Thank you Mark Storrey and April Scott for such a wonderful visit and showing me your wonderful place and introducing me to the crew at Haven Humane Society. I look forward to working with you guys in the future to making you Best of the North State in adopting animals. I know handsome Brad Pitt will be adopted before I get a chance to see him again. I really love the way you are working so hard to be a no kill shelter. Great things our happening.
Good things are happening at Haven Humane Society thanks to our dedicated sponsors, donors, supporters, volunteers, and staff. In 2016 we set a new record by achieving a 92% live release rate for dogs and have placed thousands of pets into loving, forever homes through adoption, rescue, and foster care. All of these activities help us move closer to our goal of becoming No Kill by 2021, but we cannot achieve this alone.
We cherish partnerships with local businesses and would like to offer you the opportunity to support shelter animals by becoming a sponsor at one or more of our 2018 events. Your financial support will help us fund our daily operations, establish a new kitten nursery, and fund a variety of programs that reach thousands of at-risk pets each year and move us closer to our ultimate goal of a North State with no more homeless pets!
For those of you who were not sure exactly what our department team does on a weekly basis we have many tasks. The Development team is responsible for reaching out and partnering with business owners and community members on behalf of the homeless animals in the North State in order to raise money and bring awareness. We offer and manage a variety of sponsorship marketing opportunities, fundraisers, support programs and creating new financial avenues within the community to help place animals into their loving, forever homes.
As the new Director of Development I am extremely excited about all of our upcoming events for 2018!
We are always in need of business sponsors for these wonderful events which we provide several marketing benefits in return. Including Media – TV, Radio and Print. Social Media, Signage at all of our events and of course incredible PPI! (Pawsitive Public Image). If you own a business and are considering becoming a sponsor or have questions about sponsoring a specific event please call our Development Department at: 530-241-5262 or Email us at: firstname.lastname@example.org
Starting in February we have our annual Haven Humane Society Open House. This is a free family and community friendly event that takes place on Saturday, February 24th-2018 (10am to 12pm) We will have refreshments and tours of the facility provided by our CEO, Mark Storrey. There will also be adoption specials when you adopt a dog or cat into your loving home during the event.
On March 24th, 2018 at Turtle Bay we have our Certified 5k and 10k dog-friendly race, Doggie Dash. Doggie Dash will take place on Saturday, March 24th at Turtle Bay and is fun for the entire family! We expect approximately 300 participants this year and man Zumba Bash 2018! Need we say more? This is a fun, high energy, evening event at Win River Casino Events Center! Dancing, drinks, door prizes, raffle prizes and of course an amazing Zumba Instructor, Jennifer Lozoya! Don’t forget to purchase your tickets in advance and join the party on August 11th 2018!
Our biggest and most exciting event of the year is our 11th Annual Bark Wine and Brew Gala. This elegant evening event features wine and beer tasting, a four course dinner, silent and live auctions, Viva la photo, Dj, dancing, champagne and more. This amazing evening will take place on Saturday, October 6th, 2018 at the Win River Events Center. Tickets sold out early last year so be sure to get yours in advance!
North State Giving Tuesday takes place the Tuesday after Thanksgiving weekend. This national day of giving is an online networking and giving the event that provides nonprofit organizations the opportunity to gain exposure and start relationships with new donors, and for the people in Shasta and Siskiyou counties to come together to raise as much money as possible for participating organizations within a 14 -hour period. The effort is organized and implemented by Shasta Regional Community Foundation with sponsorship provided by Redding Bank of Commerce. The online event takes place on Tuesday, November 28th, 2018 from 6:00 AM to 8:00 PM. We invite you to give where you live and support
Barney (286864) is an 11 month old male white boxer mix. This athletic boy is very friendly, loves to play, and is rated for a family with children ages 8 years and older. Barney is available for adoption at Haven Humane Society and can’t wait to find his Forever Home! A proper introduction with any other dogs in the household is required. All feline and canine adoptions at the shelter include spaying or neutering, vaccinations and a microchip. To see Barney or any of our other companion animals available for adoption at the shelter, please visit us at 7449 Eastside Road, Anderson, or call (530) 241-1653. You can also check out our website at www.havenhumane.org.
Chip (286638) is a 4-year-old male brown and black brindle hound mix. This playful boy gets along well with children and other dogs, knows “sit”and “down”, and is rated for an experienced family with children ages 5 years and older. Chip is available for adoption at Haven Humane Society and can’t wait to find his Forever Home! A proper introduction with any other dogs in the household is required. All feline and canine adoptions at the shelter includes spaying or neutering, vaccinations and a microchip. To see
Chip or any of our other companion animals available for adoption at the shelter, please visit us at 7449 Eastside Road, Anderson, or call (530) 241-1653. You can also check out our website at www.havenhumane.org.
Check out this adorable pup! Jax (278319) is a 3-year-old male black and tan Australian cattle dog and Rottweiler mix. Jax loves to play ball, knows “sit”, “down”, and “shake”, and is rated for a family with children ages 12 years and older. Jax is available for adoption at Haven Humane Society and can’t wait to find his Forever Home! A proper introduction with any other dogs in the household is required. All feline and canine adoptions at the shelter include spaying or neutering, vaccinations, and a microchip. To see Jax or
any of our other companion animals available for adoption at the shelter,
please visit us at 7449 Eastside Road, Anderson, or call (530) 241-1653.
Twenty years young, I was living life and having fun, with not a care in the world with my best friend and the love of my life. It couldn’t get any better than that. Then suddenly, on one chilly day, things I would have never dreamed of to happen would change my life forever. I had noticed a strange numbing/ tingling sensation in my hands… they were blue! I knew they were cold, but I’ve never seen them turn like that before. Was this normal? It was a little surprising, but I brushed it off and didn’t worry about it too much. As days passed, weeks, to months, I kept getting random attacks of this strange blue tint and numbing to my hands. Not only was it the strange color changing, but I was noticing that my hands were becoming weaker and weaker. Once before I could open a pickle jar no problem, it became an impossible task. I knew I needed to be seen by the doctor… there’s only so much of WebMD one can handle before thinking the worst-case scenario!
As weeks go by, symptoms were getting worse and really becoming a problem for me. It felt as if my muscles were a very short stretchy band that I could only stretch so far. I ached, I was fatigued, I kept having the sensation of wanting to pass out at random moments. My arms, shoulders, and fingers hurt so bad I couldn’t even raise my arms high enough to wash, dry or style my hair! The dressing was close to impossible. I couldn’t button any dang buttons on my clothes! My fiancé, Manuel, had to help me with a lot of chores I was once able to do no problem. I finally took my butt into the doctors, ready for them to tell me that I had rheumatoid arthritis (that was my self-diagnosis thanks to WebMD). I told the doctor all my symptoms, so he ordered me to get a blood test. A few weeks went by, I got my test results back. The rheumatoid factor was negative! I felt so defeated, so confused, so lost… The doctor referred me to a local rheumatologist, and that was just the beginning of it all.
I was finally established with my rheumatologist. Lots of blood work done, x-rays, ultrasounds, all kinds of tests to narrow down the cause of my extreme pain and fatigue. In January of 2011, I was then diagnosed with systemic lupus, and scleroderma. I had an autoimmune mixed connective tissue disease. Lupus is an inflammatory disease that affects the joints, skin, kidneys, blood cells, brain, heart, and lungs. The immune system attacks your organs because it sees them as foreign substance or infection. Scleroderma/ CREST is also an immune disorder that attacks the body, where there is an overproduction of collagen causing scar tissue on the organs and blood vessels, and narrowing of the blood vessels: GERD, digestive issues, heart, lung, and kidney problems, and Raynaud’s phenomenon (the bluing of the fingers due to cold and stress) are all part of the package.
Treatment started right away, as I was put on steroids, and immunosuppressant medication to slow my immune system down from doing any more damage to my body. The first medication my rheumy put me on, I had an allergic reaction within one week… very itchy rash spots, so we had to discontinue that one and try another, methotrexate. The steroid and methotrexate were making me feel sicker than anything! My hair was starting to fall out, and I was constantly feeling nauseous and tired all the time. I literally felt like I was dying! I knew that my body wasn’t used to such strong medication and that I would just have to be strong and suffer through it until I may wake up one day feeling better. Then, amid the starting of the treatment, the doctor visits, and pushing through one day at a time…. Surprise!!!! Manuel and I had a baby on the way! With being pregnant, I knew that I wouldn’t be able to be on the medications I was on because it would cause serious birth defects. I wasn’t going to risk it.
So, I talked to my doctor, and he suggested that it would be fine coming off the medication, we would just keep a close eye on it. Most of the time Lupus/ Scleroderma have been known to go into “remission”, where your symptoms kind of go into hibernation mode. Sure enough, by the grace of God, my symptoms were going away and the pain was pretty much gone! Wow, who could have thought to get pregnant would have made me feel better?! It was time to start the OB-GYN visits, the baby shopping, baby showers, and preparing to bring this little one into the world!
In November 2011, about 2 weeks before my due date, it was my soon to be a father in laws birthday dinner at his house. I was getting down on some really tasty, hot salsa when BAM! It hit me, the first big contraction I had ever felt. It took me by surprise, but I wasn’t going to get too excited yet. 5 minutes passed and another contraction rocked me again, then another. This time, I knew it was time to start counting and keeping track! I told everyone, “I think this is it!” The contractions were coming in strong, with fewer and fewer minutes apart. I made it through a couple of hours more, when I decided that the pain was just too painful not to take myself into the hospital. Manuel and my best friend Allison grabbed my overnight and baby bag, and out the door, we went.
It was a ten-minute drive to the hospital that couldn’t have felt any longer. Once we got there, I was admitted. They checked my cervix and told me the one thing I was dreading to hear. “You’re not dilated enough, go home.” What!! With how much pain I was clearly in they were going to send me home?! So, with nothing else to do otherwise, we drove all the way back home. I laid down on my bed trying to fall asleep as best as I could. Every 5 minutes or less I was being woken up with the most painful contractions. I told Manuel, “We’re going in whether they like it or not and I’m not leaving!” In tears and excruciating pain, we loaded up into the car and drove that hundred miles back to the hospital.
It was obvious that I was in that much pain because once I walked through the doors, they admitted me once again and hooked me up to the monitors and started prepping the room for the birth of my beautiful baby daughter! Gosh, I couldn’t wait to hold her in my arms. Eight hours later, I finally gave birth to my little bundle of joy. My son, Heath, was two years old at the time and so excited that he got to be the big brother! My life was complete. I had my fiancé, Manuel, and two beautiful children, Heath and Jada. We moved in with Manuel’s parents, where I would have a ton of help. Everything was going great. I almost forgot about the Lupus and Scleroderma! I kept busy planning my and Manuel’s wedding and taking care of the kids. Until one day, a distant old friend came knocking at my door. Pain. Everywhere. Once again, my body wasn’t liking me very much and I was beginning to become tormented by the pain I once felt before, although this time it was centralized in my wrists and my ankles. The pain was so excruciating that I couldn’t walk on my feet! I literally had to hobble around and even use crutches just to get off the couch to go to the bathroom. I was so fatigued I would fall asleep for hours throughout the day. I did become pregnant again after a year but miscarried due to the horrendous pain that I was enduring at the time. It was time to take myself back to the doctors.
I went through two years of treatment with the local rheumatologist. He was an out of town doctor so he only came once a month, and tried to see all his medical patients in one day. I was seeing my doctor probably for 10 minutes’ max, every 6 months. I was having these horrible symptoms, but I felt like every time I went in to talk to him about it, he just breezed through the appointment giving me another medication to try out to see if it would “help”. I was fed up at not being heard at that point. I felt like I was not getting my needs met and I was not being listened to. I knew something was wrong that just shoving pills down my throat wouldn’t fix.
I made an appointment to see my primary care provider, to see if there was any other option available for me. I wanted to see a different rheumatologist! It was my lucky day and I had wished I had gone in to see her earlier. She referred me to the best rheumatologists in the state… UCSF San Francisco! I was so relieved, now it was just a waiting game to hear that I was accepted. Soon enough, 3 months later I was accepted to be seen by them and made my first appointment. What was so great about going down there was that they just brought a rheumatologist/ scleroderma specialist from the east coast just to open and run the new scleroderma department at their clinics! It was perfect timing.
My new rheumatologist was amazing! He knew exactly what he was talking about, he listened, and made me feel like my health was his number one priority. It was awesome. He got me started on the right treatment plan, and 3 to 6 months my husband and I would go down there for regular checkups. I was doing fine, taking my medications like I was supposed to. Had a pain here and there of course but nothing that a pain pill or hot bath couldn’t take care of to ease some of it. Manuel and I got married, we moved into our own home, I got a job working as an instructor taking care of intellectually disabled adults at a day program, I was taking it one day at a time. Things were starting to become smooth sailing for us as we went on with our life.
January 2016, I became ill. I was experiencing a terrible cough, shortness of breath, extreme fatigue, body sweats and fever, I thought yep, sure enough, I probably have pneumonia! My mother in law was worried about me, so she took me into the local hospital where I was admitted for a week, where they diagnosed me with sepsis (blood poisoning) and pneumonia. They gave me an antibiotic while I was staying in the hospital, and pumping me full of fluids to keep me hydrated. They didn’t give me any kind of Lasix or diuretic because they said that my kidneys were failing and that if they gave me the Lasix it would just damage my kidneys further. S, because of all the excess fluids they gave me, I walked out of the hospital with 25 pounds of extra water weight!! I felt like a balloon ready to pop. I felt like death but still took myself into work the next day. Halfway into the work day, I knew that I had to leave and admit myself back into the hospital. I mean, I really felt like I was going to die! I called my mother in law to come pick me up from work and take me back to the hospital.
The hospital admitted me, and saw sure enough that I needed that water off! After a week of Lasix treatment, the “big wig” doctor came in before I was released from the hospital, and told me that, from the tests they had run from my time of being in there, I never had sepsis or pneumonia, to begin with, and that they think it was something a lot bigger than that. He said that he thought I may have a possible blood clot in my heart. Whoa, okay now. So, we go from pneumonia to blood clot in the heart? I almost lost it. When was there ever going to be an end to hearing the unwelcome news! So, for a week more, I stayed in the hospital where they ran blood clot tests, and believe it or not, there were no clots to be found. Hmmm… so what could it possibly be then? That’s when they decided that they would rather I go down to UCSF and be seen by my doctors down there.
I waved goodbye to my husband, children, and in-laws as they saw me off to the helicopter, where they emergency flew me down to UCSF medical center. Once I arrived at the hospital, they started performing all kinds of heart tests and blood tests right away. From one of the tests, they discovered that I had a lot of pressure in the right side of my heart. They gave me a right sided heart catheter test to measure the pressures in my heart and lungs. That’s when they discovered that I had developed pulmonary arterial hypertension (caused by the scleroderma). (Pulmonary Arterial Hypertension “PAH” is a type of high blood pressure that affects the arteries in the lungs and heart. The tiny arteries in the lungs become narrow or blocked.) My life was crashing down all around me at that point. It had already been 3 weeks of being away from my family, I was already fighting lupus and scleroderma battle, now come to add more problems and grief to the pile?
The doctors were very kind and very understanding to how I must be feeling. Defeated, sad, hopeless. They reassured me that no matter what I’m going through I have a wonderful team and support group standing right behind me to make me be the best that I can. My treatment options were to give me oral medication, or an IV pump that would be attached to me 24/7 feeding me hypertension medication through a tube placed through my chest right to the heart. I cried, I was devastated! If I had to get that pump, that means no more swimming for me, no more life the way that it once was. I was going to strapped and tied down to this, machine?! NO way. I prayed and prayed to God that the pressures in my heart and lungs weren’t so severe that I would need to have that, and I could just go home on the oral medication.
God answered my prayers and I was sent home after a month in the hospital on a handful of new medications, but thankfully, not the pump! I strongly did not want that just because I knew that it would change my lifestyle dramatically. Well, the medications were working, and I was starting to feel like my old self again. I continued working, became supervisor of the day program, and overall felt generally better.
September 2016, my friends and I decided how fun would it be to plan a girl’s weekend getaway? I thought, you know, I deserve it. I work hard, I’ve been through a lot, I need a break! So, in October, we went up to our friend’s cabins up by Mt. Shasta. It was fall, so it was cold up there. Good thing I brought my winter clothes! Well, regardless of how bundled I was, I could sure feel the cold creeping in my bones! And thanks, due to the Raynaud’s, I am always cold all the time as it is, numb blue hands and all. I could already feel myself getting sick. I got a runny nose, cough, and general all overtired feeling. Dang, it! I had a feeling I would be getting sick.
I got through the weekend, came back home and tried to doctor myself up the best that I could. I knew if I didn’t get better than I would end up in the hospital again… I was NOT about to be going back there again! I did everything I could think of to get better; soups, tea, vitamin c overload, rest… nothing was working! It went on a month of trying to doctor myself up and going to work on top of it. I was starting to get scared. All the symptoms that I was starting to experience, were the same symptoms that landed me in the hospital back in January! In the beginning of December, I finally left work and took myself into the hospital. I couldn’t go one more day of feeling so out of breath no matter what I did. Just walking down a hallway was getting me winded.
Around that time, there was horrible pneumonia and flu bug going around. All the beds in the hospital were taken up, they were even sending people home because there was nothing they could do for them! The hospital was a madhouse. Anyway, the triage nurses checked my oxygen saturation and noticed I was hanging around 85%, which is really low. Normal O2 readings are 92% to 100%. Because the hospital was completely full, and the next week was going to be Christmas, they sent me home with an oxygen tank to keep me stabilized. They told me to come back after Christmas unless of course, I felt like I was getting worse than to come back earlier.
I made it through Christmas. The very next day, I took myself right back to the hospital where they admitted me. Now, the hospital beds were still completely full, but they did keep me down in the ER to stay. A couple days later, I was on a helicopter being transported back to UCSF. It felt like Deja Vu. Once I arrived, they got me all settled in, told me that I was to get another heart catheter test done. They wanted to check to see where I was with pulmonary hypertension. They did the test, and the outcome was just what I was dreading to hear. It was worse. A lot worse. They said, “We’re sorry, but if you want to live you need to get the IV pump and breathe with an oxygen tank!” Well, my life depended on it! At that point, I didn’t even care anymore. I was so tired of being so tired and feeling like death, I wanted to do anything to make that feeling go away! They also told me I would need a double lung transplant because my lungs weren’t going to get better and that they were just going to get worse. At least I have my youth on my side! I knew it was going to be a dramatic life changing event, but I wanted to live more than anything! I could deal with it. Once the doctors told me I will die if I don’t, that just made up my mind right then and there.
A couple weeks went by, and I had surgery to get the port put into place in my chest. Once that was put in, I went to spend some time in the ICU where they could monitor me on the new IV medication. Honestly, I was so out of it I barely remember being in there at all! I know my parents came to visit- barely remember them being there, and my husband. He was there for me through the whole thing! After a few more days in ICU, I went back to my room on the other unit. From there, it was 2 weeks of the teaching of how to mix and prepare my medications, and education on lifestyle changes I would need to be making once I got home.
Finally, after a month in a half of being in the hospital, it was time to finally go home. I had to be transported by ambulance, all the way back up to Redding. It was the worst trip I had ever been on in my life! Not only was I strapped to an uncomfortable gurney for 4 hours facing the back of the ambulance, hooked up to their oxygen, bumping all over the place, but I had the worst migraine and nausea I had ever had in my life. I’m talking dry heaving the whole way home. I was a mess. We got into town finally about 10 pm, I was finally home! It felt so good to be home, although I knew that this was just the beginning of a whole new chapter in my life.
Now, 4 months down the road, I’m doing okay. I have my good days, and I have my bad days. A few incidents landed me in the hospital… but I recouped and continue on with my life. I have such a wonderful support system… my doctors, friends, family, even people I don’t even know are so supportive! We are all in this fight together. My mind keeps busy with planning fundraisers to raise money for my lung transplant and taking care of myself and my family. My life consists of taking one day at a time, being thankful every day for each breath that I take. I won’t go down without a fight! I may be breathless, but I am not hopeless. The lung transplant may fix my pulmonary hypertension problem, but I will always live with Scleroderma, and it will never again, try to take my breath away.
It’s The Third Annual
Summer Mountain Music and Arts Festival – Saturday, July 22, 2017
Summer is here, School is out, and you’re
Trying to decide the Perfect Place to Take your Family to for a Day in the Sun with lots of Fun? Well, look no more! The main fundraising event for C.S.O.T.F.A
“California state old time fiddlers association.” Have planned a day of Fun, great bands, beautiful views, Food, local wines and craft beers. Something that the whole family can come and Enjoy together, Smiles, Laughter and Making Memories that Last!
This Festival event will be the Third Annual Bluegrass, Old Time & Americana Music & Art Event venue will be held at the Cedar Crest Vineyards in Manton CA. This is a day full of great bands, beautiful views, great food, local wines and craft beers; this family fun event is guaranteed to be about 10 degrees cooler than anything that is going on down in the valley. Come and enjoy the fun and help us support Old Time, Old Time Fiddling, Bluegrass and Traditional American Acoustic Music & Education in the North State.
*Band Line-up for the Day will be as follows*
*Wood & Wire: “It’s been five years now since Wood & Wire sprouted out of the fertile musical soil of Austin, Texas. In that time, they’ve written music, recorded albums, and performed at some of the most notable festivals and venues across the country.
In the often tightly defined genre of bluegrass music, Wood & Wire’s “band-style” ethos are not a mystery. Nor are the elements of song crafting, so often associated with their Texas home, that permeates their sound. That being said, what comes out of the Wood & Wire blender is something entirely its own.”
*One Button Suit:
One Button Suit is an exciting, Sacramento-based string band with a repertoire of originals and bluegrass familiars hinting at unconventionality.
Tim Tobias – vocals, guitar
Tom Shewmake – mandolin, vocals
Melissa Lincoln – fiddle, vocals
Brian Burke – guitar, vocals
Casey Lipka – bass, vocals
*The Rock Ridge Bluegrass Band*
Rock Ridge is a bluegrass band from N. California. Their performances and recorded material include traditional & contemporary bluegrass, some originals, old time country, and gospel music with top notch vocals and instrumentation. The band’s debut CD, Drifter’s Prayer, has received praise and airplay across the US and abroad.
*The Buckhorn Mountain Stompers*
Foot stomping dance music from the Klamath Mountains.
The Buckhorn Mountain Stompers are an energetic dance band from the Klamath Mountains who pull from a variety of traditions, like alt-country, old-timey, polka, jazz, delta blues, – but maintain a unique sound of their own. Our goal is to perform fun dance songs that make people want to get up and strut their stuff. Our shows are hillbilly kitsch; with a disco light, fog machine, other theatric stage props and dance prizes.
Sweet Violin and Guitar Jazz from the 1920’s & 30’s
Jazz music was born in America between world wars, an economic boom and a great depression, as an amalgamation of traditional American musical styles. The honeybee is a Northern California jazz duo that captures the sounds and feel of Vintage Jazz in its original vibe – with emphasis on lyrical melody, dynamic harmony, and smooth rhythm using sweet vocals, violin and guitar. Honeybee performs Vintage Jazz tunes in that authentic vintage style – the song is the star!
The “Sweethearts of the SMMAF” The HappBees will be back to steal your hearts away this year. These three little Dolls are sure to Pull at your Heartstrings as they play on their fiddles!
*The Alldrin Family Band
*The Jim Cook Band
All Day Festival tickets are $20.
Advanced tickets are $18 and are available before July 15th
C.S.O.T.F.A. Member Discount Tickets are $15
Children 12 and under – FREE with adult
For our out of town guests and bands, the Comfort Inn in Red Bluff has partnered with us again this year to provide a beautiful room at a substantially reduced rate for folks coming to the festival from a long distance and needing a place to spend the night.
Contact: Darryl Concho, Manager, and ask for the“Summer Mountain Music and Arts Festival Deal.”
Phone:(530)529-7060 to reserve a room.
Festival Camping 2017 information. Reserve your spot soon!
Here’s a few Q’s & A’s guests may want to know before planning this Trip!
Q. If I order by mail or online, will I get physical tickets
in the mail?
A. Yes, and you will receive an email confirmation, and your name will be added to the Will Call list at the gate.
Q. If I change my mind or am unable to attend after I
already bought tickets, can I get a refund?
A. Nope, This is a “rain or shine” event, and refunds are not available.
Q. If it rains, will the festival be canceled?
A. No, the festival will go on rain or shine!
Q. Can I bring my dog?
A. No. We ask that you do NOT bring your dogs or other pets. Dogs are certainly not allowed in the audience or the vendor areas, and there is no place on the site for Safely Caring for your pet. Remember that the temperatures can get quite warm making it dangerous to leave your animal in your vehicle.
Q. What about parking?
A. Parking is free. But since it is somewhat limited, it will help if you carpool if you can!
Q. Can I bring my ice chest? Alcoholic beverages?
A. No. Ice chests and coolers are NOT allowed as both food and beverages will be for sale at the event. Craft Beer and Wine will be available for purchase on site from Cedar Crest Vineyards. Outside alcohol will be prohibited due to the licensing regulations.
A personal story from the heart of Robert Fetty “Project Manager Best of the North State”. Robert meet Tammy Lynn and Marcelleus, owners of “Tammy Got Stuff?” Thrift Store over 2 years ago, meeting with them on how I could help their business. They were great to talk too and I knew from the beginning we were going to be more than business associates. I have always been a big fan of Thrift Stores and always wanted them to be successful. I mean who doesn’t like finding a treasure. Tammy and Marcelleus are heard about all over Redding. Being in social media marketing you run into each other on Facebook, Yelp & Google. I soon found out that they are involved with Redding more than most mom and pop Thrift Store. They believe in helping our community. I wish more people came forward and tell their story of how they help our community. When Tammy told me they were moving down to San Bernardino, California, my first thought was, who will fill their shoes in our town of Redding?
So many people came forward and said how Tammy and Marcelleus changed their life. I know working with “Tammys Got Stuff?” Thrift Store my life has changed. The love and compassion that those two had made my day. Not only did they help out many organizations but they helped out real people with real problems. So many times I would be visiting Tammy and Marcelleus and someone would come in trying to help another person out. They would not only help them but sometimes just give them what they needed to help that person. Does not matter if they homeless, senior, or even a sad person needing someone to talk to, they were there. Their final hurrah they donated everything to #Lungs4Lindsey to raise money for Linsey Arzate double lung transplant. Tammy and Marcelleus you will truly be missed. Truly one of the Best of the North States favorite Thrift Store.#notforgotten
Love Tammy’s! Lot’s of stuff @ great prices and FABULOUS friendly owners!
Tammy and Marcelleus wanted special thanks to some dear friends:
Marie Moore kindness, help, fiendship… Randy & Gale Schmidt & Family for believing in us and treating us like family and all your support being there in every time of need… Popa John Jones for your dedication, leadership, love and understanding… Our Customers: Came in as a customer, left as a friend and kinder souls that connected… thank you for the support… Our Children: Estevan, Arturo, Kawan, Nathaniel, Azaria & Jaseman…. The many friendships we developed…
Dear Friends,What if you were living on borrowed time?
Lindsey Arzate is fighting for her life. In 2012, after giving birth to her daughter, Lindsey was diagnosed with systemic scleroderma which is an autoimmune disease that affects the internal organs. During a subsequent hospitalization in March 2016, she found out she had heart failure and pulmonary arterial hypertension. Nine months later, Lindsey was hospitalized with advanced severe pulmonary hypertension and is on oxygen and IV medications 24/7. Now doctors say a double lung transplant is critical.
This has been an extremely challenging time for Lindsey and her husband, Manuel, who are parents of two young children. Lindsey’s illness has had a major impact on her family emotionally, mentally and financially. She describes her situation as a huge roller coaster ride, but remains hopeful for a second chance at life. Before her health began to decline, Lindsey loved hiking, swimming, and traveling, but these days her activities are extremely limited. She is still able to enjoy cooking, crafting, movies, shopping and just being with friends and family. Lindsey looks forward to one day being able to breathe on her own and being free from the IV, so she can do all the things a young wife and mother dreams of doing with her family.
Unfortunately, Lindsey’s hope for a new life comes at a very high price.
The average double lung transplant costs over $1 million. And, that’s only the beginning. Even with insurance, which will cover a portion of the transplant costs, she still faces significant expenses related to the surgery. For the rest of her life, she will need follow-up care and anti-rejection medications. Post-transplant medications are very expensive, and they’re as critical to her survival as the transplant itself.
When she receives her transplant, Lindsey and Manuel must temporarily relocate over 200 miles from their home to be near the hospital for a least six weeks during the recovery process, incurring substantial expenses for travel, food and lodging. Because of her declining health, she had to leave a job she loved as a supervisor of a day program for intellectually disabled adults adding to the financial strain. What if your life depended on the compassion and generosity of others?
The National Foundation for Transplants (NFT) is working with volunteers and supporters to help relieve the growing burden of expenses for Lindsey. NFT has been assisting transplant patients with fundraising support for more than 30 years. Your gift—of $25, $50, $100 or more—will enable NFT to provide Lindsey with the financial support she desperately needs.
You can help by visiting http://give.transplants.org/goto/lindseyarzate to make a tax-deductible donation to NFT to help with her expenses.
If you have any questions about NFT, feel free to contact the staff at 800-489-3863.
– See more at: http://give.transplants.org/site/TR?px=1011425&fr_id=1040&pg=personal#sthash.mpaOeKaZ.dpuf
Need a Day Spa near you? Wave Lengths is a day spa in Redding,
And they’re So much more than just Hair! Wave Lengths has been in business since 1996; Located at the North end of the Downtown Promenade. We can accommodate all your beauty needs, Specializing in color, haircuts, straightening, extensions, special occasion styles, waxing, nail and foot care, facials, even spray tanning All in a One Stop Beauty Shop, Who could Ask for More! Not only is Wave Lengths Day Spa the Ideal Place to go for Glam, but Business Owner Tracey Lynn also visit’s a Local Elementary School 3 times a year on her Days off, to Volunteer her time giving Free haircuts to Special needs Children!
For the parents of these kids, something as seemingly routine as getting a haircut can be a laborious and sometimes embarrassing process;
“It’s hard,” said Tracey Lynn, “I know it’s difficult for these children to sit still, I’m just here to help the families out,” she said.
For appointments or prices call Wave Lengths at (530) 247-1897. Wave Lengths hours are below:
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WaveLengths Salon & Day Spa
Nail Salon, Day Spa, Hair Salon
1459 Market St
Redding, CA 96001 Redding, CA
*Ranked #7 out of 31 nail salons near Redding*