scott started having neurological issues again and began dropping things. When he worked at the coffeehouse he would drop plates, cups and a pitcher full of milk. His weakness increased on the right side of his body and the pain returned. From the day he returned from Alaska his health steadily declined until we were sitting in the doctors office in March of 06, discussing Lyme Disease. We went to several doctors, neurologists and had tests, tests and more tests done...the same thing he had pursued during 1997-2002. As his symptoms got worse, he worked less and less and we started antibiotics to kill Lyme. We had no idea how tricky Lyme was at the time and were so relieved that it wasn't really MS. Ha. Little did we know....it would be the biggest fight of his life.
In March of 07, it was recommended that Scott apply for disability because his symptoms continued to get worse and worse. He began spending days at a time in bed and couldn't function many days without help due to the pain and brain fog. We found new doctors, ran more tests and after he lost feeling in his legs we pursued a more aggressive treatment. In Oct. of 2007 we found an amazing dr. here in KC and by Dec. of 07 he had started 2 a day IV treatments. He has been in IV treatments for the past 25 months and we don't have an end date yet. When we filed for disability, we were told that we would be turned down several times before we got our approval and they were right. He was denied 3 or 4 times and each time we appealed. During each waiting period, we continued to get more tests run and each month brought a more complete understanding of what was happening in Scott's body. We decided it would be best to hire a disability rep and we found one in July of 2007.
We made appeals to ODAR and I worked overtime pulling together all of the relevant medical files and our rep. continued to tell us over and over that we would know any week...we of course had no idea how SLOW the SS office was and we passed this same info on to everyone we knew. So, if you have managed to read this far...you may be wondering if I am ever going to get to WHY I was/am reluctant to put Scott on our blog....this is why... In may of 2008, Scott had been in treatment for 6 months and was on the verge of organ failure. His liver was failing, his body was flooded with Ammonia and he felt like he was dieing. We had struggled with his child support from day one and although he tried to get it righted and based on his actual income, he couldn't afford the legal counsel to get this done. It was a long and hard battle for him and when we filed for disability we hoped that this would help him pay cs until he could recover...but the timing never worked out. Scott hadn't spent as much time with the kids because he was so sick and he was really missing them and feeling like a bad dad. We decided to go to 2 field trips with the boys. One afternoon I drove him to the zoo and pushed him around in a wheelchair for 2 hours and the other afternoon we went to a museum where I again pushed him around in a wheelchair for 2 hours. It was painful for him but it was important that he got to see the boys and the boys loved it.
Two weeks later Scott had a court date for CS that he was too sick to attend. He of course was in treatment 6 hours a day still, so I went in his place. We had just filed another off the record appeal with ODAR and were told we would get our answer in 2-4 weeks. We were hopeful that disability would be taken care of soon and we wouldn't have to keep defending his illness and treatment to people who only cared about money. While we were in court, the opposing lawyer stated that Scott wasn't sick because he had just gone to two field trips and spent all day at the zoo and the museum. I was shocked! I hadn't mentioned it to our lawyer because 1. it wasn't an all day event 2. it didn't seem relevant 3. i PUSHED him in a wheelchair because he couldn't walk and 4. Just because you are disabled doesn't mean you can't leave the house! The judge looked at us, I explained the situations quickly to our lawyer and she set the record straight. Yes, he had gone to the zoo but I had pushed him in a wheelchair and he could only handle 2 hours. Yes we went to the museum but I pushed him in a wheelchair and it was also just 2 hours...not all day. I realize that lawyers like to embellish facts but the other side chose to use these 2 events to try and prove that Scott was not sick and that he should be able to get a job. They were not happy that we were asking for Scott's cs to be suspended until we got his disability decision. Thankfully, the judge did not fall for the ugliness and she stayed all activity until a disability decision came thru...
So, because of that one little event, I have been reluctant to post anything about Scott. Yes, sometimes Scott has good moments where his symptoms are manageable and he can participate in our family activities but that is just a snapshot of his day. I am also reluctant to post about many of his bad days/moments because that same summer we were threatened that if Scott was so sick he shouldn't have regular access to his kids. So really, we were screwed either way. Either Scott had a good moment he could share with his kids, and then be accused of not being sick, or he would have bad moments that fueled the fire and caused threats...it was such a stressful mess and I am thankful that our marriage and Scott's body survived the poison...
Whew! Did you manage to read this far? It did indeed turn into a novel and I'm not even done yet!!
So, in our fight for disability our time line looks like this...
• January 2006- Scott is no longer able to work.
• March 2006- Scott was diagnosed with Lyme Disease instead of MS
• March 2007- We filed for disability.
• July 2007- Hired a disability rep.
• July 2007- Off The Record request thru ODAR.
• September 2007- 2nd Off The Record request thru ODAR.
• October 2007- Found a local LD doctor.
• December 2007- Started 2 a day IV treatments.
• June(ish) 2008- 3rd Off The Record request thru ODAR.
• July 2008- Got our KS rep involved in our disability case.
• October 2008- Fired worthless disability rep and hired a new one from KC.
• December 2008- Scott's 1 year anniversary at the IV clinic
• May 2009- We received a letter from SS saying we finally had a hearing for July 9th.
• July 2009- 1st disability hearing. The judge decided she needed more info. on LD so she set up another hearing for August. 19th.
• August 2009- 2nd disability hearing with a medical expert and a vocational expert. We are told that we will have a decision within 6-8 weeks.
• October 2009- We get a letter saying another hearing has been set and will be the day before Thanksgiving. The next week we got a call from our lawyer saying the judge had called her and said we didn't need another hearing because she had made her decision. We are told it would take 4 weeks to get the decision.
• November 2009- We called our lawyer and were told that our decision had to be sent to a Decision Writer who would write up the judge's decision and it should be sent any day.
• December 2009- We called our lawyer again, right before Christmas and they in turn called ODAR. ODAR said that they would try and mail our decision before Christmas...
• January 5, 2010- Our letter was started.....
• January 14, 2010- Our letter arrived in the mail and Scott was too nervous to open the letter so he had me do it. From this point we had been waiting for this decision for 2 months shy of 3 years but it has been 4 years since he was able to work. The letter is 16 pages long and discusses everything....but the most important part is that the judge gave us a partially favorable decision. It is partially favorable because instead of back dating the disability to the date we filed, she made it retroactive to Oct. of 2007 when we had more lab tests and evidence of the illness.
That brings us to today, Jan. 28th. We called the SS office the week we got our letter and were told that it will take 6-8 weeks for the decision to be entered and before we would get our first monthly check...so all in all it WILL BE 3 full years! HOLY COW! No wonder families end up losing everything during the process! Kansas is one of the worst states when it comes to pushing along disability cases and the average backlog is 15,000! It took 5 months for our decision to be written up, submitted and sent to us. THAT IS BEYOND RIDICULOUS!!! We have also heard that it will take about 6 months for our backpay to be released so we are anxiously awaiting that check...where we can finally pay off the debt we have been unable to pay off for the past 3 years.
So, all of that to say that now that we have finally been approved for disability, I am considering adding more posts about Scott. He feels vindicated and justified with his new title and knows it is one step closer to getting back to zero. He no longer needs to defend his illness to those who don't believe him because the State of Kansas has agreed with him and approved his benefits. He no longer feels the need to prove to them that yes, even with good moments, he is still disabled. To celebrate this GIGANTIC victory, we made him a red velvet cake with an apricot sour cream frosting. The boys lit the sparkler candles and we sang, "Happy Disability To You, Happy Disability To You, Happy Disability Dear Daddy, Happy Disability To You!" It was a sweet little moment in a long battle for Health, Disability and Credibility...






























